<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>60</volume><submitter>Cham S</submitter><pubmed_abstract>&lt;h4>Purpose&lt;/h4>Uterine carcinosarcoma (UCS) is a rare but aggressive tumor with high rates of recurrence and poor prognosis, and novel therapies are urgently needed. P53 mutations are identified in over 90% of cases, and other cell cycle alterations are commonly found indicating potential vulnerability to Wee1 kinase inhibition. The purpose of this study was to determine the activity and safety of adavosertib, a Wee1 inhibitor, in recurrent or persistent UCS.&lt;h4>Patients and methods&lt;/h4>This was a phase II single-institution study of patients with persistent or recurrent UCS. Eligible patients had a confirmed &lt;i>TP53&lt;/i> alteration, RECIST measurable disease, and prior treatment with platinum based systemic therapy. Patients were treated with adavosertib at a starting dose of 300 mg orall</pubmed_abstract><journal>Gynecologic oncology reports</journal><pagination>101796</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12269869</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Phase 2 study of Wee1 inhibitor adavosertib in recurrent uterine carcinosarcoma.</pubmed_title><pmcid>PMC12269869</pmcid><pubmed_authors>Sawyer H</pubmed_authors><pubmed_authors>Tayob N</pubmed_authors><pubmed_authors>Matulonis UA</pubmed_authors><pubmed_authors>Xiong N</pubmed_authors><pubmed_authors>Mathews C</pubmed_authors><pubmed_authors>Lee EK</pubmed_authors><pubmed_authors>Konstantinopoulos PA</pubmed_authors><pubmed_authors>Liu JF</pubmed_authors><pubmed_authors>Krasner C</pubmed_authors><pubmed_authors>Wright AA</pubmed_authors><pubmed_authors>Cham S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Phase 2 study of Wee1 inhibitor adavosertib in recurrent uterine carcinosarcoma.</name><description>&lt;h4>Purpose&lt;/h4>Uterine carcinosarcoma (UCS) is a rare but aggressive tumor with high rates of recurrence and poor prognosis, and novel therapies are urgently needed. P53 mutations are identified in over 90% of cases, and other cell cycle alterations are commonly found indicating potential vulnerability to Wee1 kinase inhibition. The purpose of this study was to determine the activity and safety of adavosertib, a Wee1 inhibitor, in recurrent or persistent UCS.&lt;h4>Patients and methods&lt;/h4>This was a phase II single-institution study of patients with persistent or recurrent UCS. Eligible patients had a confirmed &lt;i>TP53&lt;/i> alteration, RECIST measurable disease, and prior treatment with platinum based systemic therapy. Patients were treated with adavosertib at a starting dose of 300 mg orall</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Aug</publication><modification>2026-03-27T15:50:36.159Z</modification><creation>2025-08-27T03:06:59.038Z</creation></dates><accession>S-EPMC12269869</accession><cross_references><pubmed>40678577</pubmed><doi>10.1016/j.gore.2025.101796</doi></cross_references></HashMap>