BREAST CANCER THERAPEUTIC AGENT

Abstract

Provided is a therapeutic agent for treating breast cancer that has developed resistance to administration of CDK4/6 inhibitors and estrogen antagonists, the agent containing 5-((2-(4-(1-(2-hydroxyethyl)piperidin-4-yl)benzamide)pyridin-4-yl)oxy)-6-(2-methoxyethox y)-N-methyl-1H-indole-1-carboxamide or a pharmacologically acceptable salt thereof.

Claims

1.-15. (canceled)

16. A method for treating breast cancer that has developed resistance to CDK4/6 inhibitors and estrogen receptor antagonists in a patient in need thereof, wherein the method includes administering to the patient 5-((2-(4-(1-(2-hydroxyethyl)piperidin-4-yl)benzamide)pyridin-4-yl)oxy)-6-(2-methoxyethoxy)-N-methyl-1H-indole-1-carboxamide represented by formula (I) or a pharmacologically acceptable salt thereof ##STR00006##

17. A method for treating breast cancer in a patient in need thereof, which includes administering to the patient 5-((2-(4-(1-(2-hydroxyethyl)piperidin-4-yl)benzamide)pyridin-4-yl)oxy)-6-(2-methoxyethoxy)-N-methyl-1H-indole-1-carboxamide represented by formula (I) or a pharmacologically acceptable salt thereof, a CDK4/6 inhibitor and an estrogen receptor antagonist ##STR00007##

18. The method according to claim 17, which includes administering 5-((2-(4-(1-(2-hydroxyethyl)piperidin-4-yl)benzamide)pyridin-4-yl)oxy)-6-(2-methoxyethoxy)-N-methyl-1H-indole-1-carboxamide represented by formula (I) or a pharmacologically acceptable salt thereof to the patient after administering the CDK4/6 inhibitor and estrogen receptor antagonist.

19. The method according to claim 16, wherein the pharmacologically acceptable salt is a 1.5 succinate.

20. The method according to claim 16, wherein the breast cancer is estrogen receptor-positive.

21. The method according to claim 16, wherein the breast cancer is human epidermal growth factor receptor type 2 (HER2)-positive.

22. The method according to claim 16, wherein the CDK4/6 inhibitor is one or more selected from the group consisting of palbociclib, abemaciclib and ribociclib.

23. The method according to claim 22, wherein the CDK4/6 inhibitor is palbociclib.

24. The method according to claim 16, wherein the estrogen receptor antagonist is one or more selected from the group consisting of tamoxifen, fulvestrant and mepitiostane.

25. The method according to claim 24, wherein the estrogen receptor antagonist is fulvestrant.

26. The method according to claim 16, wherein the breast cancer is locally advanced breast cancer, metastatic breast cancer, recurrent breast cancer or unresectable breast cancer.

27. The method according to claim 16, wherein the breast cancer expresses fibroblast growth factor receptor (FGFR).

28. The method according to claim 27, wherein the FGFR is FGFR1, FGFR2 or FGFR3.

Description

BRIEF DESCRIPTION OF DRAWINGS

[0020] FIG. 1 is a graph showing transition of mean tumor volume of different groups after initiating drug administration.

[0021] FIG. 2 is a graph showing transition of mean tumor volume of different groups after initiating drug administration.

DESCRIPTION OF EMBODIMENTS

[0022] The compound represented by formula (I) and its pharmacologically acceptable salts according to the present invention can be produced by the method described in PTL 1.

[0023] As used herein, “pharmacologically acceptable salt” refers to a salt of an inorganic acid, a salt of an organic acid, or a salt of an acidic amino acid, for example.

[0024] Preferred examples of salts with inorganic acids include salts with hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid and phosphoric acid.

[0025] Preferred examples of salts with organic acids include salts with acetic acid, succinic acid, fumaric acid, maleic acid, tartaric acid, citric acid, lactic acid, stearic acid, benzoic acid, methanesulfonic acid, ethanesulfonic acid and p-toluenesulfonic acid.

[0026] Preferred examples of salts with acidic amino acids include salts with aspartic acid and glutamic acid.

[0027] Preferred pharmacologically acceptable salts are succinic acid salts or maleic acid salts, with succinic acid salts being more preferred. Particularly preferred are 1.5 succinic acid salts (hereunder, the 1.5 succinic acid salt of the compound represented by formula (I) will be listed as compound A).

