Tahan Veysel, Ozaras Resat, Karaca Cetin, Uraz Suleyman, Eren Fatih, Danalioglu Ahmet, Avsar Erol, Turkoglu Salih, Midilli Kenan, Tabak Fehmi, Ozturk Recep, Mert Ali, Senturk Hakan, Tozun Nurdan
Marmara University Institute of Gastroenterology, Istanbul.
Hepatogastroenterology. 2009 Sep-Oct;56(94-95):1425-8.
BACKGROUND/AIMS: The management of chronic hepatitis C virus (HCV) infection is costly. Genotyping determines the indication, probability of response, and duration of treatment and the dose of ribavirin. Although genotyping is accepted cost-effective, the cost of genotyping in all of the patients to find out a minority may offset the gain. The present study aimed; (1) to determine the frequency rate of HCV genotypes and (2) to compare the cost of HCV treatment tailored according to the genotype versus that planned supposing it to be genotype 1.
Six centers were included into the study. Name, age, genotype, and serotype of each patient were entered. For genotyping, HCV-RNA was extracted by acid-guanidium-phenol-chloroform method. Cost of genotyping, HCV-RNA studies and the treatment with pegylated interferon and ribavirin was estimated. The cost was determined according to two scenarios: (A) To manage patients as if all had genotypes other than 2-3. (B) To manage them after determining the geno type. The management was assumed to be made by current guidelines.
The data of 834 patients were analyzed: Genotypel was predominant: 730 (87.5%). The rest was composed of G2:26 (3.1%), G3:26 (3.1%), G4:14 (1.7%), mixed: 13 (1.6%), undetermined: 25(3%). The cost of approach A (for 100 patients) was 1,718,200 USD; that of approach B (for 100 patients) was 1,671,900 USD. With genotype targeted therapy, every 100 patient would save 46,300 USD.
The prevalent genotype in our country is genotypel. The sum of genotypes 2 and 3 corresponds to 6%. Genotyping HCV and tailoring the treatment thereafter are cost-effective even in the countries where prevalence of these genotypes is low.
背景/目的:慢性丙型肝炎病毒(HCV)感染的治疗成本高昂。基因分型可确定治疗指征、应答概率、治疗持续时间以及利巴韦林的剂量。尽管基因分型被认为具有成本效益,但对所有患者进行基因分型以找出少数患者的成本可能会抵消收益。本研究旨在:(1)确定HCV基因型的频率;(2)比较根据基因型定制的HCV治疗成本与假设为基因型1时计划的治疗成本。
本研究纳入了6个中心。记录每位患者的姓名、年龄、基因型和血清型。对于基因分型,采用酸胍-苯酚-氯仿法提取HCV-RNA。估算基因分型、HCV-RNA检测以及聚乙二醇干扰素和利巴韦林治疗的成本。成本根据两种情况确定:(A)假设所有患者的基因型均不是2-3型来管理患者。(B)在确定基因型后管理患者。假设管理方式遵循现行指南。
对834例患者的数据进行了分析:基因型1占主导:730例(87.5%)。其余包括:G2:26例(3.1%),G3:26例(3.1%),G4:14例(1.7%),混合基因型:13例(1.6%),未确定:25例(3%)。方法A(针对100例患者)的成本为1,718,200美元;方法B(针对100例患者)的成本为1,671,900美元。采用基因型靶向治疗,每100例患者可节省46,300美元。
我国流行的基因型是基因型1。基因型2和3的总和占6%。即使在这些基因型流行率较低的国家,对HCV进行基因分型并据此定制治疗也是具有成本效益的。