Emrelis: A New Approach in Treating MET-high Locally Advanced or Metastatic Non-squamous NSCLC; A Mini Review

Saim Mahmood Khan1, Areeba Naveed2, Aleena Amir2

  • 1Karachi Medical and Dental College, Department of Medicine, Karachi, Pakistan.

PubMed

Insights

Telisotuzumab vedotin (TV-t) shows promise for advanced non-small cell lung cancer (NSCLC) with c-MET alterations. This c-MET inhibitor offers therapeutic potential for patients with limited options, demonstrating notable response rates and manageable toxicity.

Area of Science:

  • Oncology
  • Pharmacology
  • Genetics

Background:

  • Non-small cell lung cancer (NSCLC) comprises 85% of lung cancers.
  • Alterations in the c-MET pathway, including MET exon 14-skipping mutations, drive tumor progression and treatment resistance in a subset of NSCLC patients.
  • Epidermal growth factor receptor (EGFR)-targeted therapies can be ineffective due to c-MET pathway activation.

Purpose of the Study:

  • To evaluate the therapeutic potential of telisotuzumab vedotin (TV-t), a novel c-MET inhibitor, for advanced NSCLC.
  • To highlight TV-t as a targeted therapy option for NSCLC patients with limited post-treatment choices.
  • To review clinical and preclinical data on TV-t's efficacy, safety, and pharmacology in c-MET-altered NSCLC.

Main Methods:

  • A targeted literature review was performed using PubMed and ClinicalTrials.gov (2018-2025).
  • Search terms included "Telisotuzumab Vedotin," "c-MET," "c-MET-high," "c-MET overexpression," "MET exon 14," and "NSCLC."
  • Inclusion criteria encompassed clinical and preclinical studies detailing TV-t's efficacy, safety, and pharmacological properties, particularly in c-MET-altered NSCLC.

Main Results:

  • The LUMINOSITY phase II trial reported a 28.6% overall response rate (ORR) in EGFR-wildtype, c-MET-overexpressing NSCLC and 34.6% ORR in c-MET-high patients.
  • Median outcomes for c-MET-high patients included 9.0 months duration of response, 14.5 months overall survival, and 5.7 months progression-free survival (PFS).
  • Combination therapy with osimertinib yielded a 50% ORR and 7.4-month PFS; combination with nivolumab showed a 7.2-month median PFS but low ORR (7.4%). Common grade 3+ toxicities (27.9%) included neuropathy, anemia, and pulmonary embolism, with notable cardiac safety and no hepatotoxicity.

Conclusions:

  • Telisotuzumab vedotin demonstrates promising efficacy and tolerability in advanced NSCLC patients with c-MET alterations.
  • TV-t represents a potential targeted therapy for patients with limited treatment options.
  • Further research is necessary to confirm survival benefits, response durability, long-term safety, and clinical utility for routine practice.