Early HBeAg Loss During Peginterferon α-2b Therapy Predicts HBsAg Loss: Results of a Long-Term Follow-Up Study in Chronic Hepatitis B Patients

被引:25
作者
Buster, Erik H. C. J. [1 ]
Flink, Hajo J. [1 ]
Simsek, Halis [2 ]
Heathcote, E. Jenny [3 ]
Sharmila, Sachithanandan [4 ]
Kitis, George E. [5 ]
Gerken, Guido [6 ]
Buti, Maria [7 ,8 ]
de Vries, Richard A. [9 ]
Verhey, Elke [1 ]
Hansen, Bettina E. [1 ,10 ]
Janssen, Harry L. A. [1 ]
机构
[1] Univ Med Ctr Rotterdam, Erasmus MC, Dept Gastroenterol & Hepatol, NL-3015 CE Rotterdam, Netherlands
[2] Hacettepe Univ, Fac Med, TR-06100 Ankara, Turkey
[3] Toronto Western Hosp, Dept Med, Univ Hlth Network, Toronto, ON M5T 2S8, Canada
[4] Hosp Selayang, Hepatol Unit, Selangor, Malaysia
[5] George Papanikolaou Gen Reg Hosp, Dept Gastroenterol, Thessaloniki, Greece
[6] Univ Hosp, Dept Gastroenterol & Hepatol, Essen, Germany
[7] Hosp Gen Univ Vall Hebron, Liver Unit, Barcelona, Spain
[8] CIBEREHD, Barcelona, Spain
[9] Rijnstate Hosp, Dept Gastroenterol & Hepatol, Arnhem, Netherlands
[10] Univ Med Ctr Rotterdam, Erasmus MC, Dept Epidemiol & Biostat, NL-3015 CE Rotterdam, Netherlands
关键词
POSITIVE PATIENTS; INTERFERON TREATMENT; VIRUS DNA; ANTIGEN; COMBINATION; SUPPRESSION; PREVENTION; LAMIVUDINE;
D O I
10.1038/ajg.2009.371
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
OBJECTIVES: Treatment with pegylated interferon (PEG-IFN) alpha-2b results in hepatitis B e antigen (HBeAg) loss in 36% of patients at 6 months post treatment. The aim of this study was to determine whether a long-term response to PEG-IFN is dependent on the timing of HBeAg loss. METHODS: A total of 91 patients treated with PEG-IFN alpha-2b alone (100 mu g per week) and 81 patients treated with PEG-IFN alpha-2b and lamivudine (100 mg/day) for 52 weeks were enrolled in this study. Patients were initially followed up at 4-week intervals and had one additional long-term follow-up (LTFU) visit (mean: 3.03 +/- 0.77 years 26 weeks post treatment). RESULTS: Of the 172 patients included, 78 patients (46%) did not have loss of HBeAg, 47 (27%) lost HBeAg within 32 weeks, and 47 patients (27%) had loss of HBeAg after week 32. At LTFU, patients with HBeAg loss <= 32 weeks had hepatitis B virus DNA of <400 copies/ml significantly more often than did those who lost HBeAg after week 32 (47 vs. 21%, respectively; P=0.009). Hepatitis B surface antigen (HBsAg) negativity was also observed significantly more often in patients with early HBeAg loss (36 vs. 4%, respectively, P<0.001). Early HBeAg loss tended to occur more often in patients treated with PEG-IFN and lamivudine combination therapy than in those treated with PEG-IFN alone (35 vs. 21%; P=0.10), as did HBsAg loss (15 vs. 8%; P=0.14). CONCLUSIONS: Early PEG-IFN-induced HBeAg loss results in a high likelihood of HBsAg loss and may be associated with more profound viral suppression during the first 32 weeks of therapy in patients treated with lamivudine combinations.
引用
收藏
页码:2449 / 2457
页数:9
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