WO2006066267A2 - Cancer treatment method - Google Patents
Cancer treatment method Download PDFInfo
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- WO2006066267A2 WO2006066267A2 PCT/US2005/046350 US2005046350W WO2006066267A2 WO 2006066267 A2 WO2006066267 A2 WO 2006066267A2 US 2005046350 W US2005046350 W US 2005046350W WO 2006066267 A2 WO2006066267 A2 WO 2006066267A2
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- breast cancer
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- compound
- mammal
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—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
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
- A61K31/52—Purines, e.g. adenine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/473—Quinolines; Isoquinolines ortho- or peri-condensed with carbocyclic ring systems, e.g. acridines, phenanthridines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—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
- A61K31/513—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim having oxo groups directly attached to the heterocyclic ring, e.g. cytosine
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- 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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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
Definitions
- the present invention relates to a method of treating breast cancer that has metastasized to the brain in a mammal by administration of 4-quinazolinamines and pharmaceutical compositions containing the same.
- the method relates to methods of treating breast cancer brain metastases which overexpress erbB2 by administration of N- ⁇ 3-chloro-4-[(3-fluorobenzyl) oxy]phenyl ⁇ -6-[5-( ⁇ [2- (methanesulphonyl) ethyljamino ⁇ methyl)-2-furyl]-4-quinazolinamine and salts and solvates thereof.
- Trastuzumab-based regimens have improved both systemic control and overall survival in patients with metastatic ErbB2 overexpressing breast cancer.
- Trastuzumab does not cross the blood-brain barrier and ErbB2-positive breast cancer may have a predilection to metastasize to distant organs, including the the brain.
- CNS progression is emerging as a major clinical problem.
- the initial treatment of brain metastases depends upon their multiplicity, location, size, and upon the status of a patient's systemic disease.
- Options may include surgical resection, stereotactic radiosurgery (SRS), and whole brain radiotherapy (WBRT).
- SRS stereotactic radiosurgery
- WBRT whole brain radiotherapy
- CNS progression after WBRT and/or SRS is a significant clinical problem.
- SRS stereotactic radiosurgery
- WBRT whole brain radiotherapy
- Temozolomide is an orally bioavailable alkylating agent that readily crosses the blood-brain barrier. Phase Il trials have reported inconsistent activity with temozolomide in this population (Christodoulou C.
- the blood-brain barrier (BBB) excludes many therapeutic agents from the
- the BBB is formed by the complex tight junctions between the endothelial cells of the brain capillaries and their low endocytic activity (Potschka et al, Journal of Pharm. And Exp. Therapeutics 306(1): 124-131 , 2003 July). This results in a capillary wall that behaves as a continuous lipid bilayer and prevents the passage of polar and lipid-insoluble substances. Additionally, ATP-dependent multidrug transporters such as P-glycoprotein (Pgp; ABCB1) and multidrug resistance protein MRP2 (ABCC2), which are found in the membranes of brain capillary endothelial cells, are thought to play an important role in BBB function by limiting drug penetration into the brain.
- Pgp P-glycoprotein
- ABCC2 multidrug resistance protein
- Brain tumors may disrupt the function of the BBB locally and nonhomogeneously.
- CNS activity with a variety of chemotherapeutic regimens (cytoxan/methotrexate/5-fluorouracil, doxorubicin/cytoxan, capecitabine, cisplatin/etoposide) has been reported, despite the fact that none of these agents cross the intact blood brain barrier at the doses used.
- chemotherapeutic regimens cytoxan/methotrexate/5-fluorouracil, doxorubicin/cytoxan, capecitabine, cisplatin/etoposide
- Small molecule tyrosine kinase inhibitors may cross a disrupted blood brain barrier.
- a 69% partial response rate and 80% systemic disease control rate with first- line gefitinib in Asian, female, non-smokers with NSCLC adenocarcinoma was recently reported (Lee Jun-Soo, International Assoc, for the Study of Lung Cancer, Baltimore, July 2004).
- Gefitinib (Iressa ⁇ ) is an inhibitor of the epidermal growth factor receptor (EGFR) and is indicated as monotherapy for the treatment of patients with locally advanced or metastatic non-small cell lung cancer after failure of both platinum-based and docetaxel chemotherapies.
- EGFR epidermal growth factor receptor
- Another potential mechanism of resistance to trastuzumab therapy is a discordance in ErbB2 expression between the primary tumor and sites of metastases e.g. ErbB2 non-overexpressing cells escape systemic therapy with trastuzumab.
- the transcriptional expression of ErbB2 in brain metastases has been shown to routinely exceed that of the primary breast cancer (Steeg P., Third Int'l. Symp. On Translational Res. In One, Santa Barbara CA, Oct9-12, 2003; and Steeg P. et al, Eur. J. Cancer 2(8): 142, Sept 2004, abstract 468).
- clones that metastasize to the CNS may be resistant to trastuzumab via mechanisms such as upregulation of the truncated ErbB2 receptor p95 or a PTEN deficiency (Nagata Y. et al, Cancer Cell 6(2):117-127, 2004; and Christianson T. A. et al, Cancer Research 58(22):5123-5129, 1998).
