<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Fiorentino F</submitter><funding>Takeda Pharmaceuticals U.S.A.</funding><funding>Calithera Biosciences, Inc</funding><pagination>261</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8980506</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>23(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>The standard initial treatment for ovarian cancer is surgery and platinum-based chemotherapy and potentially maintenance therapy with avastin or inhibitors of poly-ADP ribose polymerase (PARP). While a proportion of women are cured by this approach, the vast majority will relapse and become resistant to platinum chemotherapy either initially or on subsequent treatment. There is an unmet need to improve response to treatment and quality of life in these women. TAK228 is a novel therapy that can be added to standard treatment in the participant population and the aim of the DICE trial is to assess its effectiveness. Laboratory and clinical research has shown that these ovarian cancers may respond to the molecular target of a drug such as TAK228, and there have been studies</pubmed_abstract><journal>Trials</journal><pubmed_title>DICE: Dual mTorc Inhibition in advanCed/recurrent Epithelial ovarian cancer resistant to standard treatment-a study protocol for a randomised trial investigating a novel therapy called TAK228.</pubmed_title><pmcid>PMC8980506</pmcid><funding_grant_id>IISR-2012-M000691</funding_grant_id><pubmed_authors>de la Rosa CN</pubmed_authors><pubmed_authors>Krell J</pubmed_authors><pubmed_authors>Fiorentino F</pubmed_authors><pubmed_authors>Webber L</pubmed_authors></additional><is_claimable>false</is_claimable><name>DICE: Dual mTorc Inhibition in advanCed/recurrent Epithelial ovarian cancer resistant to standard treatment-a study protocol for a randomised trial investigating a novel therapy called TAK228.</name><description>&lt;h4>Background&lt;/h4>The standard initial treatment for ovarian cancer is surgery and platinum-based chemotherapy and potentially maintenance therapy with avastin or inhibitors of poly-ADP ribose polymerase (PARP). While a proportion of women are cured by this approach, the vast majority will relapse and become resistant to platinum chemotherapy either initially or on subsequent treatment. There is an unmet need to improve response to treatment and quality of life in these women. TAK228 is a novel therapy that can be added to standard treatment in the participant population and the aim of the DICE trial is to assess its effectiveness. Laboratory and clinical research has shown that these ovarian cancers may respond to the molecular target of a drug such as TAK228, and there have been studies</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Apr</publication><modification>2025-04-04T07:57:53.461Z</modification><creation>2024-11-15T17:04:22.632Z</creation></dates><accession>S-EPMC8980506</accession><cross_references><pubmed>35382842</pubmed><doi>10.1186/s13063-022-06201-3</doi></cross_references></HashMap>