Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B5/00—Measuring for diagnostic purposes; Identification of persons
  • A61B5/44—Detecting, measuring or recording for evaluating the integumentary system, e.g. skin, hair or nails
  • A61B5/441—Skin evaluation, e.g. for skin disorder diagnosis
  • A61B5/444—Evaluating skin marks, e.g. mole, nevi, tumour, scar
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B5/00—Measuring for diagnostic purposes; Identification of persons
  • A61B5/0059—Measuring for diagnostic purposes; Identification of persons using light, e.g. diagnosis by transillumination, diascopy, fluorescence
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B5/00—Measuring for diagnostic purposes; Identification of persons
  • A61B5/41—Detecting, measuring or recording for evaluating the immune or lymphatic systems
  • A61B5/414—Evaluating particular organs or parts of the immune or lymphatic systems
  • A61B5/415—Evaluating particular organs or parts of the immune or lymphatic systems the glands, e.g. tonsils, adenoids or thymus
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B5/00—Measuring for diagnostic purposes; Identification of persons
  • A61B5/41—Detecting, measuring or recording for evaluating the immune or lymphatic systems
  • A61B5/414—Evaluating particular organs or parts of the immune or lymphatic systems
  • A61B5/418—Evaluating particular organs or parts of the immune or lymphatic systems lymph vessels, ducts or nodes
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B5/00—Measuring for diagnostic purposes; Identification of persons
  • A61B5/44—Detecting, measuring or recording for evaluating the integumentary system, e.g. skin, hair or nails
  • A61B5/441—Skin evaluation, e.g. for skin disorder diagnosis
  • A61B5/445—Evaluating skin irritation or skin trauma, e.g. rash, eczema, wound, bed sore
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B5/00—Measuring for diagnostic purposes; Identification of persons
  • A61B5/44—Detecting, measuring or recording for evaluating the integumentary system, e.g. skin, hair or nails
  • A61B5/441—Skin evaluation, e.g. for skin disorder diagnosis
  • A61B5/446—Scalp evaluation or scalp disorder diagnosis, e.g. dandruff
• • 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
  • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B18/00—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body
  • A61B18/02—Surgical instruments, devices or methods for transferring non-mechanical forms of energy to or from the body by cooling, e.g. cryogenic techniques

Definitions

• Nonmelanoma skin cancer is the most common cancer in the United States, with an estimated annual incidence of more than 1,000,000 cases.
• Basal cell carcinomas (BCC) account for 70 to 80% of nonmelanoma skin cancers.
• Squamous cell carcinoma (SCC) while representing only about 20% of nonmelanoma skin cancers, are significant because of their ability to metastasize and accounts for over 2300 deaths annually.
• the incidence of nonmelanoma skin cancer continues to increase. Early diagnosis can be lifesaving and it is important that physicians know what treatment modalities will be the most effective.
• Nonmelanoma skin cancers may be treated using various procedures that excise or kill the cancerous cells. Removal of the entire tumor is essential to prevent tumor recurrence and, in some cases, metastasis. However, the clinically visible portion of a lesion may represent only a fraction of the total lesion, making excision of the entire lesion difficult. Currently, even with a precise preoperative diagnosis, complete excision of nonmelanoma skin cancer is not always achieved. Incomplete excision of these carcinomas requires further treatment such as, for example, a second excision procedure to remove the residual tumor. Thus, improved methods of diagnosis that identify the complete margins of such lesions are needed.
• the present invention provides a method of diagnosing a skin lesion. Generally, the method includes administering to a treatment area of the skin an IRM compound for a period of time and in an amount sufficient to permit visualization of a skin lesion in the treatment area.
• the present invention provides a method of visualizing the margins of a skin lesion. Generally, the method includes administering to a treatment area of the skin an LRM compound for a period of time and in an amount sufficient to permit visualization of the margins of a skin lesion in the treatment area.
• the present invention provides a method of visibly accentuating the margins of a skin lesion.
• the method includes administering to a treatment area that includes a clinically visible skin lesion an IRM compound for a period of time and in an amount sufficient to visibly accentuate the margins of the skin lesion.
• the present invention provides a method of pretreating a skin lesion prior to an ablation procedure.
• the method includes administering to a treatment area that includes a skin lesion an JJ M compound for a period of time and in an amount sufficient to visibly accentuate the margins of the skin lesion.
• the present invention provides methods of visualizing a subclinical skin lesion.
