Iguchi Tomohiro, Shirabe Ken, Aishima Shinichi, Wang Huanlin, Fujita Nobuhiro, Ninomiya Mizuki, Yamashita Yo-ichi, Ikegami Toru, Uchiyama Hideaki, Yoshizumi Tomoharu, Oda Yoshinao, Maehara Yoshihiko
1 Department of Surgery and Science, Kyushu University, Fukuoka, Japan. 2 Department of Anatomic Pathology, Kyushu University, Fukuoka, Japan. 3 Department of Molecular Imaging and Diagnosis, Kyushu University, Fukuoka, Japan.
Transplantation. 2015 Jun;99(6):1236-42. doi: 10.1097/TP.0000000000000489.
Vascular invasion of hepatocellular carcinoma (HCC) has a high incidence of recurrence after liver transplantation. Patients with microvascular invasion (MVI) show a high tumor grade; however, some show a good prognosis. This retrospective study aimed to investigate whether the degree of MVI affects prognosis after living-donor liver transplantation.
A total of 142 patients with HCC who had undergone living-donor liver transplantation were histologically evaluated about the number of invaded vessels and the maximum number of invading carcinoma cells. Patients with MVI were classified into two subgroups: high MVI group (n = 38), which showed more than 50 carcinoma cells in the vessels, with multiple invaded vessels; and low MVI group (n = 17), which showed MVI, but not high MVI.
Analysis of recurrence-free survival showed that high MVI group had significantly poorer outcomes than the other groups (P < 0.001). High MVI group had significantly higher α-fetoprotein levels, des-γ-carboxy prothrombin levels, number of tumors, a larger tumor size, and a higher percentage of poorly differentiated HCC than non-MVI group. High MVI was an independent prognostic factor for recurrence-free survival (P = 0.030). Among patients exceeding the Milan criteria (n = 61), high MVI group had significantly poorer outcomes than the other groups for recurrence-free survival (P = 0.003). Patients in high MVI group had significantly higher des-γ-carboxy prothrombin levels and a larger tumor size than non-MVI group. High MVI was an independent prognostic factor for recurrence-free survival (P = 0.014).
In living-donor liver transplantation for HCC, high MVI is a novel pathologic marker for predicting prognosis.
肝细胞癌(HCC)的血管侵犯在肝移植后复发率很高。微血管侵犯(MVI)患者的肿瘤分级较高;然而,一些患者预后良好。本回顾性研究旨在探讨MVI程度是否影响活体肝移植后的预后。
对142例行活体肝移植的HCC患者进行组织学评估,观察侵袭血管数量及侵袭癌细胞的最大数量。MVI患者分为两个亚组:高MVI组(n = 38),血管内癌细胞超过50个,且有多条侵袭血管;低MVI组(n = 17),有MVI但不属于高MVI。
无复发生存分析显示,高MVI组的预后明显比其他组差(P < 0.001)。高MVI组的甲胎蛋白水平、异常凝血酶原水平、肿瘤数量、肿瘤大小以及低分化HCC的比例均显著高于无MVI组。高MVI是无复发生存的独立预后因素(P = 0.030)。在超过米兰标准的患者(n = 61)中,高MVI组的无复发生存预后明显比其他组差(P = 0.003)。高MVI组患者的异常凝血酶原水平和肿瘤大小显著高于无MVI组。高MVI是无复发生存的独立预后因素(P = 0.014)。
在HCC的活体肝移植中,高MVI是预测预后的一种新的病理标志物。