Successful treatment of hepatic veno-occlusive disease after myeloablative allogeneic hematopoietic stem cell transplantation by early administration of a short course of methylprednisolone

Bone Marrow Transplant. 2008 Feb;41(3):287-91. doi: 10.1038/sj.bmt.1705896. Epub 2007 Nov 5.

Abstract

Hepatic veno-occlusive disease (VOD) is one of the most common and important regimen-related toxicities observed after hematopoietic stem cell transplantation (HSCT). There are no universally accepted preventative or therapeutic approaches for VOD. We prospectively evaluated the safety and efficacy of a short course of methylprednisolone (MP) in 48 patients undergoing allogeneic HSCT who were diagnosed with hepatic VOD. MP was administered at a dose of 0.5 mg/kg i.v. every 12 h for a total of 14 doses, and then discontinued without taper. Thirty (63%) patients responded with a reduction in total serum bilirubin of 50% or more after 10 days of treatment. In univariate analysis, non-responders had a higher total bilirubin at the start of MP therapy, more weight gain, evidence of fungal infection and platelet refractoriness. High SGPT and early engraftment were significant factors among responders. Twenty-five of the 30 responders survived up to day +100, whereas all but three non-responders died within 100 days post-HSCT, for a probability of survival of 58% among responders and 10% for non-responders. Prospective comparative studies are needed to confirm the observed encouraging outcome of MP therapy for VOD.

Publication types

  • Clinical Trial

MeSH terms

  • Anti-Inflammatory Agents / administration & dosage*
  • Drug Administration Schedule
  • Female
  • Hematopoietic Stem Cell Transplantation / adverse effects*
  • Hepatic Veno-Occlusive Disease / drug therapy*
  • Humans
  • Male
  • Methylprednisolone / administration & dosage*
  • Myeloablative Agonists / adverse effects
  • Pilot Projects
  • Prospective Studies
  • Transplantation Conditioning / adverse effects
  • Transplantation, Homologous / adverse effects

Substances

  • Anti-Inflammatory Agents
  • Myeloablative Agonists
  • Methylprednisolone