• the method includes administering to a treatment area an IRM compound for a period of time and in an amount sufficient to cause a subclinical skin lesion in the treatment area to become apparent, and then visualizing the skin lesion.
• the present invention provides a method of treating a skin lesion.
• the method includes administering to a treatment area that includes at least one skin lesion an IRM compound for a period of time and in an amount sufficient to permit visualization of the margins of the skin lesion, and then subjecting the skin lesion to an ablation procedure.
• the various methods may further include subjecting the skin lesion to an ablation procedure such as, for example, Mohs micrographic surgery, surgical excision, cryotherapy, or radiotherapy.
• the skin lesion may be a neoplastic skin lesion, a subclinical lesion, a nonmelanoma skin cancer, or a premalignant skin lesion.
• the skin lesion may be a basal cell carcinoma, a squamous cell carcinoma, lentigo maligna, Bowen's disease, or actinic keratoses.
• the IRM may be an agonist of at least one TLR; including an agonist of TLR4, TLR7, TLR8 or both TLR7 and TLR8.
• the present invention provides methods for diagnosing skin lesions, accentuating the margins of skin lesions, visualizing subclinical skin lesions, and treating skin lesions.
• the methods include administering an LRM compound to a treatment area that includes a skin lesion.
• Administering an IRM compound to a lesion whether or not the lesion is clinically visible when the IRM compound is administered, can induce a subject's immune system to respond to immunologic stimuli of the lesion, thereby initiating or enhancing a localized immune response against the lesion. This localized immune response can lead to visible changes in the appearance of the lesion (including, if the lesion is subclinical, making the lesion apparent).
• Such visible changes may result from, for example, inflammation and/or infiltration of immune cells into the lesion, and may include one or more of, for example, erosion, erythema (redness), and edema (swelling).
• Unaffected tissues surrounding the lesion are not targeted by the immune response that is induced by administering the IRM compound.
• the unaffected tissues surrounding the lesion do not manifest the visible changes observed in the lesion (e.g., erosion, redness, and/or increased swelling) when the IRM compound is administered.
• the erosion, increased swelling and/or redness of the lesion can be used to visually distinguish the tissue of the lesion from the surrounding unaffected tissue.
• the visible change in the appearance of the lesion can accentuate the margins of the lesion, allowing one to more accurately determine the margins of a lesion.
• Admimstering an IRM compound can induce visible changes in the appearance of lesions that already are clinically visible.
• Administering an IRM compound also can induce changes in subclinical lesions that render the subclinical lesions visible and, therefore, can assist in the detection and diagnosis of subclinical lesions.
• “clinically visible” lesions are lesions that are visible, apparent, or otherwise detected without administering an IRM compound.
• “subclinical” lesions are lesions that are present, but because of their location or small size are not visible, apparent, or otherwise detected - i.e., lesions that are not clinically visible.
• subclinical lesions that become visible as a result of administering and IRM compound may still be referred to as subclinical lesions even though, after administering an IRM compound, the lesions have become visible, apparent, or otherwise detected.
• margin refers to the tissue surrounding a tumor or lesion. More particularly, as used herein, “margins” refers to the edges, borders, or boundaries of a lesion.
• the margin is the region surrounding a lesion in which the normal, healthy tissue may have been altered by the presence of the lesion.
• a tumor margin can include tumor cells that have grown beyond the visibly discernable edge of the tumor and can also include stromal regions that have been altered due to the presence of the tumor.
• the margin includes tissues that usually appear to be normal to the naked eye that are removed along with the discernible lesion.
• the margin can generally extend from about 0.2 cm to about 3 cm from a primary lesion, but can be greater depending upon the size of the primary lesion.
• a "treatment area" is an area of the skin to which an IRM compound is administered.
• a treatment area may be defined by the presence of one or more clinically visible lesions.
• the treatment area may include the clinically visible lesions, including the margins, as well as tissue located between clinically visible lesions.
• a treatment area may be any area to which an LRM compound is administered that lacks clinically visible lesions.
• a treatment area may be selected because the area is at risk for developing certain types of skin lesions - e.g., areas of the face, scalp, neck, and hands may be at particular risk for developing actinic keratoses, basal cell carcinoma, melanoma, etc.
• IRM compound may be administered to such areas periodically as a treatment to make diagnosis of such lesions more sensitive.
• Lesions that may be diagnosed by the methods of the present invention include lesions of the skin, mucosal surfaces, tissues, and organs. Lesions maybe of any known histological form such as, for example, tumors, macules, papules, nodules, plaques, vesicles, bullas, blisters, wheals, scale, erosions, and ulcers.
