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Treatment
with Tenofovir Results in a Rapid Decrease of HBV-DNA Viral Load in Patients
with Resistance or Sub-optimal Response to Adefovir Adefovir dipivoxil [Hepsera] has demonstrated activity against lamivudine [Epivir-HBV]- resistant strains of hepatitis B virus (HBV). However, the N236T mutation in domain D of the hepatitis B virus (HBV) polymerase is associated with phenotypic resistance to adefovir [Hepsera]. In vitro data suggest that the N236T mutant exhibits
only a 4.5 fold decrease in sensitivity to tenofovir.
J Villeneuve and colleagues at CHUM - Hôpital Saint-Luc in [They] also explored the usefulness of tenofovir in patients with suboptimal response to adefovir, but without genotypic resistance. Two patients who were receiving adefovir because of lamivudine resistance developed resistance to adefovir, after 36 and 12 months of treatment respectively. The first case was receiving lamivudine + adefovir and the second case adefovir monotherapy. The N236T mutation of the HBV-polymerase was demonstrated by the INNO-LiPA test (HBV DR v2, Innogenetics). They were treated with tenofovir 300mg id plus lamivudine 100mg id and adefovir was stopped. Four additional patients without genotypic resistance, but with sub-optimal response to adefovir were also switched to tenofovir 300mg id. They were also receiving adefovir + lamivudine because of lamivudine resistance. These 4 cases had HBV-DNA viral loads of 97 x 106, 42 x 106, 14 x 106 and 3.6 x 106 millions copies/ml after 13, 23, 29 and 25 months of treatment with adefovir respectively. HBV-DNA viral loads were measured by the Bayer b-DNA assay (lower limit of detection = 2000 copies/ml). Results
[The authors conclude], “Treatment with tenofovir induces a rapid decrease of HBV-DNA viral load in patients with resistance or sub-optimal response to adefovir.” 11/16/05 Reference
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