EP1732539A2 - Utilisation de beta-lapachone pour le traitement du cancer du colon - Google Patents

Utilisation de beta-lapachone pour le traitement du cancer du colon

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Publication number
EP1732539A2
EP1732539A2 EP05723505A EP05723505A EP1732539A2 EP 1732539 A2 EP1732539 A2 EP 1732539A2 EP 05723505 A EP05723505 A EP 05723505A EP 05723505 A EP05723505 A EP 05723505A EP 1732539 A2 EP1732539 A2 EP 1732539A2
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EP
European Patent Office
Prior art keywords
lapachone
pharmaceutically acceptable
acceptable salt
cell
colon cancer
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Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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EP05723505A
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German (de)
English (en)
Inventor
Chiang J. Li
Youzhi Li
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Arqule Inc
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Arqule Inc
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Priority to EP08164577A priority Critical patent/EP2033639A2/fr
Publication of EP1732539A2 publication Critical patent/EP1732539A2/fr
Ceased legal-status Critical Current

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/35—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
    • A61K31/352—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. methantheline 
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/04—Antineoplastic agents specific for metastasis

Definitions

  • Colorectal cancer is the third most common cancer and the second leading cause of cancer mortality in the United States ("Cancer Facts and Figures 2003," American Cancer Society). Colon cancer is particularly insidious because of the lack of symptoms during the early-stage of development. Survival rates of individuals with colorectal cancer are dependent on the stage at which the cancer is detected. Only about one third of colorectal cancers are identified in an early, localized stage. If colorectal cancer is identified in such a stage, the 5-year survival rate is about 90%.
  • Cancer cells are by definition heterogeneous. For example, within a single tissue or cell type, multiple mutational 'mechanisms' may lead to the development of cancer. As such, heterogeneity frequently exists between cancer cells taken from tumors of the same tissue and same type that have originated in different individuals. Frequently-observed mutational
  • ⁇ -lapachone is an agent with a reported anti-cancer activity in a limited number of non- colon cancers.
  • ⁇ -lapachone for use in treatment of human prostate disease.
  • ⁇ -lapachone has also been reported to decrease the number of tumors, reduce tumor size, or increase survival time, or a combination of these, in xenotransplant mouse models of human ovarian cancer (Li, C.J. et al, (1999) Proc. Natl. Acad. Sci.
  • the present invention provides a method of treating colon cancer, comprising administering to a subject in need thereof a therapeutically effective amount of ⁇ -lapachone, or a pharmaceutically acceptable salt thereof, in combination with a pharmaceutically acceptable carrier, where the colon cancer is treated.
  • the present invention also provides a method of treating metastatic colon cancer, comprising administering to a subject in need thereof a therapeutically effective amount of ⁇ - lapachone, or a pharmaceutically acceptable salt thereof, in combination with a pharmaceutically acceptable carrier, where the metastatic colon cancer is treated.
  • the present invention also provides a method of treating or preventing a cell proliferative disorder of the colon, comprising administering to a subject in need thereof a therapeutically effective amount of ⁇ -lapachone, or a pharmaceutically acceptable salt thereof, in combination with a pharmaceutically acceptable carrier, where the cell proliferative disorder of the colon is treated or prevented.
  • the present invention also provides a method for inducing cell death in a colon cancer cell, comprising contacting the colon cancer cell with an effective amount of ⁇ -lapachone, or a pharmaceutically acceptable salt thereof, where the contacting induces the cell death in the colon cancer cell.
  • the present invention provides a method of treating colon cancer, comprising administering to a subject in need thereof a therapeutically effective amount of ⁇ -lapachone, or a pharmaceutically acceptable salt, prodrug, metabolite, analog or derivative thereof, in combination with a pharmaceutically acceptable carrier, where the colon cancer is treated.
  • the present invention also provides a method of treating metastatic colon cancer, comprising administering to a subject in need thereof a therapeutically effective amount of ⁇ - lapachone, or a pharmaceutically acceptable salt, prodrug, metabolite, analog or derivative thereof, in combination with a pharmaceutically acceptable carrier, where the metastatic colon cancer is treated.
  • the present invention also provides a method of treating or preventing a cell proliferative disorder of the colon, comprising administering to a subject in need thereof a therapeutically effective amount of ⁇ -lapachone, or a pharmaceutically acceptable salt, prodrug, metabolite, analog or derivative thereof, in combination with a pharniaceutically acceptable carrier, where the cell proliferative disorder of the colon is treated or prevented.
  • the present invention also provides a method for inducing cell death in a colon cancer cell, comprising contacting the colon cancer cell with an effective amount of ⁇ -lapachone, or a pharmaceutically acceptable salt, prodrug, metabolite, analog or derivative thereof, where the contacting induces the cell death in the colon cancer cell.
  • the present invention provides a method of treating colon cancer, comprising administering to a subject in need thereof a therapeutically effective amount of ⁇ -lapachone or pharmaceutically acceptable salt thereof, or a metabolite thereof, in combination with a pharmaceutically acceptable carrier, where the ⁇ -lapachone treats the colon cancer.
  • the present invention also provides a method of treating colon cancer, comprising administering to a subject in need thereof a therapeutically effective amount of ⁇ -lapachone or pharmaceutically acceptable salt thereof, or a metabolite thereof, in combination with a pharmaceutically acceptable carrier, and activating one or more cell cycle checkpoints in one or more colon cancer cells, where the ⁇ -lapachone or pharmaceutically acceptable salt thereof, or a metabolite thereof, treats the colon cancer.
  • the present invention further provides a method of treating colon cancer, comprising administering to a subject in need thereof a therapeutically effective amount of ⁇ -lapachone or pharmaceutically acceptable salt thereof, or a metabolite thereof, in combination with a pharmaceutically acceptable carrier, and activating one or more cell cycle checkpoint pathways in one or more colon cancer cells, where the ⁇ -lapachone or pharmaceutically acceptable salt thereof, or a metabolite thereof, treats the colon cancer.
  • the present invention also provides a method of treating colon cancer, comprising administering to a subject in need thereof a therapeutically effective amount of ⁇ -lapachone or pharmaceutically acceptable salt thereof, or a metabolite thereof, in combination with a pharmaceutically acceptable carrier, and activating one or more cell cycle checkpoint regulators in one or more colon cancer cells, where the ⁇ -lapachone or pharmaceutically acceptable salt thereof, or a metabolite thereof, treats the colon cancer.
  • the present invention further provides a method of treating colon cancer, comprising administering to a subject in need thereof a therapeutically effective amount of ⁇ -lapachone or pharmaceutically acceptable salt thereof, or a metabolite thereof, in combination with a pharmaceutically acceptable carrier, and activating cell death selectively in one or more colon cancer cells, where the ⁇ -lapachone or pharmaceutically acceptable salt thereof, or a metabolite thereof, treats the colon cancer.
  • the present invention also provides a method of treating or preventing a cell proliferative disorder of the colon, comprising administering to a subject in need thereof a therapeutically effective amount of ⁇ -lapachone or pharmaceutically acceptable salt thereof, or a metabolite thereof, in combination with a pharmaceutically acceptable carrier, where the ⁇ -lapachone or pharmaceutically acceptable salt thereof, or a metabolite thereof, treats or prevents the cell proliferative disorder of the colon.
  • the present invention provides a method of treating colon cancer, comprising administering to a subject in need thereof a therapeutically effective amount of a derivative or analog of ⁇ -lapachone or pharmaceutically acceptable salt thereof, or a metabolite thereof, in combination with a pharmaceutically acceptable carrier, where the derivative or analog of ⁇ - lapachone or pharmaceutically acceptable salt thereof, or a metabolite thereof, treats the colon cancer.
  • the present invention also provides a method of treating colon cancer, comprising administering to a subject in need thereof a therapeutically effective amount of a derivative or analog of ⁇ -lapachone or pharmaceutically acceptable salt thereof, or a metabolite thereof, in combination with a pharmaceutically acceptable carrier, and activating one or more cell cycle checkpoints in one or more colon cancer cells, where the derivative or analog of ⁇ -lapachone or pharmaceutically acceptable salt thereof, or a metabolite thereof, treats the colon cancer.
  • the present invention further provides a method of treating colon cancer, comprising administering to a subject in need thereof a therapeutically effective amount of a derivative or analog ⁇ -lapachone or pharmaceutically acceptable salt thereof, or a metabolite thereof, in combination with a pharmaceutically acceptable carrier, and activating one or more cell cycle checkpoint pathways in one or more colon cancer cells, where the ⁇ -lapachone or pharmaceutically acceptable salt thereof, or a metabolite thereof, treats the colon cancer.
  • the present invention also provides a method of treating colon cancer, comprising administering to a subject in need thereof a therapeutically effective amount of a derivative or analog of ⁇ -lapachone or pharmaceutically acceptable salt thereof, or a metabolite thereof, in combination with a pharmaceutically acceptable carrier, and activating one or more cell cycle checkpoint regulators in one or more colon cancer cells, where the derivative or analog of ⁇ - lapachone or pharmaceutically acceptable salt thereof, or a metabolite thereof, treats the colon cancer.
  • the present invention further provides a method of treating colon cancer, comprising administering to a subject in need thereof a therapeutically effective amount of a derivative or analog of ⁇ -lapachone or pharmaceutically acceptable salt thereof, or a metabolite thereof, in combination with a pharmaceutically acceptable carrier, and activating cell death selectively in one or more colon cancer cells, where the derivative or analog of ⁇ -lapachone or pharmaceutically acceptable salt thereof, or a metabolite thereof, treats the colon cancer.
  • the present invention also provides a method of treating or preventing a cell proliferative disorder of the colon, comprising administering to a subj ect in need thereof a therapeutically effective amount of a derivative or analog of ⁇ -lapachone or pharaiaceutically acceptable salt thereof, or a metabolite thereof, in combination with a pharmaceutically acceptable carrier, where the derivative or analog of ⁇ -lapachone or pharmaceutically acceptable salt thereof, or a metabolite thereof, treats or prevents the cell proliferative disorder of the colon.
  • the present invention also provides a method of treating or preventing a cell proliferative disorder of the colon, comprising administering to a subject in need thereof a therapeutically effective amount of ⁇ -lapachone or pharmaceutically acceptable salts thereof, or a metabolite thereof, in combination with a pharmaceutically acceptable carrier, and activating one or more cell cycle checkpoints in a colon cell, where the ⁇ -lapachone or pharmaceutically acceptable salts thereof, or a metabolite thereof, treats or prevents a cell proliferative disorder of the colon.
  • the present invention also provides a method of treating or preventing a cell proliferative disorder of the colon, comprising administering to a subject in need thereof a therapeutically effective amount of ⁇ -lapachone or pharmaceutically acceptable salts thereof, or a metabolite thereof, in combination with a pharmaceutically acceptable carrier, and activating one or more cell cycle checkpoint pathways in a colon cell, where the ⁇ -lapachone or pharmaceutically acceptable salts thereof, or a metabolite thereof, treats or prevents a cell proliferative disorder of the colon.
  • the present invention also provides a method of treating or preventing a cell proliferative disorder of the colon, comprising administering to a subject in need thereof a therapeutically effective amount of ⁇ -lapachone or pharmaceutically acceptable salts thereof, or a metabolite thereof, in combination with a pharmaceutically acceptable carrier, and activating one or more cell cycle checkpoint regulators in a colon cell, where the ⁇ -lapachone or pharmaceutically acceptable salts thereof, or a metabolite thereof, treats or prevents a cell proliferative disorder of the colon.
  • the present invention also provides a method of treating or preventing a cell proliferative disorder of the colon, comprising administering to a subject in need thereof a therapeutically effective amount of ⁇ -lapachone or phannaceutically acceptable salts thereof, or a metabolite thereof, in combination with a phannaceutically acceptable carrier, and activating cell death selectively in colon cell, where the ⁇ -lapachone or pharmaceutically acceptable salts thereof, or a metabolite thereof, treats or prevents a cell proliferative disorder of the colon.
  • FIGURES Figure 1 sets forth a schematic of the proposed points of action of ⁇ -Lapachone and
  • Taxol on the cell cycle sets forth an effect of ⁇ -Lapachone on survival of human colon cancer cell lines in the NCI60 in vitro screen.
  • Figure 3 sets forth an effect of ⁇ -Lapachone on the growth of xenografted HT-29 human colon tumors in an athymic nude mouse model.
  • the present invention provides a method of treating colon cancer, including metastatic colon cancer, comprising administering to a subject in need thereof a therapeutically effective amount of ⁇ -lapachone, or a pharmaceutically acceptable salt, prodrug, metabolite, analog or derivative thereof, in combination with a pharmaceutically acceptable carrier, where the colon cancer is treated.
  • the present invention also provides a method of treating or preventing a cell proliferative disorder of the colon, comprising administering to a subject in need thereof a therapeutically effective amount of ⁇ -lapachone, or a pharmaceutically acceptable salt, prodrug, metabolite, analog or derivative thereof, in combination with a pharmaceutically acceptable carrier, where the cell proliferative disorder of the colon is treated or prevented.
  • the invention also provides the use of ⁇ -lapachone for the preparation of a medicament useful for the treatment of colon cancer.
