Kondo C, Atsukawa M, Tsubota A, Shimada N, Abe H, Aizawa Y
Department of Internal Medicine, Division of Gastroenterology, Nippon Medical School Chiba Hokusoh Hospital, Inzai, Japan.
J Postgrad Med. 2016 Jan-Mar;62(1):20-5. doi: 10.4103/0022-3859.173191.
Most patients with chronic hepatitis C show virological response to telaprevir-based triple therapy, and achieve an end-of-treatment response (ETR). However, some patients showing ETR develop virological relapse. This study was carried out to evaluate factors associated with relapse after triple therapy.
A prospective, multicentric study was conducted in chronic hepatitis C patients who received telaprevir-based triple therapy. We evaluated independent variables such as age, with or without cirrhosis, prior treatment response to interferon (IFN) therapy, IL28B genotype, core amino acid (aa) 70 mutation, drug adherence, white blood cell counts, hemoglobin level, and serum low-density lipoprotein (LDL) cholesterol level. The characteristics of the patients who relapsed after achieving ETR were compared with those who did not.
Among 168 patients, 157 patients achieved ETR (93.5%) and 11 discontinued. Of these 157 patients, relapse occurred in 21 patients (13.4%). Nineteen patients (90.5%) of 21 relapsed patients had the IL28B non-TT genotype (P = 1.79 × 10 -9 ). Multivariate analysis identified core amino acid 70 [P = 0.018, crude odds ratio (OR): 6.927] and the IL28B genotype (P = 3.758 × 10 -5 , crude OR: 39.311) as significantly independent factors that influenced the relapse-related variables. Among the 49 patients with the IL28B non-TT, 18 patients had core aa70 mutation and 31 patients had core aa70 wild-type. In addition, 66.7% (12/18) of those with core aa70 mutation and 22.6% (7/31) of those with core aa70 wild-type developed relapse (P = 0.005).
Core aa70 mutation and the IL28B non-TT genotype were identified as independent factors that influenced relapse after achievement of ETR for telaprevir-based triple therapy.
大多数慢性丙型肝炎患者对基于特拉匹韦的三联疗法呈现病毒学应答,并实现治疗结束时的应答(ETR)。然而,一些出现ETR的患者会发生病毒学复发。开展本研究以评估三联疗法后复发相关的因素。
对接受基于特拉匹韦三联疗法的慢性丙型肝炎患者进行一项前瞻性、多中心研究。我们评估了独立变量,如年龄、有无肝硬化、既往对干扰素(IFN)治疗的应答、IL28B基因型、核心氨基酸(aa)70突变、药物依从性、白细胞计数、血红蛋白水平及血清低密度脂蛋白(LDL)胆固醇水平。将实现ETR后复发的患者特征与未复发的患者进行比较。
168例患者中,157例实现ETR(93.5%),11例中断治疗。在这157例患者中,21例(13.4%)出现复发。21例复发患者中有19例(90.5%)具有IL28B非TT基因型(P = 1.79×10⁻⁹)。多变量分析确定核心氨基酸70[P = 0.018,粗比值比(OR):6.927]和IL28B基因型(P = 3.758×10⁻⁵,粗OR:39.311)是影响复发相关变量的显著独立因素。在49例IL28B非TT患者中,18例有核心aa70突变,31例有核心aa70野生型。此外,核心aa70突变患者中有66.7%(12/18)复发,核心aa70野生型患者中有22.6%(7/31)复发(P = 0.005)。
核心aa70突变和IL28B非TT基因型被确定为基于特拉匹韦的三联疗法实现ETR后影响复发的独立因素。