<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>127(8)</volume><submitter>Musacchio L</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Low-grade serous ovarian and peritoneal cancer (LGSC) is a rare disease and few data on the clinical and genomic landscape have been published.&lt;h4>Methods&lt;/h4>A retrospective analysis of patients diagnosed with LGSC between 1996 and 2019 was conducted in MITO centers. Objective Response Rate (ORR) to treatments, progression-free survival (PFS) and overall survival (OS) were assessed. Additionally, the tumor molecular profile of 56 patients was evaluated using the Next Generation Sequencing (NGS) FoundationOne CDX (Foundation Medicine®).&lt;h4>Results&lt;/h4>A total of 128 patients with complete clinical data and pathologically confirmed diagnosis of LGSC were identified. ORR to first and subsequent therapies were 23.7% and 33.7%, respectively. PFS was 43.9 months (95% CI:32.4-</pubmed_abstract><journal>British journal of cancer</journal><pagination>1479-1486</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9553882</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Clinical characteristics and molecular aspects of low-grade serous ovarian and peritoneal cancer: a multicenter, observational, retrospective analysis of MITO Group (MITO 22).</pubmed_title><pmcid>PMC9553882</pmcid><pubmed_authors>Russo D</pubmed_authors><pubmed_authors>Perrone F</pubmed_authors><pubmed_authors>Del Vecchio V</pubmed_authors><pubmed_authors>Scalone S</pubmed_authors><pubmed_authors>Musacchio L</pubmed_authors><pubmed_authors>Casanova C</pubmed_authors><pubmed_authors>Zannoni GF</pubmed_authors><pubmed_authors>Raspagliesi F</pubmed_authors><pubmed_authors>Priolo D</pubmed_authors><pubmed_authors>Tuninetti V</pubmed_authors><pubmed_authors>Scambia G</pubmed_authors><pubmed_authors>Losito NS</pubmed_authors><pubmed_authors>Valabrega G</pubmed_authors><pubmed_authors>Ferrau F</pubmed_authors><pubmed_authors>Pisano C</pubmed_authors><pubmed_authors>Spina A</pubmed_authors><pubmed_authors>Canzonieri V</pubmed_authors><pubmed_authors>Ducceschi M</pubmed_authors><pubmed_authors>Pignata S</pubmed_authors><pubmed_authors>Salutari V</pubmed_authors><pubmed_authors>Lorusso D</pubmed_authors><pubmed_authors>Ghizzoni V</pubmed_authors><pubmed_authors>Cormio G</pubmed_authors><pubmed_authors>Greggi S</pubmed_authors><pubmed_authors>Bartoletti M</pubmed_authors><pubmed_authors>Del Sesto M</pubmed_authors><pubmed_authors>Loizzi V</pubmed_authors><pubmed_authors>Califano D</pubmed_authors><pubmed_authors>Arenare L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Clinical characteristics and molecular aspects of low-grade serous ovarian and peritoneal cancer: a multicenter, observational, retrospective analysis of MITO Group (MITO 22).</name><description>&lt;h4>Background&lt;/h4>Low-grade serous ovarian and peritoneal cancer (LGSC) is a rare disease and few data on the clinical and genomic landscape have been published.&lt;h4>Methods&lt;/h4>A retrospective analysis of patients diagnosed with LGSC between 1996 and 2019 was conducted in MITO centers. Objective Response Rate (ORR) to treatments, progression-free survival (PFS) and overall survival (OS) were assessed. Additionally, the tumor molecular profile of 56 patients was evaluated using the Next Generation Sequencing (NGS) FoundationOne CDX (Foundation Medicine®).&lt;h4>Results&lt;/h4>A total of 128 patients with complete clinical data and pathologically confirmed diagnosis of LGSC were identified. ORR to first and subsequent therapies were 23.7% and 33.7%, respectively. PFS was 43.9 months (95% CI:32.4-</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2026-07-14T23:32:45.94Z</modification><creation>2025-04-04T20:07:27.508Z</creation></dates><accession>S-EPMC9553882</accession><cross_references><pubmed>35869143</pubmed><doi>10.1038/s41416-022-01897-1</doi></cross_references></HashMap>