- agata Y. et al, Cancer Cell 6(2):117-127, 2004; and Christianson T. A. et al, Cancer Research 58(22):5123-5129, 1998 As indicated above, brain metastases typically develop while systemic disease is well controlled with trastuzumab. Hence, the most reasonable assumption is the large monoclonal antibody trastuzumab cannot access the CNS regardless of the blood-brain-barrier status.
- the present inventor has now identified novel treatment methods for breast cancer that has metastasized to the brain.
- Such method includes administration of N- ⁇ 3-chloro-4-[(3-fluorobenzyl) oxy]phenyl ⁇ -6-[5-( ⁇ [2-(methanesulphonyl) ethyl]amino ⁇ methyl)-2-furyl]-4-quinazolinamine (GW572016) as well as salts and/or solvates thereof to a mammal in need thereof.
- a method of treating breast cancer that has metastasized to the brain in a mammal comprising: administering to said mammal therapeutically effective amounts of a compound of formula (I)
- a method of treating breast cancer that has metastasized to the brain in a mammal comprising: administering to said mammal therapeutically effective amounts of a compound of formula (I 1 )
- a method of treating breast cancer that has metastasized to the brain in a mammal comprising: administering to said mammal therapeutically effective amounts of the compound of formula (I")
- neoplasm refers to an abnormal growth of cells or tissue and is understood to include benign, i.e., non-cancerous growths, and malignant, i.e., cancerous growths including primary or metastatic cancerous growths.
- malignant i.e., cancerous growths including primary or metastatic cancerous growths.
- neoplastic means of or related to a neoplasm.
- EGFR also known as “erbB-1”, and “erbB-2” are protein tyrosine kinase transmembrane growth factor receptors of the erbB family. Protein tyrosine kinases catalyse the phosphorylation of specific tyrosyl residues in various proteins involved in the regulation of cell growth and differentiation (A.F. Wilks, Progress in Growth Factor Research, 1990, 2, 97-111 ; S.A. Courtneidge, Dev. Supp.l, 1993, 57-64; J.A. Cooper, Semin. Cell Biol., 1994, 5(6), 377-387; R. F. Paulson, Semin.
- the ErbB family of type I receptor tyrosine kinases includes ErbB1 (also known as the epidermal growth factor receptor (EGFR or HER1)), ErbB2 (also known as Her2), ErbB3, and ErbB4. These receptor tyrosine kinases are widely expressed in epithelial, mesenchymal, and neuronal tissues where they play a role in regulating cell proliferation, survival, and differentiation (Sibilia and Wagner, Science, 269: 234 (1995); Threadgill et al., Science, 269: 230 (1995)).
- a cell "overexpressing" ErbB2 refers to a cell having a significantly increased number of functional ErbB2 receptors, compared to the average number of receptors that would be found on a cell of that same type.
- Overexpression of ErbB2 may be assessed by any suitable method as is known in the art, including but not limited to imaging, gene amplification, number of cell surface receptors present, protein expression, and mRNA expression. See e.g., Piffanelli et al., Breast Cancer Res. Treatment 37:267 (1996).
- the term "effective amount” means that amount of a drug or pharmaceutical agent that will elicit the biological or medical response of a tissue, system, animal or human that is being sought, for instance, by a researcher or clinician.
- therapeutically effective amount means any amount which, as compared to a corresponding subject who has not received such amount, results in improved treatment, healing, prevention, or amelioration of a disease, disorder, or side effect, or a decrease in the rate of advancement of a disease or disorder.
- the term also includes within its scope amounts effective to enhance normal physiological function.
- treating breast cancer that is metastasized to the brain includes within its scope treatment of the primary sites of the breast cancer, treatment of systemic breast cancer metastatic sites, and treatment of breast cancer metastatic sites in the brain.
- prevention of breast cancer brain metastases includes within its scope preventing as well as stopping, delaying, or slowing the progression of breast cancer metastases.
- solvate refers to a complex of variable stoichiometry formed by a solute (in this invention, compounds of formula (I) or a salt thereof) and a solvent.
- solvents for the purpose of the invention may not interfere with the biological activity of the solute.
- suitable solvents include, but are not limited to, water, methanol, ethanol and acetic acid.
- the solvent used is a pharmaceutically acceptable solvent.
- suitable pharmaceutically acceptable solvents include, without limitation, water, ethanol and acetic acid. Most preferably the solvent used is water.
- the methods of cancer treatment disclosed herein includes administering a compound of formula (I):
- the compound is a compound of formula (I 1 ) which is the ditosylate salt of the compound of formula (I) and anhydrate or hydrate forms thereof.
- the ditosylate salt of the compound of formula (I) has the chemical name N- ⁇ 3-chloro-4-[(3-fluorobenzyl) oxy]phenyl ⁇ -6-[5-( ⁇ [2-(methanesulphonyl) ethyl]amino ⁇ methyl)-2-furyl]-4-quinazolinamine (GW572016) ditosylate and is also known as lapatinib.
