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MET Exon 14 Skipping in NSCLC: A Systematic Literature Review of Epidemiology, Clinical Characteristics, and Outcomes
Julien Mazieres1, Helene Vioix2, Boris M Pfeiffer2
1CHU de Toulouse, Université Paul Sabatier, Toulouse, France.
Introduction:
MET exon 14 (METex14) skipping is a rare oncogenic driver in non-small-cell lung cancer (NSCLC) for which targeted therapy with MET tyrosine kinase inhibitors (TKIs) was recently approved. Given the heterogeneity in published data of METex14 skipping NSCLC, we conducted a systematic literature review to evaluate its frequency, patient characteristics, and outcomes.
Methods:
On June 13, 2022 we conducted a systematic literature review of publications and conference abstracts reporting frequency, patient characteristics, or outcomes of patients with METex14 skipping NSCLC.
Results:
We included 139 studies reporting frequency or patient characteristics (350,997 patients), and 39 studies reporting clinical outcomes (3989 patients). Median METex14 skipping frequency was 2.0% in unselected patients with NSCLC, with minimal geographic variation. Median frequency was 2.4% in adenocarcinoma or nonsquamous subgroups, 12.0% in sarcomatoid, and 1.3% in squamous histology. Patients with METex14 skipping NSCLC were more likely to be elderly, have adenocarcinoma histology; there was no marked sex or smoking status distribution. In first line of treatment, median objective response rate ranged from 50.7% to 68.8% with targeted therapies (both values correspond to MET TKIs), was 33.3% with immunotherapy, and ranged from 23.1% to 27.0% with chemotherapy.
Conclusions:
Patients with METex14 skipping are more likely to have certain characteristics, but no patient subgroup can be ruled out; thus, it is crucial to test all patients with NSCLC to identify suitable candidates for MET inhibitor therapy. MET TKIs appeared to result in higher efficacy outcomes, although no direct comparison with chemotherapy or immunotherapy regimens was found.
Insights
MET exon 14 skipping is a rare driver in non-small-cell lung cancer (NSCLC). Testing all NSCLC patients is crucial, as MET tyrosine kinase inhibitors (TKIs) show higher efficacy in this subgroup.
Area of Science:
- Oncology
- Genetics
- Pharmacology
Background:
- MET exon 14 (METex14) skipping is an oncogenic driver in non-small-cell lung cancer (NSCLC).
- Targeted therapy with MET tyrosine kinase inhibitors (TKIs) is approved for METex14 skipping NSCLC.
- Published data on METex14 skipping NSCLC exhibit heterogeneity.
Purpose of the Study:
- To evaluate the frequency of METex14 skipping in NSCLC.
- To characterize patients with METex14 skipping NSCLC.
- To assess clinical outcomes for patients with METex14 skipping NSCLC.
Main Methods:
- Systematic literature review of publications and conference abstracts.
- Data collected included frequency, patient characteristics, and clinical outcomes.
- Included 139 studies for frequency/characteristics (350,997 patients) and 39 for outcomes (3989 patients).
Main Results:
- Median METex14 skipping frequency was 2.0% in unselected NSCLC patients.
- Higher frequency observed in adenocarcinoma (2.4%) and sarcomatoid (12.0%) histology compared to squamous (1.3%).
- MET TKIs demonstrated higher objective response rates (50.7%-68.8%) compared to immunotherapy (33.3%) and chemotherapy (23.1%-27.0%).
Conclusions:
- Patients with METex14 skipping NSCLC often present with specific characteristics but can occur in any subgroup.
- Universal testing for METex14 skipping is recommended to identify candidates for MET inhibitor therapy.
- MET TKIs show promising efficacy, though direct comparative data against other treatments are limited.
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