Liquid and Tissue Biopsies for Identifying <i>MET</i> Exon 14 Skipping NSCLC: Analyses from the Phase II VISION Study of Tepotinib

Tepotinib had robust, durable activity in TBx-positive/LBx-negative and TBx-positive/LBx-positive patients. Although LBx is a complementary method to TBx for detecting METex14, it may preferentially select patients with higher tumor burden and poorer prognosis. Undetectable METex14 in baseline ctDNA (due to low ctDNA shedding) may define more favorable treatment outcomes.

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Publication Details

Journal
Clinical Cancer Research
Published
2025-05-01
DOI
https://doi.org/10.1158/1078-0432.ccr-24-4097
Citations
3
Primary Topic
Lung Cancer Treatments and Mutations
Type
article
Field-Weighted Citation Impact
4.56

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article

Liquid and Tissue Biopsies for Identifying MET Exon 14 Skipping NSCLC: Analyses from the Phase II VISION Study of Tepotinib

Paul K. Paik, Andreas Johne, Christopher Stroh, Aurora O’Brate et al.
3 citations
Clinical Cancer Research
Lung Cancer Treatments and Mutations
4.56
article

Liquid and Tissue Biopsies for Identifying MET Exon 14 Skipping NSCLC: Analyses from the Phase II VISION Study of Tepotinib

Paul K. Paik, Andreas Johne, Christopher Stroh, Aurora O’Brate, Dilafruz Juraeva, Rolf Bruns, Christian Diego Rolfo, Christoph Menzel
article en
3 citations

Abstract

Tepotinib had robust, durable activity in TBx-positive/LBx-negative and TBx-positive/LBx-positive patients. Although LBx is a complementary method to TBx for detecting METex14, it may preferentially select patients with higher tumor burden and poorer prognosis. Undetectable METex14 in baseline ctDNA (due to low ctDNA shedding) may define more favorable treatment outcomes.

Clinical Cancer ResearchVol. 31(13)
Memorial Sloan Kettering Cancer Center (US), Merck KGaA, Darmstadt (Germany) (DE), Cornell University (US), Tisch Hospital (US), Icahn School of Medicine at Mount Sinai (US)
AstraZeneca, Merck KGaA, National Institutes of Health, EMD Serono, National Cancer Institute
Openalex Percentile: Top 6%
Lung Cancer Treatments and Mutations
4.56
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