  • the invention also provides the use of ⁇ -lapachone for the preparation of a medicament useful for the treatment or prevention of a cell proliferative disorder of the colon.
  • the invention also provides the use of an analog or derivative of ⁇ - lapachone for the preparation of a medicament useful for the treatment of colon cancer.
  • the invention also provides the use of an analog or derivative of ⁇ -lapachone for the preparation of a medicament useful for the treatment or prevention of a cell proliferative disorder of the colon.
  • the present invention includes and is based in part on an understanding of, and methods for, the activation of cell cycle checkpoints by modulators of cell cycle checkpoint activation (e.g., ⁇ -lapachone, or a pharmaceutically acceptable salt, prodrug, metabolite, analog or derivative thereof).
  • the activation of cell cycle checkpoints in general is referred to as Activated Checkpoint TherapyTM, or ACTTM.
  • cancer cells are defective in their cell cycle checkpoint functions secondary to mutations in one of their molecular modulators, e.g., p53. It is in part, for this reason, that cancer cells have accumulated genetic enors during the carcinogenic process.
  • Therapeutic agents that activate cell cycle checkpoint functions can selectively promote cell death in cancer cells, since cell death appears to be induced at least in part by the conflict between the uncontrolled-proliferation drive in cancer cells and the checkpoint delays induced artificially.
  • ACTTM takes advantage of the tendency of cell death to occur at checkpoints during the cell proliferation cycle by activating one or more checkpoints, thereby producing conflicting signals regarding cell cycle progression versus arrest.
  • ACTTM offers selectivity against cancer cells as compared to normal cells and is therefore safer than less selective therapies.
  • the ACTTM method activates but does not disrupt cell cycle checkpoints.
  • normal cells with well-controlled proliferation signals can be delayed at checkpoints in a regulated fashion, resulting in no cell death-prone collisions.
  • normal cells with intact Gl checkpoint control are expected to arrest in Gl .
  • Cancer cells are expected to be delayed in S-, G2-, and M-phases, since most cancer cells harbor Gl checkpoint defects, making cancer cells more sensitive to drugs imposing S and M phase checkpoints, ⁇ -lapachone is a Gl and S phase compound, and contacting a cell with ⁇ - lapachone results in activation of a Gl or S cell cycle checkpoint.
  • Figure 1 sets forth a schematic of the proposed points of action of ⁇ -lapachone and Taxol on the cell cycle.
  • modulator of cell cycle checkpoint activation refers to a compound capable of altering checkpoint activation in cells (in prefened embodiments, activating one or more cell cycle checkpoints), preferably by activating checkpoint-mediated DNA repair mechanisms, or by reinstating checkpoint activity that has been lost due to a malfunction or mutation in the cellular pathways that regulate cell cycle activity.
  • major cell cycle checkpoints occur at Gj/S phase and at the G 2 /M phase transitions.
  • four major cell cycle checkpoints monitor the integrity of genetic material. DNA- synthesis begins only past the restriction point (R point), where the cell determines if preparation during Gl has been satisfactory for cell cycle continuation.
  • the second checkpoint occurs during replication initiation in S phase.
  • the third and fourth checkpoints take place in Gr2 phase and M phase, respectively. Modulation of cell cycle checkpoint activation is further discussed in, e.g., C.J. Li et al. Proc. Natl. Acad. Sci. USA (1999), 96(23), 13369-13374, and Y. Li et al. Proc. Natl. Acad. Sci. USA (2003), 100(5), 2674-2678, and PCT Publication WO 00/61142 (Pardee et al).
  • Preferred modulators of cell cycle checkpoint activation for use in the present invention induce checkpoint activation (i.e., activate one or more cell cycle checkpoints, preferably at Gi/S phase), preferably without causing substantial DNA damage.
  • certain preferred modulators of cell cycle checkpoint activation are capable of increasing the level or activity of E2F (more preferably E2F1) in a cell.
  • Methods for screening for modulators of cell cycle checkpoint activation include those that are disclosed in PCT Patent Application No. PCT/US03/22631 to Li et al.
  • preferred modulators of cell cycle checkpoint activation are capable of increasing the level or activity of E2F in a cell by an amount sufficient to cau.se cell death (e.g., apoptosis) if the cell is a cancerous cell. More prefened modulators of cell cycle checkpoint activation are capable of raising the level or activity of E2F1 in a cell by an amount sufficient to cause cell death (e.g., apoptosis) if the cell is a cancerous cell.
  • a modulator of cell cycle checkpoint activation is not ⁇ -lapachone.
  • ATM and ATR are protein kinases of "the phosphatidyl-inositol-3 kinase family (PI3K).
  • PI3K phosphatidyl-inositol-3 kinase family
  • Chk2 has also been shown to stabilize p53 both by directly phosphorylating p53, and by inhibiting Mdm2, a ubiquitin ligase that targets p53 for degradation. Under such conditions, increased levels of p53 lead to Gl/S anest, DNA repair, and apoptosis in cells with ineparable DNA damage. Again not limited by theory, it is believed that Chk2 is an important cell cycle regulator, which, depending on the conditions, can induce cell cycle anest and DNA repair, or initiate cell death (e.g., apoptosis) if DNA damage is too severe.
  • preferred modulators of cell cycle checkpoint activation are capable of increasing the level or activity of Chk2 in a cell by an amount sufficient to cause cell death (e.g., apoptosis) if the cell is a cancerous cell.
  • E2F1 is one of related proteins in the E2F family of nuclear transcription factors, which family is critically important in regulation of the cell cycle. E2F1 is required for cellular proliferation by promoting passage through the Gl/S checkpoint. During proliferation of normal cells, transcriptionally active E2F1 is liberated from an inactive E2F1/Rb complex following phosphorylation of Rb. E2F1 levels rise, promoting progression through Gl .
  • E2F1 levels must decline for progress to continue. Sustained elevation of E2F1 at this point in the cell cycle causes activation of the S phase checkpoint, and subsequent cell death (e.g., by apoptosis).
  • this regulatory protein may either promote cellular proliferation, induce cell cycle delay, DNA repair or cell death.
  • phosphorylation of Rb results in dissociation of Rb-E2F1 complexes, liberating active E2F1, which then stimulates entry into S phase by promoting transcription of key cell cycle effectors.
  • E2F1 must be degraded for progress to continue.
  • E2F is the E2F transcription factor family (including but not limited to E2F-1, E2F-2, E2F-3).
  • a cell cycle checkpoint pathway refers to a biochemical pathway that is involved in modulation of a cell cycle checkpoint.
  • a cell cycle checkpoint pathway may have stimulatory or inhibitory effects, or both, on one or more functions comprising a cell cycle checkpoint.
  • a cell cycle checkpoint pathway is comprised of at least two compositions of matter, preferably proteins, both of which contribute to modulation of a cell cycle checkpoint.
  • a cell cycle checkpoint pathway may be activated through an activation of one or more members of the cell cycle checkpoint pathway.
  • a cell cycle checkpoint pathway is a biochemical signaling pathway.
  • cell cycle checkpoint regulator refers to a composition of matter that can function, at least in part, in modulation of a cell cycle checkpoint.
  • a cell cycle checkpoint regulator may have stimulatory or inhibitory effects, or both, on one or more functions comprising a cell cycle checkpoint.
  • a cell cycle checkpoint regulator is a protein.
  • a cell cycle checkpoint regulator is a not a protein.
  • a cell cycle checkpoint regulator is selected from the group consisting of ATM, ATR, Chkl, Chk2, E2F1, BRCA1, Rb, p53, p21, Mdm2, Cdc2, Cdc25, and 14-4-3 [sigma].
  • ⁇ -lapachone refers to 3,4-dihydro-2,2-dimethyl-2H- naphtho[l,2-b]pyran-5,6-dione and derivatives and analogs thereof, and has the chemical structure:
  • ⁇ -Lapachone (3,4-dihydro-2, 2-dimethyl-2H-naphtho [1,2-b] pyran-5, 6-dione), a simple non- water soluble orthonapthoqumone, was first isolated in 1882 by Paterno from the heartwood of the lapacho tree (See Hooker, SC, (1936) I. Am. Chem. Soc. 58:1181-1190; Goncalves de Lima, O, et al, (1962) Rev. Inst. Antibiot. Univ. Recife. 4:3-17).
  • ⁇ -Lapachone The structure of ⁇ -Lapachone was established by Hooker in 1896 and it was first synthesized by Fieser in 1927 (Hooker, SC, (1936) 7. Am. Chem. Soc. 58:1181-1190).
  • ⁇ -Lapachone can, for example, be obtained by simple sulfuric acid treatment of the naturally occurring lapachol, which is readily isolated from Tabebuia avellenedae growing mainly in Brazil, or is easily synthesized from seeds of lomatia growing in Australia (Li, CJ, et al, (1993) J. Biol Chem. 268:22463-33464). Methods for fonnulating ⁇ -Lapachone or its derivatives or analogs can be accomplished as described in U.S. Patent No.
  • derivatives or analogs of ⁇ -Lapachone include, for example, 3,4-dihydro- 2,2-dimethyl-3 -(3 -methyl-2-butenyl)-2H-naphtho[ 1 ,2-b]pyran-5 , 6-dione, 3 ,4-dihydro-2,2- dimethyl-2H-naphtho[l,2-b]thiopyran-5,6-dione and 3,4-dihydro-4,4-dimethyl-2H-naphtho[l,2- b]thiopyran-5,6-dione.
  • Other derivatives or analogs of ⁇ -lapachone are described in PCT
  • PCT International Application PCT/US93/07878 (WO94/04145), and U.S. Pat. No. 6,245,807.
  • PCT International Application PCT/USOO/10169 (WO 00/61142), discloses ⁇ -lapachone, which may have a variety of substituents at the 3- position as well as in place of the methyl groups attached at the 2-position.
  • U.S. Patent Nos. 5,763,625, 5,824,700, and 5,969,163, disclose analogs and derivatives with a variety of substituents at the 2-, 3- and 4-positions.
  • derivatives or analogs of ⁇ -lapachone include reduced ⁇ -lapachone (e.g., Formula la, in which R' and R" are both hydrogen) and derivatives of reduced ⁇ -lapachone (see, e.g., Formula la, in which R' and R" are each independently hydrogen, C ⁇ -C 6 alkyl, C ⁇ -C 6 alkylcarbonyl, or a pharmaceutically acceptable salt).
  • reduced ⁇ -lapachone e.g., Formula la, in which R' and R" are both hydrogen
  • derivatives of reduced ⁇ -lapachone see, e.g., Formula la, in which R' and R" are each independently hydrogen, C ⁇ -C 6 alkyl, C ⁇ -C 6 alkylcarbonyl, or a pharmaceutically acceptable salt.
  • ⁇ -lapachone is the prefereed Gl/S-phase compound for use in the composition in accordance with the present invention
  • the invention is not limited in this respect, and ⁇ - lapachone derivatives or analogs, such as lapachol, and pharmaceutical compositions and formulations thereof are part of the present invention.
  • ⁇ -lapachone analogs include those recited in PCT International Application PCT/US93/07878 (WO 94/04145), which discloses compounds of the formula: Formula II where R and Ri are each independently hydrogen, substituted and unsubstituted aryl, substituted and unsubstituted alkenyl, substituted and unsubstituted alkyl and substituted or unsubstituted alkoxy.
  • the alkyl groups preferably have from 1 to about 15 carbon atoms, more preferably from 1 to about 10 carbon atoms, still more preferably from 1 to about 6 carbon atoms.
  • the term alkyl unless otherwise modified refers to both cyclic and noncyclic groups, although of course cyclic groups will comprise at least three carbon ring members.
  • Straight or branched chain noncyclic alkyl groups are generally more prefereed than cyclic groups.
  • Straight chain alkyl groups are generally more prefereed than branched.
  • the alkenyl groups preferably have from 2 to about 15 carbon atoms, more preferably from 2 to about 10 carbon atoms, still more preferably from 2 to 6 carbon atoms.
  • alkenyl groups have 3 carbon atoms (i.e., 1-propenyl or 2-propenyl), with the allyl moiety being particularly prefereed.
  • Phenyl and napthyl are generally prefereed aryl groups.
  • Alkoxy groups include those alkoxy groups having one or more oxygen linkage and preferably have from 1 to 15 carbon atoms, more preferably from 1 to about 6 carbon atoms.
  • the substituted R and Ri groups may be substituted at one or more available positions by one or more suitable groups such as, for example, alkyl groups such as alkyl groups having from 1 to 10 carbon atoms or from 1 to 6 carbon atoms, alkenyl groups such as alkenyl groups having from 2 to 10 carbon atoms or 2 to 6 carbon atoms, aryl groups having from six to ten carbon atoms, halogen such as fluoro, chloro and bromo, and N, O and S, including heteroalkyl, e.g., heteroalkyl having one or more hetero atom linkages (and thus including alkoxy, aminoalkyl and thioalkyl) and from 1 to 10 carbon atoms or from 1 to 6 carbon atoms.
