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新型靶向治疗策略在胆管癌和肝细胞癌中的应用。

Novel targeted therapy strategies for biliary tract cancers and hepatocellular carcinoma.

机构信息

Division of Hematology Oncology, Department of Medicine, Mayo Clinic, Scottsdale, AZ 85259, USA.

Department of Cancer Biology, Mayo Clinic, Jacksonville, FL 32224, USA.

出版信息

Future Oncol. 2018 Mar;14(6):553-566. doi: 10.2217/fon-2017-0451. Epub 2018 Feb 20.

Abstract

Worldwide hepatobiliary cancers are the second leading cause of cancer related death. Despite their relevance, hepatobiliary cancers have a paucity of approved systemic therapy options. However, there are a number of emerging therapeutic biomarkers and therapeutic concepts that show promise. In hepatocellular carcinoma, nivolumab appears particularly promising and recently received US FDA approval. In intrahepatic cholangiocarcinoma, therapies targeting FGFR2 and IDH1 and immune checkpoint inhibitors are the furthest along and generating the most excitement. There are additional biomarkers that merit further exploration in hepatobiliary cancers including FGF19, ERRFI1, TERT, BAP1, BRAF, CDKN2A, tumor mutational burden and ERBB2 (HER2/neu). Development of new and innovative therapies would help address the unmet need for effective systemic therapies in advanced and metastatic hepatobiliary cancers.

摘要

全球范围内,肝胆癌是癌症相关死亡的第二大主要原因。尽管肝胆癌具有重要意义,但获批的系统治疗方案却寥寥无几。然而,有许多新兴的治疗生物标志物和治疗概念显示出前景。在肝细胞癌中,纳武利尤单抗尤其有前途,最近获得了美国 FDA 的批准。在肝内胆管癌中,针对 FGFR2 和 IDH1 的治疗方法以及免疫检查点抑制剂的研究进展最快,也最令人兴奋。还有其他一些生物标志物在肝胆癌中值得进一步探索,包括 FGF19、ERRFI1、TERT、BAP1、BRAF、CDKN2A、肿瘤突变负担和 ERBB2(HER2/neu)。开发新的创新疗法将有助于解决晚期和转移性肝胆癌中对有效系统治疗的未满足需求。

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