<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ji Y</submitter><funding>NCI NIH HHS</funding><pagination>4093-8</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4669593</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>33(34)</volume><pubmed_abstract>&lt;h4>Purpose&lt;/h4>Progesterone receptors are expressed in approximately 70% of meningiomas. Mifepristone is an oral antiprogestational agent reported to have modest activity in a phase II study. This multicenter, prospective, randomized, placebo-controlled phase III trial conducted by SWOG was planned to define the role of mifepristone in the treatment of unresectable meningioma.&lt;h4>Patients and methods&lt;/h4>Eligible patients were randomly assigned to receive either mifepristone or placebo for 2 years unless disease progressed. Patients who were stable or responding to protocol therapy after 2 years had the option to continue with the same blinded therapy. Serial follow-up allowed assessment of efficacy and toxicity. Time to treatment failure and overall survival were ascertained for all rand</pubmed_abstract><journal>Journal of clinical oncology : official journal of the American Society of Clinical Oncology</journal><pubmed_title>Double-Blind Phase III Randomized Trial of the Antiprogestin Agent Mifepristone in the Treatment of Unresectable Meningioma: SWOG S9005.</pubmed_title><pmcid>PMC4669593</pmcid><funding_grant_id>U10 CA035176</funding_grant_id><funding_grant_id>CA180835</funding_grant_id><funding_grant_id>CA180834</funding_grant_id><funding_grant_id>U10 CA035431</funding_grant_id><funding_grant_id>N01 CA035119</funding_grant_id><funding_grant_id>CA180830</funding_grant_id><funding_grant_id>U10 CA073590</funding_grant_id><funding_grant_id>U10 CA035192</funding_grant_id><funding_grant_id>CA67663</funding_grant_id><funding_grant_id>N01 CA045560</funding_grant_id><funding_grant_id>U10 CA020319</funding_grant_id><funding_grant_id>CA45461</funding_grant_id><funding_grant_id>U10 CA046282</funding_grant_id><funding_grant_id>U10 CA180830</funding_grant_id><funding_grant_id>CA180819</funding_grant_id><funding_grant_id>U10 CA180834</funding_grant_id><funding_grant_id>U10 CA035119</funding_grant_id><funding_grant_id>U10 CA067663</funding_grant_id><funding_grant_id>CA180818</funding_grant_id><funding_grant_id>U10 CA180835</funding_grant_id><funding_grant_id>CA73590</funding_grant_id><funding_grant_id>CA180858</funding_grant_id><funding_grant_id>CA02115</funding_grant_id><funding_grant_id>N01 CA035431</funding_grant_id><funding_grant_id>U10 CA180858</funding_grant_id><funding_grant_id>CA35192</funding_grant_id><funding_grant_id>N01 CA035176</funding_grant_id><funding_grant_id>CA180888</funding_grant_id><funding_grant_id>CA58882</funding_grant_id><funding_grant_id>N01 CA013612</funding_grant_id><funding_grant_id>CA180846</funding_grant_id><funding_grant_id>U10 CA180818</funding_grant_id><funding_grant_id>U10 CA013612</funding_grant_id><funding_grant_id>U10 CA180819</funding_grant_id><funding_grant_id>CA180801</funding_grant_id><funding_grant_id>CA180820</funding_grant_id><funding_grant_id>CA46282</funding_grant_id><funding_grant_id>U10 CA058882</funding_grant_id><funding_grant_id>U10 CA180820</funding_grant_id><funding_grant_id>U10 CA180801</funding_grant_id><funding_grant_id>UG1 CA180830</funding_grant_id><funding_grant_id>U10 CA180846</funding_grant_id><funding_grant_id>U10 CA180888</funding_grant_id><funding_grant_id>CA20319</funding_grant_id><funding_grant_id>U10 CA045560</funding_grant_id><funding_grant_id>U10 CA045461</funding_grant_id><pubmed_authors>Grunberg S</pubmed_authors><pubmed_authors>Russell CA</pubmed_authors><pubmed_authors>Verschraegen C</pubmed_authors><pubmed_authors>Fredericks RK</pubmed_authors><pubmed_authors>Kabbinavar FF</pubmed_authors><pubmed_authors>Schott A</pubmed_authors><pubmed_authors>Ahmadi J</pubmed_authors><pubmed_authors>Rankin C</pubmed_authors><pubmed_authors>Sherrod AE</pubmed_authors><pubmed_authors>Townsend JJ</pubmed_authors><pubmed_authors>Feun LG</pubmed_authors><pubmed_authors>Ji Y</pubmed_authors><pubmed_authors>Stelzer KJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Double-Blind Phase III Randomized Trial of the Antiprogestin Agent Mifepristone in the Treatment of Unresectable Meningioma: SWOG S9005.</name><description>&lt;h4>Purpose&lt;/h4>Progesterone receptors are expressed in approximately 70% of meningiomas. Mifepristone is an oral antiprogestational agent reported to have modest activity in a phase II study. This multicenter, prospective, randomized, placebo-controlled phase III trial conducted by SWOG was planned to define the role of mifepristone in the treatment of unresectable meningioma.&lt;h4>Patients and methods&lt;/h4>Eligible patients were randomly assigned to receive either mifepristone or placebo for 2 years unless disease progressed. Patients who were stable or responding to protocol therapy after 2 years had the option to continue with the same blinded therapy. Serial follow-up allowed assessment of efficacy and toxicity. Time to treatment failure and overall survival were ascertained for all rand</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Dec</publication><modification>2026-05-10T00:41:42.823Z</modification><creation>2020-10-29T10:35:49Z</creation></dates><accession>S-EPMC4669593</accession><cross_references><pubmed>26527781</pubmed><doi>10.1200/JCO.2015.61.6490</doi><doi>10.1200/jco.2015.61.6490</doi></cross_references></HashMap>