  • suitable groups such as, for example, alkyl groups such as alkyl groups having from 1 to 10 carbon atoms or from 1 to 6 carbon atoms, alkenyl groups such as alkenyl groups having from 2 to 10 carbon atoms or 2 to 6
  • R and Ri are each independently selected from hydrogen, hydroxy, sulfhydryl, halogen, substituted alkyl, unsubstituted alkyl, substituted alkenyl, unsubstituted alkenyl, substituted aryl, unsubstituted aryl, substituted alkoxy, unsubstituted alkoxy, and salts thereof, where the dotted double bond between the ring carbons represents an optional ring double bond.
  • Additional ⁇ -lapachone analogs and derivatives are recited in PCT International Application PCT/USOO/10169 (WO00/61142), which disclose compounds of the structure:
  • R 5 and R 6 may be independently selected from hydroxy, Ci -C 6 alkyl, C ⁇ -C 6 alkenyl, Ci- C 6 alkoxy, C ⁇ -C 6 alkoxycarbonyl, ⁇ (CH ) n -phenyl; and R 7 is hydrogen, hydroxyl, C ⁇ -C 6 alkyl, C ⁇ -C 6 alkenyl, C ⁇ -C 6 alkoxy, C ⁇ -C 6 alkoxycarbonyl, ⁇ (CH 2 ) n -amino, -(CFJ 2 ) n -aryl, ⁇ (CH 2 ) n - heteroaryl, ⁇ (CH 2 ) n -heterocycle, or — (CH 2 ) n -phenyl, wherein n is an integer from 0 to 10.
  • R and Ri are each independently selected from hydrogen, hydroxy, sulfhydryl, halogen, substituted alkyl, unsubstituted alkyl, substituted alkenyl, unsubstituted alkenyl, substituted aryl, unsubstituted aryl, substituted alkoxy, unsubstituted alkoxy, and salts thereof.
  • the alkyl groups preferably have from 1 to about 15 carbon atoms, more preferably from 1 to about 10 carbon atoms, still more preferably from 1 to about 6 carbon atoms.
  • alkyl refers to both cyclic and noncyclic groups.
  • Straight or branched chain noncyclic alkyl groups are generally more prefereed than cyclic groups.
  • Straight chain alkyl groups are generally more prefereed than branched.
  • the alkenyl groups preferably have from 2 to about 15 carbon atoms, more preferably from 2 to about 10 carbon atoms, still more preferably from 2 to 6 carbon atoms.
  • Especially prefereed alkenyl groups have 3 carbon atoms (i.e., 1-propenyl or 2- propenyl), with the allyl moiety being particularly prefereed.
  • Phenyl and napthyl are generally prefereed aryl groups.
  • Alkoxy groups include those alkoxy groups having one or more oxygen linkage and preferably have from 1 to 15 carbon atoms, more preferably from 1 to about 6 carbon atoms.
  • the substituted R and Ri groups may be substituted at one or more available positions by one or more suitable groups such as, for example, alkyl groups having from 1 to 10 carbon atoms or from 1 to 6 carbon atoms, alkenyl groups having from 2 to 10 carbon atoms or 2 to 6 carbon atoms, aryl groups having from six to ten carbon atoms, halogen such as fluoro, chloro and bromo, and N, O and S, including heteroalkyl, e.g., heteroalkyl having one or more hetero atom linkages (and thus including alkoxy, aminoalkyl and thioalkyl) and from 1 to 10 carbon atoms or from 1 to 6 carbon atoms; and where R 5 and R 6 may be independently selected from hydroxy, C ⁇ -C 6 alkyl, C ⁇ -C 6 alkenyl, C ⁇ -C 6 alkoxy, C ⁇ -C 6 alkoxycarbonyl, ⁇ (CH 2 ) n -aryl, — (CH 2 )
  • Ri is (CH 2 ) n -R 2 , where n is an integer from 0-10 and R 2 is hydrogen, an alkyl, an aryl, a heteroaromatic, a heterocyclic, an aliphatic, an alkoxy, an allyloxy, a hydroxyl, an amine, a thiol, an amide, or a halogen.
  • Analogs and derivatives also contemplated by the invention include 4-acetoxy- ⁇ - lapachone, 4-acetoxy-3-bromo- ⁇ -lapachone, 4-keto- ⁇ -lapachone, 7-hydroxy- ⁇ -lapachone, 7- methoxy- ⁇ -lapachone, 8 -hydroxy- ⁇ -lapachone, 8-methoxy- ⁇ -lapachone, 8-chloro- ⁇ -lapachone, 9-chloro- ⁇ -lapachone, 8-methyl- ⁇ -lapachone and 8,9-dimethoxy- ⁇ -lapachone.
  • Preferred analogs and derivatives also contemplated by the invention include compounds of the following general formula VIII:
  • R1-R 4 are each, independently, selected from the group consisting of H, C ⁇ -C 6 alkyl, - C 6 alkenyl, C ⁇ -C 6 alkoxy, C ⁇ -C 6 alkoxycarbonyl, ⁇ (CH 2 ) n -aryl, -(CH 2 ) n -heteroaryl, ⁇ (CH ) n - heterocycle, or ⁇ (CH 2 ) n -phenyl; or Ri and R 2 combined are a single substituent selected from the above group, and R 3 and R 4 combined are a single substituent selected from the above groups, in which case — is a double bond.
  • Preferred analogs and derivatives also contemplated by this invention include dunnione and 2-ethyl-6-hydroxynaphtho [2, 3 -b] -furan-4, 5 -dione.
  • Prefereed analogs and derivatives also contemplated by the invention include compounds of the following general formula IX:
  • Formula IX where Ri is selected from H, CH 3 , OCH 3 and NO 2 .
  • Additional preferred ⁇ -lapachone analogs useful in the methods and kits of the invention are represented by Formula X (see also the co-owned PCT patent application entitled “NOVEL LAPACHONE COMPOUNDS AND METHODS OF USE THEREOF", PCT/US2003/037219, filed November 18, 2003, and claiming priority to U.S. provisional application no.
  • R1-R6 are each, independently, selected from the group consisting of H, OH, substituted and unsubstituted C ⁇ -C 6 alkyl, substituted and unsubstituted C ⁇ .
  • R7-R10 are each, independently, hydrogen, hydroxyl, halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkoxy, nitro, cyano or amide; and n is an integer from 0 to 10.
  • RI and R2 are alkyl
  • R3-R6 are, independently, H, OH, halogen, alkyl, alkoxy, substituted or unsubstituted acyl, substituted alkenyl or substituted alkyl carbonyl
  • R7-R10 are hydrogen.
  • RI and R2 are each methyl and R3-R10 are each hydrogen.
  • R1-R4 are each hydrogen
  • R5 and R6 are each methyl and R7-R10 are each hydrogen.
  • R1-R4 are each, independently, selected from the group consisting of H, OH, substituted and unsubstituted C ⁇ -C 6 alkyl, substituted and unsubstituted C ⁇ -C 6 alkenyl, substituted and unsubstituted C ⁇ -C 6 alkoxy, substituted and unsubstituted C ⁇ -C 6 alkoxycarbonyl, substituted and unsubstituted C ⁇ -C 6 acyl, -(CH 2 ) n -amino, -(CH 2 ) n -aryl, -(CH 2 ) n -heterocycle, and -(CH 2 ) n -phenyl; or one of RI or R2 and one of R3 or R4 form a fused ring, wherein the ring has 4-8 ring members; R5-R8 are each, independently, hydrogen, hydroxyl,
  • R6, R7 and R8 are not each simultaneously H.
  • All stereoisomers of the compounds of the instant invention are contemplated, either in admixture or in pure or substantially pure form.
  • the definition of the compounds according to the invention embraces all possible stereoisomers (e.g., the R and S configurations for each asymmetric center) and their mixtures. It very particularly embraces the racemic forms and the isolated optical isomers having a specified activity.
  • the racemic forms can be resolved by physical methods, such as, for example, fractional crystallization, separation or crystallization of diastereomeric derivatives or separation by chiral column chromatography.
  • the individual optical isomers can be obtained from the racemates by conventional methods, such as, for example, salt formation with an optically active acid followed by crystallization. Furthermore, all geometric isomers, such as E- and Z-configurations at a double bond, are within the scope of the invention unless otherwise stated. Certain compounds of this invention may exist in tautomeric forms. All such tautomeric forms of the compounds are considered to be within the scope of this invention unless otherwise stated.
  • the present invention also includes one or more regioisomeric mixtures of an analog or derivative of ⁇ -Lapachone.
  • salt is a pharmaceutically acceptable salt and can include acid addition salts including hydrochlorides, hydrobromides, phosphates, sulphates, hydrogen sulphates, alkylsulphonates, arylsulphonates, acetates, benzoates, citrates, maleates, fumarates, succinates, lactates, and tartrates; alkali metal cations such as Na, K, Li, alkali earth metal salts such as Mg or Ca, or organic amine salts.
  • the term “metabolite” means a product of metabolism of ⁇ -lapachone, or a pharmaceutically acceptable salt, analog or derivative thereof, that exhibits a similar activity in vivo to ⁇ -lapachone.
  • the term “prodrug” means a compound of the present invention covalently linked to one or more pro-moieties, such as an amino acid moiety or other water solubilizing moiety. A compound of the present invention may be released from the pro-moiety via hydrolytic, oxidative, and/or enzymatic release mechanisms. In an embodiment, a prodrug composition of the present invention exhibits the added benefit of increased aqueous solubility, improved stability, and improved pharmacokinetic profiles.
  • the pro-moiety may be selected to obtain desired prodrug characteristics.
  • the pro-moiety e.g., an amino acid moiety or other water solubilizing moiety may be selected based on solubility, stability, bio availability, and/or in vivo delivery or uptake.
  • a "subject” can be any mammal, e.g., a human, a primate, mouse, rat, dog, cat, cow, horse, pig, sheep, goat, camel, h a preferred aspect, the subject is a human.
  • a "subject in need thereof is a subject having a cell proliferative disorder of the colon, or a subject having an increased risk of developing a cell proliferative disorder of the colon relative to the population at large.
  • a subject in need thereof has a precancerous condition of the colon.
  • a subject in need thereof has colon cancer.
  • the subject may be suffering from a known (i.e., diagnosed) condition characterized by cell hyperproliferation (e.g., cancer) of the colon.
  • a known (i.e., diagnosed) condition characterized by cell hyperproliferation (e.g., cancer) of the colon characterized by cell hyperproliferation (e.g., cancer) of the colon.
  • cell proliferative disorder refers to conditions in which unregulated or abnormal growth, or both, of cells can lead to the development of an unwanted condition or disease, which may or may not be cancerous.
  • a cell proliferative disorder includes, for example, colon cancer and precancerous conditions of the colon.
  • a "cell proliferative disorder of the colon” is a cell proliferative disorder involving cells of the colon.
  • a cell proliferative disorder includes a pre-cancer or precancerous condition of the colon.
  • a cell proliferative disorder of the colon includes a non-cancerous cell proliferative disorder of the colon.
  • a cell proliferative disorder includes colon cancer, including metastatic lesions in other tissues or organs distant from the primary tumor site.
  • a "precancer cell” or “precancerous cell” is a cell manifesting a cell proliferative disorder that is a precancer or a precancerous condition.
  • a "cancer cell” or “cancerous cell” is a cell manifesting a cell proliferative disorder that is a cancer. Any reproducible means of measurement may be used to identify cancer cells or precancerous cells.
  • cancer cells or precancerous cells are identified by histological typing or grading of a tissue sample (e.g., a biopsy sample). In another aspect, cancer cells or precancerous cells are identified through the use of appropriate molecular markers.
  • the cell proliferative disorder of the colon is colon cancer.
  • compositions of the present invention may be used to treat colon cancer or cell proliferative disorders of the colon.
  • colon cancer includes all forms of cancer of the colon.
  • a colon cancer to be treated includes carcinoma, sarcoma, and adenocarcinoma.
  • colon cancer includes sporadic and hereditary colon cancers.
  • colon cancer includes malignant colon neoplasms, carcinoma in situ, leiomyosarcomas, typical carcinoid tumors, and atypical carcinoid tumors.
  • colon cancer includes adenocarcinoma, squamous cell carcinoma, signet ring cell adenocarcinoma and adenosquamous cell carcinoma.
  • colon cancer is associated with a hereditary syndrome selected from the group consisting of hereditary nonpolyposis colorectal cancer (HNPCC), familial adenomatous polyposis (TAP), Gardner's syndrome, Peutz-Jeghers syndrome, Turcot's syndrome and juvenile polyposis.
  • HNPCC hereditary nonpolyposis colorectal cancer
  • TAP familial adenomatous polyposis
  • Gardner's syndrome adenomatous polyposis
  • Turcot's syndrome and juvenile polyposis.
  • colon cancer is caused by a hereditary syndrome selected from the group consisting of hereditary nonpolyposis colorectal cancer (HNPCC), familial adenomatous polyposis (FAP), Gardner's syndrome, Peutz-Jeghers syndrome, Turcot's syndrome and juvenile polyposis.
  • HNPCC hereditary nonpolyposis colorectal cancer
  • FAP familial adenomatous polyposis
  • Gardner's syndrome adenomatous polyposis
  • Gardner's syndrome adenomatous polyposis
  • Turcot's syndrome a hereditary nonpolyposis colorectal cancer
  • cell proliferative disorders of the colon include all forms of cell proliferative disorders affecting colon cells.
