WO2006110175A2 - Combined treatment with bortezomib and an epidermal growth factor receptor kinase inhibitor - Google Patents
Combined treatment with bortezomib and an epidermal growth factor receptor kinase inhibitor Download PDFInfo
- Publication number
- WO2006110175A2 WO2006110175A2 PCT/US2005/037324 US2005037324W WO2006110175A2 WO 2006110175 A2 WO2006110175 A2 WO 2006110175A2 US 2005037324 W US2005037324 W US 2005037324W WO 2006110175 A2 WO2006110175 A2 WO 2006110175A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- cancer
- bortezomib
- kinase inhibitor
- egfr kinase
- erlotinib
- Prior art date
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Classifications
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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- 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
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
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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
- A61K31/69—Boron compounds
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Definitions
- the present invention is directed to compositions and methods for treating cancer patients.
- the present invention is directed to methods for manufacturing medicaments comprising bortezomib and an epidermal growth factor receptor (EGFR) kinase inhibitor.
- EGFR epidermal growth factor receptor
- Cancer is a generic name for a wide range of cellular malignancies characterized by unregulated growth, lack of differentiation, and the ability to invade local tissues and metastasize. These neoplastic malignancies affect, with various degrees of prevalence, every tissue and organ in the body.
- DNA-alkylating agents e.g., cyclophosphamide, ifosfamide
- antimetabolites e.g., methotrexate, a folate antagonist, and 5-fluorouracil, a pyrimidine antagonist
- microtubule disrupters e.g., vincristine, vinblastine, paclitaxel
- DNA intercalators e.g., doxorubicin, daunomycin, cisplatin
- hormone therapy e.g., tamoxifen, flutamide
- lung cancer is the single largest cause of cancer deaths in the United States and is responsible for nearly 30% of cancer deaths in the country. According to the World Health Organization, there are more than 1.2 million cases worldwide of lung and bronchial cancer each year, causing approximately 1.1 million deaths annually. NSCLC is the most common form of lung cancer and accounts for almost 80 percent of all cases. Treatment options for lung cancer are surgery, radiation therapy, and chemotherapy, either alone or in combination, depending on the form and stage of the cancer. For advanced NSCLC, agents that have been shown to be active include cisplatin, carboplatin, paclitaxel, docetaxel, topotecan, irinotecan, vinorelbine, gemcitabine (e.g.
- Erlotinib HCl also known as OSI-774 or TarcevaTM
- OSI-774 or TarcevaTM is a quinazoline that inhibits the tyrosine kinase activity of EGFR and induces apoptosis and cell cycle arrest
- Cisplatin-containing and carboplatin- containing combination chemotherapy regimens have been shown to produce objective response rates that are higher than those achieved with single-agent chemotherapy (Weick, J.K., et al. (1991) J. Clin. Oncol. 9(7): 1157-1162). It has been reported that paclitaxel has single-agent activity in stage IV patients, with response rates in the range of 21% to 24% (Murphy W.K., et al. (1993) J. Natl. Cancer Inst. 85(5):384-388). Paclitaxel combinations have shown relatively high response rates, significant 1 year survival, and palliation of lung cancer symptoms (Johnson D.H., et al. (1996) J. Clin. Oncol.
- EGFR epidermal growth factor receptor
- EGFR stimulated signaling pathways promote multiple processes that are potentially cancer-promoting, e.g. proliferation, angiogenesis, cell motility and invasion, decreased apoptosis and induction of drug resistance.
- Activation of EGFR stimulated signaling pathways promote multiple processes that are potentially cancer-promoting, e.g. proliferation, angiogenesis, cell motility and invasion, decreased apoptosis and induction of drug resistance.
- the development for use as anti-tumor agents of compounds that directly inhibit the kinase activity of the EGFR, as well as antibodies that reduce EGFR kinase activity by blocking EGFR activation, are areas of intense research effort (de Bono J.S. and Rowinsky, E.K. (2002) Trends in MoI. Medicine 8:S19-S26; Dancey, J. and Sausville, E.A. (2003) Nature Rev. Drug Discovery 2:92-313).
- EGFR kinase inhibitors can improve tumor cell or neoplasia killing when used in combination with certain other anti-cancer or chemotherapeutic agents or treatments (e.g. Raben, D. et al. (2002) Semin. Oncol. 29:37-46; Herbst, R.S. et al. (2001) Expert Opin. Biol. Ther. 1:719-732; Magne, N et al. (2003) Clin. Can. Res. 9:4735-4732; Magne, N. et al.
- bortezomib Another novel compound with profound cytotoxicity against lung and other tumor cells is bortezomib (Adams, J. et al. (2003) Drug Discovery Today 8(7):307-315; Lenz, HJ. (2003) Cancer Treat. Rev. 29(Suppl.l):41-48).
- Bortezomib also known as Velcade® or PS- 341
- Velcade® a small molecule proteasome inhibitor that was recently approved by the FDA for treatment of refractory multiple myeloma. It has been reported that bortezomib has activity in NSCLC cell lines, where it was found to induce concentration and time-dependent G2/M cell cycle arrest (Ling, Y-H. et al. (2003) Clin. Cancer Res.
- An anti-neoplastic drug would ideally kill cancer cells selectively, with a wide therapeutic index relative to its toxicity towards non-malignant cells. It would also retain its efficacy against malignant cells, even after prolonged exposure to the drug.
- none of the current chemotherapies possess such an ideal profile. Instead, most possess very narrow therapeutic indexes.
- cancerous cells exposed to slightly sub-lethal concentrations of a chemotherapeutic agent will very often develop resistance to such an agent, and quite often cross-resistance to several other antineoplastic agents as well.
- This invention provides anti-cancer combination therapies that reduce the dosages for individual components required for efficacy, thereby decreasing side effects associated with each agent, while maintaining or increasing therapeutic value.
- the invention described herein provides new drug combinations, and methods for using drug combinations in the treatment of NSCLC and other cancers.
- the present invention provides a method for manufacturing a medicament intended for treating tumors or tumor metastases, characterized in that a therapeutically effective amount of an EGFR kinase inhibitor and bortezomib combination is used.
- a therapeutically effective amount of an EGFR kinase inhibitor and bortezomib is intended for administration to the patient simultaneously or sequentially, with or without additional agents or treatments, such as other anti-cancer drugs or radiation therapy.
- the invention also encompasses a pharmaceutical composition that is comprised of an EGFR kinase inhibitor and bortezomib combination in combination with a pharmaceutically acceptable carrier.
- a preferred example of an EGFR kinase inhibitor that can be used in practicing this invention is the compound erlotinib HCl (also known as TarcevaTM).
- Figure 1 Sensitivity of NSCLC cell lines to erlotinib and bortezomib.
- Figure 2 Combined cytotoxic effect of erlotinib and bortezomib on four human NSCLC cell lines (Combination Index (CI)).
- Figure 3 Combined effect of erlotinib and bortezomib on H358 blonchealveolar cell line. A) Fractional cell count plotted against time, B) Apoptosis percentage plotted for three time periods.
- cancer in an animal refers to the presence of cells possessing characteristics typical of cancer-causing cells, such as uncontrolled proliferation, immortality, metastatic potential, rapid growth and proliferation rate, and certain characteristic morphological features. Often, cancer cells will be in the form of a tumor, but such cells may exist alone within an animal, or may circulate in the blood stream as independent cells, such as leukemic cells.
- abnormal cell growth refers to cell growth that is independent of normal regulatory mechanisms (e.g., loss of contact inhibition). This includes the abnormal growth of: (1) tumor cells (tumors) that proliferate by expressing a mutated tyrosine kinase or overexpression of a receptor tyrosine kinase; (2) benign and malignant cells of other proliferative diseases in which aberrant tyrosine kinase activation occurs; (4) any tumors that proliferate by receptor tyrosine kinases; (5) any tumors that proliferate by aberrant serine/threonine kinase activation; and (6) benign and malignant cells of other proliferative diseases in which aberrant serine/threonine kinase activation occurs.
- treating means reversing, alleviating, inhibiting the progress of, or preventing, either partially or completely, the growth of tumors, tumor metastases, or other cancer-causing or neoplastic cells in a patient.
- treatment refers to the act of treating.
- a method of treating when applied to, for example, cancer refers to a procedure or course of action that is designed to reduce or eliminate the number of cancer cells in an animal, or to alleviate the symptoms of a cancer.
- a method of treating does not necessarily mean that the cancer cells or other disorder will, in fact, be eliminated, that the number of cells or disorder will, in fact, be reduced, or that the symptoms of a cancer or other disorder will, in fact, be alleviated.
- a method of treating cancer will be performed even with a low likelihood of success, but which, given the medical history and estimated survival expectancy of an animal, is nevertheless deemed an overall beneficial course of action.
- the term "therapeutically effective agent” means a composition that will elicit the biological or medical response of a tissue, system, animal or human that is being sought by the researcher, veterinarian, medical doctor or other clinician.
- the term "method for manufacturing a medicament” relates to the manufacturing of a medicament for use in the indication as specified herein and in particular for use in tumors, tumor metastases, ' or cancer in general.
- the term relates to the so-called “Swiss-type” claim format in the indication specified.
