New Drug: Telisotuzumab vedotin for cMET Amplified NSCLC


  • Study

    Phase 2, non-randomized, multicenter study (LUMINOSITY)
    Previously treated c-Met overexpressing NSQ EGFR wildtype advanced NSCLC (≤2 prior lines, ≤1 chemo)
    Telisotuzumab vedotin 1.9 mg/kg IV every 2 wks



  • Efficacy

    ORR: 34.6% vs. 22.9% (c-Met high vs. c-Met intermediate)
    mDoR: 9.0 mos vs. 7.2 mos (c-Met high vs. c-Met intermediate)
    mOS: 14.6 mos vs. 14.2 mos



  • Safety

    Any-grade TRAEs: peripheral sensory neuropathy (30%), peripheral edema (16%), fatigue (14%)
    Grade 5 TRAEs: 2 pts (interstitial lung disease, respiratory failure)



  • J Clin Oncol 2024;42(16_suppl):103

    Camidge DR,Bar J,Horinouchi H Telisotuzumab vedotin monotherapy in patients with previously treated c-Met–overexpressing non-squamous EGFR wildtype advanced NSCLC: Primary analysis of the LUMINOSITY trial

    http://doi.org/10.1200/JCO.2024.42.16_suppl.103

    Reviewed by Ulas D. Bayraktar, MD on Jun 9, 2025

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