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Comprehensive Genome Profiling for Treatment Decisions in Patients with Metastatic Tumors: Real-World Evidence Meta-Analysis and Registry Data Implementation
Department of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden; Theme Cancer, Karolinska University Hospital and Comprehensive Cancer Center, Stockholm, Sweden.
Department of Medical Oncology, Medical School, University of Ioannina, Ioannina, Greece; Department of Hygiene and Epidemiology, School of Medicine, University of Ioannina, Ioannina, Greece.
Örebro University, School of Medical Sciences. Department of Oncology, Faculty of Medicine and Health, Örebro University, Örebro, Sweden; Department of Oncology, Örebro University Hospital, Örebro, Sweden.ORCID iD: 0000-0002-6357-4605
Department of Oncology, Faculty of Medicine and Health, Örebro University, Örebro, Sweden; Department of Oncology, Örebro University Hospital, Örebro, Sweden.
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2025 (English)In: Journal of the National Cancer Institute, ISSN 0027-8874, E-ISSN 1460-2105, Vol. 117, no 6, p. 1117-1124Article, review/survey (Refereed) Published
Abstract [en]

BACKGROUND: Although precision oncology has rapidly been developed in recent years, its real-world impact and challenges in healthcare implementation remain underexplored. Through a meta-analysis of real-world evidence (RWE), we aimed at investigating the applicability and clinical impact of comprehensive cancer genome profiling (CGP) in cancer patients with metastatic solid tumors.

METHODS: We systematically searched Medline, Embase, and Web of Science for RWE studies on CGP and matched therapies in metastatic solid tumors (publication period: 2012-2023). Pooled proportions of actionable genomic alterations, patients treated with matched targeted therapies, treatment, and survival outcomes were calculated. Data from Swedish cancer registries were used as a case-study for nationwide CGP implementation.

RESULTS: Out of the 7218 identified studies, 144 were included in our analysis. 59.8% of CGP-tested patients had actionable genomic alterations, with 15.6% (95% Confidence Interval (CI) 13.4-18.2%) of them having received targeted therapy. Objective response was seen in 23.9% (95% CI 20.8-27.3%). Overall, CGP-guided treatment was correlated with prolonged progression-free survival (pooled Hazard Ratio (HR) = 0.63; 95% CI, 0.56-0.70; 18 studies) and overall survival (pooled HR = 0.60; 95% CI, 0.51-0.70; 21 studies) when compared to conventional treatment. Meta-regression time projections analyses showed that these rates will steadily increase by 2030.

CONCLUSIONS: Pooled analyses of RWE studies indicate that approximately one-fourth of the patients receiving CGP-matched treatment have an objective response. By utilizing meta-regression projections, our nationwide cancer registry case-study offers insights into the potential of precision oncology for patients with metastatic cancer and to inform future healthcare strategies.

Place, publisher, year, edition, pages
Oxford University Press, 2025. Vol. 117, no 6, p. 1117-1124
National Category
Cancer and Oncology
Identifiers
URN: urn:nbn:se:oru:diva-118850DOI: 10.1093/jnci/djaf015ISI: 001436597200001PubMedID: 39842854OAI: oai:DiVA.org:oru-118850DiVA, id: diva2:1931456
Funder
Region Stockholm, FoUI-977295
Note

I.Z. is supported by the Region Stockholm (clinical postdoctorial appointment, FoUI-977295). A.D. is supported by the National Institute for Health Research (NIHR) Imperial BRC, by grant funding from the European Association for the Study of the Liver (2021 Andrew Burroughs Fellowship) and from Cancer Research UK (RCCPDB-Nov21/100008).

Available from: 2025-01-27 Created: 2025-01-27 Last updated: 2025-08-25Bibliographically approved

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Fountoukidis, GeorgiosSmith, DanielValachis, Antonis

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