- the compound is the anhydrous ditosylate salt of the compound of formula (I 1 ). In another embodiment, the compound is a compound of formula (I") which is the monohydrate ditosylate salt of the compound of formula (I 1 ).
- the free base, HCI salts, and ditosylate salts of the compound of Formula (I) may be prepared according to the procedures of International Patent Application No. PCT/EP99/00048, filed January 8, 1999, and published as WO 99/35146 on July 15, 1999, referred to above and International Patent Application No. PCT/U S01/20706, filed June 28, 2001 and published as WO 02/02552 on January 10, 2002 and according to the appropriate Examples recited below.
- One such procedure for preparing the ditosylate salt of the compound of formula (I) is presented following in Scheme 1.
- the preparation of the ditosylate salt of the compound of formula (III) proceeds in four stages: Stage 1 : Reaction of the indicated bicyclic compound and amine to give the indicated iodoquinazoline derivative; Stage 2: preparation of the corresponding aldehyde salt; Stage 3: preparation of the quinazoline ditosylate salt; and Stage 4: monohydrate ditosylate salt preparation.
- the salts of the present invention are pharmaceutically acceptable salts. Salts encompassed within the term "pharmaceutically acceptable salts" refer to non-toxic salts of the compounds of this invention. Salts of the compounds of the present invention may comprise acid addition salts derived from a nitrogen on a substituent in a compound of the present invention.
- Representative salts include the following salts: acetate, benzenesulfonate, benzoate, bicarbonate, bisulfate, bitartrate, borate, bromide, calcium edetate, camsylate, carbonate, chloride, clavulanate, citrate, dihydrochloride, edetate, edisylate, estolate, esylate, fumarate, gluceptate, gluconate, glutamate, glycollylarsanilate, hexylresorcinate, hydrabamine, hydrobromide, hydrochloride, hydroxynaphthoate, iodide, isethionate, lactate, lactobionate, laurate, malate, maleate, mandelate, mesylate, methylbromide, methylnitrate, methylsulfate, monopotassium maleate, mucate, napsylate, nitrate, N- methylglucamine, ox
- the invention further provides pharmaceutical compositions, which may be administered in the cancer treatment methods of the present invention.
- the pharmaceutical compositions include therapeutically effective amounts of a compound of formula (I) and salts or solvates thereof, and one or more pharmaceutically acceptable carriers, diluents, or excipients.
- the carrier(s), diluent(s) or excipient(s) must be acceptable in the sense of being compatible with the other ingredients of the formulation and not deleterious to the recipient thereof. .
- compositions may be presented in unit dose forms containing a predetermined amount of active ingredient per unit dose.
- a unit may contain, for example, 0.5mg to 1g, preferably 1mg to 700mg, more preferably 5mg to 100mg of a compound of formula (I), depending on the condition being treated, the route of administration and the age, weight and condition of the patient, or pharmaceutical formulations may be presented in unit dose forms containing a predetermined amount of active ingredient per unit dose.
- Preferred unit dosage formulations are those containing a daily dose or sub-dose, as herein above recited, or an appropriate fraction thereof, of an active ingredient.
- such pharmaceutical formulations may be prepared by any of the methods well known in the pharmacy art.
- the compound of formula (I) may be administered by any appropriate route. Suitable routes include oral, rectal, nasal, topical (including buccal and sublingual), vaginal, and parenteral (including subcutaneous, intramuscular, intraveneous, intradermal, intrathecal, and epidural). It will be appreciated that the preferred route may vary with, for example, the condition of the recipient of the combination.
- the method of the present invention may also be employed with other therapeutic methods of cancer treatment.
- combination therapy with other chemotherapeutic, hormonal, antibody agents as well as surgical and/or radiation treatments other than those mentioned above are envisaged.
- Anti-neoplastic therapies are described for instance in International Application No. PCT US 02/01130, filed January 14, 2002, which application is incorporated by reference to the extent that it discloses anti-neoplastic therapies.
- Combination therapies according to the present invention thus include the administration of at least one compound of formula (I) as well as optional use of other therapeutic agents including other anti-neoplastic agents.
- Such combination of agents may be administered together or separately and, when administered separately this may occur simultaneously or sequentially in any order, both close and remote in time.
- the amounts of the compound of formula (I) and the other pharmaceutically active agent(s) and the relative timings of administration will be selected in order to achieve the desired combined therapeutic effect.
- compositions adapted for oral administration may be presented as discrete units such as capsules or tablets; powders or granules; solutions or suspensions in aqueous or non-aqueous liquids; edible foams or whips; or oil-in-water liquid emulsions or water-in-oil liquid emulsions.
- the active drug component can be combined with an oral, non-toxic pharmaceutically acceptable inert carrier such as ethanol, glycerol, water and the like.
- Powders are prepared by comminuting the compound to a suitable fine size and mixing with a similarly comminuted pharmaceutical carrier such as an edible carbohydrate, as, for example, starch or mannitol. Flavoring, preservative, dispersing and coloring agent can also be present.
- Capsules are made by preparing a powder mixture as described above, and filling formed gelatin sheaths.