  • cell proliferative disorders of the colon include colon cancer, precancerous conditions of the colon, adenomatous polyps of the colon and metachronous lesions of the colon.
  • a cell proliferative disorder of the colon includes adenoma.
  • cell proliferative disorders of the colon are characterized by hyperplasia, metaplasia, and dysplasia of the colon.
  • prior colon diseases that may predispose individuals to development of cell proliferative disorders of the colon include prior colon cancer.
  • current disease that may predispose individuals to development of cell proliferative disorders of the colon include Crohn's disease and ulcerative colitis.
  • a cell proliferative disorder of the colon is associated with a mutation in a gene selected from the group consisting of p53, ras, FAP and DCC.
  • an individual has an elevated risk of developing a cell proliferative disorder of the colon due to the presence of a mutation in a gene selected from the group consisting of p53, ras, FAP and DCC.
  • a colon cancer that is to be treated has arisen in a subject equal to or older than 30 years old, or a subject younger than 30 years old.
  • a colon cancer that is to be treated has arisen in a subject equal to or older than 50 years old, or a subject younger than 50 years old.
  • a colon cancer that is to be treated has arisen in a subject equal to or older than 70 years old, or a subject younger than 70 years old.
  • a colon cancer that is to be treated has been typed to identify a familial or spontaneous mutation in p53, Rb, myc or ras.
  • a colon cancer that is to be treated is associated with a mutation in a gene selected from the group consisting of MSH2, MSH6, MLH1, PMS1, PMS2, TGFBR2, BAX, and APC.
  • a colon cancer that is to be treated is associated with a mutation selected from the group consisting of de(lp),del(8p), del(8q21), del(17p), LOH17p, and chrmosome 18q allelic loss.
  • a colon cancer that is to be treated has been typed as having the replication error phenotype RER+. In one aspect, a colon cancer that is to be treated has been typed as CpG island methylator phenotype positive (CEV1P+) or CpG island methylator phenotype negative (CEVIP-). In one aspect, a colon cancer that is to be treated is associated with elevated levels of CEA (carcinoembryonic antigen). In one aspect, a colon cancer that is to be treated includes a localized tumor of the colon.
  • a colon cancer that is to be treated includes a tumor of the colon that is associated with a negative regional lymph node biopsy. In one aspect, a colon cancer that is to be treated includes a tumor of the colon that is associated with a positive regional lymph node biopsy. In another aspect, a colon cancer that is to be treated includes a tumor of the colon that has been typed as having nodal negative status (e.g., node-negative) or nodal positive status (e.g., node- positive). In another aspect, a colon cancer that is to be treated includes a tumor of the colon that has metastasized to other locations in the body.
  • a colon cancer that is to be treated is classified as having metastasized to a location selected from the group consisting of lymph node, stomach, bile duct, liver, bone, ovary, peritoneum and brain.
  • a colon cancer that is to be treated is classified according to a characteristic selected from the group consisting of metastatic, limited stage, extensive stage, unresectable, resectable, localized, regional, local-regional, locally advanced, distant, multicentric, bilateral, ipsilateral, contralateral, newly diagnosed, recurrent, and inoperable.
  • a colon cancer that is to be treated has been staged according to the American Joint Committee on Cancer (AJCC) TNM classification system, where the tumor (T) has been assigned a stage of Tx, Tis, TI, T2, T3, T4; and where the regional lymph nodes (N) have been assigned a stage of NX, NO, NI, N2, N2a, N2b, N3, N3a, N3b, or N3c; and where distant metastasis (M) has been assigned a stage of MX, M0, or Ml.
  • AJCC American Joint Committee on Cancer
  • a colon cancer that is to be treated has been staged according to an American Joint Committee on Cancer (AJCC) classification as Stage 0, 1, II, IIA, IB, III, IIIA, hlB, HIC and IV colon cancer.
  • AJCC American Joint Committee on Cancer
  • a colon cancer that is to be treated has been assigned a grade according to an AJCC classification as Grade GX (e.g., grade cannot be assessed), Grade 1, Grade 2, Grade 3 or Grade 4.
  • a colon cancer that is to be treated has been assigned a grade according to the Dukes staging system of A, B, or C.
  • a colon cancer that is to be treated has been assigned a grade according to the Astler-Coller staging system of A, Bl, B2, B3 or Cl, C2, C3, or D.
  • a colon cancer that is to be treated includes a tumor that has been determined to be less than or equal to about 2 centimeters in diameter. In another aspect, a colon cancer that is to be treated includes a tumor that has been determined to be from about 2 to about 5 centimeters in diameter. In another aspect, a colon cancer that is to be treated includes a tumor that has been determined to be greater than or equal to about 2 centimeters in diameter. In another aspect, a colon cancer that is to be treated includes a tumor that has been determined to be greater than 5 centimeters in diameter. In another aspect, a colon cancer that is to be treated is classified by microscopic appearance as well differentiated, moderately differentiated, poorly differentiated, or undifferentiated.
  • a colon cancer that is to be treated is classified by microscopic appearance with respect to mitosis count (e.g., amount of cell division) or nuclear pleiomorphism (e.g., change in cells).
  • a colon cancer that is to be treated is classified by microscopic appearance as being associated with areas of necrosis (e.g., areas of dying or degenerating cells).
  • a colon cancer that is to be treated is classified as having an abnonnal karyotype, having an abnormal number of chromosomes, or having one or more chromosomes that are abnormal in appearance.
  • a colon cancer that is to be treated is classified as being aneuploid, triploid, tetraploid, or as having an altered ploidy.
  • a colon cancer that is to be treated is classified as having a chromosomal translocation, or a deletion or duplication of an entire chromosome, or a region of deletion, duplication or amplification of a portion of a chromosome.
  • a colon cancer that is to be treated is evaluated by DNA cytometry, flow cytometry, or image cytometry.
  • a colon cancer that is to be treated has been typed as having 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, or 90% of cells in the synthesis stage of cell division (e.g., in S phase of cell division).
  • a colon cancer that is to be treated has been typed as having a low S-phase fraction or a high S-phase fraction.
  • a "normal cell” is a cell that cannot be classified as part of a "cell proliferative disorder.”
  • a normal cell lacks unregulated or abnormal growth, or both, that can lead to the development of an unwanted condition or disease.
  • a normal cell possesses normally functioning cell cycle checkpoint control mechanisms.
  • contacting a cell refers to a condition in which a compound or other composition of matter is in direct contact with a cell, or is close enough to induce a desired biological effect in a cell.
  • monotherapy refers to administration of a single active or therapeutic compound to a subject in need thereof. Preferably, monotherapy will involve administration of a therapeutically effective amount of an active compound.
  • ⁇ -lapachone monotherapy for cancer comprises administration of a therapeutically effective amount of ⁇ - lapachone, or a pharmaceutically acceptable salt, prodrug, metabolite, analog or derivative thereof, to a subject in need of treatment of cancer.
  • Monotherapy may be contrasted with combination therapy, in which a combination of multiple active compounds is administered, preferably with each component of the combination present in a therapeutically effective amount.
  • ⁇ -lapachone montherapy is more effective than combination therapy in inducing a desired biological effect.
  • combination therapy includes ⁇ -lapachone with taxol; ⁇ -lapachone with docetaxel; ⁇ -lapachone with vincristin; ⁇ -lapachone with vinblastin; ⁇ -lapachone with nocodazole; ⁇ -lapachone with teniposide; ⁇ -lapachone with etoposide; ⁇ -lapachone with adriamycin; ⁇ -lapachone with epothilone; ⁇ -lapachone with navelbine; ⁇ -lapachone with camptothecin; ⁇ -lapachone with daunorabicin; ⁇ -lapachone with dactinomycin; ⁇ -lapachone with mitoxantrone; ⁇ -lapachone with amsacrine; ⁇ -lapachone with epirubicin; or ⁇ -lapachone with idarubicin.
  • combination therapy includes ⁇ -lapachone with gemcitabine.
  • combination therapy includes reduced ⁇ -lapachone with taxol; reduced ⁇ -lapachone with docetaxel; reduced ⁇ -lapachone with vincristin; reduced ⁇ -lapachone with vinblastin; reduced ⁇ -lapachone with nocodazole; reduced ⁇ -lapachone with teniposide; reduced ⁇ -lapachone with etoposide; reduced ⁇ -lapachone with adriamycin; reduced ⁇ - lapachone with epothilone; reduced ⁇ -lapachone with navelbine; reduced ⁇ -lapachone with camptothecin; reduced ⁇ -lapachone with daunorabicin; reduced ⁇ -lapachone with dactinomycin; reduced ⁇ -lapachone with mitoxantrone; reduced ⁇ -lapachone with amsacrine; reduced ⁇ - lapachone with epirubicin; or reduced ⁇ -lap
  • combination therapy includes reduced ⁇ -lapachone with gemcitabine.
  • treating describes the management and care of a patient for the purpose of combating a disease, condition, or disorder and includes the administration of a compound of the present invention to prevent the onset of the symptoms or complications, alleviating the symptoms or complications, or eliminating the disease, condition or disorder.
  • treating a colon cancer of the present invention results in a reduction in size of a tumor.
  • a reduction in size of a tumor may also be referred to as "tumor regression.”
  • tumor size is reduced by 5% or greater relative to its size prior to treatment; more preferably, tumor size is reduced by 10% or greater; more preferably, reduced by 20% or greater; more preferably, reduced by 30% or greater; more preferably, reduced by 40% or greater; even more preferably, reduced by 50% or greater; and most preferably, reduced by greater than 75% or greater.
  • Size of a tumor may be measured by any reproducible means of measurement. In a prefereed aspect, size of a tumor may be measured as a diameter of the tumor. In another aspect, treating a colon cancer of the present invention results in a reduction in tumor volume.
  • tumor volume is reduced by 5% or greater relative to its size prior to treatment; more preferably, tumor volume is reduced by 10% or greater; more preferably, reduced by 20%) or greater; more preferably, reduced by 30% or greater; more preferably, reduced by 40% or greater; even more preferably, reduced by 50% or greater; and most preferably, reduced by greater than 75% or greater.
  • Tumor volume may be measured by any reproducible means of measurement.
  • treating a colon cancer of the present invention results in a decrease in number of tumors.
  • tumor number is reduced by 5% or greater relative to number prior to treatment; more preferably, tumor number is reduced by 10% or greater; more preferably, reduced by 20% or greater; more preferably, reduced by 30% or greater; more preferably, reduced by 40% or greater; even more preferably, reduced by 50% or greater; and most preferably, reduced by greater than 75%.
  • Number of tumors may be measured by any reproducible means of measurement. In a prefereed aspect, number of tumors may be measured by counting tumors visible to the naked eye or at a specified magnification. In a prefereed aspect, the specified magnification is 2x, 3x, 4x, 5x, lOx, or 50x.
  • treating a colon cancer of the present invention results in a decrease in number of metastatic lesions in other tissues or organs distant from the primary tumor site.
  • the number of metastatic lesions is reduced by 5% or greater relative to number prior to treatment; more preferably, the number of metastatic lesions is reduced by 10%) or greater; more preferably, reduced by 20% or greater; more preferably, reduced by 30% or greater; more preferably, reduced by 40% or greater; even more preferably, reduced by 50% or greater; and most preferably, reduced by greater than 75%.
  • the number of metastatic lesions may be measured by any reproducible means of measurement.
  • the number of metastatic lesions may be measured by counting metastatic lesions visible to the naked eye or at a specified magnification.
  • the specified magnification is 2x, 3x, 4x, 5x, lOx, or 50x.
  • treating a colon cancer of the present invention results in an increase in average survival time of a population of treated subjects in comparison to a population receiving carrier alone.
  • the average survival time is increased by more than 30 days; more preferably, by more than 60 days; more preferably, by more than 90 days; and most preferably, by more than 120 days.
  • An increase in average survival time of a population may be measured by any reproducible means.
  • an increase in average survival time of a population may be measured, for example, by calculating for a population the average length of survival following initiation of treatment with an active compound.
  • an increase in average survival time of a population may also be measured, for example, by calculating for a population the average length of survival following completion of a first round of treatment with an active compound.
  • treating a colon cancer of the present invention results in an increase in average survival time of a population of treated subjects in comparison to a population of untreated subjects.
  • the average survival time is increased by more than 30 days; more preferably, by more than 60 days; more preferably, by more than 90 days; and most preferably, by more than 120 days.
  • An increase in average survival time of a population may be measured by any reproducible means.
  • an increase in average survival time of a population may be measured, for example, by calculating for a population the average length of survival following initiation of treatment with an active compound.
  • an increase in average survival time of a population may also be measured, for example, by calculating for a population the average length of survival following completion of a first round of treatment with an active compound.
  • treating a colon cancer of the present invention results in increase in average survival time of a population of treated subjects in comparison to a population receiving monotherapy with a drug that is not ⁇ -lapachone, or a pharmaceutically acceptable salt, metabolite, analog or derivative thereof
  • the average survival time is increased by more than 30 days; more preferably, by more than 60 days; more preferably, by more than 90 days; and most preferably, by more than 120 days.
