A predictive model of response to peginterferon ribavirin in chronic hepatitis C using classification and regression tree analysis

被引:45
作者
Kurosaki, Masayuki [1 ]
Matsunaga, Kotaro [2 ]
Hirayama, Itsuko [1 ]
Tanaka, Tomohiro [1 ]
Sato, Mitsuaki [1 ]
Yasui, Yutaka [1 ]
Tamaki, Nobuharu [1 ]
Hosokawa, Takanori [1 ]
Ueda, Ken [1 ]
Tsuchiya, Kaoru [1 ]
Nakanishi, Hiroyuki [1 ]
Ikeda, Hiroki [1 ]
Itakura, Jun [1 ]
Takahashi, Yuka [1 ]
Asahina, Yasuhiro [1 ]
Higaki, Megumu [4 ]
Enomoto, Nobuyuki [3 ]
Izumi, Namiki [1 ]
机构
[1] Musashino Red Cross Hosp, Div Gastroenterol & Hepatol, Musashino, Tokyo 1808610, Japan
[2] Musashino Red Cross Hosp, Div Pathol, Musashino, Tokyo 1808610, Japan
[3] Univ Yamanashi, Dept Internal Med 1, Tamaho, Yamanashi, Japan
[4] Jikei Med Univ, Dept Med Sci, Tokyo, Japan
关键词
data mining; decision tree; HCV; low-density-lipoprotein-cholesterol; steatosis; INTERFERON-ALPHA-2B PLUS RIBAVIRIN; LIPOPROTEIN CHOLESTEROL LEVELS; GAMMA-GLUTAMYL-TRANSFERASE; INSULIN-RESISTANCE; ALANINE AMINOTRANSFERASE; VIROLOGICAL RESPONSE; FIBROSIS PROGRESSION; SURVIVAL ANALYSIS; THERAPY; VIRUS;
D O I
10.1111/j.1872-034X.2009.00607.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Aim: Early disappearance of serum hepatitis C virus (HCV) RNA is the prerequisite for achieving sustained virological response (SVR) in peg-interferon (PEG-IFN) plus ribavirin (RBV) therapy for chronic hepatitis C. This study aimed to develop a decision tree model for the pre-treatment prediction of response. Methods: Genotype 1b chronic hepatitis C treated with PEG-IFN alpha-2b and RBV were studied. Predictive factors of rapid or complete early virological response (RVR/cEVR) were explored in 400 consecutive patients using a recursive partitioning analysis, referred to as classification and regression tree (CART) and validated. Results: CART analysis identified hepatic steatosis (< 30%) as the first predictor of response followed by low-density-lipoprotein cholesterol (LDL-C) (>= 100 mg/dL), age (< 50 and < 60 years), blood sugar (< 120 mg/dL), and gamma-glutamyltransferase (GGT) (< 40 IU/L) and built decision tree model. The model consisted of seven groups with variable response rates from low (15%) to high (77%). The reproducibility of the model was confirmed by the independent validation group (r2 = 0.987). When reconstructed into three groups, the rate of RVR/cEVR was 16% for low probability group, 46% for intermediate probability group and 75% for high probability group. Conclusions: A decision tree model that includes hepatic steatosis, LDL-C, age, blood sugar, and GGT may be useful for the prediction of response before PEG-IFN plus RBV therapy, and has the potential to support clinical decisions in selecting patients for therapy and may provide a rationale for treating metabolic factors to improve the efficacy of antiviral therapy.
引用
收藏
页码:251 / 260
页数:10
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