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Early HBeAg Loss During Peginterferon α -2b Therapy Predicts HBsAg Loss
被浏览了 次,发表时间:2010-04-28 14:37:00,来自: Erik H.C.J. Buster , MD
OBJECTIVES: Treatment with pegylated interferon (PEG-IFN) -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 -2b alone (100 μ g per week) and 81 patients
treated with PEG-IFN -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 signifi cantly 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 signifi cantly 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 fi rst 32 weeks of therapy in patients
treated with lamivudine combinations.
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 -2b alone (100 μ g per week) and 81 patients
treated with PEG-IFN -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 signifi cantly 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 signifi cantly 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 fi rst 32 weeks of therapy in patients
treated with lamivudine combinations.
中华医学会感染病学会分会