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The choice for the optimal therapy in advanced biliary tract cancers: Chemotherapy, targeted therapies or immunotherapy
被引:14
|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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