d'Arienzo Paolo D, MacDonald Alan R, Patel Virjen, Ma Yuk T, Pihlak Rille, Starling Naureen
GI Cancers Unit, The Royal Marsden NHS Foundation Trust, London, UK.
Clinical Radiology Department, The Royal Marsden NHS Foundation Trust, London, UK.
Onco Targets Ther. 2024 Jun 13;17:489-496. doi: 10.2147/OTT.S434449. eCollection 2024.
Multiple FGFR inhibitors have demonstrated significant activity in pretreated advanced fusion-positive intrahepatic cholangiocarcinoma. The irreversible pan-FGFR inhibitor futibatinib has the potential to overcome acquired resistance to ATP-competitive FGFR inhibitors in a subset of patients. We present a case of prolonged clinical benefit using FGFR inhibitors sequentially, initially an ATP-competitive inhibitor followed by futibatinib upon progression, for a total of 36 months of FGFR-targeting therapy. This case supports sequential FGFR-targeting therapies for fusion-positive cholangiocarcinoma, with futibatinib acting as rescue therapy after failure of ATP-competitive inhibitors.
多种FGFR抑制剂已在经治的晚期融合阳性肝内胆管癌中显示出显著活性。不可逆的泛FGFR抑制剂futibatinib有可能克服一部分患者对ATP竞争性FGFR抑制剂产生的获得性耐药。我们报告了一例序贯使用FGFR抑制剂获得长期临床获益的病例,最初使用ATP竞争性抑制剂,疾病进展后使用futibatinib,FGFR靶向治疗共计36个月。该病例支持对融合阳性胆管癌采用序贯FGFR靶向治疗,其中futibatinib可作为ATP竞争性抑制剂治疗失败后的挽救疗法。