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核苷(酸)类似物诱导乙肝 e 抗原血清学转换后肝细胞癌和乙肝表面抗原血清学清除的累积发生率。

Cumulative incidence of hepatocellular carcinoma and hepatitis B surface antigen Seroclearance after Nucleos(t) ide analogue-induced hepatitis B e antigen Seroclearance.

机构信息

Department of Internal Medicine, Gangnam Severance Hospital, Yonsei University College of Medicine, 211 Eonju-ro, Gangnam-gu, Seoul, 06273, South Korea.

出版信息

BMC Gastroenterol. 2020 Apr 18;20(1):113. doi: 10.1186/s12876-020-01236-9.

DOI:10.1186/s12876-020-01236-9
PMID:32305059
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7166314/
Abstract

BACKGROUND

Hepatitis B e antigen (HBeAg) seroclearance has been considered as the treatment endpoint in HBeAg-positive patients with chronic hepatitis B (CHB). Although HBeAg seroclearance has been accomplished, some aspects are yet unclear. We investigated the cumulative incidence of hepatocellular carcinoma (HCC) and evaluated hepatitis B surface antigen (HBsAg) seroclearance in patients undergoing nucleos(t) ide analogue (NA)-induced HBeAg seroclearance.

METHODS

In this retrospective cohort study, 203 patients with CHB were HBsAg and HBeAg seropositive before NA (entecavir or tenofovir) treatment. All patient who experienced NA -induced HBeAg seroclearance were recruited. Patients with documented HBeAg seroclearance were followed-up every 6 months. Baseline characteristics and laboratory results were recorded.

RESULTS

The mean age at HBeAg seroclearance was 40 years (range, 20-84), and the mean follow-up duration was 5 years (range, 2-11). The cumulative incidence of HCC was 1.5 to 11.5% at 1 to 8 years after HBeAg seroclearance. Cirrhosis was the only significant factor for HCC development (hazard ratio [HR], 24.651; confidence interval [CI], 3.018 to 201.365; P = 0.003). The cumulative incidence of HBsAg seroclearance was 3.5 to 18.7% after 1 to 8 years from HBeAg seroclearance.

CONCLUSIONS

A significant proportion of patients developed HCC after NA-induced HBeAg seroclearance. The presence of liver cirrhosis at the time of HBeAg seroclearance serves as an independent factor for HCC development. Some patients with NA-induced HBeAg seroclearance achieved HBsAg seroclearance.

摘要

背景

乙肝 e 抗原(HBeAg)血清学转换已被认为是慢性乙型肝炎(CHB)HBeAg 阳性患者的治疗终点。尽管已经实现了 HBeAg 血清学转换,但仍有一些方面尚不清楚。我们调查了接受核苷(酸)类似物(NA)诱导 HBeAg 血清学转换的患者中肝细胞癌(HCC)的累积发生率,并评估了乙型肝炎表面抗原(HBsAg)血清学转换。

方法

在这项回顾性队列研究中,203 名 CHB 患者在 NA(恩替卡韦或替诺福韦)治疗前 HBsAg 和 HBeAg 均为阳性。所有经历过 NA 诱导 HBeAg 血清学转换的患者均被招募。有记录的 HBeAg 血清学转换的患者每 6 个月随访一次。记录了基线特征和实验室结果。

结果

HBeAg 血清学转换时的平均年龄为 40 岁(范围,20-84),平均随访时间为 5 年(范围,2-11)。HBeAg 血清学转换后 1 至 8 年 HCC 的累积发生率为 1.5%至 11.5%。肝硬化是 HCC 发展的唯一显著因素(风险比[HR],24.651;置信区间[CI],3.018 至 201.365;P=0.003)。HBeAg 血清学转换后 1 至 8 年,HBsAg 血清学转换的累积发生率为 3.5%至 18.7%。

结论

相当一部分患者在 NA 诱导的 HBeAg 血清学转换后发生 HCC。HBeAg 血清学转换时存在肝硬化是 HCC 发展的独立因素。一些接受 NA 诱导的 HBeAg 血清学转换的患者实现了 HBsAg 血清学转换。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b753/7166314/6b0e74cab440/12876_2020_1236_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b753/7166314/a0b76d1e6623/12876_2020_1236_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b753/7166314/f316f2b889d4/12876_2020_1236_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b753/7166314/6b0e74cab440/12876_2020_1236_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b753/7166314/a0b76d1e6623/12876_2020_1236_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b753/7166314/f316f2b889d4/12876_2020_1236_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b753/7166314/6b0e74cab440/12876_2020_1236_Fig3_HTML.jpg

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