- terapéuticaally effective amount or “effective amount” means the amount of the subject compound or combination that will elicit the biological or medical response of a tissue, system, animal or human that is being sought by the researcher, veterinarian, medical doctor or other clinician.
- EGFR kinase inhibitor refers to any EGFR kinase inhibitor that is currently known in the art or that will be identified in the future, and includes any chemical entity that, upon administration to a patient, results in inhibition of a biological activity associated with activation of the EGF receptor in the patient, including any of the downstream biological effects otherwise resulting from the binding to EGFR of its natural ligand.
- Such EGFR kinase inhibitors include any agent that can block EGFR activation or any of the downstream biological effects of EGFR activation that are relevant to treating cancer in a patient. Such an inhibitor can act by binding directly to the intracellular domain of the receptor and inhibiting its kinase activity.
- such an inhibitor can act by occupying the ligand binding site or a portion thereof of the EGFR receptor, thereby making the receptor inaccessible to its natural ligand so that its normal biological activity is prevented or reduced.
- such an inhibitor can act by modulating the dimerization of EGFR polypeptides, or interaction of EGFR polypeptide with other proteins, or enhance ubiquitination and endocytotic degradation of EGFR.
- EGFR kinase inhibitors include but are not limited to low molecular weight inhibitors, antibodies or antibody fragments, antisense constructs, small inhibitory RNAs (i.e. RNA interference by dsRNA; RNAi), andribozymes.
- the EGFR kinase inhibitor is a small organic molecule or an antibody that binds specifically to the human EGFR.
- EGFR kinase inhibitor refers to any EGFR kinase inhibitor that is currently known in the art or that will be identified in the future, and includes any chemical entity that, upon administration to a patient, results in inhibition of a biological activity associated with activation of the EGF receptor in the patient, including any of the downstream biological effects otherwise resulting from the binding to EGFR of its natural ligand.
- Such EGFR kinase inhibitors include any agent that can block EGFR activation or any of the downstream biological effects of EGFR activation that are relevant to treating cancer in a patient. Such an inhibitor can act by binding directly to the intracellular domain of the receptor and inhibiting its kinase activity.
- such an inhibitor can act by occupying the ligand binding site or a portion thereof of the EGFR receptor, thereby making the receptor inaccessible to its natural ligand so that its normal biological activity is prevented or reduced.
- such an inhibitor can act by modulating the dimerization of EGFR polypeptides, or interaction of EGFR polypeptide with other proteins, or enhance ubiquitination and endocytotic degradation of EGFR.
- EGFR kinase inhibitors include but are not limited to low molecular weight inhibitors, antibodies or antibody fragments, antisense constructs, small inhibitory RNAs (i.e. RNA interference by dsRNA; RNAi), andribozymes.
- the EGFR kinase inhibitor is a small organic molecule or an antibody that binds specifically to the human EGFR.
- EGFR kinase inhibitors that include, for example quinazoline EGFR kinase inhibitors, pyrido-pyrimidine EGFR kinase inhibitors, pyrimido-pyrimidine EGFR kinase inhibitors, pyrrolo-pyrimidine EGFR kinase inhibitors, pyrazolo-pyrimidine EGFR kinase inhibitors, phenylamino-pyrimidine EGFR kinase inhibitors, oxindole EGFR kinase inhibitors, indolocarbazole EGFR kinase inhibitors, phthalazine EGFR kinase inhibitors, isofiavone EGFR kinase inhibitors, quinalone EGFR kinase inhibitors, and tyrphostin EGFR kinase inhibitors, such as those described in the following patent publications, and all pharmaceutically acceptable salts and solvates of
- Additional non-limiting examples of low molecular weight EGFR kinase inhibitors include any of the EGFR kinase inhibitors described in Traxler, P., 1998, Exp. Opin. Ther. Patents 8(12): 1599-1625.
- an "EGFR kinase inhibitor” is a preferably a compound of formula 1 : wherein ni is 1, 2, or 3; each R 1 is independently selected from hydrogen, halo, hydroxy, amino, hydroxyamino, carboxy, (Ci-C 4 )alkoxycarbonyl, nitro, guanidino, ureido, carbamoyl, cyano, trifluoromethyl,
- R 6 is hydrogen or R 5 wherein the R 5 S are the same or different;
- R 7 is R 5 , R 5 O or
- R 6 2 N
- A is selected from piperidino-, morpholino, pyrrolidine and 4-R 6 -piperazin-l-yl, imidazol-1-yl, 4-pyridon-l-yl, carboxy-(C r C 4 )-alkyl, phenoxy, phenyl, phenylsulfanyl, (C 2 -
- R 9 and R 6 are defined as above, and wherein the resulting groups are optionally substituted with halo or R 9 with the proviso that a nitrogen, oxygen or sulfur atom and another heteroatom cannot be attached to the same carbon atom, and with the further proviso that no more than three "R 9 " units may comprise R 1 ; or each R 1 is independently selected from R 5 -sulfonylamino, phthalimido-(C ! -C 4 )-alkylsulfonylamino, benzamido, benzenesulfonylamino,
- R 2 is selected from hydrogen and optionally substituted (Ci-C 6 )-alkyl; n is 1 or 2 and each R 3 is independently selected from hydrogen, (Cr C 6 )-alkyl, amino, halo, hydroxy;
- R 4 is azido or R ⁇ -ethynyl wherein R 11 is selected from hydrogen, optionally substituted (C 1 -
- the EGFR kinase inhibitor according to the invention relates to compounds of formula 1 wherein m, n, R 1 and R 3 are as defined above and R 2 is hydrogen and R 4 is R ⁇ -ethynyl wherein R 11 is selected from hydrogen, optionally substituted (Ci-C 6 )- alkyl wherein the substituents are selected from hydrogen, amino, hydroxy, R 5 O, R 5 NH and (R 5 ) 2 N or R 4 is azido.
- (R 6 ) 2 N(C O), R 5 ONH, R 5 S, (C r C 4 )-alkylsulfonylamino, phthalimido-(Ci-C 4 )-alkylsulfonylamino, 3-phenylureido, 2- oxopyrrolidin-1-yl, 2,5- dioxopyrrolidin-1-yl, halo-(C2-C 4 )-alkanoylamino, hydroxy-(C 2 -C 4 )- alkanoylamino, (C 2 -C 4 )-alkanoyloxy-(C 2 -C 4 )-alkanoylammo, (Ci-C 4 )-alkoxy-(C 2 -C 4 )-alkanoylamino, carboxy-(C 2 -C 4 )-alkanoylamino, (Ci-C 4 )-alkoxycarbonyl- (C 2
- low molecular weight EGFR kinase inhibitors that can be used according to the present invention include [6,7-bis(2-methoxyethoxy)-4-quinazolin-4- yl]-(3-ethynylphenyl) amine (also known as OSI-774, erlotinib, or TarcevaTM (erlotinib HCl); OSI Pharmaceuticals/Genentech/Roche) (U.S. Pat. No. 5,747,498; International Patent Publication No. WO 01/34574, and Mover, ID. et al. (1997) Cancer Res.
- CI- 1033 (formerly known as PD183805; Pfizer) (Sherwood et al., 1999, Proc. Am. Assoc. Cancer Res. 40:723); PD-158780 (Pfizer); AG-1478 (University of California); CGP-59326 (Novartis); PKI-166 (Novartis); EKB-569 (Wyeth); GW-2016 (also known as GW-572016 or lapatinib ditosylate ; GSK); and gefitinib (also known as ZDl 839 or IressaTM; Astrazeneca) (Woodburn et al., 1997, Proc. Am. Assoc. Cancer Res.
- a particularly preferred low molecular weight EGFR kinase inhibitor that can be used according to the present invention is [6,7-bis(2-methoxyethoxy)-4-quinazolin-4-yl]-(3-ethynylphenyl) amine (i.e. erlotinib), its hydrochloride salt (i.e. erlotinib HCl, TarcevaTM), or other salt forms (e.g. erlotinib mesylate).
- the EGFR kinase inhibitor according to the invention relates to the compound erlotinib HCl (also known as TarcevaTM).
- Preferred antibody-based EGFR kinase inhibitors include any anti-EGFR antibody or antibody fragment that can partially or completely block EGFR activation by its natural ligand.
- Non-limiting examples of antibody-based EGFR kinase inhibitors include those described in Modjtahedi, H., et al., 1993, Br. J. Cancer 67:247-253; Teramoto, T., et al., 1996, Cancer 77:639-645; Goldstein et al., 1995, Clin. Cancer Res. 1:1311-1318; Huang, S. M., et al., 1999, Cancer Res. 15:59(8):1935-40; and Yang, X., et al., 1999, Cancer Res.
- the EGFR kinase inhibitor can be monoclonal antibody Mab E7.6.3 (Yang, X.D. et al. (1999) Cancer Res. 59: 1236-43), or Mab C225 (ATCC Accession No. HB-8508), or an antibody or antibody fragment having the binding specificity thereof.
- Suitable monoclonal antibody EGFR kinase inhibitors include, but are not limited to, IMC-C225 (also known as cetuximab or ErbituxTM; Imclone Systems), ABX-EGF (Abgenix), EMD 72000 (Merck KgaA, Darmstadt), RH3 (York Medical Bioscience Inc.), and MDX-447 (Medarex/ Merck KgaA).
