Long-Term Orthopedic Effects Of Delaying Prophylaxis In Severe Hemophilia A Until Age 6 Years: Results Of The Joint Outcome Study Continuation (JOSc)

Author:

Manco-Johnson Marilyn J.1,Manco-Johnson Michael L2,Blades Taylor A3,Funk Sharon2,Lane Heidi4,McRedmond Kevin5,Dunn Amy L.6,Recht Michael7,Shapiro Amy D.8,Valentino Leonard A.9,Brown Deborah10

Affiliation:

1. Dept Pediatrics, University of Colorado Hemophilia and Thrombosis Center and Children's Hospital Colorado, Aurora, CO, USA,

2. Department of Pediatrics, University of Colorado Hemophilia and Thrombosis Center, Aurora, CO, USA,

3. Pediatrics, University of Colorado Hemophilia & Thrombosis Center, Aurora, CO, USA,

4. Intermountain Hemophilia and Thrombosis Center, Primary Children's Medical Center, Salt Lake City, UT, USA,

5. Hemophilia Center, Palmetto Health, Columbia, SC, USA,

6. Aflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta/Emory University, Atlanta, GA, USA,

7. The Hemophilia Center, Oregon Health & Science University, Portland, OR, USA,

8. Indiana Hemophilia & Thrombosis Center, Indianapolis, IN, USA,

9. Hemophilia and Thrombosis Center, Rush University, Chicago, IL, USA,

10. Department of Pediatrics- Hematology Division, University of Texas, Houston, TX, USA

Abstract

Abstract The Joint Outcome Study (JOS) was a randomized controlled clinical trial in boys with severe factor VIII deficiency comparing prophylaxis consisting of 25 IU/kg factor VIII every other day begun prior to age 30 months with an enhanced episodic regimen given only in response to bleeding. At JOS exit at age 6 years, joint outcome by sensitive magnetic resonance image (MRI) and joint physical examination (PE) of 6 index joints (both ankles, knees and elbows) determined superiority of prophylaxis over episodic therapy (p < 0.05). At JOS end, all parents were informed of the study results and boys in the episodic arm were counseled to initiate prophylaxis therapy; all but 1 JOS participant on episodic therapy switched to prophylaxis. The JOS Continuation Study is being performed to determine the results of early prophylaxis on joint development until the age of 18 years and to determine the impact of delaying prophylaxis initiation until age 6 years. All boys in the original JOS were eligible to enroll in the continuation study. Study data collected includes cumulative number of index joint and total hemorrhages, joint PE score of 6 index joints using the Colorado Pediatric Joint Assessment Scale as previously described (Haemophilia 6:649) and MRI soft tissue, osteochondral and total scores of 6 index joints using the expanded MRI 45 Scale as recently presented (ISTH OP Mon 7/1/13, 9 am). Additional data are collected on prophylaxis adherence, activities, surgeries, quality of life and replacement factor utilization. To date, results of 26 (40%) of the original 65 boys (16 on early and 10 on delayed prophylaxis) including 156 index joints are available for analysis. Results, expressed as a cumulative score for all 6 index joints, are shown in Table 1. While still enrolling, the JOS Continuation Study is documenting an ongoing disparity in joint outcome in children with initiation of prophylaxis delayed until age 6 years, compared with prophylaxis started before 30 months of age. Following delayed initiation of prophylaxis, adolescents manifest increased numbers of hemarthroses and increased MRI damage particularly affecting bone and cartilage. Joint PE is less sensitive than MRI in determination of joint outcome in hemophilia. Disclosures: Manco-Johnson: Bayer HealthCare: Membership on an entity’s Board of Directors or advisory committees, Research Funding; CSL Behring: Membership on an entity’s Board of Directors or advisory committees, Research Funding; Baxter BioScience: Membership on an entity’s Board of Directors or advisory committees; Biogen Idec: Membership on an entity’s Board of Directors or advisory committees; NovoNordisk: Membership on an entity’s Board of Directors or advisory committees; Eisai: Research Funding. Manco-Johnson:Bayer HealthCare: Research Funding. Lane:Bayer HealthCare: Honoraria; Baxter BioScience: Paid travel to attend a meeting, Paid travel to attend a meeting Other. Shapiro:Bayer HealthCare: Research Funding; Baxter BioScience: Research Funding; Biogen Idec: Research Funding; Cangene: Research Funding. Valentino:Baxter BioScience: Consultancy, Membership on an entity’s Board of Directors or advisory committees, Research Funding; Bayer HealthCare: Consultancy, Membership on an entity’s Board of Directors or advisory committees, Research Funding; CSL Behring: Consultancy, Membership on an entity’s Board of Directors or advisory committees, Research Funding; GTC Biotherapeutics: Consultancy, Membership on an entity’s Board of Directors or advisory committees, Research Funding; Inspiration Bioscience: Consultancy, Membership on an entity’s Board of Directors or advisory committees, Research Funding; NovoNordisk: Consultancy, Membership on an entity’s Board of Directors or advisory committees, Research Funding; Pfizer: Consultancy, Membership on an entity’s Board of Directors or advisory committees, Research Funding. Brown:Baxter BioScience: Research Funding; Biogen Idec: Research Funding; CSL Behring: Research Funding.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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