<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Monk BJ</submitter><funding>NCI NIH HHS</funding><pagination>981-992</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11934258</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>35(11)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>The phase III PRIMA/ENGOT-OV26/GOG-3012 trial met its primary endpoint. Niraparib first-line maintenance significantly prolonged progression-free survival (PFS) among patients with newly diagnosed advanced ovarian cancer that responded to first-line platinum-based chemotherapy, regardless of homologous recombination deficiency (HRD) status. Final overall survival (OS) results are reported.&lt;h4>Patients and methods&lt;/h4>Patients were randomized 2:1 to niraparib or placebo, stratified by response to first-line treatment, receipt of neoadjuvant chemotherapy, and tumor HRD status. After reaching 60% target maturity, OS was evaluated via a stratified log-rank test using randomization stratification factors and summarized using Kaplan-Meier methodology. OS testing was hierarchic</pubmed_abstract><journal>Annals of oncology : official journal of the European Society for Medical Oncology</journal><pubmed_title>Niraparib first-line maintenance therapy in patients with newly diagnosed advanced ovarian cancer: final overall survival results from the PRIMA/ENGOT-OV26/GOG-3012 trial.</pubmed_title><pmcid>PMC11934258</pmcid><funding_grant_id>P30 CA008748</funding_grant_id><pubmed_authors>Heitz F</pubmed_authors><pubmed_authors>Vulsteke C</pubmed_authors><pubmed_authors>Perez MJR</pubmed_authors><pubmed_authors>Gaba L</pubmed_authors><pubmed_authors>Bruchim I</pubmed_authors><pubmed_authors>Barretina-Ginesta MP</pubmed_authors><pubmed_authors>O'Malley DM</pubmed_authors><pubmed_authors>Moore RG</pubmed_authors><pubmed_authors>Mirza MR</pubmed_authors><pubmed_authors>Bradley WH</pubmed_authors><pubmed_authors>Pisano C</pubmed_authors><pubmed_authors>Monk BJ</pubmed_authors><pubmed_authors>Shtessel L</pubmed_authors><pubmed_authors>Redondo A</pubmed_authors><pubmed_authors>Haslund CA</pubmed_authors><pubmed_authors>Chase DM</pubmed_authors><pubmed_authors>Malinowska IA</pubmed_authors><pubmed_authors>Lorusso D</pubmed_authors><pubmed_authors>Holman LL</pubmed_authors><pubmed_authors>Vergote I</pubmed_authors><pubmed_authors>DiSilvestro P</pubmed_authors><pubmed_authors>O'Cearbhaill RE</pubmed_authors><pubmed_authors>Pothuri B</pubmed_authors><pubmed_authors>McCormick CC</pubmed_authors><pubmed_authors>Herzog TJ</pubmed_authors><pubmed_authors>Graybill W</pubmed_authors><pubmed_authors>Gonzalez-Martin A</pubmed_authors><pubmed_authors>Compton N</pubmed_authors><pubmed_authors>Shahin MS</pubmed_authors><pubmed_authors>Freyer G</pubmed_authors></additional><is_claimable>false</is_claimable><name>Niraparib first-line maintenance therapy in patients with newly diagnosed advanced ovarian cancer: final overall survival results from the PRIMA/ENGOT-OV26/GOG-3012 trial.</name><description>&lt;h4>Background&lt;/h4>The phase III PRIMA/ENGOT-OV26/GOG-3012 trial met its primary endpoint. Niraparib first-line maintenance significantly prolonged progression-free survival (PFS) among patients with newly diagnosed advanced ovarian cancer that responded to first-line platinum-based chemotherapy, regardless of homologous recombination deficiency (HRD) status. Final overall survival (OS) results are reported.&lt;h4>Patients and methods&lt;/h4>Patients were randomized 2:1 to niraparib or placebo, stratified by response to first-line treatment, receipt of neoadjuvant chemotherapy, and tumor HRD status. After reaching 60% target maturity, OS was evaluated via a stratified log-rank test using randomization stratification factors and summarized using Kaplan-Meier methodology. OS testing was hierarchic</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Nov</publication><modification>2026-06-05T09:24:16.664Z</modification><creation>2026-05-15T03:13:01.386Z</creation></dates><accession>S-EPMC11934258</accession><cross_references><pubmed>39284381</pubmed><doi>10.1016/j.annonc.2024.08.2241</doi></cross_references></HashMap>