• Skin lesions include, but are not limited to, premalignant skin lesions, malignant skin lesions, neoplastic skin lesions, nonmelanoma skin cancers, premalignant epideraial lesions, malignant epidermal lesions, epidermal lesions, dermal lesions, and superficial skin cancers.
• Skin lesions also include non-neoplastic lesions, including subcutaneous lesions and cutaneous lesions.
• non-neoplastic lesions can include, for example, warts (caused, for example by the human papilloma virus (HPV)), epidermodysplasia verruciformis, molluscum contagiosum, the lesions of leishmaniasis, and keloids.
• Nonmelanoma skin lesions to be diagnosed by the methods of the present invention include, but are not limited to, basal cell carcinomas, squamous cell carcinomas, actinic keratosis, and in situ squamous cell carcinomas (also called Bowen's disease).
• BCC basal cell carcinoma
• BCC basal cell carcinoma
• BCC a subtype of nonmelanoma skin cancer
• BCC is a malignancy arising from epidermal basal cells.
• BCC is a potentially fatal disease linked to sun exposure.
• the natural history of BCC is that of a slowly enlarging, locally invasive neoplasm.
• the degree of destruction and risk of recurrence vary with the size, duration and location of the tumor; the histologic subtype; the presence of recurrent disease; and various patient characteristics.
• Lesions located on the central face e.g., the nose, the nasolabial fold, or the periorbital or perioral area
• the ears, or the scalp are associated with a higher risk.
• BCC Small nodular, pigmented, cystic, or superficial BCC respond well to treatments.
• Mortality rates due to BCC are low, but its increasing incidence and prolonged morbidity means the disease is costly to treat. Advanced lesions may ulcerate and extensive local invasion of bone or facial sinuses may occur. Early recognition and effective treatment are therefore important.
• the current treatments for BCC include electrodessication and curettage (ED&C), surgical excision, Mohs micrographic surgery (MMS), cryosurgery, radiation therapy, and treatment with 5-fluorouracil.
• Newer treatment modalities include photodynamic therapy and the topical application of a 5% imiquimod cream, which effectively resolves BCC lesions.
• the mode of therapy chosen depends on tumor characteristics, age, medical status, preferences of the patient, and other factors.
• ED&C is the method commonly employed for low-risk tumors (e.g., a small primary tumor of a less aggressive subtype in a favorable location).
• Surgical excision which offers the advantage of histologic control, is often selected for more aggressive tumors or those in high-risk locations, or, in many instances, for esthetic reasons. Cryosurgery using liquid nitrogen may be used in certain low-risk tumors. Radiation therapy, while not employed as often as surgical modalities, offers an excellent chance for cure in many cases of BCC. It is useful in patients not considered surgical candidates and as a surgical adjunct in high-risk tumors. MMS is a specialized type of surgical excision that permits the ultimate in histologic control and preservation of uninvolved tissue. It is preferred for recurrent lesions or lesions that are in a high-risk location or are large and ill defined, and where maximal tissue conservation is critical (e.g., the eyelids).
• Topical chemotherapy with agents such as 5-fluorouracil (5FU) cream has limited usefulness in the management of BCC, being used for treating superficial BCC.
• Photodynamic therapy which employs selective activation of a photoactive drag by visible light, may be useful in patients with numerous tumors. Lasers can also be used for the treatment of skin cancer.
• Stockfleth and Sterry Recent Results Cancer Res (2002) 160:259-68
• SCC squamous cell carcinoma
• SCC a subtype of nonmelanoma skin cancer, is the most common tumor arising in sun-exposed skin in older people. Implicated as predisposing factors, in addition to sunlight, are industrial carcinogens (tars and oils), chronic ulcers, old burn scars, ingestion of arsenicals, ionizing radiation, and (in the oral cavity) tobacco and betel nut chewing.
• Primary cutaneous SCC is a malignant neoplasm of keratinizing epidermal cells. Unlike BCC, which has very low metastatic potential, SCC can metastasize and grow rapidly. The clinical features of SCC can vary widely.
• SCC first appears as an ulcerated nodule or a superficial erosion on the skin or lower lip.
• the margins of the tumor may be ill defined, and fixation to underlying structures may occur.
• Surgical excision, MMS, and radiation are standard methods of treatment of SCC.
• Cryosurgery and ED&C can be used, particularly for the treatment of small primary tumors.
