Compositions comprising chemotherapeutic agents and checkpoint inhibitors and methods of use
Disclosed herein are methods of treating/inhibiting/reducing a non-immunogenic cancer in a subject or inducing blockade inhibitor susceptibility (such as, for example, PD-1/PDLI, CTLA-4/B7-1/2, and/or CD47/SIRPa inhibitor susceptibility) in a tumor in a subject with a cancer, said methods comprising administering to the subject a hydrogel matrix comprising a chemotherapeutic agent (including, but not limited to gemcitabine) and a blockade inhibitor (including, but not limited to a PD-1/PD-LI blockade inhibitor, such as, for example nivolumab, pembrolizumab, pidilizumab, atezolizumab, avelumab, durvalumab, and BMS-936559; a CTLA-4/B7-1/2 inhibitor such as, for example, Ipilimumab; and/or a CD47/SIRPa inhibitor such as, for example Hu5F9-G4, CVI, B6H12, 2D3, CC-90002, and TTI-621).
1. A method of treating a non-immunogenic cancer in a subject comprising administering to the subject a hydrogel matrix comprising gemcitabine and an anti-PD-1/PD-L1 antibody; wherein the hydrogel matrix comprises a reactive oxygen species (ROS) degradable hydrogel that releases the gemcitabine and the anti-PD-1/PD-L1 antibody into the tumor microenvironment upon exposure to factors within the microenvironment.
2. The method of claim 1 , wherein the anti-PD-1/PD-L1 antibody is selected from the group consisting of nivolumab, pembrolizumab, pidilizumab, atezolizumab, avelumab, durvalumab, and BMS-936559.
3. The method of claim 1 , wherein the hydrogel releases the gemcitabine and the anti-PD-1/PD-L1 antibody into the tumor microenvironment for at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, or 30 days.
4. The method of claim 1 , wherein the cancer is a cancer with low PD-L1 expression or a non-immunogenic cancer selected from the group consisting of melanoma, non-small cell lung carcinoma, renal cancer, head and neck cancer, and bladder cancer.