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Cited 19 time in webofscience Cited 21 time in scopus
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Systemic Cytotoxic Chemotherapy of Patients With Advanced Hepatocellular Carcinoma in the Era of Sorafenib Nonavailability

Authors
Yoon, Eileen L.Yeon, Jong EunLee, Hyun JungSuh, Sang JunLee, Sun JaeKang, Seong HeeKang, KeunheeYoo, Yang JaeKim, Ji HoonYim, Hyung JoonByun, Kwan Soo
Issue Date
Mar-2014
Publisher
Lippincott Williams & Wilkins Ltd.
Keywords
hepatocellular carcinoma; sorafenib; cytotoxic chemotherapy; survival rate
Citation
Journal of Clinical Gastroenterology, v.48, no.3, pp E22 - E29
Indexed
SCI
SCIE
SCOPUS
Journal Title
Journal of Clinical Gastroenterology
Volume
48
Number
3
Start Page
E22
End Page
E29
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2020.sw.kumedicine/9530
DOI
10.1097/MCG.0b013e3182a54ec8
ISSN
0192-0790
1539-2031
Abstract
Goals: The goal of the study was to compare the efficacy and safety of sorafenib with those of systemic cytotoxic chemotherapy. Background: Sorafenib treatment has shown to improve the survival in patients with advanced hepatocellular carcinoma (HCC) when compared with placebo. However, whether sorafenib controls advanced-stage HCC better than systemic cytotoxic chemotherapy has not been elucidated. Study: We retrospectively reviewed the medical records of 220 patients with measurable advanced HCC who had not received systemic treatment previously between January 2007 and April 2012. Among these patients, 78 had been treated with sorafenib. Another 14 patients who were treated with a 4-weekly regimen of adriamycin, cisplatin, and capecitabine were included as the historical control group for comparison. The median overall survival, the progression-free survival, response rates, and safety profiles were evaluated. Results: Baseline characteristics were similar between the treatment groups. The median overall survival was 7.2 months [95% confidence interval (CI), 5.6-8.8] in the sorafenib group and 11.2 months (95% CI, 8.1-14.2) in the cytotoxic chemotherapy group (P=0.10). The median progression-free survival was 3.2 months (95% CI, 2.2-4.3) in the sorafenib group and 5.9 months (95% CI, 3.6-8.2) in the cytotoxic chemotherapy group (P=0.07). The deterioration of liver function and neutropenia were the most frequent serious adverse events in the sorafenib and the systemic chemotherapy group. Conclusions: Although a direct head-to-head comparison could not be done, there were some patients who showed a good response to systemic cytotoxic chemotherapy. Further assessment is necessary to study the role of chemotherapy in patients who are intolerant or intractable to sorafenib.
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Byun, Kwan Soo
Guro Hospital (Department of Gastroenterology and Hepatology, Guro Hospital)
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