Abstract

BackgroundNucleos(t)ide analogues (NAs) cessation is not widely practiced and remains a controversial, but highly relevant subject in patients infected with hepatitis B virus (HBV). We aimed to explore the related factors for safe NAs cessation.MethodsThis is a multicenter prospective cohort study. Overall, 139 initially HBV e antigen (HBeAg)-positive patients meeting the stopping criteria were included in 12 hospitals in China. Enrolled patients ceased NAs and were followed up every 3 months for 24 months or until clinical relapse (CR).ResultsThe 24 month cumulative rates of virological relapse (VR), CR, HBeAg reversion and HBV surface antigen (HBsAg) loss were 50.4, 24.5, 11.5 and 9.4%, respectively. Patients with end of treatment (EOT) HBsAg < 100 IU/mL plus negative HBV RNA had the lowest 24 month cumulative VR rate (5 vs 58%, p < 0.001). EOT HBsAg ≥ 2 log10 IU/mL [odds ratio (OR) = 6.686, p = 0.006], EOT positive HBV RNA (OR = 3.453, p = 0.008) and EOT hepatitis B core-related antigen (HBcrAg) ≥ 4log U/mL (OR = 3.702, p = 0.002) were found to independently predict the risk of VR. To predict VR, the area under the receiver-operating characteristic (AUROC) value of the EOT HBsAg < 100 IU/mL plus EOT HBV RNA negative was 0.698 (p < 0.001), which was higher than other parameters alone or combinations.ConclusionsNAs cessation is suitable only for a small and selected patients. An EOT HBsAg < 100 IU/mL and EOT negative HBV RNA identified a patient with low risk of off-treatment VR.

Highlights

  • Long-term nucleos(t)ide analogue (NAs) treatment has been proven to delay disease progression in patients infected with hepatitis B virus (HBV) [1]

  • A total of 139 initially HBV e antigen (HBeAg)-positive chronic hepatitis B (CHB) patients without cirrhosis treated with Nucleos(t)ide analogues (NAs) for at least 4 years and who had HBeAg seroconversion for at least 3 years were included in this study

  • The results showed that the area under the receiver-operating characteristic (AUROC) value of the end of treatment (EOT) hepatitis B surface antigen (HBsAg) \ 100 IU/mL plus EOT HBV RNA negative was 0.698 (p \ 0.001), which was higher than other parameters alone or combinations

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Summary

Introduction

Long-term nucleos(t)ide analogue (NAs) treatment has been proven to delay disease progression in patients infected with hepatitis B virus (HBV) [1]. Life-long NAs treatment is necessary, but causes a financial burden and potential drug toxicity [3]. Some studies suggested high rates of virological relapse (VR) after NAs cessation [4, 5], whereas other studies found sustained virological response and hepatitis B surface antigen (HBsAg) loss in some patients who ceased NAs [6, 7]. It is meaningful to identify factors associated with safe NAs discontinuation. Nucleos(t)ide analogues (NAs) cessation is not widely practiced and remains a controversial, but highly relevant subject in patients infected with hepatitis B virus (HBV). We aimed to explore the related factors for safe NAs cessation

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