Safety and efficacy of defibrotide for the treatment of severe hepatic veno-occlusive disease

Author:

Richardson Paul G.1,Ho Vincent T.2,Giralt Sergio3,Arai Sally4,Mineishi Shin5,Cutler Corey2,Antin Joseph H.2,Stavitzski Nicole2,Niederwieser Dietger6,Holler Ernst7,Carreras Enric8,Soiffer Robert2

Affiliation:

1. Dana-Farber Cancer Institute, 450 Brookline Avenue, Boston, MA 02115, USA

2. Dana-Farber Cancer Institute, Boston, MA, USA

3. Memorial Sloan-Kettering Cancer Center, New York, NY, USA

4. Stanford University Campus, Department of Medicine, Stanford, CA, USA

5. University of Michigan Comprehensive Cancer Center, Ann Arbor, MI, USA

6. Dana-Farber Cancer Institute, Boston, MA, USA and Department of Haematology/Oncology, University of Leipzig, Leipzig, Germany

7. Regensburg University Medical Center, Regensburg, Germany

8. Haematology Department, Hospital Clinic, Barcelona, Spain

Abstract

Hepatic veno-occlusive disease (VOD), also known as sinusoidal obstruction syndrome, is a potentially life-threatening complication of chemotherapeutic conditioning used in preparation for hematopoietic stem-cell transplantation (SCT). VOD may occur in up to 62% of patients undergoing SCT, with onset generally within the first month after SCT. In severe cases, 100-day mortality is in excess of 80%. Current management consists of best supportive care, with no agents to date approved for treatment in the USA or the EU. Defibrotide, a polydisperse oligonucleotide, has been shown in phase II and III trials to improve complete response and survival in patients undergoing SCT with severe VOD. This article reviews our current understanding of VOD, and examines recent clinical findings on defibrotide for the treatment and prophylaxis of VOD.

Publisher

SAGE Publications

Subject

Hematology

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