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肝细胞癌的靶向治疗。

Targeted therapy for hepatocellular carcinoma.

机构信息

Department of Liver Surgery and Transplantation, Liver Cancer Institute, Zhongshan Hospital, Fudan University, Shanghai, China.

Key Laboratory of Carcinogenesis and Cancer Invasion (Fudan University), Ministry of Education, Shanghai, China.

出版信息

Signal Transduct Target Ther. 2020 Aug 11;5(1):146. doi: 10.1038/s41392-020-00264-x.

Abstract

The last 3 years have seen the emergence of promising targeted therapies for the treatment of hepatocellular carcinoma (HCC). Sorafenib has been the mainstay of treatment for a decade and newer modalities were ineffective and did not confer any increased therapeutic benefit until the introduction of lenvatinib which was approved based on its non-inferiority to sorafenib. The subsequent success of regorafenib in HCC patients who progress on sorafenib treatment heralded a new era of second-line treatment and was quickly followed by ramucirumab, cabozantinib, and the most influential, immune checkpoint inhibitors (ICIs). Over the same period combination therapies, including anti-angiogenesis agents with ICIs, dual ICIs and targeted agents in conjunction with surgery or other loco-regional therapies, have been extensively investigated and have shown promise and provided the basis for exciting clinical trials. Work continues to develop additional novel therapeutic agents which could potentially augment the presently available options and understand the underlying mechanisms responsible for drug resistance, with the goal of improving the survival of patients with HCC.

摘要

在过去的 3 年中,出现了一些有前途的靶向治疗药物,可用于治疗肝细胞癌 (HCC)。索拉非尼已经成为治疗 HCC 的主要方法,十年以来,新的治疗方法都没有效果,也没有带来任何额外的治疗益处,直到仑伐替尼的问世,仑伐替尼的疗效不劣于索拉非尼,因此获得了批准。随后,regorafenib 在索拉非尼治疗进展的 HCC 患者中取得成功,标志着二线治疗的新时代的到来,紧接着 ramucirumab、cabozantinib 以及最具影响力的免疫检查点抑制剂 (ICIs) 也相继问世。在此期间,联合治疗方案,包括抗血管生成药物联合 ICI、双重 ICI 和靶向药物联合手术或其他局部区域治疗,已经得到了广泛的研究,并显示出了前景,为激动人心的临床试验提供了基础。目前,工作仍在继续开发其他潜在的新型治疗药物,这些药物有可能增加目前的治疗选择,并深入了解耐药的潜在机制,以期改善 HCC 患者的生存率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/601f/7419547/539626799cc0/41392_2020_264_Fig1_HTML.jpg

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