Targeted therapy and personalized medicine in hepatocellular carcinoma: drug resistance, mechanisms, and treatment strategies

被引:51
|
作者
Galun, Danijel [1 ,2 ]
Srdic-Rajic, Tatjana [3 ]
Bogdanovic, Aleksandar [1 ]
Loncar, Zlatibor [2 ,4 ]
Zuvela, Marinko [1 ,2 ]
机构
[1] Clin Ctr Serbia, Hepatopancreatobiliary Unit, Univ Clin Digest Surg, Koste Todorovica 6, Belgrade 11000, Serbia
[2] Univ Belgrade, Med Sch, Belgrade, Serbia
[3] Inst Oncol & Radiol Serbia, Unit Expt Oncol, Belgrade, Serbia
[4] Clin Ctr Serbia, Emergency Ctr, Belgrade, Serbia
关键词
hepatocellular carcinoma; drug resistance; multimodal treatment; chemotherapy; EPITHELIAL-MESENCHYMAL TRANSITION; TIVANTINIB ARQ 197; IMMUNE CHECKPOINT BLOCKADE; RECEPTOR TYROSINE KINASE; T-CELL RESPONSES; STAGING SYSTEMS; LIVER-CANCER; PHASE-III; POSTOPERATIVE RECURRENCE; TREATMENT ALGORITHM;
D O I
10.2147/JHC.S106529
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Hepatocellular carcinoma (HCC) is characterized by a growing number of new cases diagnosed each year that is nearly equal to the number of deaths from this cancer. In a majority of the cases, HCC is associated with the underlying chronic liver disease, and it is diagnosed in advanced stage of disease when curative treatment options are not applicable. Sorafenib is a treatment of choice for patients with performance status 1 or 2 and/or macrovascular invasion or extrahepatic spread, and regorafenib is the only systemic treatment found to provide survival benefit in HCC patients progressing on sorafenib treatment. Other drugs tested in different trials failed to demonstrate any benefit. Disappointing results of numerous trials testing the efficacy of various drugs indicate that HCC has low sensitivity to chemotherapy that is in great part caused by multidrug resistance. Immunotherapy for HCC is a new challenging treatment option and involves immune checkpoint inhibitors/antibody-based therapy and peptide-based vaccines. Another challenging approach is microRNA-based therapy that involves two strategies. The first aims to inhibit oncogenic miRNAs by using miRNA antagonists and the second strategy is miRNA replacement, which involves the reintroduction of a tumor-suppressor miRNA mimetic to restore a loss of function.
引用
收藏
页码:93 / 103
页数:11
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