Villavicencio Mauricio A, Li Selena S, Leifer Ann Marie, Gustafson Jenna L, Osho Asishana, Wolfe Stanley, Raz Yuval, Griffith Jason, Neuringer Isabel, Bethea Emily, Gift Thais, Waldman Georgina, Astor Todd, Langer Nathaniel B, Chung Raymond T
Department of Cardiovascular Surgery, Mayo Clinic, Rochester, Minn.
Division of Cardiac Surgery, Department of Surgery, Massachusetts General Hospital, Boston, Mass.
JTCVS Open. 2023 Mar 10;14:602-614. doi: 10.1016/j.xjon.2023.02.014. eCollection 2023 Jun.
The study objective was to assess the safety and efficacy of a preemptive direct-acting antiviral therapy in lung transplants from hepatitis C virus donors to uninfected recipients.
This study is a prospective, open-label, nonrandomized, pilot trial. Recipients of hepatitis C virus nucleic acid test positive donor lungs underwent preemptive direct-acting antiviral therapy with glecaprevir 300 mg/pibrentasvir 120 mg for 8 weeks from January 1, 2019, to December 31, 2020. Recipients of nucleic acid test positive lungs were compared with recipients of lungs from nucleic acid test negative donors. Primary end points were Kaplan-Meier survival and sustained virologic response. Secondary outcomes included primary graft dysfunction, rejection, and infection.
Fifty-nine lung transplantations were included: 16 nucleic acid test positive and 43 nucleic acid test negative. Twelve nucleic acid test positive recipients (75%) developed hepatitis C virus viremia. Median time to clearance was 7 days. All nucleic acid test positive patients had undetectable hepatitis C virus RNA by week 3, and all alive patients (n = 15) remained negative during follow-up with 100% sustained virologic response at 12 months. One nucleic acid test positive patient died of primary graft dysfunction and multiorgan failure. Three of 43 nucleic acid test negative patients (7%) had hepatitis C virus antibody positive donors. None of them developed hepatitis C virus viremia. One-year survival was 94% for nucleic acid test positive recipients and 91% for nucleic acid test negative recipients. There was no difference in primary graft dysfunction, rejection, or infection. One-year survival for nucleic acid test positive recipients was similar to a historical cohort of the Scientific Registry of Transplant Recipients (89%).
Recipients of hepatitis C virus nucleic acid test positive lungs have similar survival as recipients of nucleic acid test negative lungs. Preemptive direct-acting antiviral therapy results in rapid viral clearance and sustained virologic response at 12 months. Preemptive direct-acting antiviral may partially prevent hepatitis C virus transmission.
本研究的目的是评估在将丙型肝炎病毒(HCV)供体的肺移植给未感染受体时,抢先使用直接作用抗病毒疗法的安全性和有效性。
本研究是一项前瞻性、开放标签、非随机的试点试验。2019年1月1日至2020年12月31日,丙型肝炎病毒核酸检测呈阳性的供体肺的受体接受了8周的抢先直接作用抗病毒治疗,使用glecaprevir 300毫克/ pibrentasvir 120毫克。将核酸检测呈阳性的肺的受体与核酸检测呈阴性的供体肺的受体进行比较。主要终点是Kaplan-Meier生存率和持续病毒学应答。次要结局包括原发性移植物功能障碍、排斥反应和感染。
纳入了59例肺移植:16例核酸检测呈阳性,43例核酸检测呈阴性。12例核酸检测呈阳性的受体(75%)发生了丙型肝炎病毒血症。清除的中位时间为7天。所有核酸检测呈阳性的患者在第3周时丙型肝炎病毒RNA检测不到,所有存活患者(n = 15)在随访期间仍为阴性,12个月时持续病毒学应答率为100%。1例核酸检测呈阳性的患者死于原发性移植物功能障碍和多器官衰竭。43例核酸检测呈阴性的患者中有3例(7%)供体丙型肝炎病毒抗体呈阳性。他们均未发生丙型肝炎病毒血症。核酸检测呈阳性的受体1年生存率为94%,核酸检测呈阴性的受体为91%。原发性移植物功能障碍、排斥反应或感染方面无差异。核酸检测呈阳性的受体1年生存率与移植受者科学注册库的历史队列相似(89%)。
丙型肝炎病毒核酸检测呈阳性的肺的受体与核酸检测呈阴性的肺的受体生存率相似。抢先直接作用抗病毒疗法可导致病毒快速清除,并在12个月时实现持续病毒学应答。抢先直接作用抗病毒疗法可能部分预防丙型肝炎病毒传播。