肝移植后肝细胞癌复发:澳大利亚单中心研究。

Matthew G Garas, Luis Calzadilla-Bertot, Briohny W Smith, Luc Delriviere, Byron Jaques, Lingjun Mou, Leon A Adams, Gerry C MacQuillan, George Garas, Gary P Jeffrey, Michael C Wallace
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引用次数: 0

摘要

背景:肝细胞癌(HCC)是世界范围内癌症相关死亡的主要原因。肝移植(LT)是最有效的治疗方法。HCC复发是肝移植患者肝移植后生存率降低的最大危险因素。文献报道的HCC复发率一般为8%-20%。许多HCC的预测因素已经被研究过,然而,据我们所知,还没有发表过使用澳大利亚数据的关于这一主题的研究。目的:确定当代西澳大利亚LT队列中HCC复发率和确定预测因素。方法:我们对2006年至2021年在查尔斯·盖尔德纳爵士医院接受肝移植的所有HCC患者进行了回顾性队列研究。数据收集自各种健康记录数据库,包括受者人口统计学、血清生化、放射学、手术记录、外植体组织病理学和复发细节。肝细胞癌患者肝移植后的总生存期,按复发分层,通过Kaplan Meier分析计算。采用单因素和多因素Cox回归来确定肝移植后HCC复发的预测因素。结果:2006年1月1日至2021年12月31日期间,119例患者接受肝细胞癌移植。8.4%的受试者在肝移植后复发HCC,中位随访时间为5.4年。中位复发时间为2.9年±0.75年。当比较基线特征时,更大比例的复发患者具有外植体组织病理学的共同特征,包括bbb3活结节(P = 0.001)、血管浸润(P = 0.003)和低分化HCC (P = 0.03)。未经调整的生存曲线显示,HCC复发患者的1年、3年、5年和10年生存率低于无HCC复发患者(分别为90%对92%,70%对88%,42%对80%,14%对76%;log rank P < 0.001)。结论:在当代澳大利亚队列中,HCC复发率很低,为8.4%,但它显著影响了肝移植后的生存。需要进一步的研究来确认复发的预测因素并改善接受者的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hepatocellular carcinoma recurrence after liver transplant: An Australian single-centre study.

Background: Hepatocellular carcinoma (HCC) is a leading cause of cancer-related deaths worldwide. Liver transplantation (LT) offers the most effective treatment. HCC recurrence is the strongest risk factor that decreases post-LT survival in patients transplanted for HCC. The rate of HCC recurrence is generally reported as 8%-20% in the literature. Many predictors of HCC have already been researched, however, to our knowledge there are no published studies on this topic using Australian data.

Aim: To determine the rate and identify predictors of HCC recurrence in a contemporary Western Australian LT cohort.

Methods: We performed a retrospective cohort study of all liver transplants in patients with HCC at Sir Charles Gairdner Hospital between 2006 and 2021. Data was collected from various health record databases and included recipient demographics, serum biochemistry, radiology, operation notes, explant histopathology and details of recurrence. Overall survival of HCC patients post-LT, stratified for recurrence, was calculated by Kaplan Meier analysis. Univariate and multivariate Cox regression was used to determine predictors of HCC recurrence post-LT.

Results: Between 1/1/2006 and 12/31/2021, 119 patients were transplanted with HCC. 8.4% of subjects developed recurrent HCC after LT with median follow-up time of 5.4 years. The median time to recurrence was 2.9 years ± 0.75 years. When comparing baseline characteristics, a greater proportion of subjects with recurrence had common characteristics on explant histopathology, including > 3 viable nodules (P = 0.001), vascular invasion (P = 0.003) and poorly differentiated HCC (P = 0.03). Unadjusted survival curves showed lower 1-year, 3-year, 5-year and 10-year survival rates in subjects with HCC recurrence compared to those without HCC recurrence (90% vs 92%, 70% vs 88%, 42% vs 80%, 14% vs 76%, respectively; log rank P < 0.001).

Conclusion: HCC recurrence was low at 8.4% in this contemporary Australian cohort, however it significantly impacted post-LT survival. Further studies are required to confirm predictors of recurrence and improve recipient outcomes.

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