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Efficacy of consensus interferon in treatment of HbeAg-positive chronic hepatitis B: a multicentre, randomized
YongLi Zheng1, LianSan Zhao, TaiXiang Wu
1Infectious Disease Centre, West China Hospital, Sichuan University, No. 37, Guo Xue Xiang, Chengdu, Sichuan Province, PR China. zhyl1973@live.com
Insights
Consensus interferon (CIFN) showed comparable efficacy to interferon alpha-1b in treating chronic hepatitis B. Both treatments gradually improved liver enzymes and reduced viral DNA and HBeAg levels.
Area of Science:
- Hepatology
- Virology
- Immunology
Background:
- Consensus interferon (CIFN) is a novel type I interferon formulation.
- Chronic hepatitis B infection remains a significant global health concern, particularly HBeAg-positive cases.
Purpose of the Study:
- To evaluate the efficacy of CIFN compared to interferon alpha-1b (IFN-alpha1b) in treating HBeAg-positive chronic hepatitis B.
- To assess treatment outcomes including serological, virological, and biochemical parameters.
Main Methods:
- A multicentre, controlled trial involving 144 patients with HBeAg-positive chronic hepatitis B.
- Randomized assignment to receive either 9 microg CIFN or 50 microg IFN-alpha1b subcutaneously three times weekly for 24 weeks.
- Efficacy assessment based on normalization of ALT levels and undetectable HBV DNA or HBeAg at the end of treatment and 24 weeks post-treatment.
Main Results:
- No statistically significant differences were observed in serological, virological, or biochemical parameters between the CIFN and IFN-alpha1b groups.
- Similar rates of complete or partial response were noted at the end of treatment and during the follow-up period for both groups (p > 0.05).
Conclusions:
- The study suggests that 9 microg CIFN is an effective treatment option for HBeAg-positive chronic hepatitis B.
- CIFN demonstrated the ability to induce gradual ALT normalization, HBV DNA clearance, and HBeAg loss or seroconversion.
Background:
Consensus interferon (CIFN) is a newly developed type I interferon.
Aims:
This multicentre, controlled trial was conducted to determine the efficacy of CIFN and to compare it with alpha-1b-interferon (IFN-alpha1b) in the treatment of patients with hepatitis B e antigen (HBeAg)-positive chronic hepatitis B.
Methods:
144 Patients were randomly assigned to receive 9 microg CIFN (CIFN group) or 50 microg INF-alpha1b (IFN-alpha group) subcutaneously 3 times weekly for 24 weeks, followed by 24 weeks of observation. Efficacy was assessed by normalization of serum alanine transaminase (ALT) levels and the non-detectability of serum hepatitis B virus DNA or HBeAg at the end of treatment and 24 weeks after stopping treatment.
Results:
There was no statistically significant difference in the serological, virological and biochemical parameters between CIFN and IFN-alpha1b groups at the end of the therapy and follow-up period (p > 0.05). Overall, at the end of treatment, 7.0% (5/71) and 35.2% (25/71) of patients in the CIFN group showed a complete or partial response compared with 7.4% (5/68) and 33.8% (23/68) of the IFN-alpha group (p = 0.10). At 24 weeks after stopping treatment, 6.9% (5/72) and 37.5% (27/72) of patients in the CIFN group showed complete response or partial response compared with 7.1% (5/70) and 34.3% (24/70) of the IFN-alpha group (p = 0.10).
Conclusion:
These findings suggest that 9 microg CIFN is effective in the treatment of patients with HBeAg-positive chronic hepatitis B. It can gradually induce ALT normalization and HBV DNA clearance and HBeAg loss or HBeAg/HBeAb seroconversion.
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