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Living donor liver transplantation for hepatocellular carcinoma: a single-center experience in Taiwan
Authors:Concejero Allan  Chen Chao-Long  Wang Chih-Chi  Wang Shih-Ho  Lin Chih-Che  Liu Yueh-Wei  Yang Chin-Hsiang  Yong Chee-Chien  Lin Tsan-Shiun  Jawan Bruno  Huang Tung-Liang  Cheng Yu-Fan  Eng Hock-Liew
Affiliation:Liver Transplantation Program, Chang Gung Memorial Hospital-Kaohsiung Medical Center, and Chang Jung University College of Medicine Kaohsiung, Taiwan.
Abstract:BACKGROUND: Living donor liver transplantation (LDLT) demonstrates certain survival benefits over deceased donor liver transplantation for hepatocellular carcinoma (HCC) but there is no consensus on criteria for the use of LDLT for HCC for hepatocellular carcinoma (HCC) taking into account strategies to improve survival. METHODS: Thirty-five patients (89% men) underwent LDLT for HCC. The mean age was 51 years (range, 22-61). The median disease severity scores were B, 11-20, and 2B for Child-Turcotte-Pugh, Model for End-stage Liver Disease, and United Network for Organ Sharing, respectively. The transplant records were retrospectively analyzed. RESULTS: All were within Milan criteria at time of transplantation. A novel approach to downstaging tumors initially beyond the Milan criteria was evaluated using transarterial embolization or percutaneous ethanol injection. Our initial results were encouraging as recipients whose tumors had been downstaged had not had recurrence to date. Seven (20%) patients underwent hepatectomy for HCC before undergoing transplant. The overall mean posttransplant follow-up in this series was 40.3 months (range, 23-75). The overall posttransplant complication rate requiring intervention was 11%. There was only one malignancy recurrence for an overall recurrence rate of 3%. Vascular invasion and small- for-size transplants did not seem to influence tumor recurrence. The nonestimated recipient 1-year, 3-year, and 5-year survivals were 98%, 96%, and 90%, respectively. CONCLUSION: This review emphasizes the need for early disease recognition and prompt intervention when Milan criteria are met to improve survival from HCC after LDLT.
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