  • An increase in average survival time of a population may be measured by any reproducible means.
  • an increase in average survival time of a population may be measured, for example, by calculating for a population the average length of survival following initiation of treatment with an active compound.
  • an increase in average survival time of a population may also be measured, for example, by calculating for a population the average length of survival following completion of a first round of treatment with an active compound.
  • treating a colon cancer of the present invention results in a decrease in the mortality rate of a population of treated subjects in comparison to a population receiving carrier alone.
  • treating colon cancer results in a decrease in the mortality rate of a population of treated subjects in comparison to an untreated population.
  • treating colon cancer results a decrease in the mortality rate of a population of treated subjects in comparison to a population receiving monotherapy with a drug that is not ⁇ -lapachone, or a pharmaceutically acceptable salt, metabolite, analog or derivative thereof.
  • the mortality rate is decreased by more than 2%; more preferably, by more than 5%; more preferably, by more than 10%; and most preferably, by more than 25%.
  • a decrease in the mortality rate of a population of treated subj ects may be measured by any reproducible means.
  • a decrease in the mortality rate of a population may be measured, for example, by calculating for a population the average number of disease- related deaths per unit time following initiation of treatment with an active compound.
  • a decrease in the mortality rate of a population may also be measured, for example, by calculating for a population the average number of disease-related deaths per unit time following completion of a first round of treatment with an active compound.
  • treating a colon cancer of the present invention results in a decrease in tumor growth rate.
  • tumor growth rate is reduced by at least 5% relative to number prior to treatment; more preferably, tumor growth rate is reduced by at least 10%; more preferably, reduced by at least 20% ⁇ ; more preferably, reduced by at least 30%; more preferably, reduced by at least 40%; more preferably, reduced by at least 50%; even more preferably, reduced by at least 50%; and most preferably, reduced by at least 75%.
  • Tumor growth rate may be measured by any reproducible means of measurement.
  • tumor growth rate is measured according to a change in tumor diameter per unit time.
  • treating a colon cancer of the present invention results in a decrease in tumor regrowth.
  • tumor regrowth is less than 5%; more preferably, tumor regrowth is less than 10%; more preferably, less than 20%; more preferably, less than 30%; more preferably, less than 40%; more preferably, less than 50%; even more preferably, less than 50%; and most preferably, less than 75%.
  • Tumor regrowth may be measured by any reproducible means of measurement.
  • tumor regrowth is measured, for example, by measuring an increase in the diameter of a tumor after a prior tumor shrinkage that followed treatment.
  • a decrease in tumor regrowth is indicated by failure of tumors to reoccur after treatment has stopped.
  • treating or preventing a cell proliferative disorder of the present invention results in a reduction in the rate of cellular proliferation.
  • the rate of cellular proliferation is reduced by at least 5%; more preferably, by at least 10%; more preferably, by at least 20%; more preferably, by at least 30%; more preferably, by at least 40%; more preferably, by at least 50%; even more preferably, by at least 50%; and most preferably, by at least 75%.
  • the rate of cellular proliferation may be measured by any reproducible means of measurement.
  • the rate of cellular proliferation is measured, for example, by measuring the number of dividing cells in a tissue sample per unit time.
  • treating or preventing a cell proliferative disorder of the present invention results in a reduction in the proportion of proliferating cells.
  • the proportion of proliferating cells is reduced by at least 5%; more preferably, by at least 10%; more preferably, by at least 20%; more preferably, by at least 30%; more preferably, by at least 40%>; more preferably, by at least 50%; even more preferably, by at least 50%; and most preferably, by at least 75%.
  • the proportion of proliferating cells may be measured by any reproducible means of measurement.
  • the proportion of proliferating cells is measured, for example, by quantifying the number of dividing cells relative to the number of nondividing cells in a tissue sample.
  • the proportion of proliferating cells is equivalent to the mitotic index.
  • treating or preventing a cell proliferative disorder of the present invention results in a decrease in size of an area or zone of cellular proliferation.
  • size of an area or zone of cellular proliferation is reduced by at least 5%> relative to its size prior to treatment; more preferably, reduced by at least 10%; more preferably, reduced by at least 20%; more preferably, reduced by at least 30%; more preferably, reduced by at least 40%; more preferably, reduced by at least 50%; even more preferably, reduced by at least 50%; and most preferably, reduced by at least 75%.
  • Size of an area or zone of cellular proliferation may be measured by any reproducible means of measurement.
  • size of an area or zone of cellular proliferation may be measured as a diameter or width of an area or zone of cellular proliferation.
  • treating or preventing a cell proliferative disorder of the present invention results in a decrease in the number or proportion of cells having an abnormal appearance or morphology.
  • the number of cells having an abnormal morphology is reduced by at least 5% relative to its size prior to treatment; more preferably, reduced by at least 10%; more preferably, reduced by at least 20%; more preferably, reduced by at least 30%; more preferably, reduced by at least 40%; more preferably, reduced by at least 50%; even more preferably, reduced by at least 50%; and most preferably, reduced by at least 75%.
  • An abnormal cellular appearance or morphology may be measured by any reproducible means of measurement.
  • an abnormal cellular morphology is measured by microscopy, e.g., using an inverted tissue culture microscope.
  • an abnormal cellular morphology takes the form of nuclear pleiomorphism.
  • the term "selectively" means tending to occur at a higher frequency in one population than in another population.
  • the compared populations are cell populations.
  • ⁇ -lapachone, or a pharmaceutically acceptable salt, metabolite, analog or derivative thereof acts selectively on a cancer or precancer cell but not on a normal cell.
  • a compound of the present invention acts selectively to modulate one molecular target (e.g., E2F-1) but does not significantly modulate another molecular target (e.g., Protein Kinase C).
  • the invention provides a method for selectively inhibiting the activity of an enzyme, such as a kinase.
  • an event occurs selectively in population A relative to population B if it occurs greater than two times more frequently in population A as compared to population B. More preferably, an event occurs selectively if it occurs greater than five times more frequently in population A.
  • an event occurs selectively if it occurs greater than ten times more frequently in population A; more preferably, greater than fifty times; even more preferably, greater than 100 times; and most preferably, greater than 1000 times more frequently in population A as compared to population B.
  • cell death would be said to occur selectively in cancer cells if it occurred greater than twice as frequently in cancer cells as compared to normal cells.
  • a compound of the present invention or a pharmaceutically acceptable salt, prodrug, metabolite, analog or derivative thereof modulates the activity of a molecular target (e.g., E2F-1).
  • modulating refers to stimulating or inhibiting an activity of a molecular target.
  • a compound of the present invention modulates the activity of a molecular target if it stimulates or inhibits the activity of the molecular target by at least 10% relative to the activity of the molecular target under the same conditions but lacking only the presence of said compound. More preferably, a compound of the present invention modulates the activity of a molecular target if it stimulates or inhibits the activity of the molecular target by at least 25%, at least 50%, at least 2-fold, at least 5-fold, at least 10-fold, at least 20-fold, at least 50-fold, at least 100-fold relative to the activity of the molecular target under the same conditions but lacking only the presence of said compound.
  • the activity of a molecular target may be measured by any reproducible means.
  • the activity of a molecular target may be measured in vitro or in vivo.
  • the activity of a molecular target may be measured in vitro by an enzymatic activity assay or a DNA binding assay, or the activity of a molecular target may be measured in vivo by assaying for expression of a reporter gene.
  • a compound of the present invention, or a pharmaceutically acceptable salt, prodrug, metabolite, analog or derivative thereof does not significantly modulate the activity of a molecular target if the addition of the compound stimulates or inhibits the activity of the molecular target by less than 10% relative to the activity of the molecular target under the same conditions but lacking only the presence of said compound.
  • a compound of the present invention demonstrates a minimum of a four fold differential, preferably a ten fold differential, more preferably a fifty fold differential, in the dosage required to achieve a biological effect.
  • a compound of the present invention demonstrates this differential across the range of inhibition, and the differential is exemplified at the IC 50 , i.e., a 50% inhibition, for a molecular target of interest.
  • administering ⁇ -lapachone, or a pharmaceutically acceptable salt, prodrug, metabolite, analog or derivative thereof, to a cell or a subject in need thereof results in modulation (i. e., stimulation or inhibition) of an activity of a member of the E2F family of transcription factors (e.g., E2F-1, E2F-2, or E2F-3).
  • an activity of a member of the E2F family of transcription factors refers to any biological function or activity that is carried out by an E2F family member.
  • a function of E2F-1 includes binding of E2F-1 to its cognate DNA sequences.
  • Other functions of E2F-1 include migrating to the cell nucleus and activating transcription.
  • treating colon cancer or a cell proliferative disorder results in cell death, and preferably, cell death results in a decrease of at least 10% in number of cells in a population.
  • cell death means a decrease of at least 20%; more preferably, a decrease of at least 30%; more preferably, a decrease of at least 40%; more preferably, a decrease of at least 50%; most preferably, a decrease of at least 75%>.
  • Number of cells in a population may be measured by any reproducible means. In one aspect, number of cells in a population is measured by fluorescence activated cell sorting (FACS). In another aspect, number of cells in a population is measured by immunofluorescence microscopy, hi another aspect, number of cells in a population is measured by light microscopy. In another aspect, methods of measuring cell death are as shown in Li et al, (2003) Proc Natl Acad Sci USA. 100(5): 2674-8.
  • cell death results from apoptosis.
  • an effective amount of ⁇ -lapachone, or a pharmaceutically acceptable salt, metabolite, analog or derivative thereof is not significantly cytotoxic to normal cells.
  • a therapeutically effective amount of a compound is not significantly cytotoxic to normal cells if administration of the compound at a therapeutically effective amount does not induce apoptosis in greater than 10%) of normal cells.
  • a therapeutically effective amount of a compound does not significantly affect the viability of normal cells if administration of the compound at a therapeutically effective amount does not induce cell death in greater than 10% of normal cells.
  • activating refers to placing one or more compositions of matter (e.g., protein or nucleic acid) in a state suitable for carrying out a desired biological function.
  • a composition of matter capable of being activated also has an unactivated state.
  • an activated composition of matter may have an inhibitory or stimulatory biological function, or both.
  • elevation refers to an increase in a desired biological activity of a composition of matter (e.g., a protein or a nucleic acid). In one aspect, elevation may occur through an increase in concentration of a composition of matter.
  • stimulation of unscheduled expression of a checkpoint molecule by ⁇ - lapachone, or a pharmaceutically acceptable salt, metabolite, analog or derivative thereof triggers cell death in cells with defective checkpoints, a hallmark of cancer and pre-cancer cells.
  • contacting a cell with ⁇ -lapachone, or a pharmaceutically acceptable salt, metabolite, analog or derivative thereof stimulates unscheduled expression of the checkpoint molecule E2F.
  • contacting a cell with ⁇ -lapachone, or a pharmaceutically acceptable salt, metabolite, analog or derivative thereof results in activation of an E2F checkpoint pathway.
  • administering results in activation of an E2F checkpoint pathway.
  • E2F pathway activity is increased by more than
  • E2F activity is increased by more than 10%; more than 25%; more than 50%; more than 2-fold; more than 5-fold; and most preferably, by more than 10-fold.
  • Methods of measuring induction of E2F activity and elevation of E2F levels are as shown in Li et al, (2003) Proc Natl Acad Sci USA. 100(5): 2674-8.
  • contacting a cell with ⁇ -lapachone, or a pharmaceutically acceptable salt, metabolite, analog or derivative thereof results in elevation of an E2F transcription factor.
  • administering to a subject in need thereof ⁇ -lapachone, or a pharmaceutically acceptable salt, metabolite, analog or derivative thereof results in elevation of an E2F transcription factor.
  • contacting a cell with ⁇ -lapachone, or a pharmaceutically acceptable salt, metabolite, analog or derivative thereof results in elevation of an E2F transcription factor selectively in colon cancer cells but not in normal cells.
  • administering to a subject in need thereof ⁇ -lapachone, or a pharmaceutically acceptable salt, metabolite, analog or derivative thereof results in elevation of an E2F transcription factor selectively in colon cancer cells but not in normal cells.
  • contacting a cell with ⁇ -lapachone, or a pharmaceutically acceptable salt, metabolite, analog or derivative thereof stimulates unscheduled activation of an E2F transcription factor.
  • administering to a subject in need thereof ⁇ -lapachone, or a pharmaceutically acceptable salt, metabolite, analog or derivative thereof stimulates unscheduled activation of an E2F transcription factor.
  • contacting a cell with ⁇ -lapachone, or a pharmaceutically acceptable salt, metabolite, analog or derivative thereof stimulates unscheduled activation of an E2F transcription factor selectively in colon cancer cells but not in normal cells.
  • administering to a subject in need thereof ⁇ -lapachone, or a pharmaceutically acceptable salt, metabolite, analog or derivative thereof stimulates unscheduled activation of an E2F transcription factor selectively in colon cancer cells but not in normal cells.
  • imposed expression of a checkpoint molecule e.g., as induced by contacting a cell with ⁇ -lapachone, or a pharmaceutically acceptable salt, metabolite, analog or derivative thereof results in an expression pattern that is not reported to be of substantial consequence.
