Dongelmans Edo J, Hirode Grishma, Hansen Bettina E, Chen Chien-Hung, Su Tung-Hung, Seto Wai-Kay, Furquim d'Almeida Arno, van Hees Stijn, Papatheodoridi Margarita, Lens Sabela, Wong Grace L H, Brakenhoff Sylvia M, Chien Rong-Nan, Feld Jordan J, Chan Henry L Y, Forns Xavier, Papatheodoridis George V, Vanwolleghem Thomas, Yuen Man-Fung, Hsu Yao-Chun, Kao Jia-Horng, Cornberg Markus, Sonneveld Milan J, Jeng Wen-Juei, Janssen Harry L A
Department of Gastroenterology and Hepatology, Erasmus MC University Medical Center, Rotterdam, the Netherlands.
Toronto Centre for Liver Disease, Toronto General Hospital, University Health Network, Toronto, Canada; The Toronto Viral Hepatitis Care Network (VIRCAN), Toronto, Canada; Institute of Medical Science, University of Toronto, Toronto, Canada.
J Hepatol. 2025 Mar;82(3):446-455. doi: 10.1016/j.jhep.2024.08.015. Epub 2024 Aug 31.
BACKGROUND & AIMS: Flares after nucleos(t)ide analogue (NA) cessation are common and potentially harmful. Predictors of flares are required for risk stratification and to guide off-treatment follow-up.
This multicenter cohort study included virally suppressed patients with chronic hepatitis B (CHB) who were hepatitis B e antigen negative at NA cessation. Hepatic flares were defined based on ALT levels of ≥5x, 10x or 20x the upper limit of normal (ULN). Multivariable Cox regression analyses were performed with censoring at retreatment, HBsAg loss or loss to follow-up. A sub-analysis was performed including HBV DNA levels within the first 12 weeks as a time-dependent covariate.
Of the 1,552 included patients, 350 developed a flare (ALT ≥5x ULN), of whom 70.6% did within the first year. One-year cumulative incidences for ALT flares ≥5x, ≥10x, ≥20x ULN were 18.6%, 10.2% and 3.4%, respectively. Severity of flares decreased over time, but severe flares still occurred after 1 year. Thirteen patients decompensated after a flare, of whom three died. Flares did not seem to be associated with increased rates of HBsAg loss (adjusted hazard ratio [aHR] 1.42, p = 0.28). Multivariable analyses showed that older age (aHR 1.02, p = 0.001), male sex (aHR 1.57, p = 0.003), HBsAg levels at NA withdrawal (100-1,000 IU/ml; aHR 1.99, p <0.001; >1,000 IU/ml; aHR 2.65, p <0.001) and tenofovir disoproxil fumarate vs. entecavir therapy (aHR 2.99, p <0.001) were predictive of flares (≥5x ULN). Early HBV DNA levels >5log IU/ml were associated with the highest risk of flares (aHR 2.36, p <0.001).
Flares are common after NA withdrawal, especially within the first year and can result in hepatic decompensation and death. Older age, male sex, higher HBsAg levels at end of treatment and tenofovir therapy were associated with a higher risk of flares. Close monitoring and retreatment should be considered if HBV DNA levels exceed 5log IU/ml within the first 12 weeks.
This is the first large global multi-centered cohort study which provides detailed data about flares after nucleos(t)ide analogue cessation in patients with chronic hepatitis B. Older age, male sex, higher HBsAg levels at end of treatment and tenofovir therapy were associated with a higher risk of flares. These results could guide follow-up after withdrawal, helping clinicians identify high-risk patients and decide when to restart anti-viral therapy, which we recommend if HBV DNA levels exceed 5log IU/ml within the first 12 weeks.
not applicable.
核苷(酸)类似物(NA)停药后肝炎发作很常见且可能有害。需要确定肝炎发作的预测因素,以便进行风险分层并指导停药后的随访。
这项多中心队列研究纳入了在NA停药时乙肝e抗原阴性、病毒得到抑制的慢性乙型肝炎(CHB)患者。肝发作根据谷丙转氨酶(ALT)水平高于正常上限(ULN)的5倍、10倍或20倍来定义。进行多变量Cox回归分析,并在重新治疗、乙肝表面抗原(HBsAg)消失或失访时进行删失。进行了一项亚分析,将前12周内的乙肝病毒(HBV)DNA水平作为时间依存性协变量纳入分析。
在纳入研究的1552例患者中,350例出现了肝炎发作(ALT≥5倍ULN),其中70.6%在第一年发作。ALT发作≥5倍、≥10倍、≥20倍ULN的1年累积发生率分别为18.6%、10.2%和3.4%。肝炎发作的严重程度随时间下降,但1年后仍有严重发作。13例患者在肝炎发作后出现肝功能失代偿,其中3例死亡。肝炎发作似乎与HBsAg消失率增加无关(校正风险比[aHR]为1.42,p = 0.28)。多变量分析显示,年龄较大(aHR为1.02,p = 0.001)、男性(aHR为1.57,p = 0.003)、NA停药时的HBsAg水平(100 - 1000 IU/ml;aHR为1.99,p <0.001;>1000 IU/ml;aHR为2.65,p <0.001)以及替诺福韦酯与恩替卡韦治疗相比(aHR为2.99,p <0.001)是肝炎发作(≥5倍ULN)的预测因素。早期HBV DNA水平>5 log IU/ml与肝炎发作风险最高相关(aHR为2.36,p <0.001)。
NA停药后肝炎发作很常见,尤其是在第一年,并且可能导致肝功能失代偿和死亡。年龄较大、男性、治疗结束时较高的HBsAg水平以及替诺福韦治疗与肝炎发作风险较高相关。如果前12周内HBV DNA水平超过5 log IU/ml,应考虑密切监测和重新治疗。
这是第一项大型全球多中心队列研究,提供了慢性乙型肝炎患者核苷(酸)类似物停药后肝炎发作的详细数据。年龄较大、男性、治疗结束时较高的HBsAg水平以及替诺福韦治疗与肝炎发作风险较高相关。这些结果可指导停药后的随访,帮助临床医生识别高危患者并决定何时重新开始抗病毒治疗,我们建议如果前12周内HBV DNA水平超过5 log IU/ml则重新开始治疗。
不适用。