Late HDV RNA Relapse After Peginterferon Alpha-Based Therapy of Chronic Hepatitis Delta

被引:238
作者
Heidrich, Benjamin [1 ,2 ]
Yurdaydin, Cihan [3 ]
Kabacam, Gokhan [3 ]
Ratsch, Boris A. [4 ]
Zachou, Kalliopi [1 ,5 ,6 ]
Bremer, Birgit [1 ]
Dalekos, George N. [5 ,6 ]
Erhardt, Andreas [7 ]
Tabak, Fehmi [8 ]
Yalcin, Kendal [9 ]
Gurel, Selim [10 ]
Zeuzem, Stefan [11 ]
Cornberg, Markus [1 ,12 ]
Bock, C. -Thomas [4 ]
Manns, Michael P. [1 ,2 ,12 ]
Wedemeyer, Heiner [1 ,2 ,12 ]
机构
[1] Hannover Med Sch, Dept Gastroenterol Hepatol & Endocrinol, D-30625 Hannover, Germany
[2] Hannover Med Sch, Integrated Res & Treatment Ctr Transplantat IFB T, D-30625 Hannover, Germany
[3] Ankara Univ, Sch Med, Dept Gastroenterol, TR-06100 Ankara, Turkey
[4] Robert Koch Inst, Dept Infect Dis, Berlin, Germany
[5] Univ Thessaly, Sch Med, Dept Med, Larisa, Greece
[6] Univ Thessaly, Sch Med, Res Lab Internal Med, Larisa, Greece
[7] Univ Dusseldorf, Dept Gastroenterol Hepatol & Infect Dis, Dusseldorf, Germany
[8] Istanbul Univ, Cerrahpasa Med Sch, Dept Infect Dis, Istanbul, Turkey
[9] Dicle Univ, Sch Med, Div Hepatol, Diyarbakir, Turkey
[10] Uludad Univ, Fac Med, Dept Gastroenterol, Bursa, Turkey
[11] Goethe Univ Frankfurt, Med Klin 1, D-60054 Frankfurt, Germany
[12] Partner Site Hannover Braunschweig, German Ctr Infect Res DZIF, Braunschweig, Germany
关键词
B-VIRUS; NATURAL-HISTORY; PLUS ADEFOVIR; INTERFERON; RESOLUTION; RIBAVIRIN; PATTERNS; DECLINE;
D O I
10.1002/hep.27102
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Interferon alpha is the only treatment option for hepatitis delta virus (HDV). Trials investigating the efficacy of pegylated interferon alpha (PEG-IFNa) showed HDV RNA negativity rates of 25-30% 24 weeks after therapy. However, the clinical and virological long-term outcome of HDV-infected patients treated with PEG-IFNa is unknown. We performed a retrospective-prospective follow-up of 77 patients treated for 48 weeks with either PEG-alfa-2a and adefovir (ADV) or either drug alone in the Hep-Net-International-Delta-Hepatitis-Intervention-Study 1 (HIDIT-1) trial. Long-term follow-up data were available for 58 out of 77 patients (75%) with a median time of follow-up of 4.5 (0.5-5.5) years and a median 3 visits per patient. Patients treated with ADV alone received retreatment with PEG-IFNa (48% versus 19%; P = 0.02) more often. Hepatitis B virus surface antigen (HBsAg) became negative in six PEG-IFNa-treated patients until the end of long-term follow-up (10%). Sixteen patients tested HDV RNA-negative 6 months after PEG-IFNa treatment who were entered in the long-term follow-up study. Out of these, nine individuals tested HDV RNA-positive at least once during further long-term follow-up, with seven patients being HDV RNA-positive at the most recent visit. Clinical endpoints (liver-related death, liver transplantation, hepatic decompensation, hepatocellular carcinoma) were observed in three PEG-IFNa-treated (8%) and three ADV-treated (14%) patients during posttreatment long-term follow-up with an overall annual event rate of 2.5% (4.9% in cirrhosis). Sequencing confirmed the reappearance of pretreatment virus strains in all cases. Conclusion: Late HDV RNA relapses may occur after PEG-IFNa therapy of hepatitis delta and thus the term sustained virological response should be avoided in HDV infection. The annual posttreatment rate of clinical events in hepatitis delta patients eligible for PEG-IFNa therapy is about 2.5% and 4.9% in patients with cirrhosis.
引用
收藏
页码:87 / 97
页数:11
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