Chinese Journal of Tissue Engineering Research ›› 2011, Vol. 15 ›› Issue (31): 5879-5882.doi: 10.3969/j.issn.1673-8225.2011.31.043

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Utilization of arsenious acid chemotherapy for hepatocellular carcinoma following liver transplantation

Wu Lin-wei, Hu Xiao-kun, He Xiao-shun, Tai Qiang, Ju Wei-qiang, Wang Dong-ping, Ma Yi, Zhu Xiao-feng   

  1. Organ Transplantation Center, the First Affiliated Hospital of Sun Yat-sen University, Guangzhou  510080, Guangdong Province, China
  • Received:2011-01-22 Revised:2011-03-06 Online:2011-07-30 Published:2011-07-30
  • Contact: He Xiao-shun, Organ Transplantation Center, the First Affiliated Hospital of Sun Yat-sen University, Guangzhou 510080, Guangdong Province, China gdtrc@163.com
  • About author:Wu Lin-wei☆, Doctor, Attending physician, Organ Transplantation Center, the First Affiliated Hospital of Sun Yat-sen University, Guangzhou 510080, Guangdong Province, China lw97002@163.com Hu Xiao-kun☆, Studying for doctorate, Organ Transplantation Center, the First Affiliated Hospital of Sun Yat-sen University, Guangzhou 510080, Guangdong Province, China Wu Lin-wei and Hu Xiao-kun contributed equally to this paper.
  • Supported by:

    the Science and Technology Plan of Guangdong Province, No. 200813030301308*

Abstract:

BACKGROUND: Tumor recurrence in liver transplant recipients greatly affects prognosis of liver transplantation with hepatocellular carcinoma (HCC). How to prevent tumor recurrence has aroused increasing attention. Arsenious acid chemotherapy is considered effective on treating moderate or advanced liver cancer, but its utilization following liver transplantation remains few.
OBJECTIVE: To explore the role of arsenious acid on tumor recurrence in liver transplant patients with primary HCC extending Milan criteria.
METHODS: Twenty-three patients with HCC extending Milan criterion received intravenous arsenious acid chemotherapy after orthotopic liver transplantation (OLT), that is, intravenous injection, 10 mg per day, for 7 successive days, followed by 7-day interval, and a course comprised 4 durations. Each patient treated for 1-4 courses. Other 16 patients did not received chemotherapy served as controls. The difference of patients’ survival, tumor recurrence and adverse reaction were compared. 
RESULTS AND CONCLUSION: All patients were routinely followed up for 3-32 months. Thirty recipients were presented with tumor recurrence, 16 in the chemotherapy group and 14 in the non-chemotherapy group. Tumor recurred in lung, liver graft and bones in most cases. The total recurrence rate was similar in these two groups, but chemotherapy could delay recurrence after transplantation (P=0.026). There was no significance in 6-month, 1-year survival rate between two groups, but the 2-year survival in the chemotherapy group was higher (P=0.037); 6-month tumor-free survival rates in the two groups had no significance, 1-year and 2-year tumor-free in the chemotherapy group were significantly higher than those in the non-chemotherapy group (P=0.030, 0.023). Intravenous arsenious acid chemotherapy can delay tumor recurrence and prolong survival in liver transplant patients with HCC extending Milan criteria.

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