MET 抑制剂之间在患有 MET 14 号外显子跳越突变的非小细胞肺癌患者身上没有交叉毒性。

IF 1.1 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL
Acta Clinica Belgica Pub Date : 2024-04-01 Epub Date: 2024-03-18 DOI:10.1080/17843286.2024.2330137
Ariane Vanderick, Benoît Colinet
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引用次数: 0

摘要

导言:选择性酪氨酸激酶抑制剂被证明对MET 14外显子跳越突变的非小肺癌(NSCLC)患者有效:患者为转移性肺腺癌,伴有MET 14外显子跳越突变。她曾接受过 1b MET 抑制剂卡马替尼的治疗,但因出现严重肝毒性而不得不停药。几个月后,她开始服用另一种1b MET抑制剂特罗替尼,这次没有出现肝毒性:讨论:1b MET 抑制剂经常会出现不良反应。讨论:1b MET 抑制剂的不良反应很常见,但患者之间的差异很大。卡马替尼和泰泊替尼之间没有交叉毒性被误解,但这可以用药物动力学和药代动力学的细微差别来解释。必须提醒从业人员注意严重的不良反应,必要时停药或换药:这是首个显示 1b MET 抑制剂之间不存在交叉毒性的病例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Absence of cross-toxicity between MET inhibitors in a non-small-cell lung cancer with a MET exon 14 skipping mutation.

Introduction: Selective tyrosine kinase inhibitors are proven effective in patients with non-small lung cancer (NSCLC) with a MET exon 14 skipping mutation.

Case presentation: The patient developed a metastatic lung adenocarcinoma with a MET exon 14 skipping mutation. She was treated with a first 1b MET inhibitor, Capmatinib, but had to stop the drug because of major hepatotoxicity. A few months later, she started Tepotinib, another 1b MET inhibitor with this time, no sign of hepatotoxicity.

Discussion: Adverse events are frequent with 1b MET inhibitors. However, there is a wide interpatient variability. Absence of cross-toxicity between Capmatinib and Tepotinib is misunderstood but can be explained by slight differences in phamarcodynamics and pharmacokinetics. Practitionners have to be warned about severe adverse events to stop or change the drug if necessary.

Conclusion: This is the first case showing the absence of cross-toxicity between 1b MET inhibitors.

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来源期刊
Acta Clinica Belgica
Acta Clinica Belgica MEDICINE, GENERAL & INTERNAL-
CiteScore
3.50
自引率
0.00%
发文量
44
期刊介绍: Acta Clinica Belgica: International Journal of Clinical and Laboratory Medicine primarily publishes papers on clinical medicine, clinical chemistry, pathology and molecular biology, provided they describe results which contribute to our understanding of clinical problems or describe new methods applicable to clinical investigation. Readership includes physicians, pathologists, pharmacists and physicians working in non-academic and academic hospitals, practicing internal medicine and its subspecialties.
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