Transplanting hepatitis C virus-infected hearts into uninfected recipients: A single-arm trial

Am J Transplant. 2019 Sep;19(9):2533-2542. doi: 10.1111/ajt.15311. Epub 2019 Mar 20.

Abstract

The advent of direct-acting antiviral therapy for hepatitis C virus (HCV) has generated tremendous interest in transplanting organs from HCV-infected donors. We conducted a single-arm trial of orthotopic heart transplantation (OHT) from HCV-infected donors into uninfected recipients, followed by elbasvir/grazoprevir treatment after recipient HCV was first detected (NCT03146741; sponsor: Merck). We enrolled OHT candidates aged 40-65 years; left ventricular assist device (LVAD) support and liver disease were exclusions. We accepted hearts from HCV-genotype 1 donors. From May 16, 2017 to May 10, 2018, 20 patients consented for screening and enrolled, and 10 (median age 52.5 years; 80% male) underwent OHT. The median wait from UNOS opt-in for HCV nucleic-acid-test (NAT)+ donor offers to OHT was 39 days (interquartile range [IQR] 17-57). The median donor age was 34 years (IQR 31-37). Initial recipient HCV RNA levels ranged from 25 IU/mL to 40 million IU/mL, but all 10 patients had rapid decline in HCV NAT after elbasvir/grazoprevir treatment. Nine recipients achieved sustained virologic response at 12 weeks (SVR-12). The 10th recipient had a positive cross-match, experienced antibody-mediated rejection and multi-organ failure, and died on day 79. No serious adverse events occurred from HCV transmission or treatment. These short-term results suggest that HCV-negative candidates transplanted with HCV-infected hearts have acceptable outcomes.

Keywords: clinical research/practice; heart (allograft) function/dysfunction; heart failure/injury; heart transplantation/cardiology; infection and infectious agents - viral; organ allocation; organ procurement and allocation; organ transplantation in general.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Amides
  • Antiviral Agents / therapeutic use
  • Benzofurans / administration & dosage
  • Carbamates
  • Cyclopropanes
  • Female
  • Genotype
  • Graft Rejection
  • Heart Failure / complications
  • Heart Failure / surgery*
  • Heart Failure / virology
  • Heart Transplantation* / adverse effects
  • Heart-Assist Devices
  • Hepacivirus / genetics
  • Hepatitis C / drug therapy
  • Hepatitis C / transmission*
  • Humans
  • Imidazoles / administration & dosage
  • Male
  • Middle Aged
  • Postoperative Period
  • Quinoxalines / administration & dosage
  • RNA, Viral / analysis
  • Sulfonamides
  • Sustained Virologic Response
  • Time Factors
  • Tissue and Organ Procurement
  • Treatment Outcome
  • Viral Load
  • Waiting Lists

Substances

  • Amides
  • Antiviral Agents
  • Benzofurans
  • Carbamates
  • Cyclopropanes
  • Imidazoles
  • Quinoxalines
  • RNA, Viral
  • Sulfonamides
  • grazoprevir
  • elbasvir

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