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Undetectable HBV DNA at month 12 of entecavir treatment predicts maintained viral suppression and HB e A g‐seroconversion in chronic hepatitis B patients at 3 years
Author(s) -
Wong G. L.H.,
Wong V. W.S.,
Chan H.Y.,
Tse P. C.H.,
Wong J.,
Chim A. M.L.,
Yiu K. K.L.,
Chu S. H.T.,
Chan H. L.Y.
Publication year - 2012
Publication title -
alimentary pharmacology and therapeutics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.308
H-Index - 177
eISSN - 1365-2036
pISSN - 0269-2813
DOI - 10.1111/j.1365-2036.2012.05098.x
Subject(s) - entecavir , medicine , seroconversion , hbeag , hepatitis b virus , gastroenterology , virology , hepatitis b , immunology , viral load , chronic hepatitis , virus , hbsag , lamivudine
Summary Background On‐treatment monitoring of serum hepatitis B virus ( HBV ) DNA to guide treatment strategy for patients on entecavir has received little attention. Aim To investigate the predictive value of on‐treatment HBV DNA levels for responses to entecavir. Methods This was a retrospective cohort study among nucleos(t)ide analogue‐naïve HBV ‐infected patients on entecavir with a minimum follow‐up of 2 years. Maintained virological suppression was defined as undetectable HBV DNA (<20 IU/mL) until the last visit. Genotypic drug resistance was screened by using the INNO ‐ LiPA DR assay. Results A total of 440 chronic hepatitis B patients (160 HB e A g‐positive) followed for 34 ± 9 months were included. The cumulative probability of maintained virological suppression at year 1, 2 and 3 were 76.5%, 83.0% and 88.3% respectively. On multivariate analysis, lower baseline HBV DNA , undetectable HBV DNA at month 12 and negative HB eAg were the independent predictors of maintained virological suppression. M12 responders (who had undetectable HBV DNA at month 12) had higher probability of maintained virological suppression at 3 years (99.1%) as compared to non responders (57.5%; P < 0.001). The cumulative probability of HB eAg‐seroconversion at year 1, 2 and 3 were 19.0%, 27.2% and 33.5% respectively. M12 responders had higher probability of HB e A g‐seroconversion at 3 years (43.2%) than the non responders (19.0%; P = 0.003). M12 responders had lower probability of drug resistance at 3 years (0%) than the non responders (2.6%; P = 0.004). Conclusion Month 12 HBV DNA responses could predict the probability of maintained virological suppression, HB e A g‐seroconversion and risk of drug resistance among patients on entecavir treatment at 3 years.