Abstract

Treatment with pegylated interferon alpha-2b (PEGIFN) plus ribavirin (RBV) is standard therapy for patients with chronic hepatitis C. Although the effectiveness, patients with high titres of group Ib hepatitis C virus (HCV) respond poorly compared to other genotypes. At present, we cannot predict the effect in an individual. Previous studies have used traditional statistical analysis by assuming a linear relationship between clinical features, but most phenomena in the clinical situation are not linearly related. The aim of this study is to predict the effect of PEG IFN plus RBV therapy on an individual patient level using an artificial neural network system (ANN). 156 patients with HCV group 1b from multiple centres were treated with PEGIFN (1.5 µg/kg) plus RBV (400–1000 mg) for 48 weeks. Data on the patients' demographics, laboratory tests, PEGIFN, and RBV doses, early viral responses (EVR), and sustained viral responses were collected. Clinical data were randomly divided into training data set and validation data set and analyzed using multiple logistic regression analysis (MLRs) and ANN to predict individual outcomes. The sensitivities of predictive expression were 0.45 for the MLRs models and 0.82 for the ANNs and specificities were 0.55 for the MLR and 0.88 for the ANN. Non-linear relation analysis showed that EVR, serum creatinine, initial dose of Ribavirin, gender and age were important predictive factors, suggesting non-linearly related to outcome. In conclusion, ANN was more accurate than MLRs in predicting the outcome of PEGIFN plus RBV therapy in patients with group 1b HCV.

Highlights

  • Chronic hepatitis C (CHC) is of global concern because CHC patients frequently develop liver cirrhosis and hepatocellular carcinoma (HCC)

  • Input factors and Outcome We used the clinical data to determine input factors X1–X21, which were used to predict the outcomes of individual patients using multiple logistic regression analysis (MLRs) and artificial neural network system (ANN) analysis

  • X17 represented the presence of diabetes mellitus, X18 represented the hepatitis C virus (HCV) RNA level, X19 and X20 represented the total amount of administered Pegylated interferon alpha-2b (PEGIFN) and RBV, respectively, and X21 represented early viral responses (EVR), defined as the a 2-log decrease in the serum HCV RNA 12 weeks after therapy began

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Summary

Introduction

Chronic hepatitis C (CHC) is of global concern because CHC patients frequently develop liver cirrhosis and hepatocellular carcinoma (HCC). Eradication of the hepatitis C virus (HCV) is an effective means of preventing CHC. Pegylated interferon alpha-2b (PEGIFN) plus ribavirin (RBV) combination therapy against the HCV is currently standard therapy for patients with CHC. This combination is effective against certain types of HCV, it is effective in only 50–60% of patients infected with the IFN-resistant strain of HCV [1]. In Japan, 70% of CHC patients are infected with HCV genotype 1b [2,3,4,5,6]. The treatment outcome of patients infected with HCV genotype 1b is poor compare to other genotypes and the virus is eradicated from only 50% of these patients [7,8,9,10,11]

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