[0028] The breast cancer therapeutic agent of the invention may be orally administered in the form of a solid formulation such as a tablet, granules, fine granules, powder or capsule, or a liquid drug, jelly or syrup. The breast cancer therapeutic agent of the invention may also be administered parenterally in the form of an injection, suppository, ointment or poultice.

[0029] The breast cancer therapeutic agent of the invention may be formulated by a method described in the Japanese Pharmacopoeia, 17th Edition.

[0030] The dose of the compound represented by formula (I) or its pharmacologically acceptable salt may be appropriately selected according to the severity of symptoms, the age, gender, body weight and sensitivity of the patient, the method of administration, the period of administration, the interval of administration and the type of medical formulation. Normally, it will be 0.5 mg to 5 g, preferably 1 mg to 1 g and more preferably 1 mg to 500 mg per day, for oral administration to adults (60 kg body weight). It may be administered in 1 to 3 dosages per day.

[0031] As used herein, a “cyclin-dependent kinase 4/6 (CDK4/6) inhibitor” is a drug that inhibits activity of CDK4 and CDK6, which are enzymes activated in cancer cells and promoting unregulated cell division.

[0032] Preferred examples of CDK4/6 inhibitors include palbociclib, abemaciclib and ribociclib. Palbociclib is most preferred among these.

[0033] The dosage and method of administration for a CDK4/6 inhibitor, using palbociclib for an ordinary adult as an example, may be oral administration of 125 mg once per day for a continuous period of 3 weeks, followed by a subsequent period of pause for one week. This cycle of administration may then be repeated.

[0034] When the CDK4/6 inhibitor is ribociclib used for an ordinary adult, it may be administered orally at 600 mg once per day for a continuous period of 3 weeks, followed by a subsequent period of pause for one week. This cycle of administration may then be repeated.

[0035] When the CDK4/6 inhibitor is abemaciclib used for an ordinary adult, it may be administered orally at 150 mg per dose, given twice per day.

[0036] As used herein, a “estrogen receptor antagonist” is a drug that binds to estrogen receptors expressed in breast cancer cells. This mechanism can be used to inhibit binding between estrogen receptors and estrogen, thereby reducing proliferation of breast cancer cells.

[0037] Preferred examples of estrogen receptor antagonists include tamoxifen, fulvestrant and mepitiostane, with fulvestrant being most preferred.

[0038] The dosage and method of administration of an estrogen receptor antagonist, using fulvestrant as an example, may be intramuscular administration of 500 mg for each dose, at the start, 2 weeks later and 4 weeks later, and every 4 weeks thereafter.

[0039] When the estrogen receptor antagonist is tamoxifen, it may be orally administered at 20 to 40 mg per day.

[0040] When the estrogen receptor antagonist is mepitiostane, it may be orally administered at 20 mg per day divided into two doses.

[0041] An aromatase inhibitor which inhibits estrogen synthesis may also be used instead of an estrogen receptor antagonist. Preferred examples of aromatase inhibitors include anastrozole, letrozole and exemestane.

[0042] As used herein, “breast cancer” means a benign or malignant tumor developing in the mammary glands (lactiferous ducts or lobules). Included in this definition are locally advanced breast cancer, metastatic breast cancer, recurrent breast cancer and unresectable breast cancer.

[0043] The term “resistance” as used herein means attenuation or loss of drug effect during the course of treatment of a breast cancer patient with a CDK4/6 inhibitor and estrogen receptor antagonist.

[0044] As used herein, the phrase “the compound represented by formula (I) or a pharmacologically acceptable salt thereof is administered after administration of a CDK4/6 inhibitor and estrogen receptor antagonist” means that the compound represented by formula (I) or its pharmacologically acceptable salt is administered alone after resistance has developed against administration of the CDK4/6 inhibitor and estrogen receptor antagonist.

EXAMPLES

[0045] The present invention will now be explained in greater detail by the following examples.

[0046] Example 1 Growth inhibition effect of compound A after palbociclib and fulvestrant administration for human breast cancer patient-derived tumor (OD-BRE-0438) Using NOD-SCID mice (NOD.CB17-Prkdcscid/J, female, Charles River Japan), with 5 to 6 mice per group, the antitumor effect of administering compound A after completion of an administration period with palbociclib and fulvestrant was evaluated.

