Use of pentoxifylline with immune checkpoint-blockade therapies for the treatment of melanoma
View Patent ↗Methods of treating a PD-1-resistant cancer are provided and comprise administering to a subject in need thereof a therapeutically effective amount of a c-Rel inhibitor and a therapeutically effective amount of a PD-1 inhibitor. A pharmaceutical combination comprising a therapeutically effective amount of a c-Rel inhibitor, and a therapeutically effective amount of a PD-1 inhibitor is also provided. Finally, methods of treating a cancer such as a CTLA-4-resistant cancer, a CD137-resistant cancer, and an OX-4-resistant cancer are provided and comprise administering to a subject in need thereof a therapeutically effective amount of a c-Rel inhibitor and a therapeutically effective amount of a CLTA-4, CD137 or OX-4 inhibitor, respectively.
1. A method of treating a PD-1-resistant cancer comprising administering to a subject in need thereof a therapeutically effective amount of a c-Rel inhibitor and a therapeutically effective amount of a PD-1 inhibitor.
2. The method of claim 1 , wherein the c-Rel inhibitor is a member selected from the group consisting of pentoxifylline, a pentoxifylline analog, dehydroxymethylepoxyquinomicin (DHMEQ), pyrimidinetrione and its derivatives including IT-603, and any combination thereof.
3. The method of claim 2 , wherein the pentoxifylline analog is selected from the group consisting of lisofylline, torbafylline, propentafylline, A81-138, IT-603, dyfylline, doxofylline, theophylline, isobutyl methylxanthine (IBMX), caffeine, and any combination thereof.
4. The method of claim 3 , wherein the pentoxifylline analog is selected from the group consisting of torbafylline, propentafylline, A81-138, and any combination thereof.
5. The method of claim 1 , wherein the PD-1 inhibitor is an anti-PD-1 antibody or an anti-PD-L1 antibody or a biologically active fragment or variant thereof.
6. The method of claim 5 , wherein the anti-PD-1 antibody or the anti-PD-L1 antibody is a humanized monoclonal antibody.
7. The method of claim 1 , wherein the effective amount of the c-Rel inhibitor is about 0.1 mg/day to about 5 g/day and the amount of the PD-1 inhibitor is about 0.1 mg/day to about 5 g/day.
8. The method of claim 7 , wherein the effective amount of the c-Rel inhibitor is about 400 mg/day to about 1800 mg/day and the amount of the PD-1 inhibitor is about 1 mg/kg/2 weeks to about 10 mg/kg/week.
9. The method of claim 1 , wherein the effective amount of the c-Rel inhibitor is about 0.5 mg/day to about 2500 mg/day, about 1 mg/day to about 750 mg/day, about 5 mg to about 500 mg/day or about 10 mg/day to about 100 mg/day.
10. The method of claim 1 , wherein the effective amount of the c-Rel inhibitor is about 2500 mg/day, about 2400 mg/day, about 2000 mg/day, about 1800 mg/day, about 1600 mg/day, about 1200 mg/day, about 1000 mg/day, about 800 mg/day, about 600 mg/day, about 500 mg/day, about 400 mg/day, about 200 mg/day, about 100 mg/day, about 50 mg/day, about 25 mg/day, about 10 mg/day, about 5 mg/day, or between about 1 mg/day and 200 mg/day.
11. The method of claim 1 , wherein the effective amount of the PD-1 inhibitor is about 1 mg/kg, about 2 mg/kg, about 5 mg/kg, about 7.5 mg/kg, or about 10 mg/kg, administered every week or every two weeks.
12. The method of claim 1 , wherein the effective amount of the PD-1 inhibitor is about 200 micrograms, given every 2-3 days by injection.
13. The method of claim 1 , wherein the PD-1-resistant cancer is a melanoma.
14. The method of claim 13 , wherein the melanoma is a B16F1 melanoma or a B16F10 metastatic melanoma.
15. The method of claim 1 , wherein the PD-1-resistant cancer is selected from the group consisting of melanoma, metastatic melanoma, ovarian cancer, fibrosarcoma, breast cancer, lung cancer, non-small cell carcinoma, and colon cancer.
16. The method of claim 1 , wherein the PD-1-resistant cancer is selected from the group consisting of B16F1 (melanoma), B16F10 (metastatic melanoma), Id8 (ovarian cancer), Sa1N (fibrosarcoma), TUBO (mammary carcinoma), TC-1 (lung sarcoma), BRaf CA , Pten loxP , Tyr::CreER T2 (melanoma), MC38 (colon carcinoma), and CT-26 (colon carcinoma).