医学
精密医学
临床试验
肝内胆管癌
靶向治疗
胆道癌
精确肿瘤学
生物信息学
临床实习
鉴定(生物学)
仿形(计算机编程)
疾病
个性化医疗
重症监护医学
肿瘤科
内科学
癌症
梅德林
计算生物学
基因组测序
全身疗法
胰腺癌
药品审批
作者
Giulia Tesini,Halima Ibrahim,Lorenza Rimassa,Chiara Braconi
出处
期刊:Hepatology
[Lippincott Williams & Wilkins]
日期:2025-09-22
被引量:3
标识
DOI:10.1097/hep.0000000000001541
摘要
The development of Next-Generation Sequencing (NGS) techniques for extended genomic profiling has led to the identification of actionable molecular alterations in approximately half of the patients with biliary tract cancer (BTC), with the highest incidences among those with intrahepatic cholangiocarcinoma. Targeted drugs have demonstrated the ability to confer clinical benefit while maintaining a manageable safety profile. As a result, despite the lack of a head-to-head comparison with standard second-line chemotherapy, they are now recommended for patients with advanced disease who are still fit after progression to first-line palliative systemic anti-cancer treatment. In this review, we will contextualize the results observed with targeted drugs in clinical trials within the framework of clinical practice. We will provide an overview of available single-gene analyses that should be considered in case of lack of access to NGS, defining testing priorities, differences in yields, and therapeutic implications. Lastly, we will discuss future perspectives in the field of precision medicine for BTC, focusing on new strategies to overcome treatment resistance, on the optimal collocation of targeted drugs in the treatment algorithm, and on newly identified actionable alterations for which compounds are currently under investigation.
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