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本帖最后由 StephenW 于 2018-5-11 07:40 编辑
World J Gastroenterol. 2018 May 7;24(17):1919-1924. doi: 10.3748/wjg.v24.i17.1919.
Development of tenofovir disoproxil fumarate resistance after complete viral suppression in a patient with treatment-naïve chronic hepatitis B: A case report and review of the literature.
Cho WH1, Lee HJ1, Bang KB1, Kim SB2, Song IH1.
Author information
1
Department of Internal Medicine, Dankook University College of Medicine, Cheonan 31116, South Korea.
2
Department of Internal Medicine, Dankook University College of Medicine, Cheonan 31116, South Korea. [email protected].
Abstract
Tenofovir disoproxil fumarate (TDF) is a potent nucleotide analogue that is recommended as first-line therapy for patients with chronic hepatitis B. The results of a longitudinal study of TDF treatment demonstrated no development of resistance. We observed one treatment-naïve chronic hepatitis B (CHB) patient who developed TDF resistance after complete viral suppression during long-term TDF treatment. A 37-year-old HBeAg-positive man received TDF 300 mg/d for 43 mo. The hepatitis B virus (HBV) DNA titer was 8 log10 copies/mL at baseline and became undetectable at 16 mo after treatment. However, the HBV DNA titer rebounded to 7.5 log10 copies/mL at 43 mo after treatment. We performed full sequencing to find mutation sites associated with virologic breakthrough. The results showed 9 mutation sites, most of which had not been well-known as mutation sites. We changed the therapy from tenofovir to entecavir with a regimen of 0.5 mg once daily. After 4 mo, the HBV DNA titer decreased to 267 copies/mL, and the liver enzyme levels were normalized.
KEYWORDS:
Chronic hepatitis B; Mutation; Resistance; Tenofovir
PMID:
29740207
PMCID:
PMC5937209
DOI:
10.3748/wjg.v24.i17.1919
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