TY - JOUR
T1 - Facts and Hopes for Immunotherapy in Renal Cell Carcinoma
AU - Yao, Chen
AU - Zhang, Tian
AU - Wu, Tuoqi
AU - Brugarolas, James
N1 - Publisher Copyright:
© 2022 American Association for Cancer Research.
PY - 2022/12/1
Y1 - 2022/12/1
N2 - Immunotherapy has made a significant impact in many tumors, including renal cell carcinoma (RCC). RCC has been known to be immunoresponsive since the cytokine era of IFNa and IL2, but only a small number of patients had durable clinical benefit. Since then, discoveries of key tumor drivers, as well as an understanding of the contribution of angiogenesis and the tumor microenvironment (TME), has led to advances in drug development, ultimately transforming patient outcomes. Combinations of anti-angiogenic agents with immune checkpoint inhibitors are now standard of care. Current challenges include patient selection for immunotherapy combinations, resistance acquisition, and optimally sequencing therapies. Further discoveries about RCC biology, the TME, and resistance mechanisms will likely pave the way for the next generation of therapies.
AB - Immunotherapy has made a significant impact in many tumors, including renal cell carcinoma (RCC). RCC has been known to be immunoresponsive since the cytokine era of IFNa and IL2, but only a small number of patients had durable clinical benefit. Since then, discoveries of key tumor drivers, as well as an understanding of the contribution of angiogenesis and the tumor microenvironment (TME), has led to advances in drug development, ultimately transforming patient outcomes. Combinations of anti-angiogenic agents with immune checkpoint inhibitors are now standard of care. Current challenges include patient selection for immunotherapy combinations, resistance acquisition, and optimally sequencing therapies. Further discoveries about RCC biology, the TME, and resistance mechanisms will likely pave the way for the next generation of therapies.
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U2 - 10.1158/1078-0432.CCR-21-2372
DO - 10.1158/1078-0432.CCR-21-2372
M3 - Review article
C2 - 35819272
AN - SCOPUS:85140614146
SN - 1078-0432
VL - 28
SP - 5013
EP - 5020
JO - Clinical Cancer Research
JF - Clinical Cancer Research
IS - 23
ER -