• Metastases can be treated with lymph node dissection, irradiation, or both.
• Systemic chemotherapy combinations that include cisplatin may also be used for the treatment of metastatic SCC.
• SCC has several premalignant forms (e.g., actinic keratosis, actinic cheilitis, and some cutaneous horns), and in situ forms (e.g., Bowen's disease) that are confined to the epidermis.
• premalignant forms e.g., actinic keratosis, actinic cheilitis, and some cutaneous horns
• in situ forms e.g., Bowen's disease
• AK actinic keratosis
• Actinic keratoses are hyperkeratotic papules and plaques that occur on sun-exposed areas. Exposure to ionizing radiation, hydrocarbons, and arsenicals may induce similar lesions. Skin sites commonly affected can include the face, arms, scalp, and dorsum of the hands. Similar lesions may develop on the lips and are called actinic cheilitis. While the potential for malignant degeneration is low in individual lesions, the risk of SCC increases with larger numbers of AK lesions. AK lesions become malignant frequently enough to warrant local eradication of these potential precursor lesions. This is usually accomplished by curettage, cryotherapy, or topical application of chemotherapeutic agents.
• Bowen's disease is a precancerous lesion, which presents as a scaling, erythematous plaque. It may develop into invasive SCC in up to 20% of cases.
• treatment of the in situ lesions of Bowen's disease reduces the subsequent risk of invasive disease. It is often treated by surgical excision and direct closure.
• Alternative treatments may include cryotherapy, curettage and cautery, radiation, ultrasonic surgical aspiration (Otani et al., Plast Reconstr Surg (2001) 108(l):68-72), and photodynamic therapy (Wong et al., Dermatol Surg (2001)
• Lesions that may be diagnosed by the methods of the present invention also include the lesions of lentigo maligna.
• Lentigo maligna is a preinvasive form of melanoma induced by long-term cumulative ultraviolet injury. Lentigo maligna typically refers to lesions that are confined to the epidermis, whereas lentigo maligna melanoma typically refers to lesions that violate the dermis, thereby establishing metastatic potential.
• the most frequent findings suggesting early melanoma are changes in size or color of a new, pigmented lesion or an existing mole.
• Lentigo maligna most commonly affects the sun-exposed skin of the head and neck, with a predilection for the nose and cheek. Less common sites include the arm, leg, and trunk.
• the conjunctivae and oral mucosa may become involved when a cutaneous lentigo maligna spreads onto mucosal surfaces. Radiotherapy, cryotherapy, chemotherapy, and/or surgical may be used to treat lentigo maligna. Because the actual margins of the lesion usually extend beyond the clinically apparent margin, removal of the entire lesion may be difficult.
• Ablation methods suitable for practicing certain embodiments of the invention include all methods used to physically remove a skin lesion from its location in situ.
• Current clinical treatments for the ablation of skin lesions include, but are not limited to, electrodessication and curettage (ED&C), cryosurgery, radiation therapy, photodynamic therapy, and excision procedures such as, for example, surgical excision and Mohs micrographic surgery (MMS).
• ED&C electrodessication and curettage
• cryosurgery radiation therapy
• photodynamic therapy photodynamic therapy
• excision procedures such as, for example, surgical excision and Mohs micrographic surgery (MMS).
• MMS is an exacting surgical technique for the removal of a nonmelanoma skin cancer. The technique requires the sequential removal of involved tissue in thin layers. Each layer undergoes a histological examination in which the layer is sectioned on a microtome and examined microscopically.
• tissue map is prepared to delineate areas of residual tumor as well as normal, uninvolved tissue. Subsequent tissue layers are removed as dictated by microscopic examination and the process is repeated until the entire tumor has been resected. Due to this microscopic control, cure rates are extremely high for basal and squamous cell cancers.
• an IRM compound admimstered to treat subjects having clinically visible AK lesions experienced an increase in the number of AK lesions during the treatment period (see Table 1, Examples).
• a surprising additional benefit of treating clinically visible AK lesions with the IRM compound was that the treatment effectively uncovered subclinical lesions.
• Subjects who experienced complete resolution of baseline AK lesions also experienced increased AK lesion counts during the treatment period at a greater rate than those who did not experience complete resolution of their baseline AK lesions.
• the increase in AK lesion counts observed in those treated with IRM appears to be due to the appearance of subclinical lesions rather than the formation of new lesions.
• the present invention provides a method for treating skin lesions.
• an IRM compound is administered to a treatment area that includes a skin lesion for a period of time and in an amount sufficient to permit visualization of the margins of the skin lesion.
