Etzion Ohad, Dahari Harel, Yardeni David, Issachar Assaf, Nevo-Shor Anat, Cohen-Naftaly Michal, Ashur Yaffa, Uprichard Susan L, Arbib Orly Sneh, Munteanu Daniela, Braun Marius, Cotler Scott J, Abufreha Naim, Keren-Naus Ayelet, Shemer-Avni Yonat, Mor Orna, Murad Jayanah, Novack Victor, Shlomai Amir
Department of Gastroenterology and Liver Diseases, Soroka University Medical Center, 151 Rager Yitzhak Blvd, 84171, Beer-Sheva, Israel.
Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Sci Rep. 2020 Oct 20;10(1):17820. doi: 10.1038/s41598-020-74568-x.
The advent of direct-acting antivirals (DAAs) has transformed the landscape of hepatitis C virus (HCV) management. We aimed to prospectively (real-time) evaluate the feasibility of using a response-guided therapy approach, based on mathematical modeling of early viral kinetics, to reduce the duration of DAAs therapy. Patients were treated with DAAs according to the physicians' preference. HCV was measured at baseline and at day 2 and weeks 1, 2 and 4 after treatment initiation. The primary endpoint was the proportion of patients with sustained-virological response (SVR) at 12 and/or 24 weeks post-treatment. Twenty-nine patients (mean age 54 ± 16, 44% females, 73% with HCV genotype 1), were enrolled and all completed therapy. Treatment duration was shortened in 11 of the 29 patients (38%). SVR was achieved in 28 of the 29 patients (97%). Relapse occurred post treatment in a single case of a non-cirrhotic male with genotype 3, who was treated with sofosbuvir/velpatasvir for 6 weeks. Virus sequencing did not identify baseline or treatment emergent resistance associated substitutions. Real-time mathematical modeling of early HCV kinetics can be utilized for shortening DAAs duration in approximately 40% of patients without compromising treatment efficacy.Clinical trial registration: ClinicalTrials.gov Identifier: NCT03603327.
直接抗病毒药物(DAAs)的出现改变了丙型肝炎病毒(HCV)的治疗格局。我们旨在基于早期病毒动力学的数学模型,前瞻性地(实时)评估采用反应导向治疗方法以缩短DAAs治疗疗程的可行性。患者根据医生的偏好接受DAAs治疗。在基线、治疗开始后第2天以及第1、2和4周测量HCV。主要终点是治疗后12周和/或24周达到持续病毒学应答(SVR)的患者比例。纳入了29例患者(平均年龄54±16岁,44%为女性,73%为HCV基因1型),所有患者均完成治疗。29例患者中有11例(38%)治疗疗程缩短。29例患者中有28例(97%)实现了SVR。1例非肝硬化基因3型男性患者在接受索磷布韦/维帕他韦治疗6周后出现治疗后复发。病毒测序未发现与基线或治疗中出现的耐药相关替代突变。早期HCV动力学的实时数学模型可用于在不影响治疗效果的情况下,将约40%患者的DAAs疗程缩短。临床试验注册:ClinicalTrials.gov标识符:NCT03603327。