[0047] OD-BRE-0438 is a tumor line from an estrogen receptor-positive breast cancer patient, established by Oncodesign Co. The tumor slices were grafted under the mouse skin and subcultured. The tumors excised from the mice were cut to about 4 mm-square, and a trocar (φ3.5 mm) was used for grafting under the skin of the right flank of each mouse.

[0048] A 1 mg/mL solution of β-estradiol (FujiFilm-Wako) was prepared with 99.5% ethanol (FujiFilm-Wako). It was then adjusted to a final concentration of 2.5 μg/mL using supply-use sterilized water. The mouse were given free access to food from the day of tumor grafting until the end of the test.

[0049] The long and short diameters of the tumors were measured using an electronic digital caliper (Digimatic™ caliper by Mitsutoyo Corp.). The tumor volumes were calculated by the following formula.

[0050] Tumor volume (mm.sup.3)=Long diameter (mm)×short diameter (mm)×short diameter (mm)/2

[0051] Commercially available palbociclib isethionate (Selleck Chemicals) was adjusted to 10 mg/mL concentration with 50 mM sodium lactate buffer (pH 4.0). A commercially available fulvestrant formulation (trade name: Faslodex Intramuscular Injection 250 mg, by AstraZeneca) was used directly.

[0052] Palbociclib and fulvestrant administration was initiated from the 26th day after tumor grafting. Palbociclib was orally administered once per day for 14 days at a dosage of 100 mg/kg (10 mL/kg). Fulvestrant was hypodermically injected on the 26th and 33rd day, at a dosage of 250 mg/kg (5 mL/kg).

[0053] On the 40th day, the mice were divided into groups in such a manner that the average tumor volumes were approximately the same in each group. The control group consisted of 6 mice, and the compound A-administered group consisted of 5 mice, at different dosages.

[0054] Compound A was dissolved in purified water to a concentration of 2.5 mg/mL. Compound A was orally administered to the mice in each group at a dose of 25 mg/kg (10 mL/kg) or 50 mg/kg (20 mL/kg), once per day for 14 days. The control group was untreated.

[0055] The tumor volume and body weight of each mouse were measured on day 3, 7, 10 and 14 after starting administration of compound A. The changes in mean tumor volume in each group are shown in Table 1 and FIG. 1.

TABLE-US-00001 TABLE 1 Changes in mean tumor volume after starting administration of compound A Day 0 Day 3 Day 7 Day 10 Day 14 Control group (mm.sup.3) 278.1 323.1 380.2 408.9 429.6 Compound A 25 mg/kg 261.4 211.9 167.6 138.3 134.1 group (mm.sup.3) Compound A 50 mg/kg 262.6 174.8 136.1 110.4 96.6 group (mm.sup.3)

[0056] Reference Example 1 Growth inhibiting effect of compound A on human breast cancer patient derived tumor (OD-BRE-0438)

The antitumor effect of administering compound A was evaluated using NOD-SCID mice (NOD.CB17-Prkdcscid/J, female, Charles River Japan), with 6 mice per group.

[0057] Tumor slices were grafted under the mouse skin and subcultured. The tumors excised from the mice were cut to about 4 mm-square, and a trocar ((φ3.5 mm) was used for grafting under the skin of the right flank of each mouse, for evaluation of the antitumor effect.

[0058] A 1 mg/mL solution of β-estradiol (FujiFilm-Wako) was prepared with 99.5% ethanol (FujiFilm-Wako). It was then adjusted to a final concentration of 2.5 g/mL using supply-use sterilized water. The mice were given free access to food from the day of tumor grafting until the end of the test.

[0059] Compound A was dissolved in purified water to a concentration of 2.5 mg/mL. On the 32nd day after tumor grafting, the mice were divided into groups in such a manner that the average tumor volumes were approximately the same in each group. The tumor volumes were calculated by the same method as Example 1.

[0060] Compound A was orally administered to the mice in each group at a dose of 50 mg/kg (20 mL/kg), once per day for 14 days. The control group was untreated.

[0061] The tumor volume and body weight of each mouse were measured on day 3, 7, 10 and 14 after starting administration of compound A. The changes in mean tumor volume in each group are shown in Table 2 and FIG. 2.

TABLE-US-00002 TABLE 2 Changes in mean tumor volume after starting administration of compound A Day 0 Day 3 Day 7 Day 10 Day 14 Control group (mm.sup.3) 237.2 352.4 466.2 530.4 675.1 Compound A 50 mg/kg 234.1 267.0 338.8 380.8 403.4 group (mm.sup.3)