<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>7(45)</volume><submitter>Perrone F</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>No biomarker is available to predict prognosis of patients with advanced ovarian cancer (AOC) and guide the choice of chemotherapy. We performed a prospective-retrospective biomarker study within the MITO2 trial on the treatment of AOC.&lt;h4>Patients and methods&lt;/h4>MITO2 is a randomised multicentre phase 3 trial conducted with 820 AOC patients assigned carboplatin/paclitaxel (carboplatin: AUC5, paclitaxel: 175 mg/m², every 3 weeks for 6 cycles) or carboplatin/PLD-pegylated liposomal doxorubicin (carboplatin: AUC5, PLD: 30 mg/m², every 3 weeks for 6 cycles) as first line treatment. Sixteen biomarkers (pathways of adhesion/invasion, apoptosis, transcription regulation, metabolism, and DNA repair) were studied in 229 patients, in a tissue microarray. Progression-free and ove</pubmed_abstract><journal>Oncotarget</journal><pagination>72654-72661</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5341934</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Biomarker analysis of the MITO2 phase III trial of first-line treatment in ovarian cancer: predictive value of DNA-PK and phosphorylated ACC.</pubmed_title><pmcid>PMC5341934</pmcid><pubmed_authors>Perrone F</pubmed_authors><pubmed_authors>Sonego M</pubmed_authors><pubmed_authors>Chiappetta G</pubmed_authors><pubmed_authors>Sorio R</pubmed_authors><pubmed_authors>Zannoni GF</pubmed_authors><pubmed_authors>Zulato E</pubmed_authors><pubmed_authors>Signoriello S</pubmed_authors><pubmed_authors>Natale D</pubmed_authors><pubmed_authors>Losito S</pubmed_authors><pubmed_authors>Scambia G</pubmed_authors><pubmed_authors>Baldassarre G</pubmed_authors><pubmed_authors>Febbraro A</pubmed_authors><pubmed_authors>Esposito F</pubmed_authors><pubmed_authors>Ferro A</pubmed_authors><pubmed_authors>Scollo P</pubmed_authors><pubmed_authors>Scognamiglio G</pubmed_authors><pubmed_authors>Gallo C</pubmed_authors><pubmed_authors>Di Maio M</pubmed_authors><pubmed_authors>Canzonieri V</pubmed_authors><pubmed_authors>Tamberi S</pubmed_authors><pubmed_authors>Pignata S</pubmed_authors><pubmed_authors>Lorusso D</pubmed_authors><pubmed_authors>Indraccolo S</pubmed_authors><pubmed_authors>Franco R</pubmed_authors><pubmed_authors>Savarese A</pubmed_authors><pubmed_authors>Canevari S</pubmed_authors><pubmed_authors>Ferrandina G</pubmed_authors><pubmed_authors>Mezzanzanica D</pubmed_authors><pubmed_authors>Breda E</pubmed_authors><pubmed_authors>Califano D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Biomarker analysis of the MITO2 phase III trial of first-line treatment in ovarian cancer: predictive value of DNA-PK and phosphorylated ACC.</name><description>&lt;h4>Background&lt;/h4>No biomarker is available to predict prognosis of patients with advanced ovarian cancer (AOC) and guide the choice of chemotherapy. We performed a prospective-retrospective biomarker study within the MITO2 trial on the treatment of AOC.&lt;h4>Patients and methods&lt;/h4>MITO2 is a randomised multicentre phase 3 trial conducted with 820 AOC patients assigned carboplatin/paclitaxel (carboplatin: AUC5, paclitaxel: 175 mg/m², every 3 weeks for 6 cycles) or carboplatin/PLD-pegylated liposomal doxorubicin (carboplatin: AUC5, PLD: 30 mg/m², every 3 weeks for 6 cycles) as first line treatment. Sixteen biomarkers (pathways of adhesion/invasion, apoptosis, transcription regulation, metabolism, and DNA repair) were studied in 229 patients, in a tissue microarray. Progression-free and ove</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Nov</publication><modification>2026-05-30T05:39:43.085Z</modification><creation>2019-03-27T02:38:07Z</creation></dates><accession>S-EPMC5341934</accession><cross_references><pubmed>27655643</pubmed><doi>10.18632/oncotarget.12056</doi></cross_references></HashMap>