<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13(1)</volume><submitter>Tashiro R</submitter><pubmed_abstract>The standard treatment for platinum-sensitive relapsed ovarian cancer (PSROC) is platinum-based chemotherapy followed by olaparib monotherapy. A retrospective study was conducted to identify factors affecting the survival of patients with PSROC undergoing olaparib monotherapy in real-world clinical settings. The study enrolled 122 patients who received olaparib monotherapy between April 2018 and December 2020 at three national centers in Japan. The study used the Kaplan-Meier method and univariable and multivariable Cox proportional hazards models to evaluate the associations between factors and progression-free survival (PFS). Patients with BRCA1/2 mutations had a significantly longer median PFS than those without these mutations. Both the BRCA1/2 mutation-positive and mutation-negative groups exhibited a prolonged PFS when the platinum-free interval (PFI) was ≥ 12 months. Cancer antigen 125 (CA-125) level within reference values was significantly linked to prolonged PFS, while a high platelet-to-lymphocyte ratio (≥ 210) was significantly associated with poor PFS in the BRCA1/2 mutation-negative group. The study suggests that a PFI of ≥ 12 months may predict survival after olaparib monotherapy in patients with PSROC, regardless of their BRCA1/2 mutation status. Additionally, a CA-125 level within reference values may be associated with extended survival in patients without BRCA1/2 mutations. A larger prospective study should confirm these findings.</pubmed_abstract><journal>Scientific reports</journal><pagination>11962</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10366208</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Clinical and biomarker factors affecting survival in patients with platinum-sensitive relapsed ovarian cancer receiving olaparib monotherapy: a multicenter retrospective study.</pubmed_title><pmcid>PMC10366208</pmcid><pubmed_authors>Yonemura M</pubmed_authors><pubmed_authors>Kawasaki T</pubmed_authors><pubmed_authors>Saito Y</pubmed_authors><pubmed_authors>Kawazoe H</pubmed_authors><pubmed_authors>Shimoi T</pubmed_authors><pubmed_authors>Yonemori K</pubmed_authors><pubmed_authors>Mamishin K</pubmed_authors><pubmed_authors>Udagawa R</pubmed_authors><pubmed_authors>Furukawa T</pubmed_authors><pubmed_authors>Nakamura T</pubmed_authors><pubmed_authors>Tashiro R</pubmed_authors><pubmed_authors>Terakado H</pubmed_authors><pubmed_authors>Nishimura T</pubmed_authors><pubmed_authors>Seto K</pubmed_authors><pubmed_authors>Hashimoto H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Clinical and biomarker factors affecting survival in patients with platinum-sensitive relapsed ovarian cancer receiving olaparib monotherapy: a multicenter retrospective study.</name><description>The standard treatment for platinum-sensitive relapsed ovarian cancer (PSROC) is platinum-based chemotherapy followed by olaparib monotherapy. A retrospective study was conducted to identify factors affecting the survival of patients with PSROC undergoing olaparib monotherapy in real-world clinical settings. The study enrolled 122 patients who received olaparib monotherapy between April 2018 and December 2020 at three national centers in Japan. The study used the Kaplan-Meier method and univariable and multivariable Cox proportional hazards models to evaluate the associations between factors and progression-free survival (PFS). Patients with BRCA1/2 mutations had a significantly longer median PFS than those without these mutations. Both the BRCA1/2 mutation-positive and mutation-negative groups exhibited a prolonged PFS when the platinum-free interval (PFI) was ≥ 12 months. Cancer antigen 125 (CA-125) level within reference values was significantly linked to prolonged PFS, while a high platelet-to-lymphocyte ratio (≥ 210) was significantly associated with poor PFS in the BRCA1/2 mutation-negative group. The study suggests that a PFI of ≥ 12 months may predict survival after olaparib monotherapy in patients with PSROC, regardless of their BRCA1/2 mutation status. Additionally, a CA-125 level within reference values may be associated with extended survival in patients without BRCA1/2 mutations. A larger prospective study should confirm these findings.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jul</publication><modification>2025-04-05T11:47:28.684Z</modification><creation>2025-04-05T11:47:28.684Z</creation></dates><accession>S-EPMC10366208</accession><cross_references><pubmed>37488223</pubmed><doi>10.1038/s41598-023-39224-0</doi></cross_references></HashMap>