  • cancer and pre-cancer cells have defective mechanisms, which result in unchecked or persistent expression, or both, of unscheduled checkpoint molecules, e.g., E2F, leading to selective cell death in cancer and pre-cancer cells.
  • the present invention includes and provides for the unchecked or persistent expression, or both, of unscheduled checkpoint molecules by the administration of ⁇ - lapachone, or a pharmaceutically acceptable salt, metabolite, analog or derivative thereof.
  • contacting a cell with ⁇ -lapachone, or a pharmaceutically acceptable salt, metabolite, analog or derivative thereof results in activation of one or more cell cycle checkpoints.
  • administering to a subject in need thereof ⁇ -lapachone, or a pharmaceutically acceptable salt, metabolite, analog or derivative thereof results in activation of one or more cell cycle checkpoints.
  • contacting a cell with ⁇ -lapachone, or a pharmaceutically acceptable salt, metabolite, analog or derivative thereof results in activation of one or more cell cycle checkpoint pathways.
  • administering to a subject in need thereof ⁇ -lapachone, or a pharmaceutically acceptable salt, metabolite, analog or derivative thereof results in activation of one or more cell cycle checkpoint pathways.
  • contacting a cell with ⁇ -lapachone, or a pharmaceutically acceptable salt, metabolite, analog or derivative thereof results in activation of one or more cell cycle checkpoint regulators.
  • administering to a subject in need thereof ⁇ -lapachone, or a pharmaceutically acceptable salt, metabolite, analog or derivative thereof results in activation of one or more cell cycle checkpoint regulators.
  • contacting a cell with ⁇ -lapachone, or a pharmaceutically acceptable salt, metabolite, analog or derivative thereof induces or activates cell death selectively in colon cancer cells.
  • administering to a subject in need thereof ⁇ -lapachone, or a pharmaceutically acceptable salt, metabolite, analog or derivative thereof induces or activates cell death selectively in colon cancer cells.
  • contacting a cell with ⁇ - lapachone, or a pharmaceutically acceptable salt, metabolite, analog or derivative thereof induces cell death selectively in one or more cells affected by a cell proliferative disorder of the colon.
  • administering to a subject in need thereof ⁇ -lapachone, or a pharmaceutically acceptable salt, metabolite, analog or derivative thereof induces cell death selectively in one or more cells affected by a cell proliferative disorder of the colon.
  • the present invention relates to a method of treating or preventing cancer by administering ⁇ -lapachone, or a pharmaceutically acceptable salt, metabolite, analog or derivative thereof to a subject in need thereof, where administration of the ⁇ -lapachone, or a pharmaceutically acceptable salt, metabolite, analog or derivative thereof results in one or more of the following: accumulation of cells in Gl and/or S phase of the cell cycle, cytotoxicity via cell death in cancer cells but not in normal cells, antitumor activity in animals with a therapeutic index of at least 2, and acitvation of a cell cycle checkpoint (e.g., activation or elevation of a member of the E2F family of transcription factors).
  • acitvation of a cell cycle checkpoint e.g., activation or elevation of a member of the E2F family of transcription factors.
  • ⁇ -lapachone or a pharmaceutically acceptable salt, metabolite, analog or derivative thereof, can be administered in combination with a chemotherapeutic agent.
  • exemplary chemotheraputics with activity against cell proliferative disorders, such as colon cancer are known to those of ordinary skill in the art, and may be found in reference texts such as the Physician 's Desk Reference, 59 th Edition, Thomson PDR (2005).
  • the chemotherapeutic agent can be a taxane, an aromatase inhibitor, an anthracycline, a microtubule targeting drug, a topoisomerase poison drug, a targeted monoclonal or polyconal antibody, an inhibitor of a molecular target or enzyme (e.g., a kinase inhibitor), or a cytidine analogue drug.
  • the chemotherapeutic agent can be, but is not restricted to, tamoxifen, raloxifene, anastrozole, exemestane, letrozole, HERCEPTIN ® (trastuzumab), GLEEVEC ® (imatanib), TAXOL ® (paclitaxel), IRESSA ® (gefitinib), TARCEVATM (erlotinib), cyclophosphamide, lovastatin, minosine, araC, 5-fluorouracil (5-FU), methotrexate (MTX), TAXOTERE ® (docetaxel), ZOLADEX ® (goserelin), AVASTINTM (bevacizumab), vincristin, vinblastin, nocodazole, teniposide, etoposide, epothilone, navelbine, camptothecin, daunonibicin, dactinomycin,
  • the chemotherapeutic agent can be a cytokine such as G-CSF (granulocyte colony stimulating factor).
  • G-CSF granulocyte colony stimulating factor
  • ⁇ -lapachone, or a pharmaceutically acceptable salt, metabolite, analog or derivative thereof may be administered in combination with radiation therapy.
  • ⁇ -lapachone, or a pharmaceutically acceptable salt, metabolite, analog or derivative thereof may be administered in combination with standard chemotherapy combinations such as, but not restricted to, CMF (cyclophosphamide, methotrexate and 5-fluorouracil), CAF (cyclophosphamide, adriamycin and 5-fluorouracil), AC (adriamycin and cyclophosphamide), FEC (5-fluorouracil, epirubicin, and cyclophosphamide), ACT or ATC (adriamycin, cyclophosphamide, and paclitaxel), or CMFP (cyclophosphamide, methotrexate, 5-fluorouracil and prednisone).
  • CMF cyclophosphamide, methotrexate and 5-fluorouracil
  • CAF cyclophosphamide, adriamycin and 5-fluorouracil
  • AC adr
  • a cell proliferative disorder of the colon is treated by administering to a patient in need thereof a therapeutically effective amount of ⁇ - lapachone, or a pharmaceutically acceptable salt, metabolite, analog or derivative thereof, in combination with a therapeutically effective amount of gemcitabine.
  • GEMZAR ® (gemcitabine HCl) is 2'-deoxy-2',2'-difluorocytidine monohydrochloride ( ⁇ -isomer), a nucleoside analog that exhibits antitumor activity.
  • Gemcitabine may be used in monotherapy, or in combination with other agents (e.g., cisplatin, carbop latin, TAXOL ® (paclitaxel)), to treat various cancers, including pancreatic cancer, breast cancer, non-small cell lung cancer, ovarian cancer, and bladder cancer.
  • Gemcitabine exhibits cell phase specificity, primarily killing cells undergoing DNA synthesis (S-phase) and also blocking the progression of cells through the Gl/S boundary. Without being limited by theory, it is believed that after a gemcitabine nucleotide is incorporated into DNA, only one additional nucleotide may be added to the growing DNA strands.
  • DNA polymerase epsilon is unable to remove the gemcitabine nucleotide and repair the growing DNA strand (e.g., masked chain termination).
  • gemcitabine induces internucleosomal DNA fragmentation, one of the characteristics of programmed cell death (e.g., apoptosis).
  • One skilled in the art may refer to general reference texts for detailed descriptions of known techniques discussed herein or equivalent techniques. These texts include Ausubel et al, Current Protocols in Molecular Biology, John Wiley and Sons, Inc.
  • compositions suitable for administration can be incorporated into pharmaceutical compositions suitable for administration.
  • Such compositions typically comprise the compound (i.e., including the active compound), and a pharmaceutically acceptable excipient or carrier.
  • pharmaceutically acceptable excipient or “pharmaceutically acceptable carrier” is intended to include any and all solvents, dispersion media, coatings, antibacterial and antifungal agents, isotonic and absorption delaying agents, and the like, compatible with pharmaceutical administration. Suitable carriers are described in the most recent edition of Remington's Pharmaceutical Sciences, a standard reference text in the field.
  • Such carriers or diluents include, but are not limited to, water, saline, ringer's solutions, dextrose solution, and 5% human serum albumin.
  • Pharmaceutically acceptable carriers include solid carriers such as lactose, terra alba, sucrose, talc, gelatin, agar, pectin, acacia, magnesium stearate, stearic acid and the like.
  • Exemplary liquid carriers include syrup, peanut oil, olive oil, water and the like.
  • the carrier or diluent may include time-delay material known in the art, such as glyceryl monostearate or glyceryl distearate, alone or with a wax, ethylcellulose, hydroxypropylmethylcellulose, methylmethacrylate or the like.
  • time-delay material such as glyceryl monostearate or glyceryl distearate, alone or with a wax, ethylcellulose, hydroxypropylmethylcellulose, methylmethacrylate or the like.
  • Other fillers, excipients, flavorants, and other additives such as are known in the art may also be included in a pharmaceutical composition according to this invention.
  • Liposomes and non-aqueous vehicles such as fixed oils may also be used.
  • the use of such media and agents for pharmaceutically active substances is well known in the art. Except insofar as any conventional media or agent is incompatible with the active compound, use thereof in the compositions is contemplated.
  • compositions of this invention which are provided as part of the combination therapies may exist in the dosage form as a solid, semi-solid, or liquid such as, e.g., suspensions, aerosols or the like.
  • the compositions are administered in unit dosage forms suitable for single administration of precise dosage amounts.
  • the compositions may also include, depending on the formulation desired, pharmaceutically-acceptable, nontoxic carriers or diluents, which are defined as vehicles commonly used to formulate pharmaceutical compositions for animal or human administration. The diluent is selected so as not to affect the biological activity of the combination.
  • diluents examples include distilled water, physiological saline, Ringer's solution, dextrose solution, and Hank's solution.
  • a prefereed carrier for the solubilization of ⁇ -lapachone is hydroxypropyl beta cyclodextrin, a water solubilizing carrier molecule.
  • Other water-solubilizing agents for combining with ⁇ -lapachone and/or an S-phase compound, such as Poloxamer, Povidone K17, Povidone K12, Tween 80, ethanol, Cremophor/ethanol, polyethylene glycol 400, propylene glycol and Trappsol, are contemplated.
  • the invention is not limited to water-solubilizing agents, and oil- based solubilizing agents such as lipiodol and peanut oil, may also be used.
  • the pharmaceutical composition or fonnulation may also include other carriers, adjuvants, or nontoxic, nontherapeutic, nonimmunogenic stabilizers and the like. Effective amounts of such diluent or carrier will be those amounts which are effective to obtain a pharmaceutically acceptable formulation in terms of solubility of components, or biological activity, and the like.
  • Liposome formulations are also contemplated by the present invention, and have been described. See, e.g., U.S. Pat. No. 5,424,073.
  • the Gl/S phase drugs or compounds, or derivatives or analogs thereof, and the S phase drugs or compounds, or derivatives or analogs thereof, described herein include their pharmacologically acceptable salts, preferably sodium; analogs containing halogen substitutions, preferably chlorine or fluorine; analogs containing ammonium or substituted ammonium salts, preferably secondary or tertiary ammonium salts; analogs containing alkyl, alkenyl, aryl or their alkyl, alkenyl, aryl, halo, alkoxy, alkenyloxy substituted derivatives, preferably methyl, methoxy, ethoxy, or phenylacetate; and natural analogs such as naphthyl acetate.
  • Gl/S phase compounds or derivatives or analogs thereof, and the S phase compounds or derivatives or analogs thereof, described herein may be conjugated to a water-soluble polymer or may be derivatized with water-soluble chelating agents or radionuclides.
  • water soluble polymers are, but not limited to: polyglutamic acid polymer, copolymers with polycaprolactone, polyglycolic acid, polyactic acid, polyacrylic acid, poly (2-hydroxyethyl 1-glutamine), carboxymethyl dextran, hyaluronic acid, human serum albumin, polyalginic acid or a combination thereof.
  • water-soluble chelating agents are, but not limited to: DIP A (diethylenetriaminepentaacetic acid), EDTA, DTTP, DOT A or their water-soluble salts, etc.
  • radionuclides include, but not limited to: fti, 90 Y, 166 Ho, 68 Ga, 99 " ! Tc, and the like. Due to the water insolubility of ⁇ -lapachone, pharmaceutical carriers or solubilizing agents may be used to provide sufficient quantities of ⁇ -lapachone for use in the treatment methods of the present invention. See, e.g., U.S. Patent Publication 20030091639 to Jiang et al, and U.S.
  • Patent Publication 20040001871 to Boothman et al. This publication describes the use of complexing agents such as cyclodextrins, including hydroxypropyl beta-cyclodextrin (HPBCD), to permit the solubilization of ⁇ -lapachone at levels sufficient for administration. See also U.S. Patent Publication 20040001871 to Boothman et al.
  • complexing agents such as cyclodextrins, including hydroxypropyl beta-cyclodextrin (HPBCD)
  • the Gl/S phase drug, or an analog or derivative thereof is administered with a pharmaceutically acceptable water solubilizing carrier molecule selected from the group consisting of Poloxamer, Povidone K17, Povidone K12, Tween 80, ethanol, Cremophor/ethanol, polyethylene glycol (PEG) 400, propylene glycol, Trappsol, alpha-cyclodextrin or derivatives or analogs thereof, beta-cyclodextrin or derivatives or analogs thereof, and gamma-cyclodextrin or derivatives or analogs thereof.
