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Coexistence of a primary ALK-positive and MET14 exon skipping mutation double-fusion in one patient with NSCLC and response to crizotinib: A case report and literature review.

Medicine 2026 Vol.105(8) p. e47628

Xu K, Wang M, Zhao J, Xu X, Song M

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[RATIONALE] Lung cancer exhibits one of the highest incidence and fatality rates globally.

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APA Xu K, Wang M, et al. (2026). Coexistence of a primary ALK-positive and MET14 exon skipping mutation double-fusion in one patient with NSCLC and response to crizotinib: A case report and literature review.. Medicine, 105(8), e47628. https://doi.org/10.1097/MD.0000000000047628
MLA Xu K, et al.. "Coexistence of a primary ALK-positive and MET14 exon skipping mutation double-fusion in one patient with NSCLC and response to crizotinib: A case report and literature review.." Medicine, vol. 105, no. 8, 2026, pp. e47628.
PMID 41731828

Abstract

[RATIONALE] Lung cancer exhibits one of the highest incidence and fatality rates globally. With the advancement of next-generation sequencing testing techniques, double or multiple gene driver mutations have been identified in certain patients.

[PATIENT CONCERNS] A 78-year-old female presented with a chest shadow.

[DIAGNOSES] In this case of lung adenocarcinoma, second-generation sequencing revealed a co-occurrence of echinoderm microtubule-associated protein-like 4-anaplastic lymphoma kinase and MET exon 14 skipping mutation.

[INTERVENTIONS] Crizotinib was administered orally on August 31, 2022, resulting in a partial response and progression-free survival for a duration of 8 months. After 8 months of treatment, the patient's disease progressed, after which the treatment dose of crizotinib was increased; the patient's condition improved again.

[OUTCOMES] Over 4 months of increased-dose oral crizotinib treatment, the patient achieved durable partial response, with significant reduction in tumor burden and without new metastases.

[LESSONS] This report supports crizotinib can provide potential benefit for anaplastic lymphoma kinase/MET14 co-mutated lung adenocarcinoma patients, but sufficient cases and further research are needed to confirm and explore the possible mechanisms involved.

MeSH Terms

Humans; Crizotinib; Female; Aged; Lung Neoplasms; Anaplastic Lymphoma Kinase; Proto-Oncogene Proteins c-met; Carcinoma, Non-Small-Cell Lung; Exons; Mutation; Antineoplastic Agents; Protein Kinase Inhibitors; Adenocarcinoma of Lung

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