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利妥昔单抗治疗淋巴瘤后 HBsAg 阴性/抗 HBc 阳性且血清 HBV DNA 不可检测的患者发生乙型肝炎病毒再激活的风险:一项荟萃分析。

Risk of hepatitis B reactivation in HBsAg-negative/HBcAb-positive patients with undetectable serum HBV DNA after treatment with rituximab for lymphoma: a meta-analysis.

机构信息

Clinical Medical School, Guilin Medical University, Guilin, 541004, Guangxi Zhuang Autonomous Region, China.

Research Center for Clinical and Translational Medicine/Institute of Infectious Diseases, Beijing 302 Hospital, Beijing, 100039, China.

出版信息

Hepatol Int. 2017 Sep;11(5):429-433. doi: 10.1007/s12072-017-9817-y. Epub 2017 Aug 30.

DOI:10.1007/s12072-017-9817-y
PMID:28856548
Abstract

BACKGROUND

Hepatitis B surface antigen (HBsAg)-negative/hepatitis B core antibody (HBcAb)-positive patients with undetectable serum hepatitis B virus (HBV) DNA have experienced and resolved hepatitis B virus (HBV) infection. Lymphoma patients with resolved HBV infection have high risk of HBV reactivation when treated with robust immunosuppressive agents, but the reported rate varies extensively between different studies. This study aims to estimate the risk of HBV reactivation in HBsAg-negative/HBcAb-positive patients receiving rituximab-containing chemotherapy for lymphoma.

METHODS

Databases were searched for papers published in English until 8 August 2016. The pooled risk of HBV reactivation was estimated using a random-effects model.

RESULTS

Data from 15 studies were retrieved, including a total of 1312 HBsAg-negative/HBcAb-positive lymphoma patients treated with rituximab-containing chemotherapy. The results revealed HBV reactivation rate of 9.0 % [95 % confidence interval (CI) 0.05-0.15]. In subgroup analysis, the reactivation rates for prospective and retrospective studies were 17 % (I  = 87.3 %; 95 % 0.08-0.39, p < 0.001) and 7 % (I  = 43.1 %; 95 % CI 0.05-0.11, p = 0.07), respectively.

CONCLUSIONS

This meta-analysis confirms a measurable and potentially substantial risk of HBV reactivation in HBsAg-negative/HBcAb-positive patients with rituximab treatment for lymphoma. Prophylactic use of anti-HBV agents should be seriously considered for such patients.

摘要

背景

乙肝表面抗原(HBsAg)阴性/乙肝核心抗体(HBcAb)阳性、血清乙型肝炎病毒(HBV)DNA 检测不到的患者曾经历过并已清除 HBV 感染。HBV 感染已清除的淋巴瘤患者在接受强效免疫抑制剂治疗时,HBV 再激活的风险较高,但不同研究报道的发生率差异很大。本研究旨在评估 HBsAg 阴性/抗-HBc 阳性接受含利妥昔单抗化疗的淋巴瘤患者发生 HBV 再激活的风险。

方法

检索英文数据库中截至 2016 年 8 月 8 日发表的文献。采用随机效应模型评估 HBV 再激活的风险。

结果

共纳入 15 项研究,包含 1312 例接受含利妥昔单抗化疗的 HBsAg 阴性/抗-HBc 阳性淋巴瘤患者。结果显示 HBV 再激活率为 9.0%(95%CI 0.05-0.15)。亚组分析显示前瞻性和回顾性研究的再激活率分别为 17%(I²=87.3%;95%CI 0.08-0.39,p<0.001)和 7%(I²=43.1%;95%CI 0.05-0.11,p=0.07)。

结论

本荟萃分析证实 HBsAg 阴性/抗-HBc 阳性接受利妥昔单抗治疗的淋巴瘤患者存在可测量且潜在较大的 HBV 再激活风险。此类患者应认真考虑预防性使用抗 HBV 药物。

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利妥昔单抗化疗停止 19 个月后乙型肝炎病毒再激活 1 例报告。
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