Improved Efficacy by Individualized Combination Therapy with Peg IFN-α 2a and ADV in HBeAg Positive Chronic Hepatitis B Patients

被引:13
|
作者
Wang, Ya-Dong [1 ]
Zhao, Cai-Yan [1 ]
Wang, Wei [1 ]
Shen, Chuan [1 ]
Lu, Hong-Zhi [1 ]
Zhang, Li [1 ]
Yu, Wei-Yan [1 ]
Zhou, Jun-Ying [1 ]
Van, Wen-Zhao [1 ]
机构
[1] Hebei Med Univ, Affiliated Hosp 3, Dept Infect Dis, Shijiazhuang, Hebei Province, Peoples R China
关键词
Chronic hepatitis B; Combination therapy; Adefovir dipivoxil; Pegylated interferon alpha; REDUCES PROGRESSION; INTERFERON THERAPY; LAMIVUDINE; PEGINTERFERON-ALPHA-2A; REDUCTION; CIRRHOSIS;
D O I
10.5754/hge12183
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: Monotherapy with pegylated interferon alpha (Peg-IFN alpha) or adefovir dipivoxil (ADV) to HBeAg-positive chronic hepatitis B (CHB) patients has limited effects. This study aims to evaluate therapeutic efficacy and safety of individualized combination therapy with Peg-IFN alpha and ADV. Methodology: HBeAg-positive CHB patients (n=160) were enrolled in this multi-center, prospective, randomized, "real-life" cohort study, of which received Peg IFN alpha-2a monotherapy or combination therapy with ADV base on the baseline features and treatment response. Results: At week 24, percentages of ALT normalization, HBV DNA undetectable were both higher in individualized treatment group (ITG, 57.50%, 43.75%) than that in standard treatment group (STG, 40.00%, 27.50%; p=0.027, 0.032). The superiority of HBeAg clearance and seroconversion rates in ITG maintained from treatment termination (63.75%, 56.25%) to 48 weeks follow-up (57.50%, 53.75%). At week 96 the combined response rates were 46.25% in ITG compared with 30.00% in STG (p=0.034). Furthermore, there was no statistically significant difference in relapse rates and adverse events between the two groups. Conclusions: Individualized combination therapy can achieve higher antiviral response rates. In particular, it can accelerate undetectable HBV DNA and elevate HBeAg clearance/seroconversion rates to a greater degree than Peg-IFN alpha-2a monotherapy.
引用
收藏
页码:680 / 686
页数:7
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