两种不同的成纤维细胞生长因子受体抑制剂对FGFR2突变肝外胆管癌患者的疗效:一份病例报告

IF 4.8 2区 医学 Q1 ONCOLOGY
Oncologist Pub Date : 2025-05-08 DOI:10.1093/oncolo/oyae294
Ilianna Galli-Vareia, Petr Szturz, Ioannis A Voutsadakis, Nicolas Villard, Georgia Tsoumakidou, Mapi Fleury, Gabriela Herrera, Francois Fasquelle, Sebastien Godat, Antonia Digklia
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引用次数: 0

摘要

胆管癌(CCA)是一种有效的全身治疗方法很少的癌症。基于下一代测序(NGS)的基因组研究阐明了该疾病的分子格局,这有助于引入新的靶向治疗方法。其中一种治疗方法包括一类靶向成纤维细胞生长因子受体(FGFRs)受体酪氨酸激酶家族成员的小分子。我们在此报告一例胆管癌患者携带FGFR2突变。患者接受2种不同的FGFR抑制剂治疗,第一种引起眼部毒性。她从两者中获得了临床益处。本病例说明了FGFR抑制剂对具有特定点突变的胆管癌的疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy of 2 different fibroblast growth factor receptor-inhibitors in a patient with extrahepatic cholangiocarcinoma harboring an FGFR2 mutation: a case report.

Cholangiocarcinoma (CCA) is a type of cancer with few effective systemic therapies. Elucidation of the molecular landscape of the disease from genomic studies based on next-generation sequencing (NGS) has contributed to the introduction of new targeted therapies. One of these treatments consists of a class of small molecules that target members of the fibroblast growth factor receptors (FGFRs) family of receptor tyrosine kinases. We report here on a patient with a cholangiocarcinoma bearing an FGFR2 mutation. The patient was treated with 2 different FGFR inhibitors, as the first caused ocular toxicity. She obtained clinical benefits from both. This case illustrates the efficacy of FGFR inhibitors on cholangiocarcinoma with specific point mutations.

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来源期刊
Oncologist
Oncologist 医学-肿瘤学
CiteScore
10.40
自引率
3.40%
发文量
309
审稿时长
3-8 weeks
期刊介绍: The Oncologist® is dedicated to translating the latest research developments into the best multidimensional care for cancer patients. Thus, The Oncologist is committed to helping physicians excel in this ever-expanding environment through the publication of timely reviews, original studies, and commentaries on important developments. We believe that the practice of oncology requires both an understanding of a range of disciplines encompassing basic science related to cancer, translational research, and clinical practice, but also the socioeconomic and psychosocial factors that determine access to care and quality of life and function following cancer treatment.
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