| Literature DB >> 33712487 |
Miguel F Sanmamed1,2,3,4,5, Ignacio Melero6,3,4,5,7, Diego Salas-Benito8,2, José L Pérez-Gracia1,2, Mariano Ponz-Sarvisé1,2, María E Rodriguez-Ruiz1,2, Iván Martínez-Forero9, Eduardo Castañón1,2, José M López-Picazo1,2.
Abstract
Checkpoint inhibitors are being added to standard-of-care chemotherapy in multiple clinical trials. Success has been reported in non-small and small cell lung carcinomas and urothelial, head and neck, gastric, and esophageal cancers, and promising results are already available in triple-negative breast and pancreatic malignancies. The potential mechanisms of synergy include immunogenic tumor cell death, antiangiogenesis, selective depletion of myeloid immunosuppressive cells, and lymphopenia, which reduces regulatory T cells and makes room for proliferation of effector T cells. However, chemotherapy regimens have not been optimized for such combinations, perhaps explaining some recent clinical trial disappointments. Approaches to make the most of chemoimmunotherapy include neoadjuvant and adjuvant schemes.Significance: Immunotherapy of cancer based on PD-1/PD-L1 blockade has prompted a revolution in cancer clinical management. Evidence in phase III clinical trials already supports combinations of immunotherapy with standard-of-care chemotherapy for a number of malignant diseases. This review focuses on such evidence and provides an overview of the potential synergistic mechanisms of action and the opportunities to optimize chemoimmunotherapy regimens. ©2021 American Association for Cancer Research.Entities:
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Year: 2021 PMID: 33712487 DOI: 10.1158/2159-8290.CD-20-1312
Source DB: PubMed Journal: Cancer Discov ISSN: 2159-8274 Impact factor: 39.397