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低病毒载量慢性乙型肝炎患者发生肝细胞癌的危险因素和列线图模型。

Risk Factors and Nomogram Model for Hepatocellular Carcinoma Development in Chronic Hepatitis B Patients with Low-Level Viremia.

机构信息

Division of Gastroenterology and Hepatology, Department of Internal Medicine, Chi Mei Medical Center, Yongkang District, Tainan, Taiwan.

Department of Internal Medicine, Chi Mei Medical Center, Yongkang District, Tainan, Taiwan.

出版信息

Int J Med Sci. 2024 Jun 17;21(9):1661-1671. doi: 10.7150/ijms.95861. eCollection 2024.

Abstract

Patients with chronic hepatitis B patients (CHB) with low-level viremia (LLV) are not necessarily at low risk of developing hepatocellular carcinoma (HCC). The question of whether CHB patients with LLV require immediate antiviral agent (AVT) or long-term AVT remains controversial. The study aims to investigate the risk of HCC development and the risk factors in CHB patients with LLV and construct a nomogram model predicting the risk of HCC. We conducted a retrospective cohort study that enrolled 16,895 CHB patients from January 2008 to December 2020. The patients were divided into three groups for comparison: the LLV group, maintained virological response (MVR) group and HBV-DNA>2000 group. The cumulative incidence of progression to HCC was assessed. Cox regression analysis was performed to determine the final risk factors, and a nomogram model was constructed. The 10-fold Cross-Validation method was utilized for internal validation. A total of 408 new cases of HCC occurred during the average follow-up period of 5.78 years. The 3, 5, and 10-year cumulative HCC risks in the LLV group were 3.56%, 4.96%, and 9.51%, respectively. There was a significant difference in the cumulative risk of HCC between the HBV-DNA level > 2000 IU/mL and LLV groups (p = 0.049). Independent risk factors for HCC development in LLV group included male gender, age, presence of cirrhosis, and platelets count. The Area Under the Curve (AUC) values for the 3-year and 5-year prediction from our HCC risk prediction model were 0.75 and 0.76, respectively. Patients with LLV and MVR are still at risk for developing HCC. The nomogram established for CHB patient with LLV, incorporating identified significant risk factors, serves as an effective tool for predicting HCC-free outcomes. This nomogram model provides valuable information for determining appropriate surveillance strategies and prescribing AVT.

摘要

慢性乙型肝炎(CHB)患者的低病毒血症(LLV)不一定处于发生肝细胞癌(HCC)的低风险中。CHB 患者的 LLV 是否需要立即进行抗病毒药物(AVT)治疗或长期 AVT 治疗仍存在争议。本研究旨在探讨 LLV 的 CHB 患者发生 HCC 的风险及危险因素,并构建预测 HCC 风险的列线图模型。

我们进行了一项回顾性队列研究,纳入了 2008 年 1 月至 2020 年 12 月期间的 16895 例 CHB 患者。将患者分为三组进行比较:LLV 组、维持病毒学应答(MVR)组和 HBV-DNA>2000 组。评估进展为 HCC 的累积发生率。采用 Cox 回归分析确定最终的危险因素,并构建列线图模型。采用 10 折交叉验证方法进行内部验证。

在平均 5.78 年的随访期间,共发生 408 例 HCC 新发病例。LLV 组的 3、5 和 10 年 HCC 累积风险分别为 3.56%、4.96%和 9.51%。HBV-DNA 水平>2000IU/mL 与 LLV 组之间 HCC 累积风险存在显著差异(p=0.049)。LLV 组 HCC 发生的独立危险因素包括男性、年龄、肝硬化和血小板计数。我们的 HCC 风险预测模型对 3 年和 5 年预测的曲线下面积(AUC)值分别为 0.75 和 0.76。

尽管 LLV 且 MVR 的患者仍有发生 HCC 的风险。为 LLV 的 CHB 患者建立的列线图模型纳入了已确定的重要危险因素,是预测 HCC 无事件生存的有效工具。该列线图模型为确定适当的监测策略和开具 AVT 提供了有价值的信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1797/11241087/03ce4109e0ed/ijmsv21p1661g001.jpg

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