• the skin lesion is subjected to an ablation procedure such as, for example, Mohs micrographic surgery, surgical excision, cryotherapy, or radiotherapy.
• an ablation procedure such as, for example, Mohs micrographic surgery, surgical excision, cryotherapy, or radiotherapy.
• IRM compounds useful in the methods of the invention include compounds that possess potent immunomodulating activity such as, for example, antiviral and antitumor activity.
• Certain IRMs modulate the production and secretion of cytokines.
• certain IRM compounds induce the production and secretion of cytokines such as, e.g., Type I interferons, TNF- ⁇ , IL-1, IL-6, IL-8, IL-10, IL-12, MIP-1, and/or MCP-1.
• certain IRM compounds can inhibit production and secretion of certain T H 2 cytokines, such as IL-4 and IL-5.
• some LRM compounds are said to suppress IL-1 and TNF (U.S. Patent No. 6,518,265).
• IRMs are small organic molecules (e.g., molecular weight under about 1000 Daltons, preferably under about 500 Daltons, as opposed to large biological molecules such as proteins, peptides, and the like) such as those disclosed in, for example, U.S. Patent Nos. 4,689,338; 4,929,624; 4,988,815; 5,037,986; 5,175,296;
• IRMs include certain purine derivatives (such as those described in U.S. Patent Nos. 6,376,501, and 6,028,076), certain imidazoquinoline amide derivatives (such as those described in U.S. Patent No. 6,069,149), certain imidazopyridine derivatives (such as those described in U.S. Patent No. 6,518,265), certain benzimidazole derivatives (such as those described in U.S.
• Patent 6,387,938 certain derivatives of a 4-ami ⁇ opyrimidine fused to a five membered nitrogen containing heterocyclic ring (such as adenine derivatives described in U. S. Patent Nos. 6,376,501; 6,028,076 and 6,329,381; and in WO 02/08595), and certain 3- jS-D-ribofuranosylthiazolo[4,5-d]pyrimidine derivatives (such as those described in U.S. Publication No. 2003/0199461).
• IRMs include large biological molecules such as oligonucleotide sequences.
• Some IRM oligonucleotide sequences contain cytosine-guanine dinucleotides (CpG) and are described, for example, in U.S. Patent Nos. 6,194,388; 6,207,646; 6,239,116; 6,339,068; and 6,406,705.
• CpG-containing oligonucleo tides can include synthetic immunomodulatory structural motifs such as those described, for example, in U.S. Patent Nos. 6,426,334 and 6,476,000.
• Other IRM nucleotide sequences lack CpG sequences and are described, for example, in International Patent Publication No. WO 00/75304.
• IRMs include biological molecules such as aminoalkyl glucosaminide phosphates (AGPs) and are described, for example, in U.S. Patent Nos. 6,113,918;
• TLR Toll-like receptor
• IRMs can function as Toll-like receptor (TLR) agonists, i.e., their immunomodulating influence is exerted through a TLR-mediated cellular pathway.
• TLR Toll-like receptor
• some small molecule IRMs have been identified as agonists of one or more members of the TLR receptor family, TLR2, TLR4, TLR6, TLR7, and
• the IRM is an agonist of at least one TLR.
• the IRM compound can be an agonist of TLR7, TLR8, and/or TLR9.
• the IRM compound is an agonist of TLR4.
• the IRM is an agonist of TLR7 or an agonist of both TLR7 and TLR8.
• the IRM may induce the production of one or more cytokines, including but not limited to, Type I interferons, TNF- ⁇ , and IL-10. See, for example, Gibson et al., Cell Immunol. 218(l-2):74-86 (2002).
• the IRM may effect the maturation, activation, and/or migration of cells of the myeloid lineage, including, but not limited to, macrophages, dendritic cells, and Langerhans cells.
• Suitable IRM compounds include, but are not limited to, the small molecule LRM compounds described above having a 2-aminopyridine fused to a five membered nitrogen-containing heterocyclic ring.
