Department of Gastroenterology, School of Medicine, Marmara University, Istanbul, Turkey.
Marmara Universitesi, Pendik Eğitim ve Araştirma Hastanesi, Gastroenteroloji Bilim Dali, Fevzi Çakmak, Muhsin Yazicioğlu.
Eur J Gastroenterol Hepatol. 2020 Jul;32(7):882-888. doi: 10.1097/MEG.0000000000001685.
Toronto hepatocellular carcinoma risk index is developed to stratify cirrhotic patients according to 10-year hepatocellular carcinoma risk. We aimed to validate the performance of Toronto hepatocellular carcinoma risk index in a large Turkish cohort.
We retrospectively reviewed the database of 1287 cirrhotic patients followed-up in a 10-year period (February 2008 to January 2018). All patients were stratified into three groups based on the Toronto hepatocellular carcinoma risk index score as follows: low-risk, < 120; intermediate risk, 120 to 240; and high risk, > 240. Area under the curve and optimal cutoff value of Toronto hepatocellular carcinoma risk index were obtained from receiver operator curve. To reveal the parameters related with hepatocellular carcinoma development, logistic regression analysis was conducted. The cumulative incidences of hepatocellular carcinoma were calculated using the Kaplan-Meier method, and the curves were compared using the log-rank test.
Out of 403 enrolled patients, 57 developed hepatocellular carcinoma. The median Toronto hepatocellular carcinoma risk index value was higher in hepatocellular carcinoma (+) group comparing to hepatocellular carcinoma (-) group [267 (70-366) vs. 224 (36-366), P < 0.001]. Out of 57 detected hepatocellular carcinomas, 45 (78.9%) were high risk, 11 (19.3%) were intermediate risk, and only one (1.8%) was low risk at the entry. The area under the curve of the Toronto hepatocellular carcinoma risk index to predict hepatocellular carcinoma was 0.750 (95% confidence interval, 0.683-0.817, P < 0.001). The optimal cutoff value of Toronto hepatocellular carcinoma risk index was 239.5, giving a sensitivity of 78.9% and specificity of 62.7%. As a result, Toronto hepatocellular carcinoma risk index remained to be the only significant parameter that has an affect on hepatocellular carcinoma development [adjusted-odds ratio: 1.016 (95% confidence interval, 1.007-1.024), P<0.001].
The present study validated the performance of Toronto hepatocellular carcinoma risk index in Turkish cirrhotic patients to predict hepatocellular carcinoma risk, which can be considered as a tool for personalized surveillance.
多伦多肝癌风险指数是根据 10 年肝癌风险对肝硬化患者进行分层的。我们旨在验证该指数在土耳其大型队列中的表现。
我们回顾性分析了 1287 例肝硬化患者的数据库,这些患者在 10 年内(2008 年 2 月至 2018 年 1 月)接受了随访。所有患者根据多伦多肝癌风险指数评分分为三组:低危组,<120;中危组,120 至 240;高危组,>240。通过接收者操作特征曲线获得多伦多肝癌风险指数的曲线下面积和最佳截断值。通过逻辑回归分析揭示与肝癌发生相关的参数。使用 Kaplan-Meier 法计算肝癌的累积发生率,并使用对数秩检验比较曲线。
在纳入的 403 例患者中,57 例发生肝癌。与肝癌(-)组相比,肝癌(+)组的多伦多肝癌风险指数中位值更高[267(70-366)比 224(36-366),P<0.001]。在 57 例检测到的肝癌中,45 例(78.9%)为高危,11 例(19.3%)为中危,仅 1 例(1.8%)为低危。多伦多肝癌风险指数预测肝癌的曲线下面积为 0.750(95%置信区间,0.683-0.817,P<0.001)。多伦多肝癌风险指数的最佳截断值为 239.5,灵敏度为 78.9%,特异性为 62.7%。因此,多伦多肝癌风险指数仍然是唯一对肝癌发生有影响的显著参数[调整优势比:1.016(95%置信区间,1.007-1.024),P<0.001]。
本研究验证了多伦多肝癌风险指数在土耳其肝硬化患者中预测肝癌风险的性能,可作为个体化监测的工具。