Intrahepatic Cholangiocarcinoma: State of the Art of FGFR Inhibitors

被引:2
|
作者
Wu, Tianyu [1 ]
Jiang, Xiaoqing [2 ]
Zhang, Xin [3 ]
Wu, Bodeng [3 ]
Xu, Bin [1 ]
Liu, Xiaoliu [3 ]
Zheng, Lei [3 ]
Wang, Yu [1 ]
机构
[1] Southern Med Univ, Nanfang Hosp, Dept Hepatobiliary Surg, 1023-1063 South Sha Tai Rd, Guangzhou 510515, Peoples R China
[2] Southern Med Univ, Nanfang Hosp, Surg Intens Care Unit, Guangzhou, Peoples R China
[3] Southern Med Univ, Nanfang Hosp, Dept Lab Med, Guangzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
intrahepatic cholangiocarcinoma (iCCA); fibroblast growth factor receptor (FGFR); cholangiocarcinoma (CCA); BGJ398; pemigatinib;
D O I
10.1177/1073274821989314
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: Intrahepatic cholangiocarcinoma (iCCA), the second most common type of primary liver tumor, has an increasing incidence in the past few decades. iCCA is highly malignant, with a 5-year survival rate of approximately 5-10%. Surgical resection is usually the prescribed treatment for patients with early stage iCCA; however, patients are usually in an advanced stage iCCA upon diagnosis. Currently, targeted therapy combined with chemotherapy and other comprehensive treatment measures have been mainly adopted as palliative treatment measures. As a common candidate of targeted therapy, FGFR inhibitors have demonstrated their unique advantages in clinical trials. At present, the prospect of FGFR targeted therapy is encouraging. The landscape of FGFR inhibitors in iCCA is needed to be showed urgently. Methods: We searched relative reports of clinical trials on FGFR inhibitors in PubMed as well as Web of Science. We also concluded other available clinical trials of FGFR inhibitors (Data were collected from clinicaltrials.gov ). Results: Several relatively effective targeted drugs are being used in clinical trials. Some preliminary results indicate the outlook of targeted therapy such as BGJ398, TASI20, and HSP90 inhibitors. Conclusions: In summary, FGFR targeted therapy has broad prospects for the treatment of iCCA.
引用
收藏
页数:13
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