  • a pharmaceutically acceptable water solubilizing carrier molecule selected from the group consisting of Poloxamer, Povidone K17, Povidone K12, Tween 80, ethanol, Cremophor/ethanol, polyethylene glycol (PEG) 400, propylene glycol, Trappsol, alpha-cyclodextrin or derivatives or analogs thereof, beta-cyclodextrin or derivatives or analogs thereof, and gamma
  • a compound of the present invention, or a pharmaceutically acceptable salt, prodrug, metabolite, analog or derivative thereof is administered in a suitable dosage form prepared by combining a therapeutically effective amount (e.g., an efficacious level sufficient to achieve the desired therapeutic effect through inhibition of tumor growth, killing of tumor cells, treatment or prevention of cell proliferative disorders, etc.) of a compound of the present invention, or a pharmaceutically acceptable salt, prodrug, metabolite, analog or derivative thereof, (as an active ingredient) with standard pharmaceutical carriers or diluents according to conventional procedures (i. e. , by producing a pharmaceutical composition of the invention).
  • a therapeutically effective amount e.g., an efficacious level sufficient to achieve the desired therapeutic effect through inhibition of tumor growth, killing of tumor cells, treatment or prevention of cell proliferative disorders, etc.
  • standard pharmaceutical carriers or diluents i. e. , by producing a pharmaceutical composition of the invention.
  • a pharmaceutical composition of the invention is formulated to be compatible with its intended route of administration.
  • routes of administration include parenteral, e.g. , intravenous, intradermal, subcutaneous, oral (e.g.,, inhalation), transdermal (topical), and transmucosal administration.
  • parenteral e.g. , intravenous, intradermal, subcutaneous, oral (e.g.,, inhalation), transdermal (topical), and transmucosal administration.
  • intravenous administration is prefereed as discussed above, the invention is not intended to be limited in this respect, and the compounds can be administered by any means known in the art.
  • Such modes include oral, rectal, nasal, topical (including buccal and sublingual) or parenteral (including subcutaneous, intramuscular, intravenous and intradermal) administration.
  • oral administration is generally preferred. However, oral administration may require the administration of a higher dose than intravenous administration. The skilled artisan can determine which form of administration is best in a particular case, balancing dose needed versus the number of times per month administration is necessary.
  • Solutions or suspensions used for parenteral, intradermal, or subcutaneous application can include the following components: a sterile diluent such as water for injection, saline solution, fixed oils, polyethylene glycols, glycerine, propylene glycol or other synthetic solvents; antibacterial agents such as benzyl alcohol or methyl parabens; antioxidants such as ascorbic acid or sodium bisulfite; chelating agents such as ethylenediammetetraacetic acid; buffers such as acetates, citrates or phosphates, and agents for the adjustment of tonicity such as sodium chloride or dextrose.
  • the pH can be adjusted with acids or bases, such as hydrochloric acid or sodium hydroxide.
  • parenteral preparation can be enclosed in ampoules, disposable syringes or multiple dose vials made of glass or plastic.
  • Solutions or suspensions used for parenteral, intradennal, or subcutaneous application can include the following components: a sterile diluent such as water for injection, saline solution, fixed oils, polyethylene glycols, glycerine, propylene glycol or other synthetic solvents; antibacterial agents such as benzyl alcohol or methyl parabens; antioxidants such as ascorbic acid or sodium bisulfite; chelating agents such as ethylenediammetetraacetic acid; buffers such as acetates, citrates or phosphates, and agents for the adjustment of tonicity such as sodium chloride or dextrose.
  • a sterile diluent such as water for injection, saline solution, fixed oils, polyethylene glycols, glycerine, propylene glycol or other synthetic solvents
  • antibacterial agents such as benzy
  • the pH can be adjusted with acids or bases, such as hydrochloric acid or sodium hydroxide.
  • the parenteral preparation can be enclosed in ampoules, disposable syringes or multiple dose vials made of glass or plastic.
  • a compound or pharmaceutical composition of the invention can be administered to a subject in many of the well-known methods cureently used for chemotherapeutic treatment.
  • a compound of the invention may be injected directly into tumors, injected into the blood stream or body cavities or taken orally or applied through the skin with patches.
  • the dose chosen should be sufficient to constitute effective treatment but not so high as to cause unacceptable side effects.
  • the state of the disease condition e.g., cancer, precancer, and the like
  • the term "therapeutically effective amount,” as used herein, refers to an amount of a pharmaceutical agent to treat, ameliorate, or prevent an identified disease or condition, or to exhibit a detectable therapeutic or inhibitory effect. The effect can be detected by any assay method known in the art.
  • the precise effective amount for a subject will depend upon the subject's body weight, size, and health; the nature and extent of the condition; and the therapeutic or combination of therapeutics selected for administration. Therapeutically effective amounts for a given situation can be determined by routine experimentation that is within the skill and judgment of the clinician.
  • the disease or condition to be treated is cancer.
  • the disease or condition to be treated is a cell proliferative disorder.
  • the therapeutically effective amount can be estimated initially either in cell culture assays, e.g., of neoplastic cells, or in animal models, usually rats, mice, rabbits, dogs, or pigs. The animal model may also be used to determine the appropriate concentration range and route of administration. Such information can then be used to determine useful doses and routes for administration in humans.
  • Therapeutic/prophylactic efficacy and toxicity may be determined by standard pharmaceutical procedures in cell cultures or experimental animals, e.g., ED 5 o (the dose therapeutically effective in 50% of the population) and LD 5 o (the dose lethal to 50%) of the population).
  • the dose ratio between therapeutic and toxic effects is the therapeutic index, and it can be expressed as the ratio, ED 5 o/LD 5 o.
  • Pharmaceutical compositions that exhibit large therapeutic indices are prefereed.
  • the dosage may vary within this range depending upon the dosage form employed, sensitivity of the patient, and the route of administration. Dosage and administration are adjusted to provide sufficient levels of the active agent(s) or to maintain the desired effect.
  • Factors which may be taken into account include the severity of the disease state, general health of the subject, age, weight, and gender of the subject, diet, time and frequency of administration, drug combination(s), reaction sensitivities, and tolerance/response to therapy.
  • Long-acting pharmaceutical compositions may be administered every 3 to 4 days, every week, or once every two weeks depending on half-life and clearance rate of the particular formulation.
  • the pharmaceutical compositions containing active compounds of the present invention may be manufactured in a manner that is generally known, e.g., by means of conventional mixing, dissolving, granulating, dragee-making, levigating, emulsifying, encapsulating, entrapping, or lyophilizing processes.
  • compositions may be formulated in a conventional manner using one or more pharmaceutically acceptable carriers comprising excipients and/or auxiliaries that facilitate processing of the active compounds into preparations that can be used pharmaceutically.
  • pharmaceutically acceptable carriers comprising excipients and/or auxiliaries that facilitate processing of the active compounds into preparations that can be used pharmaceutically.
  • suitable formulation is dependent upon the route of administration chosen.
  • Pharmaceutical compositions suitable for injectable use include sterile aqueous solutions (where water soluble) or dispersions and sterile powders for the extemporaneous preparation of sterile injectable solutions or dispersion.
  • suitable carriers include physiological saline, bacteriostatic water, Cremophor ELTM (BASF, Parsippany, N. J.) or phosphate buffered saline (PBS).
  • the carrier can be a solvent or dispersion medium containing, for example, water, ethanol, polyol (for example, glycerol, propylene glycol, and liquid polyethylene glycol, and the like), and suitable mixtures thereof.
  • the proper fluidity can be maintained, for example, by the use of a coating such as lecithin, by the maintenance of the required particle size in the case of dispersion and by the use of surfactants.
  • Prevention of the action of microorganisms can be achieved by various antibacterial and antifungal agents, for example, parabens, chlorobutanol, phenol, ascorbic acid, thimerosal, and the like.
  • isotonic agents for example, sugars, polyalcohols such as manitol, sorbitol, sodium chloride in the composition.
  • Prolonged absorption of the injectable compositions can be brought about by including in the composition an agent which delays absorption, for example, aluminum monostearate and gelatin.
  • Sterile injectable solutions can be prepared by incorporating the active compound in the required amount in an appropriate solvent with one or a combination of ingredients enumerated above, as required, followed by filtered sterilization.
  • dispersions are prepared by incorporating the active compound into a sterile vehicle that contains a basic dispersion medium and the required other ingredients from those enumerated above.
  • sterile powders for the preparation of sterile injectable solutions, methods of preparation are vacuum drying and freeze-drying that yields a powder of the active ingredient plus any additional desired ingredient from a previously sterile-filtered solution thereof.
  • Oral compositions generally include an inert diluent or an edible pharmaceutically acceptable carrier. They can be enclosed in gelatin capsules or compressed into tablets.
  • the active compound can be incorporated with excipients and used in the form of tablets, troches, or capsules.
  • Oral compositions can also be prepared using a fluid carrier for use as a mouthwash, wherein the compound in the fluid carrier is applied orally and swished and expectorated or swallowed.
  • Pharmaceutically compatible binding agents, and/or adjuvant materials can be included as part of the composition.
  • the tablets, pills, capsules, troches and the like can contain any of the following ingredients, or compounds of a similar nature: a binder such as macrocrystalline cellulose, gum tragacanth or gelatin; an excipient such as starch or lactose, a disintegrating agent such as alginic acid,
  • Primogel, or corn starch a lubricant such as magnesium stearate or Sterotes; a glidant such as colloidal silicon dioxide; a sweetening agent such as sucrose or saccharin; or a flavoring agent such as peppermint, methyl salicylate, or orange flavoring.
  • the compounds are delivered in the form of an aerosol spray from pressured container or dispenser, which contains a suitable propellant, e.g., a gas such as carbon dioxide, or a nebulizer.
  • a suitable propellant e.g., a gas such as carbon dioxide, or a nebulizer.
  • Systemic administration can also be by transmucosal or transdermal means.
  • penetrants appropriate to the barrier to be permeated are used in the formulation.
  • Such penetrants are generally known in the art, and include, for example, for transmucosal administration, detergents, bile salts, and fusidic acid derivatives. Transmucosal administration can be accomplished through the use of nasal sprays or suppositories.
  • the active compounds are formulated into ointments, salves, gels, or creams as generally known in the art.
  • the active compounds are prepared with pharmaceutically acceptable carriers that will protect the compound against rapid elimination from the body, such as a controlled release formulation, including implants and microencapsulated delivery systems.
  • Biodegradable, biocompatible polymers can be used, such as ethylene vinyl acetate, polyanhydrides, polyglycolic acid, collagen, polyorthoesters, and polylactic acid. Methods for preparation of such formulations will be apparent to those skilled in the art. The materials can also be obtained commercially from Alza Corporation and Nova Pharmaceuticals, Inc. Liposomal suspensions (including liposomes targeted to infected cells with monoclonal antibodies to viral antigens) can also be used as pharmaceutically acceptable carriers. These can be prepared according to methods known to those skilled in the art, for example, as described in U.S. Pat. No. 4,522,811. It is especially advantageous to formulate oral or parenteral compositions in dosage unit form for ease of administration and uniformity of dosage.
  • Dosage unit form as used herein refers to physically discrete units suited as unitary dosages for the subject to be treated; each unit containing a predetermined quantity of active compound calculated to produce the desired therapeutic effect in association with the required pharmaceutical carrier.
  • the specification for the dosage unit forms of the invention are dictated by and directly dependent on the unique characteristics of the active compound and the particular therapeutic effect to be achieved.
  • the dosages of the pharmaceutical compositions used in accordance with the invention vary depending on the agent, the age, weight, and clinical condition of the recipient patient, and the experience and judgment of the clinician or practitioner administering the therapy, among other factors affecting the selected dosage.
  • the dose should be sufficient to result in slowing, and preferably regressing, the growth of the tumors and also preferably causing complete regression of the cancer.
  • Dosages can range from about 0.01 mg/kg per day to about 3000 mg/kg per day. In prefereed aspects, dosages can range from about 1 mg/kg per day to about 1000 mg/kg per day.
  • the dose will be in the range of about 0.1 mg/day to about 70 g/day; about 0.1 mg/day to about 25 g/day; about 0.1 mg/day to about 10 g/day; about 0.1 mg to about 3g/day; or about 0.1 mg to about 1 g/day, in single, divided, or continuous doses (which dose may be adjusted for the patient's weight in kg, body surface area in m 2 , and age in years).
  • An effective amount of a pharmaceutical agent is that which provides an objectively identifiable improvement as noted by the clinician or other qualified observer. For example, regression of a tumor in a patient may be measured with reference to the diameter of a tumor. Decrease in the diameter of a tumor indicates regression.
  • the term "dosage effective manner" refers to amount of an active compound to produce the desired biological effect in a subject or cell.
  • a compound of the present invention may be administered in combination with an S phase compound, such as an gemcitabine, in any manner found appropriate by a clinician in generally accepted efficacious dose ranges, such as those described in the Physician 's Desk Reference, 59 th Edition, Thomson PDR (2005)("PDR").
  • gemcitabine is administered intravenously at dosages from about 10 mg/m 2 to about 10,000 mg/m 2 , preferably from about 100 mg/m 2 to about 2000 mg/m 2 , and most preferably about 500 to about 1500 mg/m 2 .
