<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>43</volume><submitter>Werner B</submitter><pubmed_abstract>&lt;h4>Objective&lt;/h4>To investigate cell-free DNA (cfDNA) in plasma and ascites and its association with clinical outcomes (paracentesis-free interval, overall survival) and CA125 level in participants with advanced ovarian cancer, treated with palliative intraperitoneal bevacizumab to delay re-accumulation of ascites.&lt;h4>Methods&lt;/h4>cfDNA was extracted from 0.3 to 1 mL samples from 20/24 participants of the REZOLVE trial. Standard and methylation-specific PCRs were performed to measure 3 biomarkers: total cfDNA (Alu), tumour-derived cfDNA (ctDNA, methylated IFFO1 promoter) and endothelium-derived cfDNA (ec-cfDNA, unmethylated CDH5 promoter). Values were correlated to clinical outcomes.&lt;h4>Results&lt;/h4>cfDNA was detected in all samples, with higher yield in ascites (mean 669 ng/mL) than plasma</pubmed_abstract><journal>Translational oncology</journal><pagination>101914</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10966381</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Cell-free DNA in plasma and ascites as a biomarker of bevacizumab response- a translational research sub-study of the REZOLVE (ANZGOG-1101) clinical trial.</pubmed_title><pmcid>PMC10966381</pmcid><pubmed_authors>Cummins MM</pubmed_authors><pubmed_authors>Shannon C</pubmed_authors><pubmed_authors>Friedlander M</pubmed_authors><pubmed_authors>Yip S</pubmed_authors><pubmed_authors>Ford CE</pubmed_authors><pubmed_authors>Espinoza D</pubmed_authors><pubmed_authors>Ananda S</pubmed_authors><pubmed_authors>Warton K</pubmed_authors><pubmed_authors>Werner B</pubmed_authors><pubmed_authors>Mileshkin L</pubmed_authors><pubmed_authors>Sjoquist KM</pubmed_authors><pubmed_authors>Chang G</pubmed_authors></additional><is_claimable>false</is_claimable><name>Cell-free DNA in plasma and ascites as a biomarker of bevacizumab response- a translational research sub-study of the REZOLVE (ANZGOG-1101) clinical trial.</name><description>&lt;h4>Objective&lt;/h4>To investigate cell-free DNA (cfDNA) in plasma and ascites and its association with clinical outcomes (paracentesis-free interval, overall survival) and CA125 level in participants with advanced ovarian cancer, treated with palliative intraperitoneal bevacizumab to delay re-accumulation of ascites.&lt;h4>Methods&lt;/h4>cfDNA was extracted from 0.3 to 1 mL samples from 20/24 participants of the REZOLVE trial. Standard and methylation-specific PCRs were performed to measure 3 biomarkers: total cfDNA (Alu), tumour-derived cfDNA (ctDNA, methylated IFFO1 promoter) and endothelium-derived cfDNA (ec-cfDNA, unmethylated CDH5 promoter). Values were correlated to clinical outcomes.&lt;h4>Results&lt;/h4>cfDNA was detected in all samples, with higher yield in ascites (mean 669 ng/mL) than plasma</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 May</publication><modification>2026-07-09T10:39:24.033Z</modification><creation>2026-07-09T10:26:11.201Z</creation></dates><accession>S-EPMC10966381</accession><cross_references><pubmed>38417292</pubmed><doi>10.1016/j.tranon.2024.101914</doi></cross_references></HashMap>