Tandoi F, Ponte E, Saffioti M C, Patrono D, Mirabella S, Lupo F, Romagnoli R, Salizzoni M
Liver Transplant Center, General Surgery Unit, A.O.-Città della Salute e della Scienza, S. Giovanni Battista Hospital, University of Turin, Italy.
Transplant Proc. 2013 Sep;45(7):2711-4. doi: 10.1016/j.transproceed.2013.07.002.
Liver transplantation (OLT) is the gold standard therapy for patients with cirrhosis complicated by hepatocellular carcinoma (HCC) within Milan Criteria (MC). We evaluated the impact of the etiology of the underlying liver disease on long-term outcomes of patients undergoing OLT for HCC within MC having a Model for End-stage Liver Disease (MELD) score < 15.
From November 2002 to December 2009, we performed 203 primary OLTs from brain-dead donors in recipients with HCC and cirrhosis with biochemical MELD scores below 15. We excluded 31 patients outside MC on the explant pathology of the native liver. The remaining 172 were divided into 3 groups according to the etiology of the underlying cirrhosis: hepatitis C virus-positive (HCV+; n = 78; 45%), hepatitis B virus-positive (HBV+; n = 65; 38%) and other indications (n = 29; 17%). The groups were compared for donor and recipient features, donor-recipient match, and transplant variables. The study endpoint was long-term patient survival.
The groups were similar, except for a greater prevalence of hepatitis B core antibody-positive grafts in the HBV+ group and less frequent HCC bridging procedures in the other indications group. After a median follow-up of 72 months, HCC recurrence was observed in 8 (4.7%) patients (6 HCV+, 2 other indications), 5 of whom died. Overall 5-year patient survival of 82%, revealed significant differences among groups: 98.3% in HBV+, 67.1% in HCV+, and 85.8% in other indications (HBV+ vs other indications: P = .01; HBV+ vs HCV+: P = .0001; HCV+ vs other indications: P = NS). In the HCV+ group, recurrent HCV hepatitis was the most frequent cause of death. Upon multivariate analysis, HBV positivity in the recipient was an independent predictor of better patient survival (hazard ratio = 0.10, 95% confidence interval 0.02-0.64, P = .013).
Etiology of the underlying cirrhosis significantly influenced the long-term survival after OLT of patients with HCC within MC and MELD < 15. It should be taken into account in estimation of survival benefit.
肝移植(OLT)是米兰标准(MC)内肝硬化合并肝细胞癌(HCC)患者的金标准治疗方法。我们评估了潜在肝脏疾病病因对终末期肝病模型(MELD)评分<15的MC内HCC患者接受OLT的长期预后的影响。
2002年11月至2009年12月,我们对203例来自脑死亡供体的原发性OLT进行了研究,受体为HCC和肝硬化患者,生化MELD评分低于15。我们根据肝移植病理排除了31例不在MC范围内的患者。其余172例根据潜在肝硬化的病因分为3组:丙型肝炎病毒阳性(HCV+;n = 78;45%)、乙型肝炎病毒阳性(HBV+;n = 65;38%)和其他指征(n = 29;17%)。比较各组的供体和受体特征、供体-受体匹配情况以及移植变量。研究终点为患者长期生存情况。
除HBV+组中乙肝核心抗体阳性移植物的患病率较高以及其他指征组中HCC桥接手术的频率较低外,各组情况相似。中位随访72个月后,8例(4.7%)患者出现HCC复发(6例HCV+,2例其他指征),其中5例死亡。总体5年患者生存率为82%,各组间存在显著差异:HBV+组为98.3%,HCV+组为67.1%,其他指征组为85.8%(HBV+组与其他指征组:P = 0.01;HBV+组与HCV+组:P = 0.0001;HCV+组与其他指征组:P = 无显著差异)。在HCV+组中,复发性丙型肝炎是最常见的死亡原因。多因素分析显示,受体HBV阳性是患者生存情况较好的独立预测因素(风险比 = 0.10,95%置信区间0.02 - 0.64,P = 0.013)。
潜在肝硬化的病因显著影响了MC内且MELD<15的HCC患者OLT后的长期生存。在评估生存获益时应予以考虑。