Claims for Patent: 9,688,665

Summary for Patent: 9,688,665

Title:	Methods of treating cancer
Abstract:	The present invention relates to methods of treating cancer by administering the EZH2 inhibitor compounds and pharmaceutical compositions to subjects in need thereof. The present invention also relates to the use of such compounds for research or other non-therapeutic purposes.
Inventor(s):	Knutson; Sarah K. (Cambridge, MA), Warholic; Natalie (Brighton, MA), Keilhack; Heike (Belmont, MA)
Assignee:	Epizyme, Inc. (Cambridge, MA)
Application Number:	14/054,646
Patent Claims:	1. A method for treating or alleviating a symptom of a SWI/SNF-mediated cancer in a subject comprising administering to a subject in need thereof a therapeutically effective amount of an EZH2 inhibitor having the following structure: ##STR00051## or pharmaceutically acceptable salt thereof, wherein the subject has a cancer selected from the group consisting of brain and central nervous system cancer, head and neck cancer, kidney cancer, ovarian cancer, pancreatic cancer, leukemia, lung cancer, lymphoma, myeloma, sarcoma, breast cancer, and prostate cancer. 2. The method of claim 1, wherein the SWI/SNF-mediated cancer is characterized by reduced expression or loss of function of the SWI/SNF complex or one or more components of the SWI/SNF complex. 3. The method of claim 1, wherein the subject has a cancer selected from the group consisting of medulloblastoma, malignant rhabdoid tumor and atypical teratoid/rhabdoid tumor. 4. The method of claim 2, wherein the one or more components are selected from the group consisting of SNF5, ATRX and ARID1A. 5. The method of claim 2, wherein the loss of function is caused by a loss of function mutation resulting from a point mutation, a deletion and/or an insertion. 6. The method of claim 1, wherein the subject has a deletion of SNF5. 7. The method of claim 1, wherein the subject has a mutation of ATRX selected from the group consisting of a substitution of asparagine (N) for the wild type residue lysine (K) at amino acid position 688 of SEQ ID NO: 5 (K688N), and a substitution of isoleucine (I) for the wild type residue methionine (M) at amino acid position 366 of SEQ ID NO: 5 (M366I). 8. The method of claim 1, wherein said subject has a mutation of ARID1A selected from the group consisting of a nonsense mutation for the wild type residue cysteine (C) at amino acid position 884 of SEQ ID NO: 11 (C884*), a substitution of lysine (K) for the wild type residue glutamic acid (E) at amino acid position 966 (E966K), a nonsense mutation for the wild type residue glutamine (Q) at amino acid position 1411 of SEQ ID NO: 11 (Q1411*), a frame shift mutation at the wild type residue phenylalanine (F) at amino acid position 1720 of SEQ ID NO: 11 (F1720fs), a frame shift mutation after the wild type residue glycine (G) at amino acid position 1847 of SEQ ID NO: 11 (G1847fs), a frame shift mutation at the wild type residue cysteine (C) at amino acid position 1874 of SEQ ID NO: 11 (C1874fs), a substitution of glutamic acid (E) for the wild type residue aspartic acid (D) at amino acid position 1957 (D1957E), a nonsense mutation for the wild type residue glutamine (Q) at amino acid position 1430 of SEQ ID NO: 11 (Q1430*), a frame shift mutation at the wild type residue arginine (R) at amino acid position 1721 of SEQ ID NO: 11 (R1721fs), a substitution of glutamic acid (E) for the wild type residue glycine (G) at amino acid position 1255 (G1255E), a frame shift mutation at the wild type residue glycine (G) at amino acid position 284 of SEQ ID NO: 11 (G284fs), a nonsense mutation for the wild type residue arginine (R) at amino acid position 1722 of SEQ ID NO: 11 (R1722*), a frame shift mutation at the wild type residue methionine (M) at amino acid position 274 of SEQ ID NO: 11 (M274fs), a frame shift mutation at the wild type residue glycine (G) at amino acid position 1847 of SEQ ID NO: 11 (G1847fs), a frame shift mutation at the wild type residue P at amino acid position 559 of SEQ ID NO: 11 (P559fs), a nonsense mutation for the wild type residue arginine (R) at amino acid position 1276 of SEQ ID NO: 11 (R1276*), a frame shift mutation at the wild type residue glutamine (Q) at amino acid position 2176 of SEQ ID NO: 11 (Q2176fs), a frame shift mutation at the wild type residue histidine (H) at amino acid position 203 of SEQ ID NO: 11 (H203fs), a frame shift mutation at the wild type residue alanine (A) at amino acid position 591 of SEQ ID NO: 11 (A591fs), a nonsense mutation for the wild type residue glutamine (Q) at amino acid position 1322 of SEQ ID NO: 11 (Q1322*), a nonsense mutation for the wild type residue serine (S) at amino acid position 2264 of SEQ ID NO: 11 (S2264*), a nonsense mutation for the wild type residue glutamine (Q) at amino acid position 586 of SEQ ID NO: 11 (Q586*), a frame shift mutation at the wild type residue glutamine (Q) at amino acid position 548 of SEQ ID NO: 11 (Q548fs), and a frame shift mutation at the wild type residue asparagine (N) at amino acid position 756 of SEQ ID NO: 11 (N756fs). 9. The method of claim 1, wherein the subject has lymphoma. 10. The method of claim 1, wherein the subject has leukemia. 11. The method of claim 1, wherein the subject has lung cancer. 12. The method of claim 1, wherein the subject has myeloma. 13. The method of claim 1, wherein the subject has sarcoma. 14. The method of claim 3, wherein the subject has medulloblastoma. 15. The method of claim 3, wherein the subject has malignant rhabdoid tumor. 16. The method of claim 3, wherein the subject has atypical teratoid/rhabdoid tumor.