Toronto Centre for Liver Disease, Toronto General Hospital, University Health Network, Toronto, Canada; Institute of Medical Science, University of Toronto, Toronto, Canada; The Toronto Viral Hepatitis Care Network, Toronto, Canada.
Toronto Centre for Liver Disease, Toronto General Hospital, University Health Network, Toronto, Canada; Institute of Medical Science, University of Toronto, Toronto, Canada.
Gastroenterology. 2022 Mar;162(3):757-771.e4. doi: 10.1053/j.gastro.2021.11.002. Epub 2021 Nov 9.
BACKGROUND & AIMS: Functional cure, defined based on hepatitis B surface antigen (HBsAg) loss, is rare during nucleos(t)ide analogue (NA) therapy and guidelines on finite NA therapy have not been well established. We aim to analyze off-therapy outcomes after NA cessation in a large, international, multicenter, multiethnic cohort of patients with chronic hepatitis B (CHB).
This cohort study included patients with virally suppressed CHB who were hepatitis B e antigen (HBeAg)-negative and stopped NA therapy. Primary outcome was HBsAg loss after NA cessation, and secondary outcomes included virologic, biochemical, and clinical relapse, alanine aminotransferase flare, retreatment, and liver-related events after NA cessation.
Among 1552 patients with CHB, cumulative probability of HBsAg loss was 3.2% at 12 months and 13.0% at 48 months of follow-up. HBsAg loss was higher among Whites (vs Asians: subdistribution hazard ratio, 6.8; 95% confidence interval, 2.7-16.8; P < .001) and among patients with HBsAg levels <100 IU/mL at end of therapy (vs ≥100 IU/mL: subdistribution hazard ratio, 22.5; 95% confidence interval, 13.1-38.7; P < .001). At 48 months of follow-up, Whites with HBsAg levels <1000 IU/mL and Asians with HBsAg levels <100 IU/mL at end of therapy had a high predicted probability of HBsAg loss (>30%). Incidence rate of hepatic decompensation and hepatocellular carcinoma was 0.48 per 1000 person-years and 0.29 per 1000 person-years, respectively. Death occurred in 7/19 decompensated patients and 2/14 patients with hepatocellular carcinoma.
The best candidates for NA withdrawal are virally suppressed, HBeAg- negative, noncirrhotic patients with CHB with low HBsAg levels, particularly Whites with <1000 IU/mL and Asians with <100 IU/mL. However, strict surveillance is recommended to prevent deterioration.
根据乙型肝炎表面抗原(HBsAg)清除定义的功能性治愈在核苷(酸)类似物(NA)治疗中很少见,并且尚未制定有限 NA 治疗的指南。我们旨在分析大型国际多中心多民族慢性乙型肝炎(CHB)患者停止 NA 治疗后的停药后结局。
这项队列研究纳入了病毒抑制的 HBeAg 阴性 CHB 患者,他们停止了 NA 治疗。主要结局是 NA 停药后 HBsAg 清除,次要结局包括病毒学、生化学和临床复发、丙氨酸氨基转移酶 flares、NA 停药后的再治疗和与肝脏相关的事件。
在 1552 例 CHB 患者中,12 个月和 48 个月随访时 HBsAg 清除的累积概率分别为 3.2%和 13.0%。白人(与亚洲人相比:亚分布风险比,6.8;95%置信区间,2.7-16.8;P<.001)和治疗结束时 HBsAg 水平<100 IU/mL 的患者(与≥100 IU/mL 相比:亚分布风险比,22.5;95%置信区间,13.1-38.7;P<.001)中 HBsAg 清除率更高。在 48 个月的随访中,治疗结束时 HBsAg 水平<1000 IU/mL 的白人患者和 HBsAg 水平<100 IU/mL 的亚洲人患者有很高的 HBsAg 清除预测概率(>30%)。肝失代偿和肝细胞癌的发生率分别为 0.48/1000 人年和 0.29/1000 人年。在 19 例失代偿患者中,有 7 例死亡,在 14 例肝细胞癌患者中,有 2 例死亡。
NA 停药的最佳候选者是病毒抑制、HBeAg 阴性、非肝硬化的 CHB 患者,且 HBsAg 水平较低,特别是 HBsAg 水平<1000 IU/mL 的白人患者和 HBsAg 水平<100 IU/mL 的亚洲人患者。然而,建议进行严格监测以防止病情恶化。