  • gemcitabine is administered intravenously at a dosage from approximately 100 mg/m 2 to about 2000 mg/m 2 . In an embodiment, gemcitabine is administered intravenously at a dosage of approximately 1000 mg/m 2 . Dosage can be repeated, e.g., once weekly, preferably for about 1 to 6 weeks. It is prefereed that dosages be administered over a time period of about 30 minutes to about 6 hours, and typically over a period of about 3 hours.
  • the S phase drug such as an gemcitabine, will be administered in a similar regimen with a Gl/S phase drug, such as ⁇ -lapachone or an analog or derivative thereof, although the amounts will preferably be reduced from that normally administered.
  • the gemcitabine be administered at the same time or after the ⁇ -lapachone has administered to the patient.
  • the gemcitabine is advantageously administered about 24 hours after the ⁇ -lapachone has been administered.
  • the combination therapy agents described herein may be administered singly and sequentially, or in a cocktail or combination containing both agents or one of the agents with other therapeutic agents, including but not limited to, immunosuppressive agents, potentiators and side-effect relieving agents.
  • the therapeutic combination if administered sequentially, may be more effective when the Gl/S phase drug component (e.g., ⁇ -lapachone) is administered prior to the S phase drug, e.g., gemcitabine.
  • the Gl/S phase drug component e.g., ⁇ -lapachone
  • a dose of the Gl/S phase drag component is administered at least one hour (more preferably at least 2 hours, 4 hours, 8 hours, 12 hours, or 24 hours) prior to administration of a dose of the S phase drug, e.g., gemcitabine.
  • a dose of the Gl/S phase drug component is administered at least one hour (more preferably at least 2 hours, 4 hours, 8 hours, 12 hours, or 24 hours) following administration of a dose of the S phase drug, e.g., gemcitabine.
  • the therapeutic agents will preferably be administered intravenously or otherwise systemically by injection intramuscularly, subcutaneously, intrathecally or intraperitoneally.
  • the S phase drag is administered simultaneously with or following administration of the Gl/S phase drug.
  • the S phase drag is administered following administration of the Gl/S phase drug, h another embodiment, the S drag is administered within 24 hours after the Gl/S phase drug is admimstered.
  • the other component of the combination therapy for combination with the S phase drag or compound is the Gl/S phase drag, which is preferably ⁇ -lapachone or an analog or derivative thereof.
  • ⁇ -lapachone has been shown to have a variety of pharmacological effects
  • ⁇ -lapachone has been shown to be a DNA repair inhibitor which sensitizes cells to DNA damaging agents
  • ⁇ -lapachone is generally well-tolerated in dogs, rats, and mice.
  • the present invention provides a method of treating cancer or a precancerous condition or preventing cancer in a subject, the method comprising administering to the subject a therapeutically effective amount of a pharmaceutical composition comprising ⁇ -lapachone, or a derivative or analog thereof, or pharmaceutically acceptable salt thereof, or a metabolite thereof, and a pharmaceutically acceptable carrier such that the composition maintains a plasma concentration of about 0.15 ⁇ M to about 50 ⁇ M and treats the cancer or precancerous condition or prevents the cancer.
  • the plasma concentration can be about 0.1 ⁇ M to about 100 ⁇ M, about 0.125 ⁇ M to about 75 ⁇ M; about 0.15 ⁇ M to about 50 ⁇ M; about 0.175 ⁇ M to about 30 ⁇ M; and about 0.2 ⁇ M to about 20 ⁇ M.
  • the pharmaceutical composition can maintain a suitable plasma concentration for at least a month, at least a week, at least 24 hours, at least 12 hrs, at least 6 lirs, at least 1 hour.
  • a suitable plasma concentration of the pharmaceutical composition can be maintained indefinitely.
  • the subject can be exposed to the pharmaceutical composition in a AUC (area under the curve) range of about 0.5 ⁇ M-hr to about 100 ⁇ M-hr, about 0.5 ⁇ M-hr to about 50 ⁇ M-hr, about 1 ⁇ M-hr to about 25 ⁇ M-hr, about 1 ⁇ M-hr to about 10 ⁇ M-hr; about 1.25 ⁇ M-hr to about 6.75 ⁇ M-hr, about 1.5 ⁇ M-hr to about 6.5 ⁇ M-hr.
  • AUC area under the curve
  • the pharmaceutical composition can be administered at a dosage from about 2 mg/m 2 to 5000 mg/m 2 per day, more preferably from about 20 mg/m 2 to 2000 mg/m 2 per day, more preferably from about 20 mg/m 2 to 500 mg/m 2 per day, most preferably from about 30 to 300 mg/m 2 per day.
  • 2 mg/m 2 to 5000 mg/m 2 per day is the administered dosage for a human.
  • the pharmaceutical composition can be administered at a dosage from about 10 to 1,000,000 ⁇ g per kilogram body weight of recipient per day; preferably about 100 to 500,000 ⁇ g per kilogram body weight of recipient per day, more preferably from about 1000 to 250,000 ⁇ g per kilogram body weight of recipient per day, most preferably from about 10,000 to 150,000 ⁇ g per kilogram body weight of recipient per day.
  • One of ordinary skill in the art can determine the appropriate dosage amount in mg/m 2 per day or ⁇ g per kilogram body weight of recipient per day depending on subject to which the pharmaceutical composition is to he administered. As with the use of other chemotherapeutic drugs, the individual patient will be monitored in a manner deemed appropriate by the treating physician.
  • Dosages can also be reduced if severe neutropenia or severe peripheral neuropathy occurs, or if a grade 2 or higher level of mucositis is observed, using the Common Toxicity Criteria of the National Cancer Institute.
  • a Gl/S phase compound such as ⁇ -lapachone
  • the normal dose of such compound individually is utilized as set forth above.
  • a lower dosage preferably 75 % or less of the individual amount, more preferably 50% or less, still more preferably 40% or less.
  • effective amount refers to an amount effective to treat the disease condition in combination with any other active agent in a combination regimen according to the invention.
  • the dosages of the agents used in accordance with the invention vary depending on the agent, the age, weight, and clinical condition of the recipient patient, and the experience and judgment of the clinician or practitioner administering the therapy, among other factors affecting the selected dosage.
  • the dose should be sufficient to result in slowing, and preferably regressing, the growth of the tumors and also preferably causing complete regression of the cancer.
  • An effective amount of a pharmaceutical agent is that which provides an objectively identifiable improvement as noted by the clinician or other qualified observer.
  • Regression of a tumor in a patient is typically measured with reference to the diameter of a tumor. Decrease in the diameter of a tumor indicates regression. Regression is also indicated by failure of tumors to reoccur after treatment has stopped. In preferred embodiments, a decrease in tumor size or burden of at least 20%, more preferably 50%, 80%, 90%, 95% or 99% is prefereed.
  • the pharmaceutical compositions can be included in a container, pack, or dispenser together with instructions for administration.
  • ⁇ -lapachone induces cell death of the HT-29 and HCT-116 colon cancer cell lines in vitro. Exponentially growing cells are seeded at 250, 1000, or 5000 cells per well (2.5 ml) in six-well plates and allowed to attach for 24 hours, ⁇ -lapachone is dissolved at a concentration of 20 rnM in DMSO and diluted in complete media, ⁇ -lapachone (0.5 ml) is added at 6-fold the final concentration to a total volume of 3.0 ml/well. Control plates receive the same volume of DMSO alone. After a 4 hour exposure the drug is carefully removed, and drag-free medium is added.
  • Example 2 ⁇ -lapachone induces cell death in colon cancer cell lines in the NCI60 in vitro screen. ⁇ -lapachone is tested in the NCI in vitro screen of 60 cancer cell lines, which allows comparison with other anti-tumor agents under standardized conditions.
  • the NCI assays are performed under standardized conditions not designed to mimic the conditions of dosing and use the sulforhodamine B assay as the endpoint.
  • the NCI set of 60 lines includes nine colon cancer cell lines (COLO 205, DLD-1, HCC-2998, HCT-116, HCT-15, HT29, KM12, KM20L2, and SW-620).
  • ⁇ -lapachone is broadly active against many cell types, with LC 50 (loglO molar concentration causing 50% lethality) between -4.5 and -5.3, and mean of -5.07 across all cells.
  • LC 50 loglO molar concentration causing 50% lethality
  • mean of -5.07 across all cells When compared to many FDA approved chemotherapeutic agents for common cancer types with publicly available data, none of the compared approved drugs exceed the mean of ⁇ - lapachone across all cells and only mitoxantrone equals it.
  • Example 3 ⁇ -lapachone induces E2F expression in colon cancer cells.
  • Compounds of the present invention have demonstrated potent antiproliferative activity against a variety of cancer cell lines, including SW-480, HT-29, DLD1 and HCT-116 human colon carcinoma cells. Since ⁇ -lapachone selectively induces apoptosis in cancer cell lines and not in normal cells (Li et al, (2003) Proc Natl Acad Sci USA. 100(5): 2674-8), the present compounds were also tested in a panel of normal cell lines from a variety of tissues including NCM 460 normal colonic epithelial cells. Cell proliferation assays are performed as described previously (M ⁇ ller et al, (1996) J. Med. Chem.
  • Table 2 shows the concentrations of the compounds that inhibit 50% of cell growth (IC 5 o). As shown in Table 2, IC 5 o values in the low micromolar range and below were obtained for ⁇ -lapachone in three colon cancer cell lines tested.
  • Another effect of the compounds of the present invention is the induction or elevation of activity (e.g., elevation of the level) of at least one member of the E2F family of transcription factors. See Table 2. The tested compounds of the present invention do not exhibit apparent or significant toxic effects on normal colon cells in the assays utilized (See, Table 2).
  • a plus (“+”) symbol represents overexpression of E2F1 relative to a control.
  • Example 4. ⁇ -lapachone potently reduces mean tumor volume in a human colon cancer xenograft mouse model. Anti-tumor activity of ⁇ -lapachone is examined using a human colon cancer xenograft model. Athymic female nude mice (Ncr) are inoculated subcutaneously with 2x10 6 HT-29 human colon cancer cells, and the tumors are allowed to grow to 80 mm 3 in size. The animals are randomized into three groups.

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Abstract

La présente invention fournit des procédés qui utilisent des agents efficaces dans le traitement du cancer du colon et des affections précancéreuses du colon. De plus, la présente invention fournit des agents capables de servir d'inhibiteur de la prolifération des cellules dans des cellules du colon.
EP05723505A 2004-02-20 2005-02-18 Utilisation de beta-lapachone pour le traitement du cancer du colon Ceased EP1732539A2 (fr)

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Family Cites Families (15)

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Publication number Priority date Publication date Assignee Title
US4522811A (en) 1982-07-08 1985-06-11 Syntex (U.S.A.) Inc. Serial injection of muramyldipeptides and liposomes enhances the anti-infective activity of muramyldipeptides
DK0706373T3 (da) 1992-03-23 2000-09-18 Univ Georgetown Liposomindkapslet taxol og en fremgangsmåde til anvendelse heraf
WO1994004145A1 (fr) 1992-08-21 1994-03-03 Dana Farber Cancer Institute Traitement d'infections virales chez l'homme
US5763625A (en) 1995-04-25 1998-06-09 Wisconsin Alumni Research Foundation Synthesis and use of β-lapachone analogs
US6245807B1 (en) 1995-08-24 2001-06-12 Dana-Farber Cancer Institute Treatment of human prostate disease
US5824700A (en) 1996-02-20 1998-10-20 Wisconsin Alumni Research Foundation Ortho-quinone derivatives novel synthesis therefor and their use in the inhibition of neoplastic cell growth
ATE342054T1 (de) 1999-04-14 2006-11-15 Dana Farber Cancer Inst Inc Verfahren und zusammansetzung zur behandlung von krebs
MXPA02011218A (es) * 2000-05-15 2004-08-19 Celgene Corp Composiciones y metodos para el tratamiento de cancer.
JP4244141B2 (ja) 2000-11-07 2009-03-25 デイナ ファーバー キャンサー インスティチュート，インコーポレイテッド 血液腫瘍および血液癌を処置する方法
US6458974B1 (en) 2001-01-25 2002-10-01 Cyclis Pharmaceuticals, Inc. Synthesis of β-lapachone and its intermediates
US6962944B2 (en) 2001-07-31 2005-11-08 Arqule, Inc. Pharmaceutical compositions containing beta-lapachone, or derivatives or analogs thereof, and methods of using same
WO2003090710A1 (fr) 2002-04-23 2003-11-06 Case Western Reserve University Systemes d'administration de lapachone, compositions de lapachone et utilisations associees
JP2005538981A (ja) 2002-07-17 2005-12-22 アーキュル， インコーポレイテッド 活性化チェックポイント療法およびこれらの使用方法
TW200510367A (en) 2002-11-18 2005-03-16 Arqule Inc Novel lapachone compounds, their preparation, and the use thereof
EP1575580A4 (fr) * 2002-12-02 2009-06-10 Arqule Inc Methodes de traitement de cancers

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* Cited by examiner, † Cited by third party
Title
See references of WO2005082355A2 *

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