<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Lee MY</submitter><funding>Intramural NIH HHS</funding><funding>National Institutes of Health</funding><pagination>361-370</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8409092</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>31(4)</volume><pubmed_abstract>Owing to the presence of known tumor-specific viral antigens, human papillomavirus (HPV)-associated cancers are well suited for treatment with immunotherapy designed to unleash, amplify or replace the T cell arm of the adaptive immune system. Immune checkpoint blockade designed to unleash existing T cell immunity is currently Food and Drug Administration approved for certain HPV-associated cancers. More specific immunotherapies such as therapeutic vaccines and T cell receptor-engineered cellular therapy are currently in clinical development. Such therapies may offer more specific immune activation against viral tumor antigens and decrease the risk of immune-related adverse events. Current and planned clinical study of these treatments will determine their utility in the treatment of patients with newly diagnosed advanced stage or relapsed HPV-associated cancer.</pubmed_abstract><journal>Seminars in radiation oncology</journal><pubmed_title>Immunotherapy for HPV Malignancies.</pubmed_title><pmcid>PMC8409092</pmcid><funding_grant_id>ZIA DC000087</funding_grant_id><pubmed_authors>Allen CT</pubmed_authors><pubmed_authors>Lee MY</pubmed_authors></additional><is_claimable>false</is_claimable><name>Immunotherapy for HPV Malignancies.</name><description>Owing to the presence of known tumor-specific viral antigens, human papillomavirus (HPV)-associated cancers are well suited for treatment with immunotherapy designed to unleash, amplify or replace the T cell arm of the adaptive immune system. Immune checkpoint blockade designed to unleash existing T cell immunity is currently Food and Drug Administration approved for certain HPV-associated cancers. More specific immunotherapies such as therapeutic vaccines and T cell receptor-engineered cellular therapy are currently in clinical development. Such therapies may offer more specific immune activation against viral tumor antigens and decrease the risk of immune-related adverse events. Current and planned clinical study of these treatments will determine their utility in the treatment of patients with newly diagnosed advanced stage or relapsed HPV-associated cancer.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Oct</publication><modification>2025-04-22T21:48:30.197Z</modification><creation>2025-02-19T01:27:17.545Z</creation></dates><accession>S-EPMC8409092</accession><cross_references><pubmed>34455991</pubmed><doi>10.1016/j.semradonc.2021.02.008</doi></cross_references></HashMap>