# Capmatinib for the treatment of METex14 skipping non-small cell lung cancer: retrospective analysis of real-world data from patients receiving compassionate use treatment in Italy

**Authors:** Fabiana Letizia Cecere, Ettore D’Argento, Francesco Gelsomino, Francesco Pesola, Paolo Bironzo, Salvatore Grisanti, Laura Bonanno, Gianluca Spitaleri, Diletta Valsecchi, Ilaria Marcon, Diego Cortinovis

PMC · DOI: 10.1007/s10238-025-01934-2 · 2025-11-18

## TL;DR

Capmatinib is effective in treating a rare type of lung cancer with METex14 mutations, showing promising results in real-world patient data from Italy.

## Contribution

This study provides real-world evidence supporting capmatinib's effectiveness for METex14 skipping NSCLC outside of clinical trials.

## Key findings

- Capmatinib was administered to 53 patients with METex14 skipping NSCLC in Italy.
- Most patients started at the full dose and 45.3% discontinued due to disease progression.
- The median time to treatment discontinuation was 15.2 months.

## Abstract

In patients with advanced non-small cell lung cancer (NSCLC), MET exon 14 (METex14) skipping mutations are rare and are associated with a poor prognosis. Capmatinib, a selective oral MET inhibitor, was recently approved for the treatment of advanced METex14 skipping NSCLC. However, data from real-world experiences are limited. This was a retrospective analysis using real-world data from Italian patients with advanced METex14 skipping NSCLC who had received at least one treatment with immunotherapy and/or platinum-based chemotherapy and received compassionate use treatment with capmatinib. Patient characteristics, treatment details, discontinuations, and adverse events are reported. Overall, 53 patients received capmatinib after receiving treatment with immunotherapy and/or platinum-based chemotherapy in Italy. Patients had a median age of 74 years, mostly metastatic disease (92.5% of patients), and previously received one (66.0%) or more (2: 28.3%; 3: 5.7%) lines of standard treatment (immunotherapy and/or platinum-based chemotherapy). Most patients (98.1%) started treatment with capmatinib at the full recommended dose of 400 mg twice daily and 77.4% did not require a dose reduction. Twenty-four patients (45.3%) discontinued treatment; the most frequent reason for discontinuing treatment was disease progression, with a median estimated time to treatment discontinuation of 15.2 months. This real-world retrospective analysis confirms that capmatinib is a valuable treatment option for difficult-to-treat METex14 skipping NSCLC, in agreement with the data from the registration trial.

## Linked entities

- **Genes:** MET (MET proto-oncogene, receptor tyrosine kinase) [NCBI Gene 4233]
- **Chemicals:** capmatinib (PubChem CID 25145656)
- **Diseases:** non-small cell lung cancer (MONDO:0005233), NSCLC (MONDO:0005233)

## Full-text entities

- **Genes:** SLTM (SAFB like transcription modulator) [NCBI Gene 79811] {aka Met}
- **Diseases:** NSCLC (MESH:D002289)
- **Chemicals:** Capmatinib (MESH:C000613976), platinum (MESH:D010984)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12628474/full.md

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Source: https://tomesphere.com/paper/PMC12628474