- Additional antibody-based EGFR kinase inhibitors can be raised according to known methods by administering the appropriate antigen or epitope to a host animal selected, e.g., from pigs, cows, horses, rabbits, goats, sheep, and mice, among others.
- a host animal selected, e.g., from pigs, cows, horses, rabbits, goats, sheep, and mice, among others.
- Various adjuvants known in the art can be used to enhance antibody production.
- Monoclonal antibodies against EGFR can be prepared and isolated using any technique that provides for the production of antibody molecules by continuous cell lines in culture. Techniques for production and isolation include but are not limited to the hybridoma technique originally described by Kohler and Milstein (Nature, 1975, 256: 495- 497); the human B-cell hybridoma technique (Kosbor et al., 1983, Immunology Today 4:72; Cote et al., 1983, Proc. Nati. Acad. Sci. USA 80: 2026-2030); and the EBV-hybridoma technique (Cole et al, 1985, Monoclonal Antibodies and Cancer Therapy, Alan R. Liss, Inc., pp. 77-96).
- Antibody-based EGFR kinase inhibitors useful in practicing the present invention also include anti-EGFR antibody fragments including but not limited to F(ab').sub.2 fragments, which can be generated by pepsin digestion of an intact antibody molecule, and Fab fragments, which can be generated by reducing the disulfide bridges of the F(ab').sub.2 fragments.
- Fab and/or scFv expression libraries can be constructed (see, e.g., Huse et al., 1989, Science 246: 1275-1281) to allow rapid identification of fragments having the desired specificity to EGFR.
- EGFR kinase inhibitors for use in the present invention can alternatively be based on antisense oligonucleotide constructs.
- Anti-sense oligonucleotides including anti-sense RNA molecules and anti-sense DNA molecules, would act to directly block the translation of EGFR mRNA by binding thereto and thus preventing protein translation or increasing mRNA degradation, thus decreasing the level of EGFR kinase protein, and thus activity, in a cell.
- antisense oligonucleotides of at least about 15 bases and complementary to unique regions of the mRNA transcript sequence encoding EGFR can be synthesized, e.g., by conventional phosphodiester techniques and administered by e.g., intravenous injection or infusion.
- Methods for using antisense techniques for specifically inhibiting gene expression of genes whose sequence is known are well known in the art (e.g. see U.S. Patent Nos. 6,566,135; 6,566,131; 6,365,354; 6,410,323; 6,107,091; 6,046,321; and 5,981,732).
- Small inhibitory RNAs can also function as EGFR kinase inhibitors for use in the present invention.
- EGFR gene expression can be reduced by contacting the tumor, subject or cell with a small double stranded RNA (dsRNA), or a vector or construct causing the production of a small double stranded RNA, such that expression of EGFR is specifically inhibited (i.e. RNA interference or RNAi).
- dsRNA small double stranded RNA
- RNAi RNA interference
- Methods for selecting an appropriate dsRNA or dsRNA-encoding vector are well known in the art for genes whose sequence is known (e.g. see Tuschi, T., et al. (1999) Genes Dev. 13(24):3191-3197; Elbashir, S.M.
- Ribozymes can also function as EGFR kinase inhibitors for use in the present invention.
- Ribo ⁇ ymes are enzymatic RNA molecules capable of catalyzing the specific cleavage of RNA.
- the mechanism of ribozyme action involves sequence specific hybridization of the ribozyme molecule to complementary target RNA, followed by endonucleolytic cleavage.
- Engineered hammerhead motif ribozyme molecules that specifically and efficiently catalyze endonucleolytic cleavage of EGFR mRNA sequences are thereby useful within the scope of the present invention.
- ribozyme cleavage sites within any potential RNA target are initially identified by scanning the target molecule for ribozyme cleavage sites, which typically include the following sequences, GUA, GUU, and GUC. Once identified, short RNA sequences of between about 15 and 20 ribonucleotides corresponding to the region of the target gene containing the cleavage site can be evaluated for predicted structural features, such as secondary structure, that can render the oligonucleotide sequence unsuitable. The suitability of candidate targets can also be evaluated by testing their accessibility to hybridization with complementary oligonucleotides, using, e.g., ribonuclease protection assays.
- Both antisense oligonucleotides and ribozymes useful as EGFR kinase inhibitors can be prepared by known methods. These include techniques for chemical synthesis such as, e.g., by solid phase phosphoramadite chemical synthesis. Alternatively, anti-sense RNA molecules can be generated by in vitro or in vivo transcription of DNA sequences encoding the RNA molecule. Such DNA sequences can be incorporated into a wide variety of vectors that incorporate suitable RNA polymerase promoters such as the T7 or SP6 polymerase promoters. Various modifications to the oligonucleotides of the invention can be introduced as a means of increasing intracellular stability and half-life.
- Possible modifications include but are not limited to the addition of flanking sequences of ribonucleotides or deoxyribonucleotides to the 5' and/or 3' ends of the molecule, or the use of phosphorothioate or 2'-O-methyl rather than phosphodiesterase linkages within the oligonucleotide backbone.
- the present invention provides a method for manufacturing a medicament intended for treating tumors or tumor metastases in a patient, characterized in that a therapeutically effective amount of an EGFR kinase inhibitor and bortezomib combination is used.
- such combination is intended for administration to the patient simultaneously or sequentially.
- the cancer present in the patient can be any of those referred to herein below, including NSCLC, colorectal cancer or pancreatic cancer.
- when the compounds are administered sequentially bortezomib is administered prior to the EGFR kinase inhibitor.
- the tumors or tumor metastases to be treated are colorectal tumors or tumor metastases.
- the administration of agents simultaneously can be performed by separately administering agents at the same time, or together as a fixed combination. Also, in any of the methods of the present invention, the administration of agents sequentially can be in any order. [44] Preferably, in addition, one or more other cytotoxic, chemotherapeutic or anti-cancer agents, or compounds that enhance the effects of such agents are used.
- additional other cytotoxic, chemotherapeutic or anticancer agents include, for example: alkylating agents or agents with an alkylating action, such as cyclophosphamide (CTX; e.g. Cytoxan®), chlorambucil (CHL; e.g. leukeran®), cisplatin (CisP; e.g. platinol®) busulfan (e.g.
- alkylating agents or agents with an alkylating action such as cyclophosphamide (CTX; e.g. Cytoxan®), chlorambucil (CHL; e.g. leukeran®), cisplatin (CisP; e.g. platinol®) busulfan (e.g.
- myleran® myleran®
- melphalan carmustine (BCNU)
- streptozotocin triethylenemelamine (TEM)
- mitomycin C and the like
- anti-metabolites such as methotrexate (MTX), etoposide (VP 16; e.g. vepesid®), 6-mercaptopurine (6MP), 6-thiocguanine (6TG), cytarabine (Ara-C), 5-fluorouracil (5-FU), capecitabine (e.g.Xeloda®), dacarbazine (DTIC), and the like
- antibiotics such as actinomycin D, doxorubicin (DXR; e.g.
- adriamycin® daunorubicin (daunomycin), bleomycin, mithramycin and the like
- alkaloids such as vinca alkaloids such as vincristine (VCR), vinblastine, and the like
- antitumor agents such as paclitaxel (e.g. taxol®) and pactitaxel derivatives, the cytostatic agents, glucocorticoids such as dexamethasone (DEX; e.g.
- decadron® and corticosteroids such as prednisone, nucleoside enzyme inhibitors such as hydroxyurea, amino acid depleting enzymes such as asparaginase, leucovorin and other folic acid derivatives, and similar, diverse antitumor agents.
- the following agents may also be used as additional agents: arnifostine (e.g. ethyol®), dactinomycin, mechlorethamine (nitrogen mustard), streptozocin, cyclophosphamide, lornustine (CCNU), doxorubicin lipo (e.g. doxil®), gemcitabine (e.g. gemzar®), daunorubicin lipo (e.g.
- daunoxome® procarbazine, mitomycin, docetaxel (e.g. taxotere®), aldesleukin, carboplatin, oxaliplatin, cladribine, camptothecin, CPT 11 (irinotecan), 10-hydroxy 7-ethyl- camptothecin (SN38), floxuridine, fludarabine, ifosfamide, idarubicin, mesna, interferon alpha, interferon beta, mitoxantrone, topotecan, leuprolide, megestrol, melphalan, mercaptopurine, plicamycin, mitotane, pegaspargase, pentostatin, pipobroman, plicamycin, tamoxifen, teniposide, testolactone, thioguanine, thiotepa, uracil mustard, vinorelbine, chlorambucil.
- taxotere® aldes
- the present invention further provides a method for manufacturing a medicament for treating tumors or tumor metastases, characterized in that a therapeutically effective amount of an EGFR kinase inhibitor and bortezomib combination is used and is intended for administration to the patient simultaneously or sequentially, wherein in addition, one or more anti-hormonal agents are used.
- anti-hormonal agent includes natural or synthetic organic or peptidic compounds that act to regulate or inhibit hormone action on tumors.
