Unresectable Hepatocellular Carcinoma: A Review of New Advances with Focus on Targeted Therapy and Immunotherapy

被引:6
作者
Farasati Far, Bahareh [1 ]
Rabie, Dorsa [2 ]
Hemati, Parisa [2 ]
Fooladpanjeh, Parastoo [2 ]
Faal Hamedanchi, Neda [3 ]
Broomand Lomer, Nima [4 ]
Karimi Rouzbahani, Arian [5 ,6 ]
Naimi-Jamal, Mohammad Reza [1 ]
机构
[1] Iran Univ Sci & Technol, Dept Chem, Tehran 1684613114, Iran
[2] Islamic Azad Univ, Fac Pharmaceut Chem, Tehran Med Sci, Tehran 193951495, Iran
[3] Islamic Azad Univ, Fac Med, Tehran Med Sci Branch, Tehran 193951495, Iran
[4] Guilan Univ Med Sci, Fac Med, Rasht 4314637758, Iran
[5] Lorestan Univ Med Sci, Student Res Comm, Khorramabad 6718773654, Iran
[6] Lorestan Univ Med Sci, USERN Off, Khorramabad 6718773654, Iran
来源
LIVERS | 2023年 / 3卷 / 01期
关键词
hepatocellular carcinoma; unresectable treatment; chemotherapy; targeted therapy; PHASE-II TRIAL; TUMORS CLINICAL-EVIDENCE; PLUS OXALIPLATIN GEMOX; PULSED DENDRITIC CELLS; DOUBLE-BLIND; COMBINATION CHEMOTHERAPY; 1ST-LINE THERAPY; OPEN-LABEL; CHECKPOINT INHIBITORS; ANTITUMOR-ACTIVITY;
D O I
10.3390/livers3010011
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
With an expected incidence of more than 1 million cases by 2025, liver cancer remains a problem for world health. With over 90% of cases, hepatocellular carcinoma (HCC) is the most prevalent kind of liver cancer. In this review, we presented the range of experimental therapeutics for patients with advanced HCC, the successes and failures of new treatments, areas for future development, the evaluation of dose-limiting toxicity in different drugs, and the safety profile in patients with liver dysfunction related to the underlying chronic liver disease. In addition to the unmet demand for biomarkers to guide treatment decisions and the burgeoning fields of immunotherapy and systemic therapy in hepatocellular carcinoma, the development of old and new drugs, including their failures and current advancements, has been reviewed. This review aims to evaluate the updated optimal clinical treatment of unresectable hepatocellular carcinomas in clinical practice, mainly through targeted therapy. Although surgical treatment can significantly enhance the survival probability of early and intermediate-stage patients, it is unsuitable for most HCC patients due to a lack of donors. Due to their severe toxicity, the few first-line anti-HCC drugs, such as sorafenib, are often reserved for advanced HCC patients for whom other therapies have failed. The second-line drugs are usually alternatives for patients with intolerance or resistance. Consequently, the ongoing growth of possible preclinical drugs and studies on miRNAs, lncRNAs, and numerous other signaling pathway targets for developing novel drugs may introduce additional treatment prospects for HCC.
引用
收藏
页码:121 / 160
页数:40
相关论文
共 190 条
[121]   Observational registry of sorafenib use in clinical practice across Child-Pugh subgroups: The GIDEON study [J].
Marrero, Jorge A. ;
Kudo, Masatoshi ;
Venook, Alan P. ;
Ye, Sheng-Long ;
Bronowicki, Jean-Pierre ;
Chen, Xiao-Ping ;
Dagher, Lucy ;
Furuse, Junji ;
Geschwind, Jean-Francois H. ;
Ladron de Guevara, Laura ;
Papandreou, Christos ;
Takayama, Tadatoshi ;
Sanyal, Arun J. ;
Yoon, Seung Kew ;
Nakajima, Keiko ;
Lehr, Robert ;
Heldner, Stephanie ;
Lencioni, Riccardo .
JOURNAL OF HEPATOLOGY, 2016, 65 (06) :1140-1147
[122]   Pharmacokinetics of Nintedanib in Subjects With Hepatic Impairment [J].
