Combining Radiotherapy with Immunocheckpoint Inhibitors or CAR-T in Renal Cell Carcinoma

Curr Drug Targets. 2020;21(4):416-423. doi: 10.2174/1389450120666191017113051.

Abstract

Radiotherapy is considered a second life in Renal Cell Carcinoma (RCC) patients, mainly due to the introduction of immune checkpoint inhibitors, such as anti-Programmed-death (PD)-1, alone or in combination with anti-Cytotoxic T-Lymphocyte Antigen (CTLA)-4. Several trials are investigating the efficacy/safety of immune checkpoint inhibitors in sequential or combined strategies with radiotherapy. Chimeric Antigen Receptor (CAR)-T cells therapy as a promising approach in cancer patients has opened the way to novel possibilities of integrating therapies. The identification of biomarkers of tumor response to these combinations represents a challenge in RCC, together with the research for the best partner for immunotherapy in metastatic patients. In this review we illustrated preclinical/clinical data on the integration of radiotherapy with immunocheckpoint inhibitors or CART cells in RCC.

Keywords: CAR-T cells; immunocheckpoint inhibitors; immunotherapy; programmed-death-1; radiation therapy; renal cell carcinoma..

MeSH terms

  • Animals
  • CTLA-4 Antigen / antagonists & inhibitors
  • Carcinoma, Renal Cell / drug therapy
  • Carcinoma, Renal Cell / immunology
  • Carcinoma, Renal Cell / radiotherapy
  • Carcinoma, Renal Cell / therapy*
  • Clinical Trials as Topic
  • Combined Modality Therapy
  • Humans
  • Immune Checkpoint Inhibitors / therapeutic use*
  • Immunotherapy, Adoptive*
  • Kidney Neoplasms / drug therapy
  • Kidney Neoplasms / immunology
  • Kidney Neoplasms / radiotherapy
  • Kidney Neoplasms / therapy*
  • Mice
  • Programmed Cell Death 1 Receptor / antagonists & inhibitors
  • Receptors, Chimeric Antigen
  • T-Lymphocytes

Substances

  • CTLA-4 Antigen
  • Immune Checkpoint Inhibitors
  • Programmed Cell Death 1 Receptor
  • Receptors, Chimeric Antigen