- Glidants and lubricants such as colloidal silica, talc, magnesium stearate, calcium stearate or solid polyethylene glycol can be added to the powder mixture before the filling operation.
- a disintegrating or solubilizing agent such as agar-agar, calcium carbonate or sodium carbonate can also be added to improve the availability of the medicament when the capsule is ingested.
- suitable binders include starch, gelatin, natural sugars such as glucose or beta- lactose, corn sweeteners, natural and synthetic gums such as acacia, tragacanth or sodium alginate, carboxymethylcellulose, polyethylene glycol, waxes and the like.
- Lubricants used in these dosage forms include sodium oleate, sodium stearate, magnesium stearate, sodium benzoate, sodium acetate, sodium chloride and the like.
- Disintegrators include, without limitation, starch, methyl cellulose, agar, bentonite, xanthan gum and the like.
- Tablets are formulated, for example, by preparing a powder mixture, granulating or slugging, adding a lubricant and disintegrant and pressing into tablets.
- a powder mixture is prepared by mixing the compound, suitably comminuted, with a diluent or base as described above, and optionally, with a binder such as carboxymethylcellulose, an aliginate, gelatin, or polyvinyl pyrrolidone, a solution retardant such as paraffin, a resorption accelerator such as a quaternary salt and/or an absorption agent such as bentonite, kaolin or dicalcium phosphate.
- a binder such as carboxymethylcellulose, an aliginate, gelatin, or polyvinyl pyrrolidone
- a solution retardant such as paraffin
- a resorption accelerator such as a quaternary salt
- an absorption agent such as bentonite, kaolin or dicalcium phosphate.
- the powder mixture can be granulated by wetting with a binder such as syrup, starch paste, acadia mucilage or solutions of cellulosic or polymeric materials and forcing through a screen.
- a binder such as syrup, starch paste, acadia mucilage or solutions of cellulosic or polymeric materials and forcing through a screen.
- the powder mixture can be run through the tablet machine and the result is imperfectly formed slugs broken into granules.
- the granules can be lubricated to prevent sticking to the tablet forming dies by means of the addition of stearic acid, a stearate salt, talc or mineral oil.
- the lubricated mixture is then compressed into tablets.
- the compounds of the present invention can also be combined with free flowing inert carrier and compressed into tablets directly without going through the granulating or slugging steps.
- a clear or opaque protective coating consisting of a sealing coat of shellac, a coating of sugar or
- Oral fluids such as solution, syrups and elixirs can be prepared in dosage unit form so that a given quantity contains a predetermined amount of the compound.
- Syrups can be prepared by dissolving the compound in a suitably flavored aqueous solution, while elixirs are prepared through the use of a non-toxic alcoholic vehicle.
- Suspensions can be formulated by dispersing the compound in a non-toxic vehicle.
- Solubilizers and emulsifiers such as ethoxylated isostearyl alcohols and polyoxy ethylene sorbitol ethers, preservatives, flavor additive such as peppermint oil or natural sweeteners or saccharin or other artificial sweeteners, and the like can also be added.
- dosage unit formulations for oral administration can be microencapsulated.
- the formulation can also be prepared to prolong or sustain the release as for example by coating or embedding particulate material in polymers, wax or the like.
- the agents for use according to the present invention can also be administered in the form of liposome delivery systems, such as small unilamellar vesicles, large unilamellar vesicles and multilamellar vesicles.
- Liposomes can be formed from a variety of phospholipids, such as cholesterol, stearylamine or phosphatidylcholines.
- Agents for use according to the present invention may also be delivered by the use of monoclonal antibodies as individual carriers to which the compound molecules are coupled.
- the compounds may also be coupled with soluble polymers as targetable drug carriers.
- Such polymers can include polyvinylpyrrolidone, pyran copolymer, polyhydroxypropylmethacrylamide-phenol, polyhydroxyethylaspartamidephenol, or polyethyleneoxidepolylysine substituted with palmitoyl residues.
- the compounds may be coupled to a class of biodegradable polymers useful in achieving controlled release of a drug, for example, polylactic acid, polepsilon caprolactone, polyhydroxy butyric acid, polyorthoesters, polyacetals, polydihydropyrans, polycyanoacrylates and cross-linked or amphipathic block copolymers of hydrogels.
- a class of biodegradable polymers useful in achieving controlled release of a drug, for example, polylactic acid, polepsilon caprolactone, polyhydroxy butyric acid, polyorthoesters, polyacetals, polydihydropyrans, polycyanoacrylates and cross-linked or amphipathic block copolymers of hydrogels.
- compositions adapted for transdermal administration may be presented as discrete patches intended to remain in intimate contact with the epidermis of the recipient for a prolonged period of time.
- the active ingredient may be delivered from the patch by iontophoresis as generally described in Pharmaceutical Research, 3(6), 318 (1986).
- compositions adapted for topical administration may be formulated as ointments, creams, suspensions, lotions, powders, solutions, pastes, gels, sprays, aerosols or oils.
- the formulations are preferably applied as a topical ointment or cream.
- the active ingredient may be employed with either a paraffinic or a water-miscible ointment base.
