Use of HCV+ Donors Does Not Affect HCV Clearance With Directly Acting Antiviral Therapy But Shortens the Wait Time to Kidney Transplantation

Transplantation. 2017 May;101(5):968-973. doi: 10.1097/TP.0000000000001410.

Abstract

Background: Hepatitis C virus (HCV) infection is prevalent in the renal transplant population but direct acting antiviral agents (DAA) provide an effective cure of HCV infection without risk of allograft rejection.

Methods: We report our experience treating 43 renal transplant recipients with 4 different DAA regimens.

Results: One hundred percent achieved a sustained viral response by 12 weeks after therapy, and DAA regimens were well tolerated. Recipients transplanted with a HCV+ donor responded equally well to DAA therapy those transplanted with a kidney from an HCV- donor, but recipients of HCV+ organs experienced significantly shorter wait times to transplantation, 485 days (interquartile range, 228-783) versus 969 days (interquartile range, 452-2008; P = 0.02).

Conclusions: On this basis, we advocate for a strategy of early posttransplant HCV eradication to facilitate use of HCV+ organs whenever possible. Additional studies are needed to identify the optimal DAA regimen for kidney transplant recipients, accounting for efficacy, timing relative to transplant, posttransplant clinical outcomes, and cost.

MeSH terms

  • Adult
  • Aged
  • Antiviral Agents / therapeutic use*
  • Benzimidazoles / therapeutic use*
  • Drug Therapy, Combination
  • Female
  • Fluorenes / therapeutic use*
  • Follow-Up Studies
  • Hepatitis C, Chronic / drug therapy*
  • Hepatitis C, Chronic / etiology
  • Humans
  • Kidney Transplantation*
  • Male
  • Middle Aged
  • Postoperative Complications / drug therapy*
  • Retrospective Studies
  • Ribavirin / therapeutic use
  • Simeprevir / therapeutic use*
  • Sofosbuvir
  • Time Factors
  • Tissue Donors*
  • Treatment Outcome
  • Uridine Monophosphate / analogs & derivatives*
  • Uridine Monophosphate / therapeutic use

Substances

  • Antiviral Agents
  • Benzimidazoles
  • Fluorenes
  • ledipasvir, sofosbuvir drug combination
  • Ribavirin
  • Simeprevir
  • Uridine Monophosphate
  • Sofosbuvir