Related Experiment Video
Updated: Jan 7, 2026

Endobronchial Ultrasound-guided Intratumoral Injection of Cisplatin for the Treatment of Isolated Mediastinal Recurrence of Lung Cancer
Published on: February 12, 2017
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.
Abstract:
Non-small cell lung cancer (NSCLC) accounts for 85% of all lung cancers; however, a subset of patients experiences disease progression associated with alterations in the Mesenchymal-Epithelial Transition Factor (c-MET) pathway. These include MET exon 14-skipping mutations, which promote tumor growth, metastasis, and resistance to epidermal growth factor receptor (EGFR)-targeted therapies. Telisotuzumab vedotin (TV-t, Emrelis), a novel first-in-class c-MET inhibitor, is under investigation as a targeted therapy for c-MET-high NSCLC. This article highlights the therapeutic potential of TV-t as a targeted therapy for advanced NSCLC patients with limited post-treatment options. A targeted literature review was conducted using PubMed and ClinicalTrials.gov (2018 and 2025) with terms including "Telisotuzumab Vedotin," "c-MET," "c-MET-high," "c-MET overexpression," "MET exon 14," and "NSCLC." Both clinical and preclinical studies of the efficacy, safety, and pharmacological properties of TV-t were included. Also, those studies reported clinical findings relevant to TV-t in c-MET-altered NSCLC. In the pivotal LUMINOSITY phase II trial, TV-t showed a 28.6% overall response rate (ORR) in EGFR-wildtype, c-MET-overexpressing NSCLC, with 34.6% ORR in c-MET-high patients. Median duration of response was 9.0 months, overall survival 14.5 months, and progression-free survival (PFS) 5.7 months for the c-MET-high subgroup. In phase Ib studies, TV-t combined with osimertinib achieved a 50% ORR and 7.4-month PFS, while TV-t with nivolumab, the median PFS was 7.2 months, but ORR was low (7.4%). Common grade 3 or higher toxicities occurred in 27.9% of patients and included neuropathy, anemia, and pulmonary embolism, with no hepatotoxicity. Remarkable cardiac safety was observed. TV-t demonstrated promising efficacy and tolerability in patients, highlighting its clinical potential. However, further studies are needed to confirm its survival advantage, the durability of response, and safety profile, and to establish its long-term value and support its integration into routine clinical practice.
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.

