<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10(9)</volume><submitter>Martelli V</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Circulating tumor DNA (ctDNA) variations predict tumor response to systemic treatment (so-called molecular response) earlier than radiological assessment. However, a standardized categorization of molecular response is an unmet clinical need. Liquid biopsy-RECIST (LB-RECIST), based on aggregate variant allele frequency (aggVAF; sum of all detected variant allele frequencies in a sample) variations, has been proposed to stratify molecular response. Metastatic colorectal cancer (mCRC) may be an attractive clinical scenario for LB-RECIST clinical implementation; however, specific data on clinical validity is still lacking.&lt;h4>Patients and methods&lt;/h4>The prospective PLATFORM-B study enrolled 130 mCRC patients who received standard frontline treatment and underwent serial ct</pubmed_abstract><journal>ESMO open</journal><pagination>105760</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12446507</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Clinical validation of liquid biopsy-RECIST (LB-RECIST) in metastatic colorectal cancer (mCRC) patients: findings from the PLATFORM-B study.</pubmed_title><pmcid>PMC12446507</pmcid><pubmed_authors>Elez E</pubmed_authors><pubmed_authors>Ferreiro R</pubmed_authors><pubmed_authors>Manzano JL</pubmed_authors><pubmed_authors>Alonso V</pubmed_authors><pubmed_authors>Martelli V</pubmed_authors><pubmed_authors>Pineda E</pubmed_authors><pubmed_authors>Bellosillo B</pubmed_authors><pubmed_authors>Montagut C</pubmed_authors><pubmed_authors>Gibert J</pubmed_authors><pubmed_authors>Gomez-Espana MA</pubmed_authors><pubmed_authors>Toledo R</pubmed_authors><pubmed_authors>Salazar R</pubmed_authors><pubmed_authors>Losa F</pubmed_authors><pubmed_authors>Aranda E</pubmed_authors><pubmed_authors>Paez D</pubmed_authors><pubmed_authors>Guix M</pubmed_authors><pubmed_authors>Cano MT</pubmed_authors><pubmed_authors>Garcia-Alfonso P</pubmed_authors><pubmed_authors>Spanish Cooperative Group for the Treatment of Digestive Tumours (TTD)</pubmed_authors><pubmed_authors>Tabernero J</pubmed_authors><pubmed_authors>Sibilio A</pubmed_authors><pubmed_authors>Linares J</pubmed_authors><pubmed_authors>Fernandez-Rodriguez MC</pubmed_authors><pubmed_authors>Santos C</pubmed_authors><pubmed_authors>Rivera F</pubmed_authors><pubmed_authors>Vidal J</pubmed_authors><pubmed_authors>Duran G</pubmed_authors><pubmed_authors>Garcia-Carbonero R</pubmed_authors><pubmed_authors>Sastre J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Clinical validation of liquid biopsy-RECIST (LB-RECIST) in metastatic colorectal cancer (mCRC) patients: findings from the PLATFORM-B study.</name><description>&lt;h4>Background&lt;/h4>Circulating tumor DNA (ctDNA) variations predict tumor response to systemic treatment (so-called molecular response) earlier than radiological assessment. However, a standardized categorization of molecular response is an unmet clinical need. Liquid biopsy-RECIST (LB-RECIST), based on aggregate variant allele frequency (aggVAF; sum of all detected variant allele frequencies in a sample) variations, has been proposed to stratify molecular response. Metastatic colorectal cancer (mCRC) may be an attractive clinical scenario for LB-RECIST clinical implementation; however, specific data on clinical validity is still lacking.&lt;h4>Patients and methods&lt;/h4>The prospective PLATFORM-B study enrolled 130 mCRC patients who received standard frontline treatment and underwent serial ct</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-06-03T14:29:06.795Z</modification><creation>2026-04-28T03:11:41.127Z</creation></dates><accession>S-EPMC12446507</accession><cross_references><pubmed>40907207</pubmed><doi>10.1016/j.esmoop.2025.105760</doi></cross_references></HashMap>