<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Volders PJ</submitter><funding>OncoDNA, Belgium</funding><funding>Belgian Society of Medical Oncologists</funding><funding>Velsera, USA</funding><funding>European Commission</funding><funding>Illumina</funding><pagination>66</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11893761</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(1)</volume><pubmed_abstract>The Belgian Approach for Local Laboratory Extensive Tumor Testing (BALLETT) study assessed the feasibility of using comprehensive genomic profiling (CGP) in clinical decision-making for patients with advanced cancers. This multi-center study enrolled 872 patients from 12 Belgian hospitals. CGP was performed on tumor tissues using a standardized CGP panel (523 genes) across nine laboratories with success in 93% of patients and a median turnaround time of 29 days. Actionable genomic markers were identified in 81% of patients, substantially higher than the 21% using nationally reimbursed, small panels. A national molecular tumor board (nMTB) recommended treatments for 69% of patients, with 23% receiving matched therapies. Reasons for non-compliance were highly variable across clinical sites. </pubmed_abstract><journal>NPJ precision oncology</journal><pubmed_title>A nationwide comprehensive genomic profiling and molecular tumor board platform for patients with advanced cancer.</pubmed_title><pmcid>PMC11893761</pmcid><funding_grant_id>101080009</funding_grant_id><pubmed_authors>Schroder D</pubmed_authors><pubmed_authors>Van Huysse J</pubmed_authors><pubmed_authors>Van der Meulen J</pubmed_authors><pubmed_authors>De Greve J</pubmed_authors><pubmed_authors>Schreuer M</pubmed_authors><pubmed_authors>Tejpar S</pubmed_authors><pubmed_authors>Aftimos P</pubmed_authors><pubmed_authors>Van Den Bulcke M</pubmed_authors><pubmed_authors>Mebis J</pubmed_authors><pubmed_authors>Van Dam PJ</pubmed_authors><pubmed_authors>Vaeyens F</pubmed_authors><pubmed_authors>Dedeurwaerdere F</pubmed_authors><pubmed_authors>De Pauw R</pubmed_authors><pubmed_authors>Canon JL</pubmed_authors><pubmed_authors>Volders PJ</pubmed_authors><pubmed_authors>Vanden Bempt I</pubmed_authors><pubmed_authors>Prenen H</pubmed_authors><pubmed_authors>de Azambuja E</pubmed_authors><pubmed_authors>Punie K</pubmed_authors><pubmed_authors>Loontiens S</pubmed_authors><pubmed_authors>Cuppens K</pubmed_authors><pubmed_authors>Beniuga G</pubmed_authors><pubmed_authors>Lambin S</pubmed_authors><pubmed_authors>Maes B</pubmed_authors><pubmed_authors>Rutten A</pubmed_authors><pubmed_authors>van Marcke C</pubmed_authors><pubmed_authors>Martens G</pubmed_authors><pubmed_authors>Rottey S</pubmed_authors><pubmed_authors>Froyen G</pubmed_authors><pubmed_authors>Decoster L</pubmed_authors></additional><is_claimable>false</is_claimable><name>A nationwide comprehensive genomic profiling and molecular tumor board platform for patients with advanced cancer.</name><description>The Belgian Approach for Local Laboratory Extensive Tumor Testing (BALLETT) study assessed the feasibility of using comprehensive genomic profiling (CGP) in clinical decision-making for patients with advanced cancers. This multi-center study enrolled 872 patients from 12 Belgian hospitals. CGP was performed on tumor tissues using a standardized CGP panel (523 genes) across nine laboratories with success in 93% of patients and a median turnaround time of 29 days. Actionable genomic markers were identified in 81% of patients, substantially higher than the 21% using nationally reimbursed, small panels. A national molecular tumor board (nMTB) recommended treatments for 69% of patients, with 23% receiving matched therapies. Reasons for non-compliance were highly variable across clinical sites. </description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Mar</publication><modification>2026-06-02T19:16:51.376Z</modification><creation>2025-04-04T02:50:38.545Z</creation></dates><accession>S-EPMC11893761</accession><cross_references><pubmed>40065106</pubmed><doi>10.1038/s41698-025-00858-0</doi></cross_references></HashMap>