Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/49426
Title: Geneo study: Comprehensive genomic profiling versus limited local reimbursed NGS panels within the belgian Precision initiative
Authors: Toungouz, Gordana Raiceivc
Hebrant, Aline
Nannini, Simon
Van Marcke, Cedric
Maetens, Julie
Decoster, Lore
Rottey, Sylvie
Demey, Wim
Collignon, Joelle
Rutten, Annemie
Vanden Bempt, Isabelle
Vermeij, Joanna
Tejpar, Sabine
Canon, Jean-Luc.
Van den Mooter, Tom
Lybaert, Willem
Van der Meulen, Joni
D'Haene, Nicky
MEBIS, Jeroen 
Prenen, Hans
Van den Bulcke, Marc
De Greve, Jacques
MAES, Brigitte 
Punie, Kevin
Aftimos, Philippe
Issue Date: 2026
Publisher: ELSEVIER SCI LTD
Source: European journal of cancer, 240 (Art N° 116681)
Abstract: Background: Molecular diagnostics in oncology is shifting from targeted NGS panels to comprehensive genomic profiling (CGP), which detects a broader range of alterations and expands access to clinical trials and therapies. Method: This study assessed the added value of CGP compared with current Belgian practice using local NGS panels covering a minimally required set of genes set by cancer type. We prospectively recruited 1000 patients with metastatic or locally advanced cancer across 13 Belgian hospitals. Tumor tissue or liquid biopsies were analyzed with FoundationOne CDx assays. The added value over reimbursed local NGS panels was measured by additional treatments recommendations issued by the national molecular tumor board (nMTB). Results: CGP was successful in 93% of patients. Among patients tested with both local NGS and CGP, 48% received at least one additional nMTB recommendations based on CGP. Overall, CGP more than doubled targeted therapy recommendations compared with local NGS panels, with nMTB providing recommendations for 61% of patients. Of the evaluable patients (n = 586), 23% received the nMTB recommended therapy. Non-adherence was due to treatment unavailability (25%), rapid clinical deterioration (24%), patient choice (17%), or physician decision (15%). Among those treated according to nMTB recommendations, the majority participated in clinical trials (48%), followed by standard of care treatments (35%) and off-label therapies (16%). Conclusions: The GeNeo study demonstrated that CGP provides added clinical value by significantly increasing the detection of actionable alterations and targeted therapy recommendations compared with small reimbursed local NGS panels.
Notes: Aftimos, P (corresponding author), Univ Libre Bruxelles, Hop Univ Bruxelles, Inst Jules Bordet, Clin Trials Conduct Unit, Brussels, Belgium.
philippe.aftimos@hubruxelles.be
Keywords: Precision medicine;Comprehensive genomic profiling;Foundation;One CDx;Molecular Tumor Board;Target therapy;Off-label therapy
Document URI: http://hdl.handle.net/1942/49426
ISSN: 0959-8049
e-ISSN: 1879-0852
DOI: 10.1016/j.ejca.2026.116681
ISI #: 001780004700001
Rights: 2026 Published by Elsevier Ltd.
Category: A1
Type: Journal Contribution
Appears in Collections:Research publications

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