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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.
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页码:680 / 686
页数:7
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