- the active ingredient may be formulated in a cream with an oil-in-water cream base or a water-in-oil base.
- compositions adapted for topical administrations to the eye include eye drops wherein the active ingredient is dissolved or suspended in a suitable carrier, especially an aqueous solvent.
- compositions adapted for topical administration in the mouth include lozenges, pastilles and mouth washes.
- compositions adapted for rectal administration may be presented as suppositories or as enemas.
- compositions adapted for nasal administration wherein the carrier is a solid include a coarse powder having a particle size for example in the range 20 to 500 microns which is administered in the manner in which snuff is taken, i.e. by rapid inhalation through the nasal passage from a container of the powder held close up to the nose.
- Suitable formulations wherein the carrier is a liquid, for administration as a nasal spray or as nasal drops, include aqueous or oil solutions of the active ingredient.
- Fine particle dusts or mists that may be generated by means of various types of metered dose pressurised aerosols, nebulizers or insufflators.
- compositions adapted for vaginal administration may be presented as pessaries, tampons, creams, gels, pastes, foams or spray formulations.
- compositions adapted for parenteral administration include aqueous and non-aqueous sterile injection solutions which may contain antioxidants, buffers, bacteriostats and solutes which render the formulation isotonic with the blood of the intended recipient; and aqueous and non-aqueous sterile suspensions which may include suspending agents and thickening agents.
- the formulations may be presented in unit-dose or multi-dose containers, for example sealed ampoules and vials, and may be stored in a freeze-dried (lyophilized) condition requiring only the addition of the sterile liquid carrier, for example water for injections, immediately prior to use.
- Extemporaneous injection solutions and suspensions may be prepared from sterile powders, granules and tablets.
- formulations may include other agents conventional in the art having regard to the type of formulation in question, for example those suitable for oral administration may include flavoring agents.
- therapeutically effective amounts of a specific compound of formula (I) is administered to a mammal.
- the therapeutically effective amount of one of the administered agents of the present invention will depend upon a number of factors including, for example, the age and weight of the mammal, the precise condition requiring treatment, the severity of the condition, the nature of the formulation, and the route of administration. Ultimately, the therapeutically effective amount will be at the discretion of the attendant physician or veterinarian.
- the compound of formula (I) will be given in the range of 0.1 to 100 mg/kg body weight of recipient (mammal) per day and more usually in the range of 1 to 10 mg/kg body weight per day.
- the present invention is directed to novel treatment methods for breast cancer that has metastasized to the brain.
- Such method includes administration of N- ⁇ 3-chloro-4-[(3-fluorobenzyl) oxy]phenyl ⁇ -6-[5-( ⁇ [2- (methanesulphonyl) ethyl]amino ⁇ methyl)-2-furyl]-4-quinazolinamine (GW572016) as well as salts and/or solvates thereof to a mammal in need thereof.
- the breast cancer overexpresses erbB-2.
- the brain metastatic sites overexpress erbB-2.
- the mammal has previously been treated with trastuzumab.
- a method of treating breast cancer metastases in the brain of a mammal which includes administration of a compound of formula (I).
- the compound of formula (I) is a compound of formula (I 1 ). In another embodiment, the compound of formula (I) is the compound of formula (I").
- the breast cancer metastases overexpress erbB-2.
- the mammal has previously been treated with trastuzumab.
- the compounds of formulae (I), (I 1 ), and (I") if utilized to treat earlier stages of breast cancer alone or in combination with other anti-neoplasties, may prevent or delay the development of brain metastases. Accordingly, in another aspect of the present invention is provided a method for the prevention of breast cancer brain metastases, which includes administration of a compound of formula (I).
- the compound of formula (I) is a compound of formula (I 1 ).
- the compound of formula (I) is the compound of formula
- a compound of formulae (I), (I 1 ), or (I") and at least one additional cancer treatment therapy may be employed in the disclosed cancer treatment methods.
- the compounds of formulae (I), (I 1 ), and (I") may be utilized in combination concomitantly or sequentially in any therapeutically appropriate combination with such other anti-cancer therapies.
- the additional anti-cancer therapy is a radiation therapy, including stereotactic radiosurgery (SRS) and whole brain radiotherapy (WBRT).
- the other anti-cancer therapy is at least one additional chemotherapeutic therapy including administration of at least one anti-neoplastic agent.
- the administration in combination of a compound of formula (I) or salts, solvates, or physiologically functional derivatives thereof with other anti-neoplastic agents may be in combination in accordance with the invention by administration concomitantly in (1) a unitary pharmaceutical composition including both compounds, or (2) separate pharmaceutical compositions each including one of the compounds.
- the combination may be administered separately in a sequential manner wherein one anti-neoplastic agent is administered first and the other second or vice versa. Such sequential administration may be close in time or remote in time.
- Anti-neoplastic agents may induce anti-neoplastic effects in a cell-cycle specific manner, i.e., are phase specific and act at a specific phase of the cell cycle, or bind DNA and act in a non cell-cycle specific manner, i.e., are non-cell cycle specific and operate by other mechanisms.
