Defibrotide for the treatment of severe hepatic veno-occlusive disease/sinusoidal obstruction syndrome: Evidence for clinical benefit Journal Article


Authors: Richardson, P. G.; Krishnan, A.; Giralt, S.; Soiffer, R. J.
Article Title: Defibrotide for the treatment of severe hepatic veno-occlusive disease/sinusoidal obstruction syndrome: Evidence for clinical benefit
Abstract: Introduction: Veno-occlusive disease/sinusoidal obstruction syndrome (VOD/SOS), characterized by hepatic sinusoidal endothelial damage and liver dysfunction, is an unpredictable and potentially life-threatening complication of hematopoietic stem cell transplantation that occurs in an estimated 14% of these patients (range 0 - 62.3%). VOD/SOS typically occurs following high-dose radiotherapy and/or chemotherapy as conditioning. Although mild/moderate VOD/SOS may not progress in some patients and may resolve at an early stage (i.e., within 2 or 3 weeks), in others it develops into severe VOD/SOS, commonly identified by the presence of multi-organ failure (defined by pulmonary and/or renal dysfunction), which, in turn, is associated with mortality rates >80%.Areas covered: This review of severe hepatic VOD/SOS discusses the disease characteristics, diagnostic criteria, prevalence, pathogenesis and current treatment guidelines for VOD/SOS, as well as prophylactic measures. The clinical trial evidence for associated therapies is reviewed, along with evaluations of these therapies by VOD/SOS expert consensus groups. Defibrotide, the only medication approved for the treatment of severe VOD/SOS in the European Union, is discussed in detail with regard to chemistry, pharmacodynamics/pharmacokinetics, proposed mechanisms of action and evidence from clinical trials of efficacy and safety.Expert opinion: Clinical data show that defibrotide reduces the mortality associated with VOD/SOS. Given the lack of therapeutic options and the favorable benefit/risk profile of defibrotide, this agent may therefore help fill an important and unmet therapeutic need. © 2015 Taylor & Francis.
Keywords: review; drug efficacy; drug safety; radiation dose; treatment; liver toxicity; bleeding; gastrointestinal symptom; prevalence; practice guideline; hematopoietic stem cell transplantation; high risk patient; hypotension; disease severity; drug mechanism; kidney function; prophylaxis; reduced intensity conditioning; heparin; methylprednisolone; hyperbilirubinemia; drug bioavailability; drug metabolism; drug half life; tissue plasminogen activator; endothelial dysfunction; artificial ventilation; meta analysis (topic); phase 3 clinical trial (topic); phase 1 clinical trial (topic); veno-occlusive disease; liver venoocclusive disease; hemofiltration; defibrotide; multi-organ failure; fibrinolysis; sinusoidal obstruction syndrome; hematopoietic stem cell transplant; paracentesis; acetylcysteine; transjugular intrahepatic portosystemic shunt; human; priority journal; fluid balance; antithrombotic activity; pro-fibrinolysis; sodium balance
Journal Title: Expert Opinion on Orphan Drugs
Volume: 3
Issue: 12
ISSN: 2167-8707
Publisher: Taylor & Francis Group  
Date Published: 2015-01-01
Start Page: 1491
End Page: 1501
Language: English
DOI: 10.1517/21678707.2015.1114455
PROVIDER: scopus
DOI/URL:
Notes: Review -- Export Date: 3 February 2016 -- Source: Scopus
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  1. Sergio Andres Giralt
    1050 Giralt