Literature DB >> 22517493

The use of single-agent sorafenib in the treatment of advanced hepatocellular carcinoma patients with underlying Child-Pugh B liver cirrhosis: a retrospective analysis of efficacy, safety, and survival benefits.

Joanne Chiu1, Yuen Fong Tang, Tzy-Jyun Yao, Ashley Wong, Hilda Wong, Roland Leung, Pierre Chan, Tan To Cheung, Albert C Chan, Roberta Pang, Sheung-Tat Fan, Ronnie Poon, Thomas Yau.   

Abstract

BACKGROUND: This study explored the efficacy, tolerability, and survival benefits of using sorafenib in patients with Child-Pugh class B (CPB) cirrhosis.
METHODS: Patients with advanced hepatocellular carcinoma who were treated with sorafenib at Queen Mary Hospital, Hong Kong, China, were analyzed retrospectively. Treatment outcomes were analyzed according to their respective Child-Pugh status. Patients with CPB disease were further divided into CPB7 (those with a score of 7) and CPB8-9 (a score of 8 or 9) subgroups.
RESULTS: The baseline demographic parameters were comparable between 108 patients with Child-Pugh class A (CPA) disease and 64 CPB patients. Both clinical benefit rate (21.3% vs 32.4% vs 14.8%; P = .23) and progression-free survival (median: 3.2 months vs 3.2 months vs 2.3 months; P = .26) were similar among CPA, CPB7, and CPB8-9 groups, respectively. The overall survival was different among these groups (P = .002) and showed a trend toward worse outcome in CPB patients: the median was 6.1, 5.4, and 2.7 months among CPA, CPB7, and CPB8-9 patients, respectively. The commonest grade 3/4 adverse events were hand-foot syndrome (13.5%), diarrhea (9.9%), and rash (7.0%). Grade 3/4 leukopenia, thrombocytopenia, and anemia occurred in 2.9%, 5.3%, and 8.8% of the patients, respectively. Overall, the 3 groups of patients experienced similar incidence of most of these adverse events. Nonetheless, CPB patients experienced more anemia (P = .01), gastrointestinal bleeding (P = .02), and hepatic encephalopathy (P = .02).
CONCLUSIONS: CPA and CPB patients tolerated sorafenib similarly and derived similar clinical and progression-free survival benefit. Among CPB patients, most benefits were observed in patients with a score of 7. Nevertheless, CPB patients were more susceptible to developing cirrhotic complications, and thus more vigilant surveillance is needed.
Copyright © 2012 American Cancer Society.

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Year:  2012        PMID: 22517493     DOI: 10.1002/cncr.27543

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  26 in total

1.  Role of sorafenib in the treatment of advanced hepatocellular carcinoma: An update.

Authors:  Angela Gauthier; Mitchell Ho
Journal:  Hepatol Res       Date:  2012-11-12       Impact factor: 4.288

Review 2.  Sorafenib for the treatment of hepatocellular carcinoma.

Authors:  Marcus Alexander Wörns; Peter Robert Galle
Journal:  Hepat Oncol       Date:  2014-03-20

3.  Survival and tolerance to sorafenib in Child-Pugh B patients with hepatocellular carcinoma: a prospective study.

Authors:  Cassia Regina Guedes Leal; Cristiane Magalhães; Daniel Barbosa; Diogo Aquino; Bernardo Carvalho; Elizabeth Balbi; Lucio Pacheco; Renata Perez; Paulo de Tarso Pinto; Sérgio Setubal
Journal:  Invest New Drugs       Date:  2018-06-13       Impact factor: 3.850

Review 4.  Chemotherapy for hepatocellular carcinoma: The present and the future.

Authors:  Marco Le Grazie; Maria Rosa Biagini; Mirko Tarocchi; Simone Polvani; Andrea Galli
Journal:  World J Hepatol       Date:  2017-07-28

Review 5.  Hong Kong consensus recommendations on the management of hepatocellular carcinoma.

Authors:  Ronnie Tung-Ping Poon; Tom Tan-To Cheung; Philip Chong-Hei Kwok; Ann-Shing Lee; Tat-Wing Li; Kwok-Loon Loke; Stephen Lam Chan; Moon-Tong Cheung; Tak-Wing Lai; Chin-Cheung Cheung; Foon-Yiu Cheung; Ching-Kong Loo; Yiu-Kuen But; Shing-Jih Hsu; Simon Chun-Ho Yu; Thomas Yau
Journal:  Liver Cancer       Date:  2015-03       Impact factor: 11.740

Review 6.  Clinical trials of combined molecular targeted therapy and locoregional therapy in hepatocellular carcinoma: past, present, and future.

Authors:  Hwi Young Kim; Joong-Won Park
Journal:  Liver Cancer       Date:  2014-03       Impact factor: 11.740

7.  Predictors of survival in patients with established cirrhosis and hepatocellular carcinoma treated with sorafenib.

Authors:  Andrea L Inghilesi; Donatella Gallori; Lorenzo Antonuzzo; Paolo Forte; Daniela Tomcikova; Umberto Arena; Stefano Colagrande; Silvia Pradella; Bernardo Fani; Elena Gianni; Luca Boni; Giacomo Laffi; Francesco Di Costanzo; Fabio Marra
Journal:  World J Gastroenterol       Date:  2014-01-21       Impact factor: 5.742

Review 8.  Hepatocellular carcinoma: Will novel targeted drugs really impact the next future?

Authors:  Liliana Montella; Giovannella Palmieri; Raffaele Addeo; Salvatore Del Prete
Journal:  World J Gastroenterol       Date:  2016-07-21       Impact factor: 5.742

9.  GALNT14 genotype, α-fetoprotein and therapeutic side effects predict post-chemotherapy survival in patients with advanced hepatocellular carcinoma.

Authors:  Wey-Ran Lin; Chao-Wei Hsu; Yi-Cheng Chen; Ming-Ling Chang; Kung-Hao Liang; Ya-Hui Huang; Chau-Ting Yeh
Journal:  Mol Clin Oncol       Date:  2014-05-15

10.  Implications of FGF19 on sorafenib-mediated nitric oxide production in hepatocellular carcinoma cells - a short report.

Authors:  Lixia Gao; Chloe Shay; Fenglin Lv; Xuli Wang; Yong Teng
Journal:  Cell Oncol (Dordr)       Date:  2017-10-05       Impact factor: 6.730

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