• Such compounds include, for example, imidazoquinoline amines including but not limited to amide substituted imidazoquinoline amines, sulfonamide substituted imidazoquinoline amines, urea substituted imidazoquinoline amines, aryl ether substituted imidazoquinoline amines, heterocyclic ether substituted imidazoquinoline amines, amido ether substituted imidazoquinoline amines, sulfonamido ether substituted imidazoquinoline amines, urea substituted imidazoquinoline ethers, thioether substituted imidazoquinoline amines, and 6-, 7-, 8-, or 9-aryl or heteroaryl substituted imidazoquinoline amines; tetrahydroimidazoquinoline amine
• the IRM compound is an imidazoquinoline amine such as, for example, l-(2-methylpropyl)-lH-imidazo[4,5-c]quinolin-4-amine or 4-amino- _ ⁇ -dimemyl-2-ethoxymethyl-lH-imidazo[4,5-c]quinolin-l-ethanol.
• the IRM compound is l-(2-methylpropyl)-lH-imidazo[4,5-c]quinolin-4- amine.
• the IRM compound is an imidazonaphthyridine amine such as, for example, 2-methyl-l-(2-methylpropyl)-lH-imidazo[4,5- c][l,5]naphthyridin-4-amine or l-(2-methylpropyl)-lH-imidazo[4,5- c] [ 1 ,5]naphthyridin-4-amine.
• the IRM compound is a sulfonamide substituted imidazoquinoline amine such as, for example, N-[4-(4-amino-2-ethyl-lH- imidazo[4,5-c]quinolin-l -yl)butyl]methanesulfonamide.
• the IRM compound is an amide substituted imidazoquinoline amine such as, for example, N- ⁇ 2-[4-amino-2-(ethoxymethyl)-lH- imidazo[4,5-c]quinolin-l-yl]-l,l-dimethylethyl ⁇ cyclohexanecarboxamide.
• the IRM compound is a thioether substituted imidazoquinoline amine such as, for example, 2-butyl-l-[2-(propylsulfonyl)ethyl]-lH- imidazo[4,5-e]quinolin-4-amine.
• the IRM compound is an imidazopyridine amine such as, for example, N- ⁇ 2-[4-amino-2-(ethoxymethyl)-6,7- dimethyl-lH-imidazo[4,5-c]pyridin-l-yl]ethyl ⁇ benzamide.
• the IRM compound may be an imidazonaphthyridine amine, a tetrahydroimidazonaphthyridine amine, an oxazoloquinoline amine, a thiazoloquinoline amine, an oxazolopyridine amine, a thiazolopyridine amine, an oxazolonaphthyridine amine, or a thiazolonaphthyridine amine.
• the IRM compound may be a substituted imidazoquinoline amine, a tetrahydroimidazoquinoline amine, an imidazopyridine amine, a 1,2-bridged imidazoquinoline amine, a 6,7-fused cycloalkylimidazopyridine amine, an imidazonaphthyridine amine, a tetrahydroimidazonaphthyridine amine, an oxazoloquinoline amine, a thiazoloquinoline amine, an oxazolopyridine amine, a thiazolopyridine amine, an oxazolonaphthyridine amine, or a thiazolonaphthyridine amine.
• a substituted imidazoquinoline amine refers to an amide substituted imidazoquinoline amine, a sulfonamide substituted imidazoquinoline amine, a urea substituted imidazoquinoline amine, an aryl ether substituted imidazoquinoline amine, a heterocyclic ether substituted imidazoquinoline amine, an amido ether substituted imidazoquinoline amine, a sulfonamido ether substituted imidazoquinoline amine, a urea substituted imidazoquinoline ether, a thioether substituted imidazoquinoline amine, or a 6-, 7-, 8-, or 9-aryl or heteroaryl substituted imidazoquinoline amine.
• substituted imidazoquinoline amines specifically and expressly exclude l-(2-methylpropyl)-lH-imidazo[4,5-c]quinolin-4- amine and 4-amino-o Q!-dimethyl-2-ethoxymethyl-lH-imidazo[4,5-c]quinolin-l- ethanol.
• reference to a compound can include the compound in any pharmaceutically acceptable form, including any isomer (e.g., diastereomer or enantiomer), salt, solvate, polymorph, and the like.
• reference to the compound can include each of the compound's enantiomers as well as racemic mixtures of the enantiomers.
• An IRM compound may be provided in any formulation suitable for administration to a subject. Suitable types of formulations are described, for example, in U.S. Pat. No. 5,736,553; U.S. Pat. No. 5,238,944; U.S. Pat. No. 5,939,090; U.S. Pat. No. 6,365,166; U.S. Pat. No. 6,245,776; U.S. Pat. No. 6,486,186; European Patent No. EP 0394 026; and U.S. Patent Publication No. 2003/0199538.
• the compound may be provided in any suitable form including but not limited to a solution, a suspension, an emulsion, or any form of mixture.
