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   <subfield code="a">10.1007/s10620-010-1537-2</subfield>
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   <subfield code="a">The Level of HBV DNA at Month 12 Is an Important Predictor of Virological Breakthrough During Adefovir Monotherapy in Chronic Hepatitis B Patients with Lamivudine Resistance</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Moon-Chan Kim, Seok Jung, Jung Shin, Neung Park]</subfield>
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   <subfield code="a">Background and Aims: The aim of this study was to determine the optimal time and HBV DNA levels during the treatment period for prediction of virological breakthrough (VBT) 3years after adefovir monotherapy in chronic hepatitis B (CHB) patients with lamivudine resistance. Methods: We consecutively analyzed HBV DNA levels within 12months in 210 lamivudine-resistant CHB patients treated with adefovir monotherapy for more than 36months. Results: VBT, genotypic adefovir mutations, and virologic responses were observed in 52 (24.8%), 37 (17.6%), and 117 (55.7%) cases within 3years of treatment, respectively. Using receiver-operating characteristic curve analysis, HBV DNA levels at month 12 had a greater power (AUROC, 0.839; 95% CI, 0.759-0.919; p&lt;0.001) to predict VBT after 3years of treatment. The best cut-off value of HBV DNA levels at month 12 for predicting VBT at 3years of treatment was 200IU/ml with a sensitivity and negative predictive value of 88.5 and 94.3%, respectively. Using this time and cut-off value, VBT had developed in six (5.7%) of the patients with HBV DNA levels &lt;200IU/ml (n=105) and 46 (43.8%) of the patients with HBV DNA levels ≥200IU/ml (n=105) at month 12 (p&lt;0.001). Moreover, virological response or HBeAg seroconversion remained higher at 82.9 and 81.2%, respectively. Conclusions: In patients who were switched to adefovir monotherapy as rescue therapy for lamivudine resistance before the introduction of current therapeutic guidelines, measurements of HBV DNA levels at month 12 should be performed to predict VBT. Early termination of adefovir monotherapy should be considered for patients who still have HBV DNA ≥200IU/ml (3 log10 copies/ml) at 12months of treatment.</subfield>
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   <subfield code="a">Springer Science+Business Media, LLC, 2011</subfield>
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   <subfield code="a">Hepatitis B virus</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Adefovir dipivoxil</subfield>
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   <subfield code="a">Lamivudine resistance</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">HBV DNA level</subfield>
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   <subfield code="a">Kim</subfield>
   <subfield code="D">Moon-Chan</subfield>
   <subfield code="u">Department of Family Medicine, University of Ulsan College of Medicine, Ulsan University Hospital, Ulsan, South Korea</subfield>
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   <subfield code="a">Jung</subfield>
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   <subfield code="u">Department of Internal Medicine and Biomedical Research Center, University of Ulsan College of Medicine, Ulsan University Hospital, 290-3 Jeonha-dong, Dong-gu, 682-714, Ulsan, South Korea</subfield>
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   <subfield code="a">Shin</subfield>
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   <subfield code="u">Department of Internal Medicine and Biomedical Research Center, University of Ulsan College of Medicine, Ulsan University Hospital, 290-3 Jeonha-dong, Dong-gu, 682-714, Ulsan, South Korea</subfield>
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   <subfield code="u">Department of Internal Medicine and Biomedical Research Center, University of Ulsan College of Medicine, Ulsan University Hospital, 290-3 Jeonha-dong, Dong-gu, 682-714, Ulsan, South Korea</subfield>
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   <subfield code="t">Digestive Diseases and Sciences</subfield>
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   <subfield code="g">56/4(2011-04-01), 1215-1221</subfield>
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