- Antihormonal agents include, for example: steroid receptor antagonists, anti- estrogens such as tamoxifen, raloxifene, aromatase inhibiting 4(5)-imidazoles, other aromatase inhibitors, 42-hydroxytamoxifen, trioxifene, keoxifene, LY 117018, onapristone, and toremifene (e.g.
- anti-androgens such as flutamide, nilutamide, bicalutamide, leuprolide, and goserelin; and pharmaceutically acceptable salts, acids or derivatives of any of the above; agonists and/or antagonists of glycoprotein hormones such as follicle stimulating hormone (FSH), thyroid stimulating hormone (TSH), and luteinizing hormone (LH) and LHRH (leuteinizing hormone-releasing hormone); the LHRH agonist goserelin acetate, commercially available as Zoladex® (AstraZeneca); the LHRH antagonist D-alaninamide N- acetyl-3 -(2-naphthalenyl)-D-alanyl-4-chloro-D-phenylalanyl-3 -(3 -pyridinyl)-D-alanyl-L- seryl-N6-( 3-pyridinylcarbonyl)-L-lysyl-N6-(3-pyridinyl
- cytotoxic and other anticancer agents described above in chemotherapeutic regimens is generally well characterized in the cancer therapy arts, and their use herein falls under the same considerations for monitoring tolerance and effectiveness and for controlling administration routes and dosages, with some adjustments.
- the actual dosages of the cytotoxic agents may vary depending upon the patient's cultured cell response determined by using histoculture methods. Generally, the dosage will be reduced compared to the amount used in the absence of additional other agents.
- Typical dosages of an effective cytotoxic agent can be in the ranges recommended by the manufacturer, and where indicated by in vitro responses or responses in animal models, can be reduced by up to about one order of magnitude concentration or amount.
- the actual dosage will depend upon the judgment of the physician, the condition of the patient, and the effectiveness of the therapeutic method based on the in vitro responsiveness of the primary cultured malignant cells or histocultured tissue sample, or the responses observed in the appropriate animal models.
- the any one or a combination of the compounds selected from the group of gemcitabine, cisplatin and carboplatin are preferred.
- the present invention further provides a method for manufacturing a medicament for treating tumors or tumor metastases in a patient, characterized in that a therapeutically effective amount of an EGFR kinase inhibitor and bortezomib combination is used and is intended for administration to the patient simultaneously or sequentially, wherein in addition one or more angiogenesis inhibitors are used.
- Anti-angiogenic agents include, for example: VEGFR inhibitors, such as SU-5416 and SU-6668 (Sugen Inc. of South San Francisco, Calif, USA), or as described in, for example International Application Nos. WO 99/24440, WO 99/62890, WO 95/21613, WO 99/61422, WO 98/50356, WO 99/10349, WO 97/32856, WO 97/22596, WO 98/54093, WO 98/02438, WO 99/16755, and WO 98/02437, and U.S. Patent Nos.
- VEGF inhibitors such as IM862 (Cytran Inc. of Kirkland, Wash., USA); angiozyme, a synthetic ribozyme from Ribozyme (Boulder, Colo.); and antibodies to VEGF, such as bevacizumab (e.g. AvastinTM, Genentech, South San Francisco, CA), a recombinant humanized antibody to VEGF; integrin receptor antagonists and integrin antagonists, such as to c ⁇ ft, o ⁇ s and Q ⁇ S 6 integrins, and subtypes thereof, e.g.
- cilengitide EMD 12191 ⁇
- anti-integrin antibodies such as for example c ⁇ ft specific humanized antibodies (e.g. Vitaxin®); factors such as IFN-alpha (U.S. Patent Nos. 41530,901, 4,503,035, and 5,231,176); angiostatin and plasminogen fragments (e.g. kringle 1- 4, kringle 5, kringle 1-3 (O'Reilly, M. S. et al. (1994) Cell 79:315-328; Cao et al. (1996) J. Biol. Chem. 271: 29461-29467; Cao et al. (1997) J. Biol. Chem.
- IFN-alpha U.S. Patent Nos. 41530,901, 4,503,035, and 5,231,176
- angiostatin and plasminogen fragments e.g. kringle 1- 4, kringle 5, kringle 1-3 (O'Reilly, M. S.
- PF4 platelet factor 4
- plasminogen activator/urokinase inhibitors plasminogen activator/urokinase inhibitors
- urokinase receptor antagonists heparinases
- fumagillin analogs such as TNP-4701
- suramin and suramin analogs angiostatic steroids
- bFGF antagonists flk-1 and flt-1 antagonists
- anti-angiogenesis agents such as MMP-2 (matrix-metalloproteinase 2) inhibitors and MMP-9 (matrix- metalloproteinase 9) inhibitors.
- MMP-2 matrix-metalloproteinase 2 inhibitors
- MMP-2 and MMP-9 inhibitors are those that have little or no activity inhibiting MMP-I. More preferred, are those that selectively inhibit MMP-2 and/or MMP-9 relative to the other matrix- metalloproteinases (i.e. MMP-I, MMP-3, MMP-4, MMP-5, MMP-6, MMP-7, MMP-8, MMP-IO 3 MMP-I l, MMP-12, and MMP-13).
- MMP-I matrix- metalloproteinases
- the present invention further provides a method for manufacturing a medicament for treating tumors or tumor metastases in a patient, characterized in that a therapeutically effective amount of an EGFR kinase inhibitor and bortezomib combination is used and is intended for administration to the patient simultaneously or sequentially, wherein in addition one or more tumor cell pro-apoptotic or apoptosis-stimulating agents are used.
- the present invention further provides a method for manufacturing a medicament for treating tumors or tumor metastases in a patient, characterized in that a therapeutically effective amount of an EGFR kinase inhibitor and bortezomib combination is used and is intended for administration to the patient simultaneously or sequentially, wherein in addition one or more signal transduction inhibitors are used.
- Signal transduction inhibitors include, for example: erbB2 receptor inhibitors, such as organic molecules, or antibodies that bind to the erbB2 receptor, for example, trastuzumab (e.g. Herceptin®); inhibitors of other protein tyrosine-kinases, e.g. imitinib (e.g. Gleevec®); ras inhibitors; raf inhibitors; MEK inhibitors; mTOR inhibitors; cyclin dependent kinase inhibitors; protein kinase C inhibitors; and PDK-I inhibitors (see Dancey, J. and Sausville, E. A. (2003) Nature Rev. Drug Discovery 2:92-313, for a description of several examples of such inhibitors, and their use in clinical trials for the treatment of cancer).
- trastuzumab e.g. Herceptin®
- inhibitors of other protein tyrosine-kinases e.g. imitinib (e.g. Gleevec
- ErbB2 receptor inhibitors include, for example: ErbB2 receptor inhibitors, such as GW-282974 (Glaxo Wellcome pic), monoclonal antibodies such as AR-209 (Aronex Pharmaceuticals Inc. of The Woodlands, Tex., USA) and erbB2 inhibitors such as those described in International Publication Nos. WO 98/02434, WO 99/35146, WO 99/35132, WO 98/02437, WO 97/13760, and WO 95/19970, and U.S. Patent Nos. 5,587,458, 5,877,305, 6,465,449 and 6,541,481.
- the present invention further provides a method for manufacturing a medicament for treating tumors or tumor metastases in a patient, characterized in that a therapeutically effective amount of an EGFR kinase inhibitor and bortezomib combination is used and is intended for administration to the patient simultaneously or sequentially, wherein in addition an anti-HER2 antibody or an immunotherapeutically active fragment thereof is used.
- the present invention further provides a method for manufacturing a medicament for treating tumors or tumor metastases in a patient, characterized in that a therapeutically effective amount of an EGFR kinase inhibitor and bortezomib combination is used and is intended for administration to the patient simultaneously or sequentially, wherein in addition one or more anti-proliferative agents are used.
- Additional antiproliferative agents include, for example: Inhibitors of the enzyme farnesyl protein transferase and inhibitors of the receptor tyrosine kinase PDGFR, including the compounds disclosed and claimed in U.S. patent Nos. 6,080,769, 6,194,438, 6,258,824, 6,586,447, 6,071,935, 6,495,564, 6,150,377, 6,596,735 and 6,479,513, and International Patent Publication WO 01/40217.
- the present invention further provides a method for manufacturing a medicament for treating tumors or tumor metastases in a patient, characterized in that a therapeutically effective amount of an EGFR kinase inhibitor and bortezomib combination is used and is intended for administration to the patient simultaneously or sequentially, wherein in addition a COX II (cyclooxygenase II ) inhibitor is used.
- COX II cyclooxygenase II
- useful COX-II inhibitors include alecoxib (e.g. CelebrexTM), valdecoxib, and rofecoxib.
- the present invention further provides a method for manufacturing a medicament for treating tumors or tumor metastases in a patient, characterized in that a therapeutically effective amount of an EGFR kinase inhibitor and bortezomib combination is used and is intended for administration to the patient simultaneously or sequentially, wherein in addition treatment with an effective amount of ionizing radiation is carried out and/or a radiopharmaceutical is used.
- the source of radiation can be either external or internal to the patient being treated.
- the therapy is known as external beam radiation therapy (EBRT).