• the compound may be delivered in formulation with any pharmaceutically acceptable excipient, carrier, or vehicle.
• the formulation may be delivered in a conventional topical dosage form such as, for example, a cream, an ointment, an aerosol formulation, a non-aerosol spray, a gel, a foam, a solution, a suspension, a dispersion, an emulsion, a microemulsion, a paste, a powder, a solid stick (e.g., wax- or petroleum-based sticks), a wipe, an oil, a lotion, and the like.
• the IRM compound is provided in a cream formulation suitable for topical administration.
• a formulation suitable for practicing the invention may include one or more additional active ingredients such as, for example, another IRM compound, an antibiotic, a pain reliever, a skin penetration enhancer, or a topical anesthetic.
• the LRM compound may be incorporated into, for example, a sunscreen, a skin lotion, a skin moisturizer, or cosmetic.
• the IRM compound may be incorporated into any vehicle suitable for intrade ⁇ nal or transdermal delivery.
• composition of a suitable formulation may depend at least in part on many factors known in the art including, but not limited to, the physical and chemical nature of the IRM compound; the nature of the carrier; the dosing regimen; the state of the subject's immune system (e.g., suppressed, compromised, stimulated); the method of administering the LRM compound; and the desired result (e.g., accentuating margins, visualizing subclinical lesions, etc.). Accordingly it is not practical to set forth generally a single formulation suitable for diagnosing skin lesions for all possible applications. Those of ordinary skill in the art, however, can readily determine a suitable formulation with due consideration of such factors.
• a suitable formulation may contain, for example, about 0.001%, about 0.002%, about 0.005%, about 0.01%, about 0.015%, about 0.02%, about 0.025%, about 0.05%, about 0.1%, about 0.25%, about 0.5%, about 0.75%, about 1%, about 2.5%, about 5%, about 7.5%, about 10%, about 25%, or about 50% active LRM compound.
• the composition includes about 5% IRM compound.
• the amount of IRM compound administered and the period of time over which it is administered may depend, at least in part, on the particular embodiment of the invention being practiced, h one embodiment, the IRM compound may be administered to a lesion periodically for a period of time and in an amount sufficient to permit visualization of the margins of the lesion. In some cases, administering the LRM compound may permit visualization of a subclinical lesion. In other cases, applying the IRM compound may permit more accurate visualization of the actual margin of a clinically visible lesion. The treatment may cause tissue of the lesion that had not been clinically visible to become visible, thereby increasing the likelihood that the entire lesion is visible.
• pre-treatment with an JJRM compound may increase the likelihood that the entire lesion is removed during the ablation procedure, thereby improving the likelihood of a positive treatment outcome.
• Visualization of the lesion may be unaided (e.g., with the naked eye) or aided such as, for example, with a magnifying lens.
• the IRM compound may be administered to a lesion periodically for a period of time and in an amount sufficient to visibly accentuate the margins of a skin lesion, h some cases, the margin of a lesion may appear somewhat indefinite, having margins that are, for example, diffuse or irregular. Administering an IRM compound may visibly accentuate the margin of the lesion — i.e., render the margins of the lesion more definite.
• the IRM compound may be administered to a lesion periodically for a period of time and in an amount sufficient to "light up" the margins of a lesion by inducing a localized immune response within the lesion.
• the localized immune response within the lesion may be mild to moderate.
• the localized immune response within the lesion may be moderate to severe.
• the localized immune response within the lesion may result in inflammation within the lesion, which may include one or more of, for example, erosion, edema (swelling) or erythema (redness) of the lesion.
• the particular amount of IRM compound necessary to permit diagnosis of a lesion in a subject may depend, at least in part, on one or more factors. Such factors include, but are not limited to, the particular IRM compound being administered; the state of the subject's overall health; the state of the subject's immune system (e.g., suppressed, compromised, stimulated); the route of administering the IRM; the particular type of lesion; the histological subtype of the lesion; the size, duration, and location of the lesion; the subject's treatment history; the presence of recurrent disease; and the desired result (e.g., margin accentuation, visualization of subclinical lesions, etc.). Accordingly, it is not practical to set forth generally the amount that constitutes an effective amount of an IRM compound. Those of ordinary skill in the art, however, can readily determine the appropriate amount with due consideration of such factors.
