Medical Oncology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Department of Medical Oncology, Cancer Center Amsterdam, Amsterdam UMC, VU University Medical Center (VUmc), Amsterdam, The Netherlands.
Expert Rev Gastroenterol Hepatol. 2024 Oct;18(10):605-630. doi: 10.1080/17474124.2024.2416230. Epub 2024 Nov 15.
After years of treatment stagnation in biliary tract cancers (BTC), there has been a notable shift with the emergence of targeted therapies and immunotherapy, leading to substantial progress in tackling this aggressive disease.
We provide a comprehensive overview of the target therapies that are already part of the treatment algorithm for BTC, such as FGFR, IDH, and HER2 inhibitors. Additionally, we delve into some less known targets that are being explored, such as KRAS proto-oncogene, MAPK cascade, PI3K/AKT/mTOR pathway and novel molecules directed against P53, claudin, histones, and mitochondrial metabolism. Furthermore, we discuss agnostic drugs and analyze the efficacy data available for BTC specifically. We also examine the expanding world of immunotherapy, with an eye on predictive factors of response for immune checkpoint inhibitors, and on novel immune drugs such as chimeric antigen receptor (CAR)-T and vaccines.
In the expert opinion, we discuss the problem of the scarcity of patients eligible for target therapies and how can clinical trials be designed to overcome this challenge. We also summarize the most promising trials that have the potential to change clinical practice both for immunotherapies and target drugs.
经过多年的胆道癌(BTC)治疗停滞,随着靶向治疗和免疫疗法的出现,该疾病的治疗取得了显著进展。
我们全面概述了已经纳入 BTC 治疗方案的靶向治疗药物,如 FGFR、IDH 和 HER2 抑制剂。此外,我们还探讨了一些正在探索中的不太知名的靶点,如 KRAS 原癌基因、MAPK 级联、PI3K/AKT/mTOR 通路以及针对 P53、claudin、组蛋白和线粒体代谢的新型分子。此外,我们还讨论了未知靶点药物,并分析了 BTC 特定的疗效数据。我们还研究了免疫疗法的扩展领域,着眼于免疫检查点抑制剂的反应预测因素,以及新型免疫药物,如嵌合抗原受体(CAR)-T 和疫苗。
在专家意见中,我们讨论了适合靶向治疗的患者数量有限的问题,以及如何设计临床试验来克服这一挑战。我们还总结了最有前途的临床试验,这些试验有可能改变免疫疗法和靶向药物的临床实践。