- Anti-neoplastic agents useful in combination with the compounds and salts, solvates or physiologically functional derivatives thereof of formula I include the following: (1) cell cycle specific anti-neoplastic agents including, but not limited to, diterpenoids such as paclitaxel and its analog docetaxel; vinca alkaloids such as vinblastine, vincristine, vindesine, and vinorelbine; epipodophyllotoxins such as etoposide and teniposide; gemcitabine; capecitabine, fluoropyrimidines such as 5- fluorouracil and fluorodeoxyuridine ; antimetabolites such as allopurinol, fludurabine, methotrexate, cladrabine, cytarabine, mercaptopurine and thioguanine; and camptothecins such as 9-amino camptothecin, irinotecan, topotecan, CPT-11 and the various optical forms of 7-(4-methylpiperazino-
- cytotoxic chemotherapeutic agents including, but not limited to, alkylating agents such as melphalan, chlorambucil, cyclophosphamide, mechlorethamine, hexamethylmelamine, busulfan, carmustine, lomustine, and dacarbazine; anti-tumour antibiotics such as doxorubicin, daunomycin, epirubicin, idarubicin, mitomycin-C, dacttinomycin and mithramycin; and platinum coordination complexes such as cisplatin, carboplatin, and oxaliplatin; and
- anti-estrogens such as tamoxifen, toremifene, raloxifene, droloxifene and iodoxyfene
- progestrogens such as megestrol acetate
- aromatase inhibitors such as anastrozole, letrazole, vorazole, and exemestane
- antiandrogens such as flutamide, nilutamide, bicalutamide, and cyproterone acetate
- LHRH agonists and antagagonists such as goserelin acetate and luprolide, testosterone 5 ⁇ -dihydroreductase inhibitors such as finasteride
- metalloproteinase inhibitors such as marimastat
- antiprogestogens urokinase plasminogen activator receptor function inhibitors
- Bcl-2 inhibitors growth factor function inhibitors such as inhibitors of the functions of he
- the methods of the present invention will include the administration of a compound of formulae (I), (I 1 ), or (I") and an inhibitor of transport proteins such as p-glycoprotein (P-gp) and breast cancer resistant protein (BCRP).
- P-gp p-glycoprotein
- BCRP breast cancer resistant protein
- a suitable example includes elacridar which is described in U.S. Patents 5,604,237, 6,469,022, 6,803,373, and International Patent Application PCT/N LOO/00331 filed May 17, 2000 and published as WO 00/69390 on November 23, 2000.
- T r retention time
- RP reverse phase
- DCM dichloromethane
- DCE dichloroethane
- TIPS triisopropylsilyl
- TBS f-butyldimethylsilyl
- GW572016F is lapatanib whose chemical name is N- ⁇ 3-Chloro-4-[(3- fluorobenzyl)oxy]phenyl ⁇ -6-[5-( ⁇ [2-(methane sulphonyl) ethyl]amino ⁇ methyl)-2-furyl]- 4-quinazolinamine ditosylate monhydrate.
- the vessel was rinsed with IMS (2vol).
- the resulting mixture was stirred at ca 22°C for ca 2 hours then sampled for HPLC analysis.
- the reaction was quenched by addition of aqueous sodium hydroxide (25% w/w, 3 vols.) followed by water (2 vols.) and stirred for ca 30 minutes (some effervescence was seen at the start of the caustic addition).
- aqueous phase was then separated, extracted with THF (2 vols) and the combined THF extracts were then washed twice with 25% w/v aqueous ammonium chloride solution (2 x 5 vols) 2 .
- a solution of p-toluenesulfonic acid monohydrate (p- TSA, 0.74 wt, 2.5 equiv.) in water (1 vol) 1 was prepared, warmed to ca 60 0 C, and GW572016F (Compound G) (0.002 wt) seeds were added.
- the THF solution of the free base of GW572016 was added to the p-TSA solution over at least 30 minutes, while maintaining the batch temperature at 60+3 0 C.
- the resulting suspension was stirred at ca 6O 0 C for 1-2 hours, cooled to 20-25 0 C over an hour and aged at this temperature for ca 1hr.
- the solid was collected by filtration, washed with 95:5 THF:Water (3 x 2 vols) and dried in vacuo at ca 35°C to give
- the initial week 1 PET scan results on one patient showed promising activity with a dramatic change in one lesion while other brain lesions showed less change or no change at all.
- the patient had disease which had progressed through Xeloda® (capecitabine), Navelbine® (vinorelbine)/Herceptin® (trastuzumab), and single agent Herceptin® (trastuzumab) treatments. She entered the study with progression in the liver and the brain.
- the initial one week PET scans showed promising activity after treatment with lapatinib.
