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早期应用依维莫司对肝移植后肝细胞癌复发的影响。

Impact of Early Initiated Everolimus on the Recurrence of Hepatocellular Carcinoma After Liver Transplantation.

机构信息

Department of Hepatology and Liver Transplantation, Reina Sofía University Hospital, IMIBIC, CIBERehd, Córdoba, Spain.

General Surgery and Transplantation, Hospital Virgen del Rocío, IBIS, Sevilla, Spain.

出版信息

Transplantation. 2018 Dec;102(12):2056-2064. doi: 10.1097/TP.0000000000002270.

Abstract

BACKGROUND

Many centers implement everolimus-based immunosuppression in liver transplant patients with hepatocellular carcinoma. We aimed to explore the potential impact of early initiated everolimus on tumor recurrence after liver transplantation.

METHODS

This study included 192 patients with hepatocellular carcinoma undergoing liver transplantation among who 64 individuals were prospectively enrolled (2012-2015) and received early initiated everolimus (ie, started between postoperative day 15 to 21), whereas the remaining 128 patients acted as historical controls without everolimus. Propensity score matching was performed to ensure comparability. Multivariate Cox regression and competing risks analysis were used to control for potential confounders.

RESULTS

Patients with and without everolimus were comparable in terms of number of nodules (P = 0.37), total tumor diameter (P = 0.44), Milan criteria fulfillment (P = 0.56), and histological differentiation (P = 0.61), but there were increased microvascular invasion rates in the everolimus group (26.5% vs 13.3%; P = 0.026). Tumor recurrence rates were similar with and without everolimus (10.9% vs 9.9% at 36 months respectively; P = 0.18). After controlling for microvascular invasion among other potential confounders, everolimus had no significant impact on tumor recurrence, neither in the multivariate Cox regression (relative risk = 3.23; P = 0.09), nor in the competing risks analysis for tumor recurrence-death (relative risk = 1.02; P = 0.94). Patients receiving everolimus had reduced tacrolimus trough concentrations and lower serum creatinine within the first 18 months postliver transplantation.

CONCLUSION

Everolimus may not be universally prescribed to prevent tumor recurrence in liver transplant patients with hepatocellular carcinoma. Future randomized trials should be focused on patients with histological features of increased tumor aggressiveness, in whom the potential benefit would be higher.

摘要

背景

许多中心在肝癌肝移植患者中实施依维莫司为基础的免疫抑制治疗。我们旨在探讨肝移植后早期开始依维莫司对肿瘤复发的潜在影响。

方法

本研究纳入了 192 名接受肝移植的肝癌患者,其中 64 名患者前瞻性入组(2012-2015 年)并接受早期开始依维莫司治疗(即术后第 15-21 天开始),而其余 128 名患者作为无依维莫司的历史对照。采用倾向评分匹配以确保可比性。多变量 Cox 回归和竞争风险分析用于控制潜在混杂因素。

结果

依维莫司组和无依维莫司组在结节数量(P = 0.37)、总肿瘤直径(P = 0.44)、米兰标准符合率(P = 0.56)和组织学分级(P = 0.61)方面无差异,但依维莫司组的微血管侵犯率较高(26.5% vs 13.3%;P = 0.026)。两组肿瘤复发率相似(分别为 36 个月时的 10.9%和 9.9%;P = 0.18)。在控制其他潜在混杂因素中的微血管侵犯后,依维莫司对肿瘤复发无显著影响,无论是在多变量 Cox 回归中(相对风险 = 3.23;P = 0.09),还是在肿瘤复发-死亡的竞争风险分析中(相对风险 = 1.02;P = 0.94)。肝移植后 18 个月内,接受依维莫司的患者他克莫司谷浓度降低,血清肌酐水平降低。

结论

依维莫司可能不适用于普遍预防肝癌肝移植患者的肿瘤复发。未来的随机试验应集中在具有肿瘤侵袭性增加的组织学特征的患者,这些患者的潜在获益更高。

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