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慢性丙型肝炎患者直接抗病毒治疗期间乙型肝炎病毒再激活率低。

Low Rate of Hepatitis B Reactivation Among Patients with Chronic Hepatitis C During Direct Acting Antiviral Therapy.

机构信息

Liver Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD, USA.

Toronto Centre for Liver Disease, Toronto General Hospital, Toronto, Canada.

出版信息

Dig Dis Sci. 2023 Jul;68(7):3193-3198. doi: 10.1007/s10620-023-07916-2. Epub 2023 Apr 6.

Abstract

BACKGROUND AND AIMS

Hepatitis B virus (HBV) reactivation has been reported in patients co-infected with hepatitis C virus (HCV) during direct acting antiviral (DAA) therapy, leading the United States Food and Drug Administration (U.S. FDA) to issue a black box warning on all DAA drug labels recommending monitoring for HBV reactivation. We conducted a comprehensive evaluation to assess the rate of HBV reactivation among patients with chronic hepatitis C (CHC) during DAA therapy.

METHODS

Patients with CHC and recovered HBV infection (hepatitis B surface antigen negative (HBsAg)/anti-hepatitis B core positive), treated with DAAs were included if stored sera were available. Samples were tested for HBV DNA, HBsAg, and ALT. HBV reactivation was considered if (1) HBV DNA was undetectable pre-DAA therapy and became detectable post-therapy, or (2) HBV DNA was detectable pre-treatment, but not quantifiable (< 20 IU/mL) and became quantifiable post-treatment.

RESULT

79 patients with median age of 62 years were included. 68% were male and Caucasian. Various DAA regimens were administered for 12-24 weeks. Reactivation occurred in 8/79 (10%) of patients and occurred more frequently in men compared to women: 6 during treatment and 2 after treatment. Neither an ALT flare nor HBsAg seroreversion were observed. Detectable HBV DNA was transient in 5/8 and could not be determined in 3/8 but ALT flares were not observed in follow-up of these patients.

CONCLUSION

The risk of HBV reactivation was low in CHC patients with resolved HBV during DAA therapy. Our data support testing for HBV DNA only in selected patients with ALT flares or failure of ALT normalization during DAA treatment.

摘要

背景与目的

已有研究报道,在接受直接作用抗病毒药物(DAA)治疗的丙型肝炎病毒(HCV)合并乙型肝炎病毒(HBV)感染患者中,会出现 HBV 再激活,这导致美国食品药品监督管理局(U.S. FDA)在所有 DAA 药物标签上发布了关于 HBV 再激活监测的黑框警告。我们进行了一项全面评估,以评估 DAA 治疗期间慢性丙型肝炎(CHC)患者的 HBV 再激活率。

方法

纳入接受 DAA 治疗且储存血清可用的 CHC 合并 HBV 感染(乙型肝炎表面抗原阴性(HBsAg)/抗乙型肝炎核心阳性)已恢复的患者。检测 HBV DNA、HBsAg 和 ALT。如果(1)HBV DNA 在 DAA 治疗前不可检测,而在治疗后变得可检测,或(2)HBV DNA 在治疗前可检测,但不能定量(<20 IU/mL)且在治疗后可定量,则认为发生了 HBV 再激活。

结果

纳入 79 例患者,中位年龄为 62 岁,68%为男性,白种人。接受了 12-24 周的各种 DAA 方案治疗。8/79(10%)例患者发生再激活,男性发生率高于女性:6 例在治疗期间,2 例在治疗后。未观察到 ALT flares 或 HBsAg 血清学转换。5/8 例患者的 HBV DNA 可检测,但持续时间短暂,3/8 例患者的 HBV DNA 无法确定,但在这些患者的随访中未观察到 ALT flares。

结论

在 DAA 治疗期间,HBV 已恢复的 CHC 患者发生 HBV 再激活的风险较低。我们的数据支持仅在 DAA 治疗期间发生 ALT flares 或 ALT 未正常化的选定患者中检测 HBV DNA。

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