- EBRT external beam radiation therapy
- BT brachytherapy
- Radioactive atoms for use in the context of this invention can be selected from the group including, but not limited to, radium, cesium- 137, iridium-192, americium- 241, gold-198, cobalt-57, copper-67, technetium-99, iodine- 123, iodine-131, and indium-I l l.
- Radiation therapy is a standard treatment for controlling unresectable or inoperable tumors and/or tumor metastases. Improved results have been seen when radiation therapy has been combined with chemotherapy. Radiation therapy is based on the principle that high-dose radiation delivered to a target area will result in the death of reproductive cells in both tumor and normal tissues. The radiation dosage regimen is generally defined in terms of radiation absorbed dose (Gy), time and fractionation, and must be carefully defined by the oncologist.
- the amount of radiation a patient receives will depend on various considerations, but the two most important are the location of the tumor in relation to other critical structures or organs of the body, and the extent to which the tumor has spread.
- a typical course of treatment for a patient undergoing radiation therapy will be a treatment schedule over a 1 to 6 week period, with a total dose of between 10 and 80 Gy administered to the patient in a single daily fraction of about 1.8 to 2.0 Gy, 5 days a week.
- the inhibition of tumor growth by means of the agents comprising the combination of the invention is enhanced when combined with radiation, optionally with additional chemotherapeutic or anticancer agents.
- Parameters of adjuvant radiation therapies are, for example, contained in International Patent Publication WO 99/60023.
- the present invention further provides a method for manufacturing a medicament for treating tumors or tumor metastases in a patient, characterized in that a therapeutically effective amount of an EGFR kinase inhibitor and bortezomib combination is used and is intended for administration to the patient simultaneously or sequentially, wherein in addition one or more agents capable of enhancing antitumor immune responses are used.
- CTLA4 cytotoxic lymphocyte antigen 4 antibodies
- MDX-CTLA4 cytotoxic lymphocyte antigen 4 antibodies
- Specific CTLA4 antibodies that can be used in the present invention include those described in U.S. Patent No. 6,682,736.
- the present invention further provides a method for manufacturing a medicament for reducing the side effects caused by the treatment of tumors or tumor metastases, characterized in that a therapeutically effective amount of an EGFR kinase inhibitor or bortezomib combination is used and is intended for administration to the patient simultaneously or sequentially in amounts that are effective to produce an additive, or a superadditive or synergistic antitumor effect, and that are effective at inhibiting the growth of the tumor.
- the present invention further provides a method for the treatment of cancer, comprising administering to a subject in need of such treatment (i) an effective first amount of an EGFR kinase inhibitor, or a pharmaceutically acceptable salt thereof; and (ii) an effective second amount of bortezomib.
- the cancer can be any of those referred to herein below, including lung cancer, and NSCLC.
- the present invention also provides a method for the treatment of cancer, comprising administering to a subject in need of such treatment (i) a sub-therapeutic first amount of an EGFR kinase inhibitor, or a pharmaceutically acceptable salt thereof; and (ii) a subtherapeutic second amount of bortezomib.
- the cancer can be any of those referred to herein below, including lung cancer, and NSCLC.
- the order of administration of the first and second amounts can be simultaneous or sequential, i.e. bortezomib can be administered before the EGFR kinase inhibitor, after the EGFR inhibitor, or at the same time as the EGFR kinase inhibitor. In a preferred embodiment, bortezomib is administered prior to the EGFR kinase inhibitor.
- the present invention provides a pharmaceutical composition
- a pharmaceutical composition comprising an EGFR inhibitor and bortezomib in a pharmaceutically acceptable carrier.
- the present invention further provides a pharmaceutical composition, in particular for use in cancer, comprising (i) an effective first amount of an EGFR kinase inhibitor, or a pharmaceutically acceptable salt thereof; and (ii) an effective second amount of bortezomib.
- a pharmaceutical composition in particular for use in cancer, comprising (i) an effective first amount of an EGFR kinase inhibitor, or a pharmaceutically acceptable salt thereof; and (ii) an effective second amount of bortezomib.
- Such composition optionally comprises pharmaceutically acceptable carriers and / or excipients.
- the present invention further provides a pharmaceutical composition, in particular for use in cancer, comprising (i) a sub-therapeutic first amount of the EGFR kinase inhibitor erlotinib, or a pharmaceutically acceptable salt thereof; and (ii) a sub-therapeutic second amount of bortezomib.
- a pharmaceutical composition in particular for use in cancer, comprising (i) a sub-therapeutic first amount of the EGFR kinase inhibitor erlotinib, or a pharmaceutically acceptable salt thereof; and (ii) a sub-therapeutic second amount of bortezomib.
- Such composition optionally comprises pharmaceutically acceptable carriers and / or excipients.
- the EGFR kinase inhibitor is erlotinib.
- the term "patient” preferably refers to a human in need of treatment with an EGFR kinase inhibitor for any purpose, and more preferably a human in need of such a treatment to treat cancer, or a precancerous condition or lesion.
- the term “patient” can also refer to non-human animals, preferably mammals such as dogs, cats, horses, cows, pigs, sheep and non-human primates, among others, that are in need of treatment with an EGFR kinase inhibitor.
- the patient is a human in need of treatment for cancer, or a precancerous condition or lesion.
- the cancer is preferably any cancer treatable, either partially or completely, by administration of an EGFR kinase inhibitor.
- the cancer may be, for example, lung cancer, non small cell lung (NSCL) cancer, bronchioloalviolar cell lung cancer, bone cancer, pancreatic cancer, skin cancer, cancer of the head or neck, cutaneous or intraocular melanoma, uterine cancer, ovarian cancer, rectal cancer, cancer of the anal region, stomach cancer, gastric cancer, colon cancer, breast cancer, uterine cancer, carcinoma of the fallopian tubes, carcinoma of the endometrium, carcinoma of the cervix, carcinoma of the vagina, carcinoma of the vulva, Hodgkin's Disease, cancer of the esophagus, cancer of the small intestine, cancer of the endocrine system, cancer of the thyroid gland, cancer of the parathyroid gland, cancer of the adrenal gland,
- the precancerous condition or lesion includes, for example, the group consisting of oral leukoplakia, actinic keratosis (solar keratosis), precancerous polyps of the colon or rectum, gastric epithelial dysplasia, adenomatous dysplasia, hereditary nonpolyposis colon cancer syndrome (HNPCC), Barrett's esophagus, bladder dysplasia, and precancerous cervical conditions.
- the cancer is colon cancer and most preferably colorectal cancer.
- the cancer is lung cancer and most preferably non-small cell lung cancer (NSCL).
- the cancer is pancreatic cancer.
- co-administration of and “co-administering" bortezomib with an EGFR kinase inhibitor refer to any administration of the two active agents, either separately or together, where the two active agents are administered as part of an appropriate dose regimen designed to obtain the benefit of the combination therapy.
- the two active agents can be administered either as part of the same pharmaceutical composition or in separate pharmaceutical compositions.
- Bortezomib can be administered prior to, at the same time as, or subsequent to administration of the EGFR kinase inhibitor, or in some combination thereof.
- bortezomib can be administered prior to, at the same time as, or subsequent to, each administration of the EGFR kinase inhibitor, or some combination thereof, or at different intervals in relation to the EGFR kinase inhibitor treatment, or in a single dose prior to, at any time during, or subsequent to the course of treatment with the EGFR kinase inhibitor.
- the EGFR kinase inhibitor will typically be administered to the patient in a dose regimen that provides for the most effective treatment of the cancer (from both efficacy and safety perspectives) for which the patient is being treated, as known in the art, and as disclosed, e.g. in International Patent Publication No. WO 01/34574.
- the EGFR kinase inhibitor can be administered in any effective manner known in the art, such as by oral, topical, intravenous, intra-peritoneal, intramuscular, intra-articular, subcutaneous, intranasal, intra-ocular, vaginal, rectal, or intradermal routes, depending upon the type of cancer being treated, the type of EGFR kinase inhibitor being used (e.g., small molecule, antibody, RNAi or antisense construct), and the medical judgement of the prescribing physician as based, e.g., on the results of published clinical studies.
- oral topical, intravenous, intra-peritoneal, intramuscular, intra-articular, subcutaneous, intranasal, intra-ocular, vaginal, rectal, or intradermal routes, depending upon the type of cancer being treated, the type of EGFR kinase inhibitor being used (e.g., small molecule, antibody, RNAi or antisense construct), and the medical judgement of the prescribing physician
- the amount of EGFR kinase inhibitor administered and the timing of EGFR kinase inhibitor administration will depend on the type (species, gender, age, weight, etc.) and
- small molecule EGFR kinase inhibitors can be administered to a patient in doses ranging from 0.001 to 100 mg/kg of body weight per day or per week in single or divided doses, or by continuous infusion (see for example, International Patent Publication No. WO 01/34574).
- erlotinib HCl can be administered to a patient in doses ranging from 5-200 mg per day, or 100-1600 mg per week, in single or divided doses, or by continuous infusion.
- a preferred dose is 150 mg/day.
