Liver Cancer
Copyright ©The Author(s) 2003. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Dec 15, 2003; 9(12): 2666-2670
Published online Dec 15, 2003. doi: 10.3748/wjg.v9.i12.2666
Hepatic arterial infusion chemotherapy for hepatocellular carcinoma with tumor thrombosis of the portal vein tumor thrombosis
Yung-Chih Lai, Cheng-Yen Shih, Chin-Ming Jeng, Sien-Sing Yang, Jui-Ting Hu, Yung-Chuan Sung, Han-Ting Liu, Shaw-Min Hou, Chi-Hwa Wu, Tzen-Kwan Chen
Yung-Chih Lai, Cheng-Yen Shih, Sien-Sing Yang, Jui-Ting Hu, Yung-Chuan Sung, Han-Ting Liu, Chi-Hwa Wu, Tzen-Kwan Chen, Department of Internal Medicine, Cathay General Hospital, Taipei, Taiwan, China
Chin-Ming Jeng, Department of Radiology, Cathay General Hospital, Taipei, Taiwan, China
Shaw-Min Hou, Department of Surgery, Cathay General Hospital, Taipei, Taiwan, China
Author contributions: All authors contributed equally to the work.
Correspondence to: Dr. Yung-Chih Lai, Department of Internal Medicine, Cathay General Hospital, 280, Jen-Ai Road, Section 4, Taipei 106, Taiwan, China. yungchihlai@hotmail.com
Telephone: +86-2-27082121 Ext.3120 Fax: +86-2-27074949
Received: September 6, 2003
Revised: September 17, 2003
Accepted: October 12, 2003
Published online: December 15, 2003
Abstract

AIM: Hepatocellular carcinoma (HCC) with portal vein tumor thrombosis (PVTT) is associated with poor prognosis. The aim of this prospective study was to evaluate the efficacy of hepatic arterial infusion chemotherapy (HAIC) for patients with this disease.

METHODS: Eighteen HCC patients with PVTT were treated with HAIC via a subcutaneously implanted injection port. A course of chemotherapy consisted of daily cisplatin (10 mg for one hour) followed by 5-fluorouracil (250 mg for five hours) for five continuous days within a given week. The patients were scheduled to receive four consecutive courses of HAIC. Responders were defined in whom either a complete or partial response was achieved, while non-responders were defined based on stable or progressive disease status. The prognostic factors associated with survival after treatment were analyzed.

RESULTS: Six patients exhibited partial response to this form of HAIC (response rate = 33%). The 3, 6, 9, 12 and 18-month cumulative survival rates for the 18 patients were 83%, 72%, 50%, 28%, and 7%, respectively. Median survival times for the six responders and 12 non-responders were 15.0 (range, 11-18) and 7.5 (range, 1-13) months, respectively. It was demonstrated by both univariate and multivariate analyses that the therapeutic response and hepatic reserve function were significant prognostic factors.

CONCLUSION: HAIC using low-dose cisplatin and 5-fluorouracil may be a useful alternative for the treatment of patients with advanced HCC complicated with PVTT. There may also be survival-related benefits associated with HAIC.

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