<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Leung YY</submitter><funding>Janet D. Cottrelle Foundation</funding><funding>Alberta Precision Laboratories</funding><funding>Cancer Research Society</funding><funding>VGH and UBC Hospital Foundation</funding><funding>Gynecologic Cancer Initiative at the University of British Columbia</funding><funding>Cure our Ovarian Cancer</funding><funding>BC Cancer Foundation</funding><funding>NCI NIH HHS</funding><funding>Management Office at APL NASA</funding><funding>Ovarian Cancer Canada</funding><pagination>e74</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12426737</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>36(5)</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>With the development of novel antibody-drug conjugates (ADCs), folate receptor alpha (FOLR1) is a promising therapeutic target for the treatment of platinum-resistant tubo-ovarian carcinomas. The main aims of this study were to assess FOLR1 protein expression in a large cohort of ovarian carcinoma histotypes. To inform future clinical trial design we identified molecular correlates of FOLR1 expression in low-grade serous carcinoma (LGSC).&lt;h4>Methods&lt;/h4>One thousand five hundred forty-seven ovarian carcinoma samples from 5 different Canadian cohorts were successfully evaluated by immunohistochemistry for FOLR1 expression using the PS2+ system. Statistical analyses with clinicopathological parameters, LGSC molecular subtypes, and overall survival (OS) were performed.&lt;h4>Re</pubmed_abstract><journal>Journal of gynecologic oncology</journal><pubmed_title>FOLR1 as a therapeutic target in platinum-resistant ovarian carcinoma: unique expression patterns across ovarian carcinoma histotypes and molecular subtypes of low-grade serous carcinoma.</pubmed_title><pmcid>PMC12426737</pmcid><funding_grant_id>RS21-609</funding_grant_id><funding_grant_id>P30 CA118100</funding_grant_id><funding_grant_id>RS21-608</funding_grant_id><pubmed_authors>Hoenisch J</pubmed_authors><pubmed_authors>Tinker AV</pubmed_authors><pubmed_authors>Bittner M</pubmed_authors><pubmed_authors>Kobel M</pubmed_authors><pubmed_authors>Carey MS</pubmed_authors><pubmed_authors>Llaurado-Fernandez M</pubmed_authors><pubmed_authors>Kim H</pubmed_authors><pubmed_authors>Wong NKY</pubmed_authors><pubmed_authors>Schmid J</pubmed_authors><pubmed_authors>Cameron A</pubmed_authors><pubmed_authors>Da-Anoy A</pubmed_authors><pubmed_authors>Ghesquiere C</pubmed_authors><pubmed_authors>Cook LC</pubmed_authors><pubmed_authors>Gaillard S</pubmed_authors><pubmed_authors>Leung YY</pubmed_authors><pubmed_authors>Dhillion G</pubmed_authors><pubmed_authors>Dawson A</pubmed_authors></additional><is_claimable>false</is_claimable><name>FOLR1 as a therapeutic target in platinum-resistant ovarian carcinoma: unique expression patterns across ovarian carcinoma histotypes and molecular subtypes of low-grade serous carcinoma.</name><description>&lt;h4>Objective&lt;/h4>With the development of novel antibody-drug conjugates (ADCs), folate receptor alpha (FOLR1) is a promising therapeutic target for the treatment of platinum-resistant tubo-ovarian carcinomas. The main aims of this study were to assess FOLR1 protein expression in a large cohort of ovarian carcinoma histotypes. To inform future clinical trial design we identified molecular correlates of FOLR1 expression in low-grade serous carcinoma (LGSC).&lt;h4>Methods&lt;/h4>One thousand five hundred forty-seven ovarian carcinoma samples from 5 different Canadian cohorts were successfully evaluated by immunohistochemistry for FOLR1 expression using the PS2+ system. Statistical analyses with clinicopathological parameters, LGSC molecular subtypes, and overall survival (OS) were performed.&lt;h4>Re</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-04-08T18:37:06.949Z</modification><creation>2026-04-08T10:01:49.784Z</creation></dates><accession>S-EPMC12426737</accession><cross_references><pubmed>40150910</pubmed><doi>10.3802/jgo.2025.36.e74</doi></cross_references></HashMap>