- Antibody-based EGFR kinase inhibitors, or antisense, RNAi or ribozyme constructs can be administered to a patient in doses ranging from 0.1 to 100 mg/kg of body weight per day or per week in single or divided doses, or by continuous infusion. In some instances, dosage levels below the lower limit of the aforesaid range may be more than adequate, while in other cases still larger doses may be employed without causing any harmful side effect, provided that such larger doses are first divided into several small doses for administration throughout the day. [79]
- the EGFR kinase inhibitors and bortezomib can be administered either separately or together by the same or different routes, and in a wide variety of different dosage forms.
- the EGFR kinase inhibitor is preferably administered orally or parenterally.
- Bortezomib is preferably administered parenterally.
- the EGFR kinase inhibitor is erlotinib HCl (TarcevaTM)
- oral administration is preferable.
- the EGFR kinase inhibitor can be administered with various pharmaceutically acceptable inert carriers in the form of tablets, capsules, lozenges, troches, hard candies, powders, sprays, creams, salves, suppositories, jellies, gels, pastes, lotions, ointments, elixirs, syrups, and the like. Administration of such dosage forms can be carried out in single or multiple doses. Carriers include solid diluents or fillers, sterile aqueous media and various non-toxic organic solvents, etc. Oral pharmaceutical compositions can be suitably sweetened and/or flavored.
- the EGFR kinase inhibitor and bortezomib can be combined together with various pharmaceutically acceptable inert carriers in the form of sprays, creams, salves, suppositories, jellies, gels, pastes, lotions, ointments, and the like. Administration of such dosage forms can be carried out in single or multiple doses.
- Carriers include solid diluents or fillers, sterile aqueous media, and various non-toxic organic solvents, etc.
- All formulations comprising proteinaceous EGFR kinase inhibitors should be selected so as to avoid denaturation and/or degradation and loss of biological activity of the inhibitor.
- tablets containing one or both of the active agents are combined with any of various excipients such as, for example, micro- crystalline cellulose, sodium citrate, calcium carbonate, dicalcium phosphate and glycine, along with various disintegrants such as starch (and preferably corn, potato or tapioca starch), alginic acid and certain complex silicates, together with granulation binders like polyvinyl pyrrolidone, sucrose, gelatin and acacia.
- disintegrants such as starch (and preferably corn, potato or tapioca starch), alginic acid and certain complex silicates, together with granulation binders like polyvinyl pyrrolidone, sucrose, gelatin and acacia.
- lubricating agents such as magnesium stearate, sodium lauryl sulfate and talc are often very useful for tableting purposes.
- Solid compositions of a similar type may also be employed as fillers in gelatin capsules; preferred materials in this connection also include lactose or milk sugar as well as high molecular weight polyethylene glycols.
- the EGFR kinase inhibitor may be combined with various sweetening or flavoring agents, coloring matter or dyes, and, if so desired, emulsifying and/or suspending agents as well, together with such diluents as water, ethanol, propylene glycol, glycerin and various like combinations thereof.
- solutions in either sesame or peanut oil or in aqueous propylene glycol may be employed, as well as sterile aqueous solutions comprising the active agent or a corresponding water-soluble salt thereof.
- sterile aqueous solutions are preferably suitably buffered, and are also preferably rendered isotonic, e.g., with sufficient saline or glucose.
- These particular aqueous solutions are especially suitable for intravenous, intramuscular, subcutaneous and intraperitoneal injection purposes.
- the oily solutions are suitable for intra-articular, intramuscular and subcutaneous injection purposes. The preparation of all these solutions under sterile conditions is readily accomplished by standard pharmaceutical techniques well known to those skilled in the art.
- Any parenteral formulation selected for administration of proteinaceous EGFR kinase inhibitors should be selected so as to avoid denaturation and loss of biological activity of the inhibitor.
- a topical formulation comprising either an EGFR kinase inhibitor or bortezomib in about 0.1% (w/v) to about 5% (w/v) concentration can be prepared.
- the active agents can be administered separately or together to animals using any of the forms and by any of the routes described above.
- the EGFR kinase inhibitor is administered in the form of a capsule, bolus, tablet, liquid drench, by injection or as an implant.
- the EGFR kinase inhibitor can be administered with the animal feedstuff, and for this purpose a concentrated feed additive or premix may be prepared for a normal animal feed.
- the bortezomib is preferably administered in the form of liquid drench, by injection or as an implant.
- Such formulations are prepared in a conventional manner in accordance with standard veterinary practice.
- the present invention further provides a kit comprising a single container comprising both an EGFR kinase inhibitor and bortezomib.
- the present invention further provides a kit comprising a first container comprising an EGFR kinase inhibitor and a second container comprising bortezomib.
- the kit containers may further include a pharmaceutically acceptable carrier.
- the kit may further include a sterile diluent, which is preferably stored in a separate additional container.
- the kit may further include a package insert comprising printed instructions directing the use of the combined treatment as a method for treating cancer.
- the invention also encompasses a pharmaceutical composition that is comprised of an EGFR kinase inhibitor and bortezomib combination in combination with a pharmaceutically acceptable carrier.
- composition is comprised of a pharmaceutically acceptable carrier and a non-toxic therapeutically effective amount of an EGFR kinase inhibitor compound and bortezomib combination (including pharmaceutically acceptable salts of each component thereof).
- the invention encompasses a pharmaceutical composition for the treatment of disease, the use of which results in the inhibition of growth of neoplastic cells, benign or malignant tumors, or metastases, comprising a pharmaceutically acceptable carrier and a non-toxic therapeutically effective amount of an EGFR kinase inhibitor compound and bortezomib combination (including pharmaceutically acceptable salts of each component thereof).
- salts refers to salts prepared from pharmaceutically acceptable non-toxic bases or acids.
- a compound of the present invention is acidic, its corresponding salt can be conveniently prepared from pharmaceutically acceptable non-toxic bases, including inorganic bases and organic bases.
- Salts derived from such inorganic bases include aluminum, ammonium, calcium, copper (cupric and cuprous), ferric, ferrous, lithium, magnesium, manganese (manganic and manganous), potassium, sodium, zinc and the like salts. Particularly preferred are the ammonium, calcium, magnesium, potassium and sodium slats.
- Salts derived from pharmaceutically acceptable organic non-toxic bases include salts of primary, secondary, and tertiary amines, as well as cyclic amines and substituted amines such as naturally occurring and synthesized substituted amines.
- Other pharmaceutically acceptable organic non-toxic bases from which salts can be formed include ion exchange resins such as, for example, arginine, betaine, caffeine, choline, N',N'-diben2ylethylenediarnine, diethylamine, 2-diethylaminoethanol, 2- dimethylaminoethanol, ethanolamine, ethylenediamine, N-ethylmorpholine, N- ethylpiperidine, glucamine, glucosamine, histidine, hydrabamine, isopropylamine, lysine, methylglucamine, morpholine, piperazine, piperidine, polyamine resins, procaine, purines, theobromine, triethylame
- a compound of the present invention is basic, its corresponding salt can be conveniently prepared from pharmaceutically acceptable non-toxic acids, including inorganic and organic acids.
- acids include, for example, acetic, benzenesulfonic, benzoic, camphorsulfonic, citric, ethanesulfonic, fumaric, gluconic, glutamic, hydrobromic, hydrochloric, isethionic, lactic, maleic, malic, mandelic, methanesulfonic, mucic, nitric, pamoic, pantothenic, phosphoric, succinic, sulfuric, tartaric, p-toluenesulfonic acid and the like.
- Particularly preferred are citric, hydrobromic, hydrochloric, maleic, phosphoric, sulfuric and tartaric acids.
- compositions of the present invention comprise an EGFR kinase inhibitor compound and bortezomib combination (including pharmaceutically acceptable salts of each component thereof) as active ingredient, a pharmaceutically acceptable carrier and optionally other therapeutic ingredients or adjuvants.
- Other therapeutic agents may include those cytotoxic, chemotherapeutic or anti-cancer agents, or agents which enhance the effects of such agents, as listed above.
- the compositions include compositions suitable for oral, rectal, topical, and parenteral (including subcutaneous, intramuscular, and intravenous) administration, although the most suitable route in any given case will depend on the particular host, and nature and severity of the conditions for which the active ingredient is being administered.
- the pharmaceutical compositions may be conveniently presented in unit dosage form and prepared by any of the methods well known in the art of pharmacy.
- the compounds represented by an EGFR kinase inhibitor compound and bortezomib combination (including pharmaceutically acceptable salts of each component thereof) of this invention can be combined as the active ingredient in intimate admixture with a pharmaceutical carrier according to conventional pharmaceutical compounding techniques.
- the carrier may take a wide variety of forms depending on the form of preparation desired for administration, e.g. oral or parenteral (including intravenous).
- the pharmaceutical compositions of the present invention can be presented as discrete units suitable for oral administration such as capsules, cachets or tablets each containing a predetermined amount of the active ingredient.
- compositions can be presented as a powder, as granules, as a solution, as a suspension in an aqueous liquid, as a non-aqueous liquid, as an oil-in-water emulsion, or as a water-in-oil liquid emulsion.
- an EGFR kinase inhibitor compound and bortezomib combination may also be administered by controlled release means and/or delivery devices.
