A Randomized, Controlled, Clinical Study of Thymosin Alpha-1 Versus Interferon-Alpha in Chinese Patients with Chronic Hepatitis B Lacking Hepatitis B Envelope Antigen

Autor: Yong-Liang Ma, Rong-Xue Wu, J.H. Huang, Jun-Yan Qu, Yan-Wei Qiao, Guo-Bing Wu, Jing You, Hong-Ying Cheng, Lin Zhuang, Bao-Zhang Tang, Shou-Ming Yan
Jazyk: angličtina
Rok vydání: 2005
Předmět:
Zdroj: Journal of the Chinese Medical Association, Vol 68, Iss 2, Pp 65-72 (2005)
ISSN: 1726-4901
Popis: Background This study was designed to compare the efficacy and safety of thymosin-α1 (T-α1) with that of interferon-α (IFN-α) in patients with chronic hepatitis B who were positive for hepatitis B virus (HBV) DNA and hepatitis B envelope antibody (anti-Hbe). Methods Fifty-six patients were randomly divided into groups A and B. Both groups were comparable ( p > 0.05) at baseline regarding age, sex, and alanine aminotransferase (ALT) levels. Group A patients received T-α1 1.6 mg subcutaneously twice weekly, while group B patients received IFN-α 5 million IU daily for 15 days, then thrice weekly for 6 months. Results from the 2 groups were compared with data from a group of 30 patients never treated with IFN-α and who were followed-up for 12 months (historical control [HC] group); the 3 groups were comparable ( p > 0.05). Results After treatment, a complete response (ALT normalization and HBV DNA loss) occurred in 8 of 26 patients in group A (30.8%) and 14 of 30 in group B (46.7%; χ = 1.476, p = 0.224). After a follow-up period of 6 months, a complete response was observed in 11 of 26 patients in group A (42.3%) and 7 of 30 in group B (23.3%; χ = 2.299, p = 0.129). The rate of complete response was significantly greater in the IFN-α than HC group at the end of therapy (46.7% vs 3.3%; χ = 15.022, p = 0.0001), and in the T-α1 than HC group at the end of follow-up (42.3% vs 3.3%; χ = 12.566, p = 0.0001). Ten of the 12 T-α1 responders (i.e. partial responders; 83.3%) experienced sustained, non-detectable HBV DNA after 6 months' treatment; 6 of the 14 T-α1 non-responders (42.9%) showed a delayed response of non-detectable HBV DNA during the follow-up period. Corresponding values for group B patients were 50% (9/18) and 0% (0/12). The rate of delayed response was significantly higher in group A than the other 2 groups (χ = 6.686, p = 0.010; χ = 4.964, p = 0.038), whereas the rate of flare was higher in group B than in the other 2 groups (χ = 3.445, p = 0.063; χ = 7.668, p = 0.006), during the follow-up period. Unlike IFN-α, T-α1 was well tolerated, i.e. no adverse effects were noted in group A. Conclusion These results suggest that a 6-month course of T-α1 therapy is effective and safe in patients with anti-Hbe-positive chronic hepatitis B; T-α1 can reduce HBV replication in such patients. Compared with IFN-α, T-α1 is better tolerated and seems to induce a gradual and more sustained normalization of ALT and loss of HBV DNA. Combination therapy with T-α1 and IFN-α or nucleoside analogs for hepatitis B warrants further study.
Databáze: OpenAIRE
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