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Experience with Entecavir Therapy for Lamivudine-Resistant Chronic Hepatitis B in Korean Children and Adolescents
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Á¶½Â¸¸ ( Cho Seung-Man )
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ÃÖº´È£ ( Choe Byung-Ho )
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±èÁ¤¹Ì ( Kim Jung-mi )
°æºÏ´ëÇб³ ÀÇÇÐÀü¹®´ëÇпø ¼Ò¾Æ°úÇб³½Ç
Ãß¹Ì¾Ö ( Chu Mi-Ae )
°æºÏ´ëÇб³ ÀÇÇÐÀü¹®´ëÇпø ¼Ò¾Æ°úÇб³½Ç
KMID : 0816120100130010044
Abstract
Purpose: To estimate the viral suppressive effect of entecavir monotherapy in Korean children and adolescents with lamivudine-resistant chronic hepatitis B (CHB).
Methods: One milligram of entecavir was administered once daily to 6 patients (4 boys; mean age, 17.5 years; range, 15.10¡24.6 years) with lamivudine-resistant CHB for a mean duration of therapy of 13.4 months (range, 1¡21.1 months). The therapeutic results were compared with 11 patients who received adefovir (0.3 mg/kg/day [maximal dose 10 mg]) for at least 12 months (mean, 33.4 months; range, 12.4¡58.3 months). The serum HBV DNA level and serologic markers were measured every 2 months.
Results: The interval to a HBV DNA titer decrement (£¾1 log10) was 1.2¡¾0.2 and 4.4¡¾5.2 months (p=0.185) for the entecavir and adefovir groups, respectively. The interval to a HBV DNA titer decrement (£¾2 log10) was 2.4¡¾2.3 and 9.2¡¾7.3 months (p=0.025), for the entecavir and adefovir groups, respectively.
Conclusion: The therapeutic efficacy of entecavir was favorable in children and adolescents, especially in shortening the interval to a £¾2 log10 decrement in the HBV DNA titer. Long-term follow up is needed to determine the therapeutic efficacy of entecavir for lamivudine-resistant CHB in children and adolescents.
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Entecavir; Adefovir; Lamivudine; Chronic hepatitis B; Resistance
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