• the methods of the present invention include administering sufficient IRM compound to provide a dose of, for example, from about 100 ng kg to about 50 mg/kg to the subject, although in some embodiments the method may be performed by administering IRM compound in a dose outside this range. In some of these embodiments, the method includes administering sufficient IRM compound to provide a dose of from about 10 ⁇ g/kg to about 5 mg/kg to the subject, for example, a dose of from about 100 ⁇ g/kg to about 1 mg/kg.
• the dosing regimen may depend at least in part on many factors known in the art including but not limited to the physical and chemical nature of the IRM compound; the nature of the carrier; the amount of LRM being administered; the period over which the IRM compound is being administered; the state of the subject's immune system (e.g., suppressed, compromised, stimulated); the method of administering the IRM compound; and the desired result (e.g., accentuating margins of clinically visible lesions, visualizing subclinical lesions, etc.). Accordingly it is not practical to set forth a general dosing regimen effective for all possible applications. Those of ordinary skill in the art, however, can readily determine an appropriate dosing regimen with due consideration of such factors.
• the LRM compound may be administered, for example, from a single dose to multiple doses administered multiple times per day.
• the IRM compound may be administered from about once per week to about once per day.
• the IRM compound is administered once per day, two days per week.
• the IRM compound is administered once per day, three times per week.
• the period of time that is sufficient for practicing the invention may depend, at least in part, on factors such as, for example, the physical and chemical nature of the
• IRM compound the nature of the carrier; the amount of LRM being administered; the frequency with which the IRM compound is being administered; the state of the subject's immune system (e.g., suppressed, compromised, stimulated); the method of administering the LRM compound; and the desired result (e.g., accentuating margins of clinically visible lesions, visualizing subclinical lesions, etc.). Accordingly it is not practical to set forth generally a sufficient period of time for all possible applications. Those of ordinary skill in the art, however, can readily determine an appropriate time period with due consideration of such factors.
• a sufficient period of time may range from at least one day to about six months, although in some embodiments the invention may be practiced by administering IRM compound for a period outside this range.
• the IRM compound may be administered for at least one week.
• the IRM compound may be administered for at least about four weeks.
• the IRM compound may be administered for at least about eight weeks.
• the IRM compound may be administered for at least about sixteen weeks.
• Suitable subjects include, but are not limited to, animals such as, but not limited to, humans, non-human primates, rodents, dogs, cats, horses, pigs, sheep, goats, or cows.
• Example 1 Pretreatment of AK lesions with imiquimod.
• Volunteers having from four to eight clinically diagnosed AK lesions located within a 25 cm 2 treatment area were enrolled in a study.
• the study consisted of a prestudy period, a 16-week treatment period, and an 8-week post treatment period. Enrolled participants were randomized to receive either 5% imiquimod cream
• Subjects were instructed to topically administer cream from a single-use sachet.
• Sachets that contained imiquimod contained 250 mg of cream.
• One group of subjects applied cream two days per week for sixteen weeks, with dosing days occurring a minimum of three days apart.
• a second group of subjects applied cream three days per week for sixteen weeks, with dosing days occurring at least two days apart.
• a baseline AK lesion count was established for each subject. Updated AK lesion counts were calculated at visits after four weeks, eight weeks, and sixteen weeks of treatment. For each individual, "new" AK lesions were calculated as the difference between the updated AK count and the baseline AK count.
• Example 2 Pretreatment of BCC lesions with imiquimod.
• 5% imiquimod cream Prior to surgical excision of their lesions, patients with BCC lesions are prefreated with a 5% imiquimod cream, marketed as ALDARA (3M Pharmaceuticals, St. Paul, MN). Topical application of the 5% imiquimod cream to the BCC lesions five to seven times a week for five to seven weeks results in significant erosion, erythema, and/or edema of the BCC lesions, thereby accentuating the margins of the lesions.
• ALDARA 5% imiquimod cream
• Example 3 Treatment of Bowen's lesions with imiquimod.
• 5% imiquimod cream Prior to surgical excision of their lesions, patients with Bowen's disease are prefreated with a 5% imiquimod cream, marketed as ALDARA (3M Pharmaceuticals, St. Paul, MN). Topical application of the 5% imiquimod cream to the lesion two to three times a week for one to three weeks results in significant erosion, erythema, and/or edema of the lesions, thereby accentuating the margins of the lesions.
• ALDARA 5% imiquimod cream
• Example 4 Treatment of lentigo maligna lesions with imiquimod.
• Topical application of the 5% imiquimod cream to the lesion two to three times a week for one to three weeks results in significant erosion, erythema, and/or edema of the lesions, thereby accentuating the margins of the lesions.

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