Division of Gastroenterology, Hospital of the University of Pennsylvania, Philadelphia, PA.
Leonard David Institute of Health Economics, University of Pennsylvania, Philadelphia, PA.
Liver Transpl. 2020 Aug;26(8):977-988. doi: 10.1002/lt.25787.
Liver transplantation (LT) is curative for most patients with hepatocellular carcinoma (HCC). However, 10%-15% of patients experience HCC recurrence. Patients who are reported as within Milan criteria by imaging are frequently found to be outside the criteria on explant. This under-staging of HCC worsens post-LT outcomes. However, risk factors for under-staging have not been elucidated. Furthermore, it is not known if there is regional or center-level variation in under-staging. We conducted a retrospective analysis of adult patients transplanted for HCC in the United Network for Organ Sharing (UNOS) database between 2012 and 2016. Under-staging was determined on the basis of comparing pre-LT imaging to explant findings. Kaplan-Meier methods and Cox regression were used to evaluate the impact of under-staging on HCC recurrence and post-LT survival. Mixed effects logistic regression was used to identify risk factors for under-staging and to study regional and center-level variation in adjusted analyses. A total of 5424 patients were included in the cohort, of whom 24.9% (n = 1353) were under-staged. Post-LT HCC recurrence and death were significantly associated with under-staging (each P < 0.001). In adjusted analyses, independent predictors of under-staging included age (odds ratio [OR], 1.13 per 10 years; 95% confidence interval [CI], 1.03-1.25), male sex (OR, 1.61; 95% CI, 1.36-1.89), down-staging (OR, 4.03; 95% CI, 2.65-6.11), and pre-LT alpha-fetoprotein (P < 0.001). There was also significant variation in under-staging between UNOS regions and among transplant centers, ranging from 14.8% to 38.1%. We report novel risk factors for HCC under-staging, which worsens post-LT outcomes. Significant center-level and regional variation in under-staging highlights the need for standards that achieve greater uniformity in staging.
肝移植(LT)是大多数肝细胞癌(HCC)患者的治愈方法。然而,10%-15%的患者出现 HCC 复发。在影像学上报告符合米兰标准的患者,在切除标本中经常发现不符合标准。这种 HCC 的分期过低会导致 LT 后结果恶化。然而,导致分期过低的危险因素尚未阐明。此外,尚不清楚是否存在分期过低的区域或中心水平的差异。我们对 2012 年至 2016 年间在美国器官共享网络(UNOS)数据库中接受 HCC 移植的成年患者进行了回顾性分析。根据 LT 前影像学与切除标本的发现,确定分期过低。Kaplan-Meier 方法和 Cox 回归用于评估分期过低对 HCC 复发和 LT 后生存的影响。混合效应逻辑回归用于确定分期过低的危险因素,并在调整分析中研究区域和中心水平的差异。该队列共纳入 5424 例患者,其中 24.9%(n=1353)分期过低。LT 后 HCC 复发和死亡与分期过低显著相关(均 P<0.001)。在调整分析中,分期过低的独立预测因素包括年龄(优势比[OR],每增加 10 岁增加 1.13;95%置信区间[CI],1.03-1.25)、男性(OR,1.61;95%CI,1.36-1.89)、降级分期(OR,4.03;95%CI,2.65-6.11)和 LT 前甲胎蛋白(P<0.001)。UNOS 区域之间和移植中心之间的分期过低也存在显著差异,范围为 14.8%-38.1%。我们报告了 HCC 分期过低的新危险因素,这会导致 LT 后结果恶化。分期过低的显著中心和区域差异突出表明需要制定标准,以实现分期更加统一。