Treatment of cancer with TG02
The present disclosure provides therapeutic methods of treating a cancer patient with TG02 and a second therapeutic agent, e.g., TG02 and an immune checkpoint inhibitor, TG02 and a COX-2 inhibitor, or TG02 and an immune checkpoint inhibitor and a COX-2 inhibitor.
1. A method of treating a patient having cancer, the method comprising administering to the patient a therapeutically effective amount of (16E)-14-methyl-20-oxa-5,7,14,26-tetraazatetracyclo[19.3.1.1(2,6).1(8,12)]heptacosa-1(25),2(26),3,5,8(27),9,11,16,21,23-decaene and radiotherapy, wherein MYC overexpression, MCL1 overexpression, or MYC and MCL1 overexpression is differentially present in a biological sample taken from the patient as compared with a biological sample taken from a subject of another phenotypic status.
2. The method of claim 1 , wherein (16E)-14-methyl-20-oxa-5,7,14,26-tetraazatetracyclo[19.3.1.1(2,6).1(8,12)]heptacosa-1(25),2(26),3,5,8(27),9,11,16,21,23-decaene is administered to the patient before radiotherapy.
3. The method of claim 1 , wherein (16E)-14-methyl-20-oxa-5,7,14,26-tetraazatetracyclo[19.3.1.1(2,6).1(8,12)]heptacosa-1(25),2(26),3,5,8(27),9,11,16,21,23-decaene is administered to the patient after radiotherapy.
4. The method of claim 1 , wherein a therapeutically effective amount of (16E)-14-methyl-20-oxa-5,7,14,26-tetraazatetracyclo[19.3.1.1(2,6).1(8,12)]heptacosa-1(25),2(26),3,5,8(27),9,11,16,21,23-decaene is administered to the patient at the same time as radiotherapy.
5. The method of claim 1 , wherein the cancer is selected from the group consisting of acoustic neuroma, acute lymphoblastic leukemia, acute monocytic leukemia, acute promyelocytic leukemia, adenocarcinoma, adult T-cell leukemia/lymphoma, alveolar rhabdomyosarcoma, angiosarcoma, astrocytoma, B-cell chronic lymphocytic leukemia, B-cell prolymphocytic leukemia, B-cell lymphoma, basal cell carcinoma, bladder cancer, blastoma, Burkitt's lymphoma, breast cancer, brain cancer, carcinoma, carcinoma in situ, carcinosarcoma, chondroma, chordoma, choriocarcinoma, craniopharyngioma, cervical cancer, colorectal cancer, diffuse large B-cell lymphoma, embryonal carcinoma, esophageal cancer, fibrosarcoma, follicular lymphoma, follicular thyroid cancer, ganglioneuroma, germ cell tumor, gestational choriocarcinoma, glioblastoma, glioma, hemangioblastoma, head and neck cancer, hematological malignancy, hepatoblastoma, hepatocellular carcinoma, Hodgkin's lymphoma, non-Hodgkin's lymphoma, invasive lobular carcinoma, intestinal cancer, kidney cancer, laryngeal cancer, lentigo maligna, lethal midline carcinoma, leukemia, liposarcoma, lung cancer, lymphangiosarcoma, acute lymphocytic leukemia, acute myelogeous leukemia, chronic lymphocytic leukemia, liver cancer, small cell lung cancer, non- small cell lung cancer, medullary carcinoma of the breast, medulloblastoma, melanoma, meningioma, multiple myeloma, myxosarcoma, neurinoma, neuroblastoma, neuroma, nodular melanoma, oligodendroglioma, oral cancer, osteosarcoma, ovarian cancer, Pancoast tumor, papillary thyroid cancer, prostate cancer, pancreatic cancer, pharyngeal cancer, pseudomyxoma periotonei, renal cell carcinoma, retinoblastoma, rhabdomyosarcoma, Richter's transformation, rectal cancer, sarcoma, Schwannomatosis, seminoma, skin cancer, small cell carcinoma, somatostatinoma, squamous cell carcinoma, synovial sarcoma, squamous carcinoma, stomach cancer, T-cell lymphoma, testicular cancer, thyroid cancer, uterine cancer, verrucous carcinoma, Waldenstrom's macroglobulinemia, Warthin's tumor, and Wilms' tumor.
6. The method of claim 1 , wherein the cancer is selected from the group consisting of astrocytoma, hepatocellular carcinoma, lung cancer, breast cancer, head and neck cancer, prostate cancer, melanoma, multiple myeloma, glioma, glioblastoma, and colorectal cancer.
7. The method of claim 1 , wherein the cancer is glioma.
8. The method of claim 1 , wherein the cancer is glioblastoma.