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Entecavir+tenofovir vs. lamivudine/telbivudine+adefovir in chronic hepatitis B patients with prior suboptimal response

Authors :
Chang Wook Kim
Won Young Tak
Si Hyun Bae
Hyun Young Woo
Jeong Heo
Jun Yong Park
Sang Hoon Ahn
Jae Young Jang
Dong Joon Kim
In Hee Kim
Source :
Clinical and Molecular Hepatology, Vol 26, Iss 3, Pp 352-363 (2020), Clinical and Molecular Hepatology
Publication Year :
2020
Publisher :
Korean Association for the Study of the Liver, 2020.

Abstract

Background/Aims: Suboptimal responses to lamivudine or telbivudine plus adefovir (LAM/LdT+ADV) rescue therapy are common in patients with LAM-resistant hepatitis B virus (HBV) infections. We compared patients switched to entecavir plus tenofovir (ETV+TDF) to those maintained on LAM/LdT+ADV.Methods: This prospective randomized controlled trial examined 91 patients whose serum HBV DNA levels were greater than 60 IU/mL after at least 24 weeks of treatment with LAM/LdT+ADV for LAM-resistant HBV. Patients were randomized to receive a new treatment (ETV+TDF, n=45) or maintained on the same treatment (LAM/LdT+ADV, n=46) for 48 weeks. Patients with baseline ADV resistance were excluded.Results: Compared to LAM/LdT+ADV group, ETV+TDF group had more patients with a virologic response (42/45 [93.33%] vs. 3/46 [6.52%], PPP=0.005) and LAM/LdT+ADV maintenance therapy (P=0.001) were negatively associated with virologic response. At week 48, additional ADV- or ETV-associated mutations were cleared in ETV+TDF group, but such mutations were present in 4.3% of patients in LAM/LdT+ADV group (P=0.106). The two groups had similar rates of adverse events.Conclusions: ETV+TDF combination treatment led to a significantly higher rate of virologic response compared to LAM/LdT+ADV combination treatment in patients with LAM-resistant HBV who had suboptimal responses to LAM/LdT+ADV regardless of HBV genotypic resistance profile (NCT01597934).

Details

Language :
English
ISSN :
22872728
Volume :
26
Issue :
3
Database :
OpenAIRE
Journal :
Clinical and Molecular Hepatology
Accession number :
edsair.doi.dedup.....f7dc0335b7504b412207d90c4ce2f571