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用于预测慢性乙型肝炎病毒携带者肝细胞癌的临床评分系统。

Clinical scoring system to predict hepatocellular carcinoma in chronic hepatitis B carriers.

机构信息

Department of Medicine and Therapeutics and Institute of Digestive Disease, Chinese University of Hong Kong; State Key Laboratory in Oncology in South China.

出版信息

J Clin Oncol. 2010 Apr 1;28(10):1660-5. doi: 10.1200/JCO.2009.26.2675. Epub 2010 Mar 1.

Abstract

PURPOSE

Hepatitis B virus (HBV) infection is an important etiology for hepatocellular carcinoma (HCC). We aim to develop a simple clinical score in predicting the risk of HCC among HBV carriers.

PATIENTS AND METHODS

We first evaluated 1,005 patients and found that the following five factors independently predicted HCC development: age, albumin, bilirubin, HBV DNA, and cirrhosis. These variables were used to construct a prediction score ranging from 0 to 44.5. The score was validated in another prospective cohort of 424 patients.

RESULTS

During a median follow-up of 10 years, 105 patients (10.%) in the training cohort and 45 patients (10.6%) in the validation cohort developed HCC. Cutoff values of 5 and 20 best discriminated HCC risk. By applying the cutoff value of 5, the score excluded future HCC development with high accuracy (negative predictive value = 97.8% and 97.3% in the training and validation cohorts, respectively). In the validation cohort, the 5-year HCC-free survival rates were 98.3%, 90.5%, and 78.9% in the low-, medium-, and high-risk groups, respectively. The hazard ratios for HCC in the medium- and high-risk groups were 12.8 and 14.6, respectively.

CONCLUSION

A simple prediction score constructed from routine clinical and laboratory parameters is accurate in predicting HCC development in HBV carriers. Future prospective validation is warranted.

摘要

目的

乙型肝炎病毒(HBV)感染是肝细胞癌(HCC)的重要病因。我们旨在开发一种简单的临床评分,以预测 HBV 携带者发生 HCC 的风险。

患者与方法

我们首先评估了 1005 名患者,发现以下五个因素独立预测 HCC 的发生:年龄、白蛋白、胆红素、HBV DNA 和肝硬化。这些变量用于构建预测评分,范围为 0 至 44.5。该评分在另一项前瞻性队列的 424 名患者中进行了验证。

结果

在中位数为 10 年的随访期间,训练队列中有 105 名(10.0%)患者和验证队列中有 45 名(10.6%)患者发生 HCC。5 和 20 的截断值最佳区分 HCC 风险。应用 5 的截断值,评分排除了 HCC 发生的高准确率(训练和验证队列的阴性预测值分别为 97.8%和 97.3%)。在验证队列中,低、中、高危组的 5 年 HCC 无复发生存率分别为 98.3%、90.5%和 78.9%。中危和高危组 HCC 的风险比分别为 12.8 和 14.6。

结论

由常规临床和实验室参数构建的简单预测评分可准确预测 HBV 携带者 HCC 的发生。需要进一步前瞻性验证。

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