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Article: Limited Sustained Remission After Nucleos(t)ide Analog Withdrawal: Results From a Large, Global, Multiethnic Cohort of Patients With Chronic Hepatitis B (RETRACT-B Study)

TitleLimited Sustained Remission After Nucleos(t)ide Analog Withdrawal: Results From a Large, Global, Multiethnic Cohort of Patients With Chronic Hepatitis B (RETRACT-B Study)
Authors
Issue Date22-Apr-2024
PublisherLippincott, Williams & Wilkins
Citation
The American Journal of Gastroenterology, 2024 How to Cite?
Abstract

INTRODUCTION: 

Complete viral suppression with nucleos(t)ide analogs (NAs) has led to a profound reduction in hepatocellular carcinoma and mortality among patients with chronic hepatitis B. Finite therapy yields higher rates of functional cure; however, initial hepatitis B virus (HBV) DNA and alanine aminotransferase (ALT) elevations are almost certain after treatment interruption. We aimed to analyze off-treatment outcomes beyond 12 months after NA cessation.

METHODS: 

Patients with well-suppressed chronic hepatitis B who were hepatitis B e antigen-negative at NA cessation and remained off treatment without hepatitis B surface antigen (HBsAg) loss at 12 months were included (n = 945). HBV DNA and ALT fluctuations were allowed within the first 12 months. We used Kaplan-Meier methods to analyze outcomes beyond 12 months. Sustained remission was defined as HBV DNA <2,000 IU/mL and ALT <2× upper limit of normal (ULN) and an ALT flare as ALT ≥5× ULN.

RESULTS: 

Cumulative probability of sustained remission was 29.7%, virological relapse was 65.2% with a mean peak HBV DNA of 5.0 ± 1.5 log10 IU/mL, an ALT flare was 15.6% with a median peak ALT × ULN of 8.3 (5.7–11.3), HBsAg loss was 9.9% and retreatment was 34.9% at 48 months after NA cessation. A single occurrence of virological relapse or an ALT flare within the first 12 months off-treatment were associated with significantly lower rates of sustained remission beyond 12 months.

DISCUSSION: 

Despite allowing for HBV DNA and ALT fluctuations within the first 12 months off-treatment, most patients without HBsAg loss did not maintain a sustained response thereafter. The best candidates for NA withdrawal are patients with low HBsAg levels at NA cessation, and those without profound or recurrent virological and biochemical relapses in the first off-treatment year.


Persistent Identifierhttp://hdl.handle.net/10722/343565
ISSN
2023 Impact Factor: 8.0
2023 SCImago Journal Rankings: 2.391

 

DC FieldValueLanguage
dc.contributor.authorHirode, Grishma-
dc.contributor.authorHansen, Bettina E-
dc.contributor.authorChen, Chien-Hung-
dc.contributor.authorSu, Tung-Hung-
dc.contributor.authorWong, Grace LH-
dc.contributor.authorSeto, Wai-Kay-
dc.contributor.authord'Almeida, Arno Furquim-
dc.contributor.authorPapatheodoridi, Margarita-
dc.contributor.authorBrakenhoff, Sylvia M-
dc.contributor.authorLens, Sabela-
dc.contributor.authorChoi, Hannah SJ-
dc.contributor.authorChien, Rong-Nan-
dc.contributor.authorFeld, Jordan J-
dc.contributor.authorForns, Xavier-
dc.contributor.authorSonneveld, Milan J-
dc.contributor.authorPapatheodoridis, George V-
dc.contributor.authorVanwolleghem, Thomas-
dc.contributor.authorYuen, Man-Fung-
dc.contributor.authorChan, Henry LY-
dc.contributor.authorKao, Jia-Horng-
dc.contributor.authorHsu, Yao-Chun-
dc.contributor.authorCornberg, Markus-
dc.contributor.authorJeng, Wen-Juei-
dc.contributor.authorJanssen, Harry LA-
dc.contributor.authorRETRACT-B study group,-
dc.date.accessioned2024-05-21T03:11:50Z-
dc.date.available2024-05-21T03:11:50Z-
dc.date.issued2024-04-22-
dc.identifier.citationThe American Journal of Gastroenterology, 2024-
dc.identifier.issn0002-9270-
dc.identifier.urihttp://hdl.handle.net/10722/343565-
dc.description.abstract<h3>INTRODUCTION: </h3><p>Complete viral suppression with nucleos(t)ide analogs (NAs) has led to a profound reduction in hepatocellular carcinoma and mortality among patients with chronic hepatitis B. Finite therapy yields higher rates of functional cure; however, initial hepatitis B virus (HBV) DNA and alanine aminotransferase (ALT) elevations are almost certain after treatment interruption. We aimed to analyze off-treatment outcomes beyond 12 months after NA cessation.</p><h3>METHODS: </h3><p>Patients with well-suppressed chronic hepatitis B who were hepatitis B e antigen-negative at NA cessation and remained off treatment without hepatitis B surface antigen (HBsAg) loss at 12 months were included (n = 945). HBV DNA and ALT fluctuations were allowed within the first 12 months. We used Kaplan-Meier methods to analyze outcomes beyond 12 months. Sustained remission was defined as HBV DNA <2,000 IU/mL and ALT <2× upper limit of normal (ULN) and an ALT flare as ALT ≥5× ULN.</p><h3>RESULTS: </h3><p>Cumulative probability of sustained remission was 29.7%, virological relapse was 65.2% with a mean peak HBV DNA of 5.0 ± 1.5 log<sub>10</sub> IU/mL, an ALT flare was 15.6% with a median peak ALT × ULN of 8.3 (5.7–11.3), HBsAg loss was 9.9% and retreatment was 34.9% at 48 months after NA cessation. A single occurrence of virological relapse or an ALT flare within the first 12 months off-treatment were associated with significantly lower rates of sustained remission beyond 12 months.</p><h3>DISCUSSION: </h3><p>Despite allowing for HBV DNA and ALT fluctuations within the first 12 months off-treatment, most patients without HBsAg loss did not maintain a sustained response thereafter. The best candidates for NA withdrawal are patients with low HBsAg levels at NA cessation, and those without profound or recurrent virological and biochemical relapses in the first off-treatment year.</p>-
dc.languageeng-
dc.publisherLippincott, Williams & Wilkins-
dc.relation.ispartofThe American Journal of Gastroenterology-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titleLimited Sustained Remission After Nucleos(t)ide Analog Withdrawal: Results From a Large, Global, Multiethnic Cohort of Patients With Chronic Hepatitis B (RETRACT-B Study)-
dc.typeArticle-
dc.identifier.doi10.14309/ajg.0000000000002759-
dc.identifier.eissn1572-0241-
dc.identifier.issnl0002-9270-

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