Therapeutic treatment of breast cancer based on c-MAF status
The present invention relates to the design of a customized therapy for a subject with breast cancer based on the c-MAF expression level and the menopausal status of the subject. In some embodiments, the customized therapy comprises an agent for avoiding, treating or preventing bone degradation. In some embodiments, the agent for avoiding, treating or preventing bone degradation is zoledronic acid. In other embodiments, the agent is clodronate or denosumab.
1. A method for the treatment of a subject having breast cancer, comprising administering to the subject from about 1 mg to about 10 mg of zoledronic acid or administering clodronate at a dose from about 1000 mg to about 2000 mg, wherein the subject has been identified as having a not increased c-MAF gene expression level, copy number, amplification, or gain in a tumor sample compared to a control sample.
2. A method for the treatment of a subject having breast cancer, comprising:
(i) quantifying the c-MAF gene expression level, copy number, amplification, or gain in a sample of said subject, and
(ii) comparing the expression level, copy number, amplification, or gain obtained in (i) with a reference value,
wherein said subject has a not increased c-MAF gene expression level, copy number, amplification, or gain with respect to said reference value, and said subject is administered from about 1 mg to about 10 mg of zoledronic acid or administered clodronate at a dose from about 1000 mg to about 2000 mg.
3. A method for the identification of a subject having breast cancer who will benefit from treatment with zoledronic acid or clodronate, comprising:
(i) quantifying the c-MAF gene expression level, copy number, amplification, or gain in a sample of said subject, and
(ii) comparing the expression level, copy number, amplification, or gain obtained in (i) with a reference value,
wherein said subject has a not increased c-MAF gene expression level, copy number, amplification, or gain with respect to said reference value, and said subject is administered from about 1 mg to about 10 mg of zoledronic acid or administered clodronate at a dose from about 1000 mg to about 2000 mg.
4. An in vitro method for designing a customized therapy for a subject having breast cancer which comprises:
(i) quantifying the c-MAF gene expression level, copy number, amplification, or gain in a sample of said subject, and
(ii) comparing the expression level, copy number, amplification, or gain obtained in (i) with a reference value,
wherein said subject has a not increased c-MAF gene expression level, copy number, amplification, or gain with respect to said reference value, and said subject is administered clodronate at a dose of from about 1000 mg to about 2000 mg or about 1 mg to about 10 mg of zoledronic acid.
5. The method of claim 1 , wherein the subject is administered about 1 mg, about 2 mg, about 3 mg, about 4 mg, about 5 mg, about 6 mg, about 7 mg, about 8 mg, about 9 mg, or about 10 mg of zoledronic acid.
6. The method of claim 1 , wherein the zoledronic acid is administered once about every 2 weeks, 3 weeks, 4 weeks, 5 weeks, 6 weeks, 8 weeks, 10 weeks, 12 weeks, 2 months, 3 months, 4 months, 5 months, 6 months, or 1 year.
7. The method of claim 1 , wherein the zoledronic acid or clodronate is administered with an additional therapy.
8. The method of claim 1 , wherein the clodronate is administered at a dose of about 1000 mg, about 1100 mg, about 1200 mg, about 1250 mg, about 1300 mg, about 1400 mg, about 1500 mg, about 1600 mg, about 1700 mg, about 1750 mg, about 1800 mg, about 1900 mg, or about 2000 mg.
9. The method of claim 1 , wherein the clodronate is administered about once a day for at least about 1 month, about 2 months, about 3 months, about 4 months, about 6 months, about 9 months, about 1 year, about 2 years, about 3 years, about 4 years, about 5 years, or longer.
10. The method of claim 1 , wherein the breast cancer is Stage 0 breast cancer.
11. The method of claim 1 , wherein the breast cancer is Stage I, Stage II, Stage III, Stage IV, or metastatic breast cancer.
12. The method of claim 1 , wherein the method further comprises quantifying the messenger RNA (mRNA) of said c-MAF gene, or a fragment of said mRNA, the complementary DNA (cDNA) of said c-MAF gene, or a fragment of said cDNA or quantifying the level of protein encoded by said c-MAF gene.
13. The method of claim 1 , wherein the expression level, copy number, amplification or gain is quantified by means of a quantitative polymerase chain reaction (PCR) or a DNA or RNA array, FISH, in situ hybridization, or nucleotide hybridization technique.
14. The method of claim 1 , wherein the level of protein is quantified by means of western blot, ELISA, immunohistochemistry or a protein array.
15. The method of claim 1 , wherein the breast cancer is ER+ breast cancer.
16. The method of claim 1 , wherein the breast cancer is ER− breast cancer, triple negative breast cancer, of the basal-like subtype, or HER2+ breast cancer.
17. The method of claim 1 , wherein the subject is non-postmenopausal.
18. The method of claim 1 , wherein the subject is premenopausal or postmenopausal.
19. The method of claim 1 , wherein the treatment or therapy improves invasive disease free survival or disease free survival.
20. The method of claim 1 , wherein the treatment or therapy improves overall survival.