关键词: MET gene capmatinib cholangiocarcinoma met amplification targeted therapy

Mesh : Benzamides Bile Duct Neoplasms / drug therapy genetics pathology Bile Ducts, Intrahepatic / pathology Carcinoma, Non-Small-Cell Lung / pathology Cholangiocarcinoma / drug therapy genetics Humans Imidazoles Lung Neoplasms / pathology Proto-Oncogene Proteins c-met / genetics Triazines

来  源:   DOI:10.1080/15384047.2022.2029128

Abstract:
Cholangiocarcinoma is a highly morbid gastrointestinal malignancy for which available therapies are limited. Standard of care includes cytotoxic chemotherapies such as gemcitabine, platinum agents, nab-paclitaxel, and fluoropyrimidine analogues. However, tolerability of these regimens varies, and patients who do not tolerate chemotherapy have limited targeted therapies and immunotherapy options. In cholangiocarcinoma, mesenchymal-epithelial transition factor (MET) amplification may present an additional opportunity for a targeted therapeutic approach, especially considering emerging data in non-small cell lung cancer. In this case, we present a metastatic cholangiocarcinoma patient with high-level MET gene amplification for whom capmatinib, a tyrosine kinase inhibitor with activity against c-MET, provided a partial response after cessation of chemotherapy.
摘要:
胆管癌是一种高度病态的胃肠道恶性肿瘤,可用的治疗方法有限。护理标准包括细胞毒性化疗,如吉西他滨,铂剂,nab-紫杉醇,和氟嘧啶类似物.然而,这些方案的耐受性各不相同,不耐受化疗的患者的靶向治疗和免疫治疗选择有限.在胆管癌中,间充质上皮转化因子(MET)扩增可能为靶向治疗方法提供额外的机会,特别是考虑到非小细胞肺癌的新数据。在这种情况下,我们介绍了一名具有高水平MET基因扩增的转移性胆管癌患者,一种具有抗c-MET活性的酪氨酸激酶抑制剂,在化疗停止后提供了部分反应。
公众号