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Switching from entecavir to tenofovir disoproxil fumarate for HBeAg-positive chronic hepatitis B patients: a phase 4, prospective study.

Authors :
Suzuki, Fumitaka
Suzuki, Yoshiyuki
Karino, Yoshiyasu
Tanaka, Yasuhito
Kurosaki, Masayuki
Yatsuhashi, Hiroshi
Atarashi, Tomofumi
Atsukawa, Masanori
Watanabe, Tsunamasa
Enomoto, Masaru
Kudo, Masatoshi
Maeda, Naoto
Kohno, Hiroshi
Joko, Kouji
Michitaka, Kojiro
Miki, Koichiro
Takahashi, Kazuhiro
Ide, Tatsuya
Fujiyama, Shigetoshi
Kohno, Tomoko
Source :
BMC Gastroenterology. 12/20/2021, Vol. 21 Issue 1, p1-10. 10p.
Publication Year :
2021

Abstract

<bold>Background: </bold>Tenofovir disoproxil fumarate (TDF) is widely used and recommended as first-line treatment for patients infected with the hepatitis B virus (HBV). However, current data are limited regarding the efficacy and safety of switching to TDF for the treatment of chronic hepatitis B in hepatitis B e-antigen (HBeAg)-positive patients who are virologically suppressed with another nucleos(t)ide analogue. The primary objective of this study was to evaluate the hepatitis B surface antigen (HBsAg) reduction potential of switching from entecavir (ETV) to TDF at week 48 in HBeAg-positive chronic hepatitis B patients with undetectable serum HBV-DNA.<bold>Methods: </bold>In this multicenter, single-arm, open-label, phase 4 clinical study, 75 participants currently treated with ETV 0.5 mg once daily were switched to TDF 300 mg once daily for 96 weeks.<bold>Results: </bold>At week 48, 3/74 participants (4%) achieved 0.25 log10 reduction of HBsAg levels from baseline (the primary endpoint). Mean HBsAg reduction was -0.14 log10 IU/mL and 12% (9/74) achieved 0.25 log10 reduction by 96 weeks. No participants achieved HBsAg seroclearance. HBsAg reduction at weeks 48 and 96 was numerically greater in participants with higher alanine aminotransferase levels (≥ 60 U/L). Seventeen participants (25%) achieved HBeAg seroclearance up to week 96. No participants experienced viral breakthrough. All drug-related adverse events (18 participants [24%]) were mild in intensity, including an increase in urine beta-2-microglobulin (15 participants [20%]).<bold>Conclusions: </bold>In conclusion, HBsAg reduction was limited after switching from ETV to TDF in this study population. Further investigation is warranted to better understand the clinical impact of switching from ETV to TDF. ClinicalTrials.gov: NCT03258710 registered August 21, 2017. https://clinicaltrials.gov/ct2/show/NCT03258710?term=NCT03258710&draw=2&rank=1. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
1471230X
Volume :
21
Issue :
1
Database :
Academic Search Index
Journal :
BMC Gastroenterology
Publication Type :
Academic Journal
Accession number :
154212453
Full Text :
https://doi.org/10.1186/s12876-021-02008-9