Complete response to capmatinib in a patient with metastatic lung adenocarcinoma harboring CD47-MET fusion: a case report
- PMID: 38832711
- PMCID: PMC11379643
- DOI: 10.1093/oncolo/oyae106
Complete response to capmatinib in a patient with metastatic lung adenocarcinoma harboring CD47-MET fusion: a case report
Abstract
Comprehensive genomic profiling is highly recommended for treatment decision in nonsquamous, non-small cell lung cancer (NSCLC). However, rare genomic alterations are still being unveiled, with scarce data to guide therapy. Herein, we describe the treatment journey of a 56-year-old, never-smoker Caucasian woman with a metastatic NSCLC harboring a CD47-MET fusion, initially classified as a variant of unknown significance. She had undergone 3 lines of therapy over the course of 3 years, including chemotherapy, immunotherapy, and anti-angiogenic therapy. After reanalysis of her next-generation sequencing data in our service, the fusion was reclassified as likely oncogenic. The patient was started with fourth-line capmatinib, with a good tolerance so far and a complete metabolic response in the active sites of disease, currently ongoing for 18 months. In conclusion, we highlight the sensitivity of a novel MET fusion to capmatinib and emphasize the need for comprehensive panels in NSCLC and molecular tumor board discussions with specialized centers when rare findings arise.
Keywords: MET receptor tyrosine kinase; capmatinib; case report; next-generation sequencing; non-small cell lung cancer.
© The Author(s) 2024. Published by Oxford University Press.
Conflict of interest statement
The authors have no financial conflict of interest with this manuscript.
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Comment in
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Oncofusions - shaping cancer care.Oncologist. 2025 Jan 17;30(1):oyae126. doi: 10.1093/oncolo/oyae126. Oncologist. 2025. PMID: 38833619 Free PMC article.
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