Methods For Treating Cancer

Abstract

Disclosed herein are methods of treating one or more tumors by administering to the subject a therapeutically effective amount of a combination of RAD1901 or solvates (e.g., hydrate) or salts thereof and one or more second therapeutic agent(s) (e.g., everolimus). The cancer is an estrogen-dependent cancer, such as breast cancer, ovarian cancer, colon cancer, endometrial cancer, or prostate cancer.

What is claimed is: 
     
         1 - 18 . (canceled) 
     
     
         19 . A method of treating breast cancer in a subject having an estrogen receptor alpha-positive cancer that is drug-resistant and/or has a mutant estrogen receptor alpha comprising administering to said subject a therapeutically effective amount of a combination of an m-TOR inhibitor and RAD1901 having the structure: 
       
         
           
           
               
               
           
         
         or a salt or solvate thereof. 
       
     
     
         20 . The method of  claim 19  wherein said drug resistant breast cancer is resistant to one or more antiestrogen and/or or aromatase inhibitor therapies. 
     
     
         21 . The method of  claim 20  wherein said one or more antiestrogens are selected from the group consisting of tamoxifen, toremifene and fulvestrant and said one or more aromatase inhibitors are selected from the group consisting of aromasin, letrozole and anastrozole. 
     
     
         22 . The method according to  claim 19  wherein said subject expresses at least one mutant estrogen receptor alpha selected from the group consisting of D538G, Y537S, Y537N, Y537C, E380Q, S463P, L536R, L536Q, P535H, V392I and V534E. 
     
     
         23 . The method of  claim 22  wherein said mutant estrogen receptor alpha is selected from the group consisting of Y537S, Y537N, Y537C, D538G, L536R, S463P and E380Q 
     
     
         24 . The method according to  claim 22  wherein said mutant receptor alpha is Y537S. 
     
     
         25 . (canceled) 
     
     
         26 . The method according to  claim 19  wherein said RAD1901 is administered in a total daily dosage of from between 100 mg and 1,000 mg. 
     
     
         27 . The method according to  claim 26  wherein said RAD1901 is administered in a total daily dosage of 100 mg, 200 mg, 300 mg, 400 mg, 500 mg, 600 mg, 700 mg, 800 mg, 900 mg or 1,000 mg. 
     
     
         28 . The method according to  claim 22  wherein said daily dosage is delivered in two separate doses. 
     
     
         29 . The method according to  claim 28  wherein said separate doses are equal doses. 
     
     
         30 - 31 . (canceled) 
     
     
         32 . The method according to  claim 19  wherein said woman is post-menopausal. 
     
     
         33 . The method according to  claim 19  wherein said woman is first identified for treatment through measuring for increased expression of one or more genes selected from ABL1, AKT1, AKT2, ALK, APC, AR, ARID1A, ASXL1, ATM, AURKA, BAP, BAP1, BCL2L11, BCR, BRAF, BRCA1, BRCA2, CCND1, CCND2, CCND3, CCNE1, CDH1, CDK4, CDK6, CDK8, CDKN1A, CDKN1B, CDKN2A, CDKN2B, CEBPA, CTNNB1, DDR2, DNMT3A, E2F3, EGFR, EML4, EPHB2, ERBB2, ERBB3, ESR1, EWSR1, FBXW7, FGF4, FGFR1, FGFR2, FGFR3, FLT3, FRS2, HIF1A, HRAS, IDH1, IDH2, IGF1R, JAK2, KDM6A, KDR, KIF5B, KIT, KRAS, LRP1B, MAP2K1, MAP2K4, MCL1, MDM2, MDM4, MET, MGMT, MLL, MPL, MSH6, MTOR, MYC, NF1, NF2, NKX2-1, NOTCH1, NPM, NRAS, PDGFRA, PIK3CA, PIK3R1, PML, PTEN, PTPRD, RARA, RB1, RET, RICTOR, ROS1, RPTOR, RUNX1, SMAD4, SMARCA4, SOX2, STK11, TET2, TP53, TSC1, TSC2, and VHL. 
     
     
         34 . The method according to  claim 33  wherein said one or more genes is selected from AKT1, AKT2, BRAF, CDK4, CDK6, PIK3CA, PIK3R1 and MTOR. 
     
     
         35 . The method according to  claim 19  wherein said m-TOR inhibitor is selected from the group consisting of sirolimus, temsirolimus, everolimus, and ridafarolimus. 
     
     
         36 . The method according to  claim 19  wherein said m-TOR inhibitor is dosed at from between 1 mg and 500 mg daily. 
     
     
         37 . The method according to  claim 36  wherein said m-TOR inhibitor is dosed at from between 5 mg and 100 mg daily. 
     
     
         38 . (canceled) 
     
     
         39 . The method according to  claim 35  wherein said m-TOR inhibitor is everolimus. 
     
     
         40 . The method according to  claim 39  wherein said everolimus is dosed at a daily dose of 10 mg. 
     
     
         41 . The method according to  claim 39  wherein said everolimus is dosed at a daily dose from between 2.5 mg and 7.5 mg. 
     
     
         42 . (canceled) 
     
     
         43 . The method according to  claim 19  wherein said m-TOR inhibitor is dosed once per day.