## Abstract There is little clinical information on the management of hepatitis B virus (HBV) that is resistant to multiple drugs including entecavir (ETV). The present retrospective cohort study assessed the antiviral efficacy of ETV/adefovir dipivoxil (ADV) combination therapy for ETV‐resistant H
Adefovir-based combination therapy with entecavir or lamivudine for patients with entecavir-refractory chronic hepatitis B
✍ Scribed by Soon Sun Kim; Jae Youn Cheong; Dami Lee; Myoung Hee Lee; Sun Pyo Hong; Soo-Ok Kim; Sung Won Cho
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 160 KB
- Volume
- 84
- Category
- Article
- ISSN
- 0146-6615
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✦ Synopsis
This study evaluated the efficacy of adefovir (ADV) plus lamivudine (LAM) or ADV add-on therapy for patients with entecavir (ETV)-refractory hepatitis B infection. Twenty-nine ETVresistant and 8 patients with suboptimal response to ETV were enrolled. Twenty-seven patients received ADV þ LAM therapy and 10 patients received ADV þ ETV therapy for >24 weeks. In 29 patients who were ETV-resistant, the mean reduction in HBV DNA levels at 24 weeks was not different between the ADV þ LAM and ADV þ ETV groups (À1.98 log 10 IU/ml vs. À2.16 log 10 IU/ml; P ¼ 0.792). Primary nonresponse was observed in 52.2% (12/23) of ADV þ LAM group and 33.3% (2/6) of ADV þ ETV group (P ¼ 0.651). Initial virologic response (IVR) was observed in 17.4% (4/23) of ADV þ LAM group and 33.3% (2/6) of ETV þ ADV group (P ¼ 0.362). In eight patients with suboptimal response to ETV, the ADV þ ETV group had a greater reduction in HBV DNA at 24 and 48 weeks than the ADV þ LAM group (À2.29 log 10 IU/ml vs. À0.09 log 10 IU/ml and À2.04 log 10 IU/ml vs. À0.72 log 10 IU/ml; P ¼ 0.020 and P ¼ 0.012, respectively). Primary nonresponse and IVR did not significantly differ between the two groups [100% (4/4) vs. 50% (2/4) and 0% (0/4) vs. 50% (2/4); P ¼ 0.429 and P ¼ 0.429, respectively]. The antiviral efficacies of ADV-based therapy with ETV or LAM for patients with ETV-resistant hepatitis B were limited and did not differ between the two groups. However, adding ADV to ETV may be more effective than ADV þ LAM therapy in patients with suboptimal virologic response to ETV.
📜 SIMILAR VOLUMES
Entecavir (ETV) is currently recommended as a rescue therapy purely for adefovir (ADV)resistant chronic hepatitis B virus (HBV) infections. We evaluated the efficacy of ETV in patients who were resistant to lamivudine (LAM)/ADV sequential therapy and in those resistant to LAM monotherapy. Fifty LAM/
## Abstract No study has reported on the comparative effect of adefovir (ADV) add‐on lamivudine (LAM) versus switching to entecavir (ETV) in LAM‐resistant patients with chronic hepatitis B. From October 2007 to September 2008, 92 consecutive LAM‐resistant patients were enrolled (47 LAM + ADV and 45
for the AI463026 Benefits of Entecavir for Hepatitis B Liver Disease (BEHoLD) Study Group In hepatitis B e antigen (HBeAg)-positive chronic hepatitis B patients who were refractory to current lamivudine therapy, switching to entecavir was superior to continued lamivudine at week 48 for histologic i
A randomized, open-label comparative study of entecavir versus adefovir therapy was performed in subjects with chronic hepatitis B who had hepatic decompensation (Child-Turcotte-Pugh score ≥7). Adult subjects were randomized and treated (n = 191) with entecavir 1.0 mg or adefovir 10 mg daily for up
This study was undertaken to compare the early antiviral activity and viral kinetic profiles of entecavir (ETV) versus adefovir (ADV) in hepatitis B e antigen positive nucleoside-naïve adults with chronic hepatitis B (CHB). Sixty-nine nucleoside-naïve CHB patients with baseline HBV DNA of 10(8) copi