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Predictive factors for sustained response to interferon treatment in patients with chronic hepatitis C: a randomized, open, and multi-center controlled trial |
Yao Xie, Dao-Zhen Xu, Zhi-Meng Lu, Kang-Xian Luo, Ji-Dong Jia, Yu-Ming Wang, Gui-Zhen Zhao, Shu-Lin Zhang and Da-Zhi Zhang |
Beijing, China
Author Affiliations: Ninth Clinical Department, Beijing Ditan Hospital, Beijing 100011, China (Xie Y and Xu DZ); Department of Infectious Diseases, Ruijin Hospital, Shanghai 200025, China (Lu ZM); Department of Infectious Diseases, Nanfang Hospital, First Military Medical University, Guangzhou 510515, China (Luo KX); Center of Liver Diseases, Beijing Friendship Hospital, Beijing 100050, China (Jia JD); Institute of Infectious Diseases, Southwest Hospital, Third Military Medical University, Chongqing 400038, China (Wang YM); Department of Infectious Diseases, Second Hospital, China Medical University, Shenyang 110004, China (Zhao GZ); Department of Infectious Diseases, First Affiliated Hospital, Xi'an Jiaotong University, Xi'an 710061, China (Zhang SL); and Liver Disease Center of Chongqing, Second Affiliated Hospital, Chongqing Medical University, Chongqing 400010, China (Zhang DZ)
Corresponding Author: Yao Xie, MD, Ninth Clinical Department, Beijing Ditan Hospital, Beijing 100011, China (Tel: 86-10-64211031; Fax: 86-10-64227308; Email: xieyao@public.bta.net.cn) |
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Abstract BACKGROUND: This study was undertaken to investigate the predictive factors of sustained viral response in roferon-A or pegasys treated chronic hepatitis C patients after logistic regression analysis of the factors that might be associated with the therapeutic effects of interferon (IFN).
METHODS: All patients enrolled into this randomized, open and multi-center controlled trial were divided into two groups randomly and treated with pegasys and roferon-A for 24 weeks, then followed up for another 24 weeks. Before treatment, hepatitis C virus (HCV) genotype was determined, and HCV-RNA in serum was detected before and at the end of treatment and follow-up. HCV-RNA turning negative was considered the major index for evaluating the therapeutic effect. The clinical characteristics including gender, age, infection route of HCV, treatment with IFN, platelet count, AST/ALT ratio and treatment drugs were analyzed by logistic regression.
RESULTS: Intention to treat (ITT) and per-protocol (PP) population groups have 208 and 197 patients respectively. In the PP group, after treatment for 24 weeks, the response rates of female patients aged less than 50 years, infected through non-transfusion, relapsed after IFN treatment, and presented with a AST/ALT ratio≤1, virus load less than 8×105 IU/ml, and non genotype 1 HCV infection, and treated finally with pegasys were higher than those of male patients, aged more than 50 years, infected by transfusion, treated firstly with IFN, presented with a AST/ALT ratio≥1, virus load equal or more than 8×105 IU/ml, and genotype 1 infection, and treated finally with roferon-A. But, at the end of follow-up, the patients with a AST/ALT ratio≥1 and virus load more than 8×105 IU/ml had a higher rate of sustained response than did those with a AST/ALT ratio≤1 and virus load less than 8×105 IU/ml. Logistic regression analysis and control of the promiscuous factors showed that the genotype of HCV was not related to the response rate at the end of treatment (OR 0.604, 95% CI 0.271-1.349, P=0.219), but was the independent predictive factor of virus sustained response to IFN treatment (OR 0.408, 95% CI 0.189-0.881, P=0.023). The form of IFN was significantly related to viral response at the end of treatment (OR 0.105, 95% CI 0.052-0.212, P<0.001), and pegasys were an intensely predictive factor for sustained response(OR 0.255, 95% CI 0.123-0.529, P<0.001).
CONCLUSION: HCV genotype and pegasys are the predictive factors for IFN response to the IFN treatment of patients with chronic hepatitis C.
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Cite this article: |
Xie Y,
Xu DZ,
Lu ZM,
et al.
Predictive factors for sustained response to interferon treatment in patients with chronic hepatitis C: a randomized, open, and multi-center controlled trial.
Hepatobiliary Pancreat Dis Int
2005;
4(2):
213-219. DOI:
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URL: |
http://dx.doi.org/ OR http://www.hbpdint.com/EN/Y2005/V4/I2/213 |
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