The choice for the optimal therapy in advanced biliary tract cancers: Chemotherapy, targeted therapies or immunotherapy

被引:16
|
作者
Palmieri, Lola-Jade [1 ,2 ]
Lavol, J. [1 ]
Dermine, S. [1 ,2 ]
Brezault, C. [1 ]
Dhooge, M. [1 ]
Barr, A. [1 ,2 ]
Chaussade, S. [1 ,2 ]
Coriat, R. [1 ,2 ]
机构
[1] Cochin Hosp, AP HP, Gastroenterol & Digest Oncol Dept, F-75014 Paris, France
[2] Univ Paris, Unite INSERM U1016, Paris, France
关键词
Biliary tract cancers; Cholangiocarcinoma; Targeted therapy; Immunotherapy; Genome sequencing; GROWTH-FACTOR-RECEPTOR; PHASE-II TRIAL; GALLBLADDER CANCER; IMPROVES SURVIVAL; 2ND-LINE THERAPY; IDH-MUTANT; OPEN-LABEL; GEMCITABINE; COMBINATION; OXALIPLATIN;
D O I
10.1016/j.pharmthera.2020.107517
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Biliary tract cancers (BTCs) represent a heterogeneous group that includes intrahepatic cholangiocarcinomas (CCAs), perihilar-CCAs or Klatskin tumors, extrahepatic-CCAs, and gallbladder adenocarcinoma. These entities have distinct demographics, risk factors, clinical presentation, and molecular characteristics. In advanced BTCs, the recommendations are mainly supporting a doublet chemotherapy regimen using cisplatin/gemcitabine (CisGem) with a 5-year overall survival rate close to 5% and median overall survival (mOS) of less than a year. The lack of overall efficacy stresses the need for personalized therapies. Recently, whole-genome and transcriptome sequencing highlighted the diversity of BTCs' subtypes. Distinct genetic alterations were retrieved according to the localization, with a high rate of potentially actionable alterations. Targeted therapies and immunotherapy have since then been tested for BTCs, trying to propose a more personalized treatment. This review describes the different therapeutic options, validated and in development, for patients with advanced BTCs. (C) 2020 Elsevier Inc. All rights reserved.
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页数:10
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