Marzin, Kristell ;
Kretschmar, Gunther ;
Luedtke, Doreen ;
Kraemer, Sandrine ;
Kuelzer, Raimund ;
Schlenker-Herceg, Rozsa ;
Schmid, Ulrike ;
Schnell, David ;
Dallinger, Claudia .
JOURNAL OF CLINICAL PHARMACOLOGY, 2018, 58 (03) :357-363
[123]   Fraction and incidence of liver cancer attributable to hepatitis B and C viruses worldwide [J].
Maucort-Boulch, Delphine ;
de Martel, Catherine ;
Franceschi, Silvia ;
Plummer, Martyn .
INTERNATIONAL JOURNAL OF CANCER, 2018, 142 (12) :2471-2477
[124]   Advances and Challenges on Management of Gastrointestinal Stromal Tumors [J].
Mei, Lin ;
Du, Wei ;
Idowu, Michael ;
von Mehren, Margaret ;
Boikos, Sosipatros A. .
FRONTIERS IN ONCOLOGY, 2018, 8
[125]   Sorafenib in combination with transarterial chemoembolisation in patients with unresectable hepatocellular carcinoma (TACE 2): a randomised placebo-controlled, double-blind, phase 3 trial [J].
Meyer, Tim ;
Fox, Richard ;
Ma, Yuk Ting ;
Ross, Paul J. ;
James, Martin W. ;
Sturgess, Richard ;
Stubbs, Clive ;
Stocken, Deborah D. ;
Wall, Lucy ;
Watkinson, Anthony ;
Hacking, Nigel ;
Evans, T. R. Jeffry ;
Collins, Peter ;
Hubner, Richard A. ;
Cunningham, David ;
Primrose, John Neil ;
Johnson, Philip J. ;
Palmer, Daniel H. .
LANCET GASTROENTEROLOGY & HEPATOLOGY, 2017, 2 (08) :565-575
[126]   Phase I study of the antiprogrammed cell death-1 Ab spartalizumab (PDR001) in Japanese patients with advanced malignancies [J].
Minami, Hironobu ;
Doi, Toshihiko ;
Toyoda, Masanori ;
Imamura, Yoshinori ;
Kiyota, Naomi ;
Mitsuma, Ayako ;
Shimokata, Tomoya ;
Naito, Yoichi ;
Matsubara, Nobuaki ;
Tajima, Takeshi ;
Tokushige, Kota ;
Ishihara, Kae ;
Cameron, Scott ;
Ando, Yuichi .
CANCER SCIENCE, 2021, 112 (02) :725-733
[127]   Selenium nanoparticles and quercetin suppress thioacetamide-induced hepatocellular carcinoma in rats: Attenuation of inflammation involvement [J].
Mohamed, Ahmed A. ;
Zaghloul, Randa A. ;
Abdelghany, Amr M. ;
El Gayar, Amal M. .
JOURNAL OF BIOCHEMICAL AND MOLECULAR TOXICOLOGY, 2022, 36 (04)
[128]   Hallmarks of response, resistance, and toxicity to immune checkpoint blockade [J].
Morad, Golnaz ;
Helmink, Beth A. ;
Sharma, Padmanee ;
Wargo, Jennifer A. .
CELL, 2021, 184 (21) :5309-5337
[129]   A first-in-human phase 1 dose escalation study of spartalizumab (PDR001), an anti-PD-1 antibody, in patients with advanced solid tumors [J].
Naing, Aung ;
Gainor, Justin F. ;
Gelderblom, Hans ;
Forde, Patrick M. ;
Butler, Marcus O. ;
Lin, Chia-Chi ;
Sharma, Sunil ;
de Olza, Maria Ochoa ;
Varga, Andrea ;
Taylor, Matthew ;
Schellens, Jan H. M. ;
Wu, Hongqian ;
Sun, Haiying ;
Silva, Antonio P. ;
Faris, Jason ;
Mataraza, Jennifer ;
Cameron, Scott ;
Bauer, Todd M. .
JOURNAL FOR IMMUNOTHERAPY OF CANCER, 2020, 8 (01)
[130]  
O'Reilly EM, 2001, CANCER-AM CANCER SOC, V91, P101, DOI 10.1002/1097-0142(20010101)91:1<101::AID-CNCR13>3.0.CO