关键词: MET exon 14 skipping mutation interstitial lung disease invasive mucinous adenocarcinoma mesenchymal-epithelial transition factor tepotinib tyrosine kinase inhibitors

Mesh : Humans Female Aged Protein Kinase Inhibitors / therapeutic use adverse effects Lung Neoplasms / drug therapy genetics pathology Epithelial-Mesenchymal Transition / genetics drug effects Exons / genetics Mutation Adenocarcinoma, Mucinous / genetics drug therapy pathology Fatal Outcome Proto-Oncogene Proteins c-met / genetics Lung Diseases, Interstitial / genetics drug therapy diagnostic imaging Tyrosine Kinase Inhibitors

来  源:   DOI:10.2169/internalmedicine.2540-23   PDF(Pubmed)

Abstract:
Mesenchymal-epithelial transition (MET) exon 14-skipping mutation (METex14) is rare in pulmonary invasive mucinous adenocarcinomas (IMAs), and the clinical impact of MET-tyrosine kinase inhibitors (TKIs) remains unknown. We herein report a 75-year-old woman with IMA harboring METex14 who was treated with the MET-TKI tepotinib. The lung tumor regressed over six months; however, the patient ultimately died of exacerbated interstitial lung disease (ILD), possibly associated with tepotinib. An autopsy revealed diffuse alveolar damage in pre-existing chronic fibrosis. We discuss how to pre-evaluate ILD deterioration risks and monitor TKI-induced lung toxicity during treatment.
摘要:
间充质上皮转化(MET)外显子14-跳跃突变(METex14)在肺侵袭性黏液腺癌(IMAs)中很少见,而MET-酪氨酸激酶抑制剂(TKIs)的临床影响尚不清楚.我们在此报告一名携带METex14的IMA患者75岁,她接受了MET-TKI替泊替尼治疗。肺肿瘤消退超过六个月;然而,患者最终死于加剧的间质性肺病(ILD),可能与替泊替尼有关。尸检显示在先前存在的慢性纤维化中弥漫性肺泡损伤。我们讨论了如何在治疗期间预先评估ILD恶化风险并监测TKI引起的肺毒性。
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