<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10(12)</volume><submitter>Turinetto M</submitter><pubmed_abstract>&lt;h4>Introduction&lt;/h4>The introduction of poly (ADP-ribose) polymerase inhibitors (PARPi) in ovarian cancer has raised increasing concerns about PARPi-related myeloid neoplasms (PrMN). Therapy-related neoplasms, including myelodysplastic syndromes and acute myeloid leukemia, account for 10%-20% of cases. Expanding PARPi indications, longer survival, and aging populations may contribute to rising PrMN incidence. Randomized clinical trials and real-world analyses show a significant risk increase, but data on individual PARPi, treatment lines, and prior therapies are limited.&lt;h4>Methods&lt;/h4>We evaluated PrMN incidence across 17 Italian centers using a 71-item survey distributed to MITO (Multicenter Italian Trials on Ovarian cancer) and MaNGO (Mario Negri Gynecologic Oncology) centers, focusing</pubmed_abstract><journal>ESMO open</journal><pagination>105903</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12670540</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>PARPi and myeloid neoplasms; the Italian MITO-MaNGO experience based on a multicentric survey.</pubmed_title><pmcid>PMC12670540</pmcid><pubmed_authors>Fagotti A</pubmed_authors><pubmed_authors>Marchetti C</pubmed_authors><pubmed_authors>Coppola E</pubmed_authors><pubmed_authors>Abeni C</pubmed_authors><pubmed_authors>Lombardo V</pubmed_authors><pubmed_authors>DeStefanis M</pubmed_authors><pubmed_authors>Valabrega G</pubmed_authors><pubmed_authors>Scandurra G</pubmed_authors><pubmed_authors>Giordano M</pubmed_authors><pubmed_authors>Pellegrini D</pubmed_authors><pubmed_authors>Camnasio C</pubmed_authors><pubmed_authors>Distefano M</pubmed_authors><pubmed_authors>Petrella MC</pubmed_authors><pubmed_authors>Caruso G</pubmed_authors><pubmed_authors>Barberi V</pubmed_authors><pubmed_authors>Cirigliano G</pubmed_authors><pubmed_authors>Perri MT</pubmed_authors><pubmed_authors>Pignata S</pubmed_authors><pubmed_authors>Ferrero A</pubmed_authors><pubmed_authors>Chiusolo P</pubmed_authors><pubmed_authors>Cormio G</pubmed_authors><pubmed_authors>Boccia S</pubmed_authors><pubmed_authors>Cecere S</pubmed_authors><pubmed_authors>Loizzi V</pubmed_authors><pubmed_authors>De Angelis C</pubmed_authors><pubmed_authors>Turinetto M</pubmed_authors><pubmed_authors>Colombo N</pubmed_authors><pubmed_authors>Villa F</pubmed_authors><pubmed_authors>Mammoliti S</pubmed_authors><pubmed_authors>Lamia MR</pubmed_authors></additional><is_claimable>false</is_claimable><name>PARPi and myeloid neoplasms; the Italian MITO-MaNGO experience based on a multicentric survey.</name><description>&lt;h4>Introduction&lt;/h4>The introduction of poly (ADP-ribose) polymerase inhibitors (PARPi) in ovarian cancer has raised increasing concerns about PARPi-related myeloid neoplasms (PrMN). Therapy-related neoplasms, including myelodysplastic syndromes and acute myeloid leukemia, account for 10%-20% of cases. Expanding PARPi indications, longer survival, and aging populations may contribute to rising PrMN incidence. Randomized clinical trials and real-world analyses show a significant risk increase, but data on individual PARPi, treatment lines, and prior therapies are limited.&lt;h4>Methods&lt;/h4>We evaluated PrMN incidence across 17 Italian centers using a 71-item survey distributed to MITO (Multicenter Italian Trials on Ovarian cancer) and MaNGO (Mario Negri Gynecologic Oncology) centers, focusing</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Dec</publication><modification>2026-06-12T04:51:08.095Z</modification><creation>2026-06-12T03:08:06.085Z</creation></dates><accession>S-EPMC12670540</accession><cross_references><pubmed>41259900</pubmed><doi>10.1016/j.esmoop.2025.105903</doi></cross_references></HashMap>