Abstract
Description
Claims
Priority Applications (10)
Application Number | Priority Date | Filing Date | Title |
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US11/721,675 US20080306097A1 (en) | 2004-12-17 | 2005-12-16 | Cancer Treatment Method |
AU2005316238A AU2005316238B2 (en) | 2004-12-17 | 2005-12-16 | Cancer treatment method |
EP05854982.5A EP1824492B1 (en) | 2004-12-17 | 2005-12-16 | Lapatinib for treating breast cancer brain metastases |
NZ555462A NZ555462A (en) | 2004-12-17 | 2005-12-16 | Cancer treatment method |
ES05854982T ES2426007T3 (en) | 2004-12-17 | 2005-12-16 | Method for cancer treatment |
JP2007547043A JP5291345B2 (en) | 2004-12-17 | 2005-12-16 | Cancer treatment |
MX2007006043A MX2007006043A (en) | 2004-12-17 | 2005-12-16 | Cancer treatment method. |
IL183059A IL183059A0 (en) | 2004-12-17 | 2007-05-08 | Cancer treatment method |
NO20072631A NO20072631L (en) | 2004-12-17 | 2007-05-22 | Cancer Treatment Method |
US14/690,917 US20150283139A1 (en) | 2004-12-17 | 2015-04-20 | Cancer treatment method |
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US63705204P | 2004-12-17 | 2004-12-17 | |
US60/637,052 | 2004-12-17 |
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US11/721,675 A-371-Of-International US20080306097A1 (en) | 2004-12-17 | 2005-12-16 | Cancer Treatment Method |
US14/690,917 Continuation US20150283139A1 (en) | 2004-12-17 | 2015-04-20 | Cancer treatment method |
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WO2006066267A3 WO2006066267A3 (en) | 2006-12-14 |
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US (2) | US20080306097A1 (en) |
EP (1) | EP1824492B1 (en) |
JP (1) | JP5291345B2 (en) |
KR (1) | KR20070107004A (en) |
CN (1) | CN101083995A (en) |
AU (1) | AU2005316238B2 (en) |
ES (1) | ES2426007T3 (en) |
IL (1) | IL183059A0 (en) |
MX (1) | MX2007006043A (en) |
NO (1) | NO20072631L (en) |
NZ (1) | NZ555462A (en) |
RU (1) | RU2007119432A (en) |
WO (1) | WO2006066267A2 (en) |
ZA (1) | ZA200705059B (en) |
Cited By (10)
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EP1906185A1 (en) * | 2006-09-26 | 2008-04-02 | ProteoSys AG | Use of at least one isoform of progesterone receptor membrane component 1 (PGRMC1) |
EP2158913A1 (en) | 2008-08-25 | 2010-03-03 | Ratiopharm GmbH | Pharmaceutical composition comprising N-[3-chhloro-4-[(3-fluorophenyl)methoxy]phenyl]6-(5[[[2-(methylsulfonyl)ethyl]amino]methyl]-2-furyl]-4-quinazolinamine |
EP2158912A1 (en) | 2008-08-25 | 2010-03-03 | Ratiopharm GmbH | Pharmaceutical composition comprising N-[3-chhloro-4-[3-fluorophenyl)methoxy)phenyl]6-[5[[[2-(methylsulfonyl)ethyl]amino]methyl]-2-furyl]-4-quinazolinamine |
WO2010105110A1 (en) * | 2009-03-11 | 2010-09-16 | Ardea Biosciences, Inc. | Pharmaceutical combinations comprising rdea119/bay 869766 for the treatment of specific cancers |
WO2011116634A1 (en) | 2010-03-23 | 2011-09-29 | Scinopharm Taiwan Ltd. | Process and intermediates for preparing lapatinib |
WO2012010091A1 (en) * | 2010-07-23 | 2012-01-26 | 江苏豪森医药集团有限公司 | Optically pure quinazoline compound |
WO2012010088A1 (en) * | 2010-07-23 | 2012-01-26 | 江苏豪森医药集团有限公司 | Optically pure quinazoline compounds |
US8252805B2 (en) | 2008-05-07 | 2012-08-28 | Teva Pharmaceutical Industries Ltd. | Forms of lapatinib ditosylate and processes for preparation thereof |
WO2014059956A1 (en) | 2012-10-17 | 2014-04-24 | Zentiva, K.S. | A method of producing the key intermediate of lapatinib synthesis |
US8710221B2 (en) | 2010-03-23 | 2014-04-29 | Scinopharm Taiwan, Ltd. | Process and intermediates for preparing lapatinib |
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CN102146075B (en) * | 2010-02-06 | 2014-04-02 | 浙江九洲药业股份有限公司 | Preparation method of quinazoline compound |
CN102321076B (en) * | 2011-07-07 | 2013-08-21 | 中国科学技术大学 | Preparation method of lapatinib intermediate and analogues thereof |
CN106632276B (en) * | 2015-10-28 | 2021-06-15 | 上海天慈生物谷生物工程有限公司 | Preparation method of medicine for treating breast cancer |
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GB9800569D0 (en) * | 1998-01-12 | 1998-03-11 | Glaxo Group Ltd | Heterocyclic compounds |
