Togashi Junichi, Akamastu Nobuhisa, Kokudo Norihiro
Artificial Organ and Transplantation Surgery Division, Department of Surgery, University of Tokyo, Tokyo, Japan.
Hepatobiliary Surg Nutr. 2016 Oct;5(5):399-407. doi: 10.21037/hbsn.2016.08.05.
Living donor liver transplantation (LDLT) is an established treatment not only for those with end-stage liver disease but for those with hepatocellular carcinoma (HCC) developing in cirrhotic liver. The aim of this study was to present a single-center experience of LDLT for HCC at the University of Tokyo Hospital, Japan.
Among 573 liver transplant recipients from January 1996 until the end of 2015, 139 patients have been indicated LDLT for the treatment of HCC, and were the subjects of the present study. We use the expanded criteria for HCC as follows; the number of tumor should be five or less, and the maximum diameter of the tumor should be 5 cm or less, without the distant metastasis nor the vascular invasion (Tokyo criteria, 5-5 rule). We also focused on the identification of the incidental intrahepatic cholangiocarcinoma (ICC) and combined hepatocellular carcinoma/cholangiocarcinoma (cHCC-CC) in liver explants.
The overall 1-, 5-, and 10-year recurrence-free and patient survival rates were 95%, 91%, and 91%, 91%, and 80%, 78%, respectively. The 1-, 3-, and 5-year cumulative recurrence rate was 5%, 6%, and 6% for within Milan, 0%, 8%, and 8% for beyond Milan/within Tokyo, and 33%, 50%, and 50% for beyond Tokyo, respectively, demonstrating the significantly impaired outcome of those beyond Tokyo criteria (P<0.001). The high alpha-fetoprotein (AFP) value (≥400 ng/mL), the high des-gamma-carboxy prothrombin (DCP) value (≥200 mAU/mL) and beyond the Tokyo criteria were proved to be significant predictors for the HCC recurrence, but the size or the type of the partial graft was not associated. Incidental ICC and cHCC-CC were found in one and two patients, respectively, with the size of less than 2 cm in all cases. ICC was not detected in preoperative evaluation but cHCC-CCs were misdiagnosed as HCC preoperatively. All three patients were alive without recurrence with a follow-up period of 2 to 14 years.
The present results of our institution seem acceptable in terms of the recurrence-free and patient survival. The issues of the expansion of indication, living donor deceased donor for HCC, and liver transplantation (LT) for cholangiocarcinoma are still left to be investigated in future studies.
活体肝移植(LDLT)不仅是终末期肝病患者的既定治疗方法,也是肝硬化肝脏中发生肝细胞癌(HCC)患者的治疗方法。本研究的目的是介绍日本东京大学医院单中心进行的针对HCC的LDLT经验。
在1996年1月至2015年底的573例肝移植受者中,有139例患者因治疗HCC而接受LDLT,为本研究对象。我们采用以下扩大的HCC标准:肿瘤数量应在5个或以下,肿瘤最大直径应在5厘米或以下,无远处转移和血管侵犯(东京标准,5-5规则)。我们还着重于在肝外植体中识别偶然发现的肝内胆管癌(ICC)和肝细胞癌/胆管癌合并症(cHCC-CC)。
总体1年、5年和10年无复发生存率和患者生存率分别为95%、91%和91%,91%和80%,78%。米兰标准内的1年、3年和5年累积复发率分别为5%、6%和6%,米兰标准外/东京标准内为0%、8%和8%,东京标准外为33%、50%和50%,表明东京标准外患者的预后明显受损(P<0.001)。高甲胎蛋白(AFP)值(≥400 ng/mL)、高脱γ-羧基凝血酶原(DCP)值(≥200 mAU/mL)和超出东京标准被证明是HCC复发的重要预测因素,但部分移植物的大小或类型与之无关。分别在1例和2例患者中发现偶然的ICC和cHCC-CC,所有病例大小均小于2厘米。术前评估未检测到ICC,但cHCC-CC术前被误诊为HCC。所有3例患者均存活且无复发,随访期为2至14年。
就无复发生存率和患者生存率而言,本机构目前的结果似乎是可以接受的。扩大适应症、HCC的活体供体与尸体供体以及胆管癌的肝移植(LT)等问题仍有待未来研究探讨。