- the combination compositions may be prepared by any of the methods of pharmacy. In general, such methods include a step of bringing into association the active ingredients with the carrier that constitutes one or more necessary ingredients.
- the compositions are prepared by uniformly and intimately admixing the active ingredient with liquid carriers or finely divided solid carriers or both. The product can then be conveniently shaped into the desired presentation.
- the pharmaceutical compositions of this invention may include a pharmaceutically acceptable carrier and an EGFR kinase inhibitor compound and bortezomib combination (including pharmaceutically acceptable salts of each component thereof).
- An EGFR kinase inhibitor compound and bortezomib combination (including pharmaceutically acceptable salts of each component thereof) can also be included in pharmaceutical compositions in combination with one or more other therapeutically active compounds.
- Other therapeutically active compounds may include those cytotoxic, chemotherapeutic or anticancer agents, or agents which enhance the effects of such agents, as listed above.
- a pharmaceutical composition can comprise an EGFR kinase inhibitor compound and bortezomib in combination with an anticancer agent, wherein said anti-cancer agent is a member selected from the group consisting of alkylating drugs, antimetabolites, microtubule inhibitors, podophyllotoxins, antibiotics, nitrosoureas, hormone therapies, kinase inhibitors, activators of tumor cell apoptosis, and antiangiogenic agents.
- an anticancer agent is a member selected from the group consisting of alkylating drugs, antimetabolites, microtubule inhibitors, podophyllotoxins, antibiotics, nitrosoureas, hormone therapies, kinase inhibitors, activators of tumor cell apoptosis, and antiangiogenic agents.
- the pharmaceutical carrier employed can be, for example, a solid, liquid, or gas.
- solid carriers include lactose, terra alba, sucrose, talc, gelatin, agar, pectin, acacia, magnesium stearate, and stearic acid.
- liquid carriers are sugar syrup, peanut oil, olive oil, and water.
- gaseous carriers include carbon dioxide and nitrogen.
- any convenient pharmaceutical media may be employed.
- water, glycols, oils, alcohols, flavoring agents, preservatives, coloring agents, and the like may be used to form oral liquid preparations such as suspensions, elixirs and solutions; while carriers such as starches, sugars, microcrystalline cellulose, diluents, granulating agents, lubricants, binders, disintegrating agents, and the like may be used to form oral solid preparations such as powders, capsules and tablets. Because of their ease of administration, tablets and capsules are the preferred oral dosage units whereby solid pharmaceutical carriers are employed.
- tablets may be coated by standard aqueous or nonaqueous techniques.
- a tablet containing the composition of this invention may be prepared by compression or molding, optionally with one or more accessory ingredients or adjuvants.
- Compressed tablets may be prepared by compressing, in a suitable machine, the active ingredient in a free-flowing form such as powder or granules, optionally mixed with a binder, lubricant, inert diluent, surface active or dispersing agent. Molded tablets may be made by molding in a suitable machine, a mixture of the powdered compound moistened with an inert liquid diluent.
- Each tablet preferably contains from about 0.05mg to about 5g of the active ingredient and each cachet or capsule preferably containing from about 0.05mg to about 5g of the active ingredient.
- a formulation intended for the oral administration to humans may contain from about 0.5mg to about 5g of active agent, compounded with an appropriate and convenient amount of carrier material that may vary from about 5 to about 95 percent of the total composition.
- Unit dosage forms will generally contain between from about lmg to about 2g of the active ingredient, typically 25mg, 50mg, lOOmg, 200mg, 300mg, 400mg, 500mg, 600mg, 800mg, or lOOOmg.
- compositions of the present invention suitable for parenteral administration may be prepared as solutions or suspensions of the active compounds in water.
- a suitable surfactant can be included such as, for example, hydroxypropylcellulose.
- Dispersions can also be prepared in glycerol, liquid polyethylene glycols, and mixtures thereof in oils. Further, a preservative can be included to prevent the detrimental growth of microorganisms.
- compositions of the present invention suitable for injectable use include sterile aqueous solutions or dispersions.
- the compositions can be in the form of sterile powders for the extemporaneous preparation of such sterile injectable solutions or dispersions.
- the final injectable form must be sterile and must be effectively fluid for easy syringability.
- the pharmaceutical compositions must be stable under the conditions of manufacture and storage; thus, preferably should be preserved against the contaminating action of microorganisms such as bacteria and fungi.
- the carrier can be a solvent or dispersion medium containing, for example, water, ethanol, polyol (e.g., glycerol, propylene glycol and liquid polyethylene glycol), vegetable oils, and suitable mixtures thereof.
- compositions of the present invention can be in a form suitable for topical sue such as, for example, an aerosol, cream, ointment, lotion, dusting powder, or the like. Further, the compositions can be in a form suitable for use in transdermal devices. These formulations may be prepared, utilizing an EGFR kinase inhibitor compound and bortezomib combination (including pharmaceutically acceptable salts of each component thereof) of this invention, via conventional processing methods. As an example, a cream or ointment is prepared by admixing hydrophilic material and water, together with about 5wt% to about 10wt% of the compound, to produce a cream or ointment having a desired consistency.
- compositions of this invention can be in a form suitable for rectal administration wherein the carrier is a solid. It is preferable that the mixture forms unit dose suppositories. Suitable carriers include cocoa butter and other materials commonly used in the art. The suppositories may be conveniently formed by first admixing the composition with the softened or melted carrier(s) followed by chilling and shaping in molds.
- the pharmaceutical formulations described above may include, as appropriate, one or more additional carrier ingredients such as diluents, buffers, flavoring agents, binders, surface-active agents, thickeners, lubricants, preservatives (including anti-oxidants) and the like.
- additional carrier ingredients such as diluents, buffers, flavoring agents, binders, surface-active agents, thickeners, lubricants, preservatives (including anti-oxidants) and the like.
- additional carrier ingredients such as diluents, buffers, flavoring agents, binders, surface-active agents, thickeners, lubricants, preservatives (including anti-oxidants) and the like.
- additional carrier ingredients such as diluents, buffers, flavoring agents, binders, surface-active agents, thickeners, lubricants, preservatives (including anti-oxidants) and the like.
- other adjuvants can be included to render the formulation isotonic with the blood of the intended recipient
- Dosage levels for the compounds of the combination of this invention will be approximately as described herein, or as described in the art for these compounds. It is understood, however, that the specific dose level for any particular patient will depend upon a variety of factors including the age, body weight, general health, sex, diet, time of administration, route of administration, rate of excretion, drug combination and the severity of the particular disease undergoing therapy. [108] This invention will be better understood from the Experimental Details that follow. However, one skilled in the art will readily appreciate that the specific methods and results discussed are merely illustrative of the invention as described more fully in the claims which follow thereafter, and are not to be considered in any way limited thereto.
- Erlotinib was supplied by OSI Pharmaceuticals as erlotinib HCl (TarcevaTM), and clinical grade bortezomib was obtained from the Montif ⁇ ore Medical Center, NY, outpatient pharmacy. Both agents were dissolved in DMSO as stock solution and diluted to the desired concentration with PBS. Monoclonal antibodies were obtained from Santa Cruz Biotechnology, Inc. (Santa Cruz, CA), and other chemicals were obtained from Sigma- Aldrich Chemical Co. (St. Louis, MO).
- H322, H358, H661, H460, H522, H1299, A549) were obtained from American Type Culture Collection (Manassas, VA). All cells were grown in RPMI 1640 supplemented with 10% fetal bovine serum in a humidified atmosphere of 5% CO 2 and 95% air.
- Log-phase growing cells were continuously exposed to varying concentrations of erlotinib HCl and bortezomib for 72 h and drug-induced cytotoxicity was assessed by MTT assay, as described previously (Ling, Y-H et al. (1993) Cancer Res. 53(7): 1583-1589.
- Cells were treated with either erlotinib HCl or bortezomib alone or in combination given either concomitantly or sequentially 24-hour apart.
- Cells were harvested at 48 h from first drug exposure, fixed with 75% ethanol at -20C overnight, and then incubated at room temperature for 3h with 5 ⁇ g/mL propidium iodide and 5 ⁇ g/mL RNase I (Roche Molecular Biochemicals, Indianapolis, IN). The number of cells at different stages of the cell cycle, and apoptotic cells (sub-Gl), were measured by flow cytometry (Epics Profile Analyzer; Coulter Co., Miami, FL).
- Antagonistic effects of erlotinib pre-exposure is independent of p53 stabilization.
- p53 is also an important mediator to apoptosis in response to cellular stress.
- quiescence cells p53 has a very short half-life and is very closely mediated by Mdm-2. The latter binds to p53 and by its ubiquitin ligase function targets p53 to proteosomal degradation.
- Cellular stress results in a series of phosphorylation events on p53 resulting in its dissociation from Mdm-2 with activation of p53.
- the consequences of p53 activation include cell cycle arrest, DNA repair, and if DNA repair is not successful, apoptosis.
- the bortezomib exposure caused the accumulation of ubiquitinated p53, compared to positive control paclitaxel.
- Erlotinib exposure either concomitantly or sequentially has no effect on bortezomib-induced accumulation of ubiquitinated p53.
