Inhibitor Development in Patients With Hemophilia A Undergoing Surgery (PASs)
|Study Design:||Observational Model: Cohort
Time Perspective: Prospective
|Official Title:||Inhibitor Development in Patients With Hemophilia A Undergoing Surgery|
- Inhibitor development (inhibitor titer > 0.4 BU/ml) [ Time Frame: postopereratvie date 90 ]Primary Study Endpoint: Inhibitor development (inhibitor titer > 0.4 BU/ml) by post-operative (POD) day 90. Three months or 90 days was selected as the primary end point based on data collected in the case-control study where 17/18 cases had developed their inhibitor within 12 weeks of their intensive fVIII treatment and only 1 case developed the inhibitor >16 weeks after the intensive fVIII treatment.
Biospecimen Retention: Samples With DNA
Blood drawn during study includes 15 ml within 7 days prior to surgery and 15 ml drawn on post-operative days 1, 14 and 90.
Samples for DNA storage will be generated from blood draw study samples.
|Study Start Date:||November 2011|
|Estimated Study Completion Date:||March 2017|
|Primary Completion Date:||February 2016 (Final data collection date for primary outcome measure)|
Mild or moderate hemophilia A
Subjects with mild or moderate hemophilia A (fVIII activity 1-40%) who are scheduled to undergo surgery for which at least 5 consecutive days of fVIII replacement therapy is required.
The development of neutralizing anti-factor VIII (fVIII) antibodies, fVIII inhibitor, is the most significant complication affecting patients with hemophilia A (HA). Once an inhibitor develops, treatment is less effective and costly. Although inhibitors occur most commonly in those with severe HA, 25% of new inhibitors occur in those with non-severe HA. In patients with non-severe HA, the development of a fVIII inhibitor can change the course of disease from one that is easily managed to one with the potential for spontaneous life-threatening difficult to treat bleeding. Although significant advances have been made in understanding risk factors for fVIII inhibitor development in patients with severe HA, studies that seek to understand the risk for fVIII inhibitor development in those with non-severe disease have been limited to retrospective analyses. In these retrospective analyses, intensive fVIII treatment and surgery have been identified as risk factors for fVIII inhibitor development in non-severe HA. Additionally, receiving fVIII by continuous infusion has been associated with fVIII inhibitor development in non-severe HA in some but not all studies and may be due in part to a more robust proinflammatory response during continuous infusion. Accordingly, the next logical step to evaluate the risk of inhibitor development associated with continuous fVIII infusion is a prospective observational cohort study. Additionally, knowledge of the immune response to fVIII in the surgical setting is essential for identification of patients at high risk for inhibitor development and development of strategies to prevent inhibitor development and is best evaluated in the setting of an prospective cohort study.
This multicenter prospective observational cohort study will enroll a total of 140 subjects at 10 centers who have mild or moderate hemophilia a (fVIII activity 1-40%) who are scheduled to undergo surgery for which at least 5 consecutive days of fVIII replacement therapy is required. The study will gather clinical data and collect blood specimens on 4 occasions over a 3 month period. Outcomes include: inhibitor development, total fVIII usage, bleeding, and markers of T cell activation.
Please refer to this study by its ClinicalTrials.gov identifier: NCT01571934
|United States, Colorado|
|University of Colorado, Hemophilia and Thrombosis Center|
|Aurora, Colorado, United States, 80045|
|United States, Georgia|
|Emory University Comprehensive Hemophilia Treatment Center|
|Atlanta, Georgia, United States, 30322|
|United States, Indiana|
|Indiana Hemophilia and Thrombosis Center|
|Indianapolis, Indiana, United States, 46260|
|United States, North Carolina|
|University of North Carolina|
|Chapel Hill, North Carolina, United States, 27599-7035|
|United States, Oregon|
|Oregon Health & Science University|
|Portland, Oregon, United States, 97239|
|United States, Pennsylvania|
|University of Pittsburgh and Hemophilia Center of Pennsylvania|
|Pittsburgh, Pennsylvania, United States, 15213|
|United States, Texas|
|The University of Texas Health Science Center at Houston|
|Houston, Texas, United States, 77030|
|Principal Investigator:||Christine Kempton, MD, MSc||Emory University|