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Genomic Therapy Matching in Rare and Refractory Cancers

Title: Genomic Therapy Matching in Rare and Refractory Cancers
Authors: Lin, Frank P.; Thavaneswaran, Subotheni; Grady, John P.; Napier, Christine E.; Kansara, Maya; Sebastian, Lucille; Kee, Damien; Desai, Jayesh; Zaheed, Milita; Chinchen, Sarah; Oakes, Samantha R.; Blackburn, James; Scott, Hamish S.; Glover, Anthony; Fox, Stephen B.; Goldstein, David; Leo, Paul; Amanuel, Benhur; Mersiades, Antony; Millward, Michael; Brown, Michael P.; Charakidis, Michail; Pokorny, Adrian M. J.; Craft, Paul; Espinoza, David; Grimison, Peter; Harrup, Rosemary; Joshua, Anthony M.; O’Byrne, Ken; Lee, Chee Khoon; Cowley, Mark J.; Ballinger, Mandy L.; Simes, John; Thomas, David M.; Hughes, Brett G; Itchins, Malinda; Karapetis, Chris; Lane, Steven; Peters, Geoffrey; Parakh, Sagun; Ross, David; Sjoquist, Katrin; Shackleton, Mark; Nagrial, Adnan M; Moore, Melissa; Moore, Maggie; Underhill, Craig; Barker, Hayley; Collignon, Emily; Conole, Laura
Source: JAMA Oncology ; ISSN 2374-2437
Publisher Information: American Medical Association (AMA)
Publication Year: 2026
Description: Importance The clinical utility of matching therapies to genomic biomarkers based on varying levels of evidence remains uncertain, particularly for patients with rare and refractory cancers. Objective To assess whether a tiered, evidence-based framework for matching genomic biomarkers to therapies is associated with differential overall survival in patients with advanced solid tumors. Design, Setting, and Participants This multicenter cohort study was conducted within the Molecular Screening and Therapeutic program, a nationwide precision oncology program in Australia. Patients aged 18 years and older with advanced, refractory solid tumors and adequate Eastern Cooperative Oncology Group Performance Status were enrolled from June 2016 to December 2021, with follow-up through July 2022. Data were analyzed from July 2022 to July 2024. Exposures Systemic therapy following comprehensive genomic profiling. Therapies were classified as matched or unmatched using the TOPOGRAPH (Therapy-Oriented Precision Oncology Guidelines for Recommending Anticancer Pharmaceuticals) knowledge base, which stratifies biomarker-drug pairs by level of evidence (tiers 1-3A, prospective trial evidence; tiers 3B/4, investigational/repurposed). Main Outcome and Measures The primary outcome was overall survival from date of molecular profiling results. The hypothesis was tested using a time-dependent multivariable Cox proportional hazards model, adjusted for age, Eastern Cooperative Oncology Group Performance Status, cancer type, prior therapy, and prior receipt of matched therapy. Results Of 3383 patients (mean [SD] age 57.1 [14.3] years; 1792 [53.0%] female), 1270 (37.5%) had a clinically active (tiers 1-3A) biomarker. Among patients with a tier 1 to 3A biomarker receiving treatment, those receiving matched therapy had a longer median overall survival than those receiving unmatched therapy (21.2 months [95% CI, 17.1-26.8 months] vs 12.8 months [95% CI, 11.7-13.9 months]; adjusted hazard ratio [aHR], 0.60; 95% CI, 0.44-0.82; P = .001). In ...
Document Type: article in journal/newspaper
Language: English
DOI: 10.1001/jamaoncol.2026.0127
Availability: https://doi.org/10.1001/jamaoncol.2026.0127; https://jamanetwork.com/journals/jamaoncology/articlepdf/2845808/jamaoncology_lin_2026_oi_260003_1771982454.22432.pdf
Accession Number: edsbas.7A68718
Database: BASE