- This result together with the fact that we observed similar antagonistic results in p53 null H358 cells, confirmed that the antagonistic effect of erlotinib pre-exposure is independent of bortezomib-induced p53 stabilization.
- ROS reactive oxygen species
- the results of the present study demonstrate that the combination of erlotinib and bortezomib is more active than either agent alone in H358 bronchoalveolar cells, and thus may be useful in the treatment of certain NSCLC and other tumors in patients with cancer.
- the choice of schedule may be very important in combining erlotinib with bortezomib, and further in vivo studies are required to further evaluate this combination.
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Abstract
Description
Claims
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EP05857727A EP1804809A2 (en) | 2004-10-18 | 2005-10-18 | Combined treatment with bortezomib and an epidermal growth factor receptor kinase inhibitor |
BRPI0517104-0A BRPI0517104A (en) | 2004-10-18 | 2005-10-18 | combination treatment with bortezomib and an epidermal growth factor receptor kinase inhibitor |
CA002583520A CA2583520A1 (en) | 2004-10-18 | 2005-10-18 | Combined treatment with bortezomib and an epidermal growth factor receptor kinase inhibitor |
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IL182584A IL182584A0 (en) | 2004-10-18 | 2007-04-16 | Combined treatment with bortezomib and an epidermal growth factor receptor kinase inhibitor |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2010523680A (en) * | 2007-04-13 | 2010-07-15 | ダナ ファーバー キャンサー インスティテュート,インコーポレイテッド | Method for treating cancer resistant to ErbB therapy |
Families Citing this family (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101204247B1 (en) | 2003-07-22 | 2012-11-22 | 아스텍스 테라퓨틱스 리미티드 | 3,4-disubstituted 1h-pyrazole compounds and their use as cyclin dependent kinases cdk and glycogen synthase kinase-3 gsk-3 modulators |
CN1960730A (en) * | 2004-06-03 | 2007-05-09 | 霍夫曼-拉罗奇有限公司 | Treatment with irinotecan and EGFR-inhibitor |
AR054425A1 (en) | 2005-01-21 | 2007-06-27 | Astex Therapeutics Ltd | PIPERIDIN ADDITION SALTS 4-IL-ACID AMID 4- (2,6-DICLORO-BENZOILAMINO) 1H-PIRAZOL-3-CARBOXILICO. |
US8404718B2 (en) * | 2005-01-21 | 2013-03-26 | Astex Therapeutics Limited | Combinations of pyrazole kinase inhibitors |
US20070286864A1 (en) * | 2006-06-09 | 2007-12-13 | Buck Elizabeth A | Combined treatment with an EGFR kinase inhibitor and an agent that sensitizes tumor cells to the effects of EGFR kinase inhibitors |
WO2007146226A2 (en) * | 2006-06-09 | 2007-12-21 | Osi Pharmaceuticals, Inc. | Combined treatment with an egfr kinase inhibitor and an agent that sensitizes tumor cells to the effects of egfr kinase inhibitors |
WO2010022277A2 (en) * | 2008-08-20 | 2010-02-25 | O'connor Owen A | Combination of 10-propargyl-10-deazaaminopterin and bortezomib for the treatment of cancers |
EA201170527A1 (en) * | 2008-10-01 | 2011-10-31 | Др. Редди'С Лабораторис Лтд. | PHARMACEUTICAL COMPOSITIONS, INCLUDING BORONIC ACID COMPOUNDS |
US9492449B2 (en) | 2008-11-13 | 2016-11-15 | Gilead Calistoga Llc | Therapies for hematologic malignancies |
ES2674719T3 (en) * | 2008-11-13 | 2018-07-03 | Gilead Calistoga Llc | Therapies for hematologic malignancies |
RU2529800C2 (en) * | 2010-03-18 | 2014-09-27 | ИННОФАРМА, Инк. | Stable formulations of bortezomib |
US8263578B2 (en) | 2010-03-18 | 2012-09-11 | Innopharma, Inc. | Stable bortezomib formulations |
US20130211384A1 (en) * | 2010-07-28 | 2013-08-15 | Fondazione Irccs Istituto Nazionale Dei Tumori | Therapeutic agent, composition including said agent, implantable device and process for the treatment of cervical cancer and/or for the prevention of the formation of neoplasms in correspondence of the cervix in a human female genital system |
KR20140033384A (en) | 2011-05-16 | 2014-03-18 | 울리커 누베르 | Novel cancer therapies and methods |
KR101695237B1 (en) * | 2013-10-11 | 2017-01-12 | 이화여자대학교 산학협력단 | Composition for relief and treatment of liver injury comprising Bortezomib as a active ingredient |
US20190125772A1 (en) * | 2015-05-05 | 2019-05-02 | The Regents Of The University Of California | Improved drug combinations for drug-resistant and drug-sensitive multiple myeloma |
WO2019169389A1 (en) * | 2018-03-02 | 2019-09-06 | Epicentrx, Inc. | Methods and compositions for treating cancer and sensitizing tumor cells to kinase inhibitors |
CA3115038A1 (en) * | 2018-10-04 | 2020-04-09 | Inserm (Institut National De La Sante Et De La Recherche Medicale) | Egfr inhibitors for treating keratodermas |
TW202237143A (en) | 2020-12-10 | 2022-10-01 | 南韓商Lg化學股份有限公司 | Boronic acid compounds |
KR20220118247A (en) | 2021-02-18 | 2022-08-25 | 김성운 | Self Hair-cut comb |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2373815A1 (en) * | 1999-05-14 | 2000-11-23 | Imclone Systems Incorporated | Treatment of refractory human tumors with epidermal growth factor receptor antagonists |
WO2004010937A2 (en) * | 2002-07-26 | 2004-02-05 | Advanced Research & Technology Institute At Indiana University | Method of treating cancer |
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Non-Patent Citations (6)
Title |
---|
BAYES M ET AL: "GATEWAYS TO CLINICAL TRIALS" METHODS AND FINDINGS IN EXPERIMENTAL AND CLINICAL PHARMACOLOGY, PROUS, BARCELONA, ES, vol. 26, no. 3, April 2004 (2004-04), pages 211-244, XP009043087 ISSN: 0379-0355 * |
DAVIES ANGELA M ET AL: "EGFR inhibitor OSI-774 activity in non-small cell lung carcinoma (NSCLC) cells." PROCEEDINGS OF THE AMERICAN ASSOCIATION FOR CANCER RESEARCH ANNUAL MEETING, vol. 44, July 2003 (2003-07), page 752, XP001247461 & 94TH ANNUAL MEETING OF THE AMERICAN ASSOCIATION FOR CANCER RESEARCH; WASHINGTON, DC, USA; JULY 11-14, 2003 ISSN: 0197-016X * |
HIGGINS BRIAN ET AL: "Antitumor activity of erlotinib (OSI-774, Tarceva) alone or in combination in human non-small cell lung cancer tumor xenograft models" ANTI-CANCER DRUGS, vol. 15, no. 5, June 2004 (2004-06), pages 503-512, XP009053757 ISSN: 0959-4973 * |
KARASIK A ET AL: "Dexamethasone-induced changes in phosphorylation of the insulin and epidermal growth factor receptors and their substrates in intact rat hepatocytes." ENDOCRINOLOGY. NOV 1988, vol. 123, no. 5, November 1988 (1988-11), pages 2214-2222, XP009071881 ISSN: 0013-7227 * |
LARA PRIMO N JR ET AL: "Proteasome inhibition with PS-341 (bortezomib) in lung cancer therapy." SEMINARS IN ONCOLOGY, vol. 31, no. 1 Supplement 1, February 2004 (2004-02), pages 40-46, XP009071956 ISSN: 0093-7754 * |
LING YI-HE ET AL: "Mechanisms of proteasome inhibitor PS-341-induced G(2)-M-phase arrest and apoptosis in human non-small cell lung cancer cell lines." CLINICAL CANCER RESEARCH : AN OFFICIAL JOURNAL OF THE AMERICAN ASSOCIATION FOR CANCER RESEARCH. MAR 2003, vol. 9, no. 3, March 2003 (2003-03), pages 1145-1154, XP002397660 ISSN: 1078-0432 * |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2010523680A (en) * | 2007-04-13 | 2010-07-15 | ダナ ファーバー キャンサー インスティテュート,インコーポレイテッド | Method for treating cancer resistant to ErbB therapy |
US8715665B2 (en) | 2007-04-13 | 2014-05-06 | The General Hospital Corporation | Methods for treating cancer resistant to ErbB therapeutics |
US11008620B2 (en) | 2007-04-13 | 2021-05-18 | The General Hospital Corporation | Methods for treating cancer resistant to ErbB therapeutics |
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IL182584A0 (en) | 2008-04-13 |
CN101043892A (en) | 2007-09-26 |
WO2006110175A9 (en) | 2006-11-23 |
CA2583520A1 (en) | 2006-10-19 |
US20060084691A1 (en) | 2006-04-20 |
JP2008516983A (en) | 2008-05-22 |
AU2005330507A1 (en) | 2006-10-19 |
MX2007004549A (en) | 2007-07-11 |
EP1804809A2 (en) | 2007-07-11 |
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KR20070083719A (en) | 2007-08-24 |
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