Targeted therapy for hepatocellular carcinoma

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作者
Ao Huang
Xin-Rong Yang
Wen-Yuan Chung
Ashley R. Dennison
Jian Zhou
机构
[1] Fudan University,Department of Liver Surgery and Transplantation, Liver Cancer Institute, Zhongshan Hospital
[2] Key Laboratory of Carcinogenesis and Cancer Invasion (Fudan University),Shanghai Key Laboratory of Organ Transplantation, Zhongshan Hospital
[3] Ministry of Education,Department of Hepatobiliary and Pancreatic Surgery
[4] Fudan University,Institute of Biomedical Sciences
[5] University Hospitals of Leicester NHS Trust,State Key Laboratory of Genetic Engineering
[6] Fudan University,undefined
[7] Fudan University,undefined
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摘要
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.
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