Risk score based PEG Interferon alpha 2b and Ribavirin treatment response estimation model for genotype 1 chronic hepatitis C patients

被引:2
作者
Jurczyk, K. [1 ]
Laurans, L. [1 ]
Karpinska, E. [1 ]
Wawrzynowicz-Syczewska, M. [1 ]
Parczewski, M. [1 ]
Boron-Kaczmarska, A. [1 ]
机构
[1] Pomeranian Med Univ, Dept Infect Dis & Hepatol, PL-71455 Szczecin, Poland
来源
ADVANCES IN MEDICAL SCIENCES | 2011年 / 56卷 / 02期
关键词
hepatitis C; interferon alpha; ribavirin; treatment; ALPHA-2B PLUS RIBAVIRIN; PEGINTERFERON ALPHA-2A; INSULIN-RESISTANCE; COMBINATION THERAPY; ANTIVIRAL THERAPY; VIROLOGICAL RESPONSE; GENETIC-VARIATION; VIRUS; EFFICACY; PREDICTORS;
D O I
10.2478/v10039-011-0056-5
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Purpose: Attempt to create simple practical algorithm for prospective assessment of PEG interferon/ribavirin related treatment response in individuals with chronic hepatitis C (CHC) basing on the risk factors defined prior to the treatment initiation. Material/Methods: Retrospective assessment of 45 female and 39 male previously untreated CHC patients aged 20 to 73 years, with genotype 1, undergoing standard treatment with PEG-IFNa2b+RBV was performed. For the final analysis 78 patients were included (38 effectively treated and 40 treatment failures). Thirty-six sustained virological response (SVR) related factors, which were routinely measured before treatment initiation were compared (including physical, biochemical, serologic and histopathologic). From this group the risk factors of the highest predictive value for treatment failure were selected. Cut-off values for statistical significance were defined for each parameter, with risk score (RS) calculated and compared in the group with and without SVR. Results: Seven factors related to treatment failure were identified: HCV>600000 IU/L, blood platelet count <150000/ul, GGTP>45 IU/ml, total serum protein<7.8 g/dl, glycaemia>105 mg/dl, detectable HBc IgG antibodies and cirrhosis. In the group with RS 1 the likelihood of SVR was 70% (p<0.028), while in patients with RS 3 the response was reduced to 23.8% (p<0.016), with no SVR achieved among patients with RS >3. Conclusions: Low risk score (0-2) is associated with high probability of treatment success with scores >3 predictive for treatment failure. The presented model is a simple tool for prediction of treatment success for clinical use before PegIFN/RBV treatment initiation among genotype 1 CHC patients.
引用
收藏
页码:165 / 171
页数:7
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