Paradigm shift of chemotherapy and systemic treatment for biliary tract cancer

被引:0
作者
Leowattana, Wattana [1 ]
Leowattana, Tawithep [2 ]
Leowattana, Pathomthep [1 ]
机构
[1] Mahidol Univ, Fac Trop Med, Dept Clin Trop Med, 420-6 Rajavithi Rd, Bangkok 10400, Thailand
[2] Srinakharinwirot Univ, Fac Med, Dept Med, Bangkok 10110, Thailand
关键词
Biliary tract cancers; Gemcitabine and cisplatin combination; Fibroblast growth factor receptor 2 inhibitors; Isocitrate dehydrogenase 1 inhibitors; Neurotrophic tyrosine receptor kinase gene fusion inhibitors; Immune checkpoint inhibitors; Microsatellite instability high; Infrigatinib; Pemigatinib; OPEN-LABEL; SOLID TUMORS; METASTATIC CHOLANGIOCARCINOMA; IMMUNE CHECKPOINT; SINGLE-ARM; PHASE-II; MULTICENTER; GEMCITABINE; CISPLATIN; BGJ398;
D O I
10.4251/wjgo.v15.i6.959
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Biliary tract cancers (BTC) are frequently identified at late stages and have a poor prognosis due to limited systemic treatment regimens. For more than a decade, the combination of gemcitabine and cis-platin has served as the first-line standard treatment. There are few choices for second-line chemo-therapy. Targeted treatment with fibroblast growth factor receptor 2 inhibitors, neurotrophic tyrosine receptor kinase inhibitors, and isocitrate dehydrogenase 1 inhibitors has had important results. Immune checkpoint inhibitors (ICI) such as pembrolizumab are only used in first-line treatment for microsatellite instability high patients. The TOPAZ-1 trial's outcome is encouraging, and there are several trials underway that might soon put targeted treatment and ICI combos into first-line options. Newer targets and agents for existing goals are being studied, which may represent a paradigm shift in BTC management. Due to a scarcity of targetable mutations and the higher toxicity profile of the current medications, the new category of drugs may occupy a significant role in BTC therapies.
引用
收藏
页码:959 / 972
页数:14
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