<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Yao C</submitter><funding>NIA NIH HHS</funding><funding>NIAID NIH HHS</funding><funding>National Cancer Institute</funding><funding>NCI NIH HHS</funding><funding>National Institutes of Health</funding><funding>V Foundation for Cancer Research</funding><funding>Cancer Prevention and Research Institute of Texas</funding><pagination>5013-5020</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9835201</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>28(23)</volume><pubmed_abstract>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 IFNα 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.</pubmed_abstract><journal>Clinical cancer research : an official journal of the American Association for Cancer Research</journal><pubmed_title>Facts and Hopes for Immunotherapy in Renal Cell Carcinoma.</pubmed_title><pmcid>PMC9835201</pmcid><funding_grant_id>DP2 AI154450</funding_grant_id><funding_grant_id>P50 CA196516</funding_grant_id><funding_grant_id>R01 AI158294</funding_grant_id><funding_grant_id>R00 AG056524</funding_grant_id><funding_grant_id>1DP2AI154450</funding_grant_id><funding_grant_id>RR210035</funding_grant_id><funding_grant_id>V2020-05</funding_grant_id><funding_grant_id>AG056524</funding_grant_id><funding_grant_id>RR 210079</funding_grant_id><pubmed_authors>Zhang T</pubmed_authors><pubmed_authors>Brugarolas J</pubmed_authors><pubmed_authors>Yao C</pubmed_authors><pubmed_authors>Wu T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Facts and Hopes for Immunotherapy in Renal Cell Carcinoma.</name><description>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 IFNα 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.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-04-04T20:21:28.722Z</modification><creation>2025-02-19T04:20:43.584Z</creation></dates><accession>S-EPMC9835201</accession><cross_references><pubmed>35819272</pubmed><doi>10.1158/1078-0432.CCR-21-2372</doi><doi>10.1158/1078-0432.ccr-21-2372</doi></cross_references></HashMap>