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预测接受抗病毒治疗的慢性乙型肝炎患者发生肝细胞癌的风险:在中国验证 CAMD 和 AASL 评分。

Predicting the risk of hepatocellular carcinoma in chronic hepatitis B patients receiving antiviral therapy: Validating the CAMD and AASL scores in China.

机构信息

Department of Gastroenterology, China-Japan Union Hospital of Jilin University, Changchun, China.

Department of Critical Care Medicine, Affiliated Hangzhou First People's Hospital, Zhejiang University School of Medicine, Hangzhou, China.

出版信息

Saudi J Gastroenterol. 2022 Sep-Oct;28(5):362-368. doi: 10.4103/sjg.sjg_527_21.

DOI:10.4103/sjg.sjg_527_21
PMID:35170433
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9752533/
Abstract

BACKGROUND

We aimed to validate the predictive value of the cirrhosis, age, male sex, and diabetes (CAMD) score and age, albumin, sex, and liver cirrhosis (AASL) score for chronic hepatitis B (CHB) patients, treated with nucleos(t)ide analogues (NUCs) in Northeast China.

METHODS

From January 2009 to June 2020, 945 patients diagnosed with CHB who received NUC therapy at China-Japan Union Hospital of Jilin University were included. Comprehensive medical records were retrospectively analyzed, and the predictive values of the CAMD score and AASL score for hepatocellular carcinoma (HCC) were evaluated.

RESULTS

A total of 58 patients (5.94%) were diagnosed with HCC. Multivariate analysis revealed that age [odds ratio (OR) = 1.041, 95% confidence interval (CI) 1.009-1.073, P < 0.011] and cirrhosis (OR = 3.297, 95% CI 1.383-7.861, P < 0.007) were independent predictors of HCC. Either the CAMD or AASL score was significantly higher in the HCC group compared to the non-HCC group. The area under the receiver operating characteristic (ROC) curve (AUC) of CAMD and AASL was 0.721 (95% CI 0.663-0.780) and 0.718 (95% CI 0.662-0.774), respectively. Risk stratification using either CAMD or AASL revealed significant differences in the one-, three-, and five-year cumulative incidence rates of HCC between the low-, intermediate-, and high-risk groups (all P < 0.001, log-rank test).

CONCLUSIONS

Both CAMD and AASL scores have predictive value for HCC risk of CHB patients in Northeast China. In future, the optimal monitoring frequency and methods should be personalized.

摘要

背景

本研究旨在验证肝硬化、年龄、性别和糖尿病(CAMD)评分以及年龄、白蛋白、性别和肝硬化(AASL)评分对中国东北接受核苷(酸)类似物(NUCs)治疗的慢性乙型肝炎(CHB)患者的预测价值。

方法

本研究纳入了 2009 年 1 月至 2020 年 6 月期间在吉林大学中日联谊医院接受 NUC 治疗的 945 例 CHB 患者。对其进行回顾性分析,评估了 CAMD 评分和 AASL 评分对肝细胞癌(HCC)的预测价值。

结果

共有 58 例(5.94%)患者被诊断为 HCC。多因素分析显示,年龄(比值比 [OR] = 1.041,95%置信区间 [CI] 1.009-1.073,P < 0.011)和肝硬化(OR = 3.297,95% CI 1.383-7.861,P < 0.007)是 HCC 的独立预测因素。HCC 组的 CAMD 或 AASL 评分均显著高于非 HCC 组。CAMD 和 AASL 的受试者工作特征(ROC)曲线下面积(AUC)分别为 0.721(95% CI 0.663-0.780)和 0.718(95% CI 0.662-0.774)。使用 CAMD 或 AASL 进行风险分层,低、中、高危组之间的 HCC 1 年、3 年和 5 年累积发生率存在显著差异(均 P < 0.001,对数秩检验)。

结论

CAMD 和 AASL 评分均对中国东北 CHB 患者的 HCC 风险具有预测价值。未来,应根据患者的具体情况制定最佳的监测频率和方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2502/9752533/aad2c684ccfc/SJG-28-362-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2502/9752533/bee9338f3663/SJG-28-362-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2502/9752533/bee9338f3663/SJG-28-362-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2502/9752533/81ff3e4caff3/SJG-28-362-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2502/9752533/d86847ad758f/SJG-28-362-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2502/9752533/aad2c684ccfc/SJG-28-362-g004.jpg

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J Hepatol. 2021 Jul;75(1):108-119. doi: 10.1016/j.jhep.2021.01.041. Epub 2021 Feb 3.
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Five-year comparative risk of hepatocellular carcinoma development under entecavir or tenofovir treatment-naïve patients with chronic hepatitis B-related compensated cirrhosis in Taiwan.台湾地区慢性乙型肝炎相关代偿性肝硬化患者在恩替卡韦或替诺福韦治疗初治患者中 5 年肝细胞癌发展的比较风险。
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替诺福韦与恩替卡韦治疗慢性乙型肝炎患者的肝细胞癌发病率:系统评价和荟萃分析。
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Comparable Incidence of Hepatocellular Carcinoma in Chronic Hepatitis B Patients Treated with Entecavir or Tenofovir.恩替卡韦或替诺福韦治疗慢性乙型肝炎患者的肝细胞癌发病率相当。
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The effectiveness of TDF versus ETV on incidence of HCC in CHB patients: a meta analysis.TDF 与 ETV 对 CHB 患者 HCC 发生率的影响:一项荟萃分析。
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Bull World Health Organ. 2019 Mar 1;97(3):230-238. doi: 10.2471/BLT.18.219469. Epub 2019 Jan 28.
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