ES2236481T3 (en) * | 2001-01-16 | 2005-07-16 | Glaxo Group Limited | PHARMACEUTICAL COMBINATION CONTAINING A 4-QUINAZOLINAMINE AND PACLITAXEL, CARBOPLATIN OR VINORELBINE FOR CANCER TREATMENT. |
MXPA06013952A (en) * | 2004-06-04 | 2007-02-08 | Smithkline Beecham Cork Ltd | Cancer treatment method. |
-
2005
- 2005-12-16 WO PCT/US2005/046350 patent/WO2006066267A2/en active Application Filing
- 2005-12-16 JP JP2007547043A patent/JP5291345B2/en not_active Expired - Fee Related
- 2005-12-16 US US11/721,675 patent/US20080306097A1/en not_active Abandoned
- 2005-12-16 EP EP05854982.5A patent/EP1824492B1/en active Active
- 2005-12-16 CN CNA2005800434300A patent/CN101083995A/en active Pending
- 2005-12-16 RU RU2007119432/14A patent/RU2007119432A/en not_active Application Discontinuation
- 2005-12-16 ES ES05854982T patent/ES2426007T3/en active Active
- 2005-12-16 NZ NZ555462A patent/NZ555462A/en not_active IP Right Cessation
- 2005-12-16 MX MX2007006043A patent/MX2007006043A/en not_active Application Discontinuation
- 2005-12-16 KR KR1020077016268A patent/KR20070107004A/en not_active Application Discontinuation
- 2005-12-16 AU AU2005316238A patent/AU2005316238B2/en not_active Ceased
-
2007
- 2007-05-08 IL IL183059A patent/IL183059A0/en unknown
- 2007-05-22 NO NO20072631A patent/NO20072631L/en not_active Application Discontinuation
- 2007-06-11 ZA ZA200705059A patent/ZA200705059B/en unknown
-
2015
- 2015-04-20 US US14/690,917 patent/US20150283139A1/en not_active Abandoned
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EP1906185A1 (en) * | 2006-09-26 | 2008-04-02 | ProteoSys AG | Use of at least one isoform of progesterone receptor membrane component 1 (PGRMC1) |
US8252805B2 (en) | 2008-05-07 | 2012-08-28 | Teva Pharmaceutical Industries Ltd. | Forms of lapatinib ditosylate and processes for preparation thereof |
EP2158913A1 (en) | 2008-08-25 | 2010-03-03 | Ratiopharm GmbH | Pharmaceutical composition comprising N-[3-chhloro-4-[(3-fluorophenyl)methoxy]phenyl]6-(5[[[2-(methylsulfonyl)ethyl]amino]methyl]-2-furyl]-4-quinazolinamine |
EP2158912A1 (en) | 2008-08-25 | 2010-03-03 | Ratiopharm GmbH | Pharmaceutical composition comprising N-[3-chhloro-4-[3-fluorophenyl)methoxy)phenyl]6-[5[[[2-(methylsulfonyl)ethyl]amino]methyl]-2-furyl]-4-quinazolinamine |
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US9220696B2 (en) | 2009-03-11 | 2015-12-29 | Ardea Biosciences, Inc. | Pharmaceutical combinations for treatment of specific cancers |
US8673876B2 (en) | 2009-03-11 | 2014-03-18 | Ardea Biosciences Inc. | Pharmaceutical combinations for treatment of specific cancers |
WO2011116634A1 (en) | 2010-03-23 | 2011-09-29 | Scinopharm Taiwan Ltd. | Process and intermediates for preparing lapatinib |
JP2013522327A (en) * | 2010-03-23 | 2013-06-13 | サイノファーム タイワン リミテッド | Preparation process and intermediate of lapatinib |
US8563719B2 (en) | 2010-03-23 | 2013-10-22 | Scinopharm Taiwan, Ltd. | Process and intermediates for preparing lapatinib |
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CN102344445A (en) * | 2010-07-23 | 2012-02-08 | 岑均达 | Optical voidness quinazoline compound |
WO2012010088A1 (en) * | 2010-07-23 | 2012-01-26 | 江苏豪森医药集团有限公司 | Optically pure quinazoline compounds |
CN102344445B (en) * | 2010-07-23 | 2015-11-25 | 岑均达 | Optical pure quinazoline compound |
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WO2014059956A1 (en) | 2012-10-17 | 2014-04-24 | Zentiva, K.S. | A method of producing the key intermediate of lapatinib synthesis |
Also Published As
Publication number | Publication date |
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ES2426007T3 (en) | 2013-10-18 |
AU2005316238B2 (en) | 2009-05-07 |
RU2007119432A (en) | 2009-01-27 |
MX2007006043A (en) | 2007-06-13 |
JP5291345B2 (en) | 2013-09-18 |
IL183059A0 (en) | 2007-10-31 |
WO2006066267A3 (en) | 2006-12-14 |
AU2005316238A1 (en) | 2006-06-22 |
JP2008524258A (en) | 2008-07-10 |
ZA200705059B (en) | 2009-09-30 |
NZ555462A (en) | 2009-03-31 |
KR20070107004A (en) | 2007-11-06 |
NO20072631L (en) | 2007-07-02 |
US20080306097A1 (en) | 2008-12-11 |
EP1824492A2 (en) | 2007-08-29 |
US20150283139A1 (en) | 2015-10-08 |
EP1824492A4 (en) | 2009-10-28 |
CN101083995A (en) | 2007-12-05 |
EP1824492B1 (en) | 2013-07-10 |
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