Peginterferon plus Adefovir versus Either Drug Alone for Hepatitis Delta

被引:353
作者
Wedemeyer, Heiner
Yurdaydin, Cihan [6 ]
Dalekos, George N. [10 ]
Erhardt, Andreas [2 ]
Cakaloglu, Yilmaz [8 ]
Degertekin, Halil [7 ]
Gurel, Selim [9 ]
Zeuzem, Stefan [3 ]
Zachou, Kalliopi [10 ]
Bozkaya, Hakan [6 ]
Koch, Armin
Bock, Thomas [4 ]
Dienes, Hans Peter [5 ]
Manns, Michael P. [1 ]
机构
[1] Hannover Med Sch, Dept Gastroenterol Hepatol & Endocrinol, D-30625 Hannover, Germany
[2] Univ Dusseldorf, Dusseldorf, Germany
[3] Goethe Univ Frankfurt, Frankfurt, Germany
[4] Robert Koch Inst, D-1000 Berlin, Germany
[5] Univ Cologne, Cologne, Germany
[6] Ankara Univ, Sch Med, TR-06100 Ankara, Turkey
[7] Ufuk Univ, Sch Med, Ankara, Turkey
[8] Mem Hosp Istanbul, Istanbul, Turkey
[9] Uludag Univ, Sch Med, Bursa, Turkey
[10] Univ Larissa, Larisa, Greece
关键词
D VIRUS-INFECTION; B-VIRUS; COMBINATION THERAPY; VANISHING DISEASE; INTERFERON; LAMIVUDINE; RIBAVIRIN; HBEAG; PREVALENCE; DIPIVOXIL;
D O I
10.1056/NEJMoa0912696
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Chronic infection with hepatitis B virus and hepatitis delta virus (HDV) results in the most severe form of viral hepatitis. There is no currently approved treatment. We investigated the safety and efficacy of 48 weeks of treatment with peginterferon alfa-2a plus adefovir dipivoxil, peginterferon alfa-2a alone, and adefovir dipivoxil alone. METHODS We conducted a randomized trial in which 31 patients with HDV infection received treatment with 180 mu g of peginterferon alfa-2a weekly plus 10 mg of adefovir daily, 29 received 180 mu g of peginterferon alfa-2a weekly plus placebo, and 30 received 10 mg of adefovir alone weekly for 48 weeks. Follow-up was conducted for an additional 24 weeks. Efficacy end points included clearance of HDV RNA, normalization of alanine aminotransferase levels, and a decline in levels of hepatitis B surface antigen (HBsAg). RESULTS The primary end point - normalization of alanine aminotransferase levels and clearance of HDV RNA at week 48 - was achieved in two patients in the group receiving peginterferon alfa-2a plus adefovir and two patients in the group receiving peginterferon alfa-2a plus placebo but in none of the patients in the group receiving adefovir alone. At week 48, the test for HDV RNA was negative in 23% of patients in the first group, 24% of patients in the second, and none of those in the third (P=0.006 for the comparison of the first and third groups; P=0.004 for the comparison of the second and third). The efficacy of peginterferon alfa-2a was sustained for 24 weeks after treatment, with 28% of the patients receiving peginterferon alfa-2a plus adefovir or peginterferon alfa-2a alone having negative results on HDV-RNA tests; none of the patients receiving adefovir alone had negative results. A decline in HBsAg levels of more than 1 log(10) IU per milliliter from baseline to week 48 was observed in 10 patients in the first group, 2 in the second, and none in the third (P<0.001 for the comparison of the first and third groups and P=0.01 for the comparison of the first and second). CONCLUSIONS Treatment with peginterferon alfa-2a for 48 weeks, with or without adefovir, resulted in sustained HDV RNA clearance in about one quarter of patients with HDV infection.
引用
收藏
页码:322 / 331
页数:10
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