Daily low dose intravesical cidofovir for the treatment of BK virus associated hemorrhagic cystitis after allogeneic stem cell transplantation

J Infect Chemother. 2023 Jan;29(1):67-71. doi: 10.1016/j.jiac.2022.09.014. Epub 2022 Sep 24.

Abstract

Introduction: BK virus associated hemorrhagic cystitis(BKV-AHC) is a serious complication observed after allogeneic stem cell transplantation and the current therapeutic options are scarce with substantial renal side effects. Although the guidelines recommend intravenous cidofovir application with caution to nephrotoxicity, there are few studies which investigated intravesical administration and reported similar therapeutic results with less renal side effects.

Methods: We administered low dose, daily and consecutive (75 mg/day, for 5 days) intravesical cidofovir to 25 patients with BKV-AHC that developed after (ASCT).

Results: The response rate in our cohort was 92% and relapse was not encountered in 84% of the patient population during one year of follow-up. The median BK urine viral load significantly decreased from 260,000,000 IU/mL to 53,000,000 IU/mL after a week of treatment (p = 0.0001). Rise in serum creatinine was observed in 5 patients during treatment and post-treatment nephrotoxicity was seen in only 1 patient.

Conclusions: Daily low dose intravesical cidofovir might be an effective treatment option for BKV-AHC after ASCT with favorable less systemic side effects.

Keywords: BK virus; C; H; I; Low dose; S; emorrhagic cystitis; idofovir; ntravesical; tem cell transplantation.

MeSH terms

  • Antiviral Agents / adverse effects
  • BK Virus*
  • Cidofovir / pharmacology
  • Cidofovir / therapeutic use
  • Cystitis* / drug therapy
  • Cystitis* / etiology
  • Cytosine / adverse effects
  • Drug-Related Side Effects and Adverse Reactions* / etiology
  • Hematopoietic Stem Cell Transplantation* / adverse effects
  • Hematopoietic Stem Cell Transplantation* / methods
  • Hemorrhage / drug therapy
  • Hemorrhage / etiology
  • Humans
  • Organophosphonates* / adverse effects
  • Polyomavirus Infections* / drug therapy
  • Renal Insufficiency* / etiology
  • Tumor Virus Infections* / drug therapy

Substances

  • Cidofovir
  • Organophosphonates
  • Cytosine
  • Antiviral Agents