Abatacept improves health‐related quality of life, pain, sleep quality, and daily participation in subjects with juvenile idiopathic arthritis

Objective To assess health‐related quality of life (HRQOL) in abatacept‐treated children/adolescents with juvenile idiopathic arthritis (JIA). Methods In this phase III, double‐blind, placebo‐controlled trial, subjects with active polyarticular course JIA and an inadequate response/intolerance to ≥1...

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Published inArthritis care & research (2010) Vol. 62; no. 11; pp. 1542 - 1551
Main Authors Ruperto, Nicolino, Lovell, Daniel J., Li, Tracy, Sztajnbok, Flavio, Goldenstein‐Schainberg, Claudia, Scheinberg, Morton, Penades, Inmaculada Calvo, Fischbach, Michael, Alcala, Javier Orozco, Hashkes, Philip J., Hom, Christine, Jung, Lawrence, Lepore, Loredana, Oliveira, Sheila, Wallace, Carol, Alessio, Maria, Quartier, Pierre, Cortis, Elisabetta, Eberhard, Anne, Simonini, Gabriele, Lemelle, Irene, Chalom, Elizabeth Candell, Sigal, Leonard H., Block, Alan, Covucci, Allison, Nys, Marleen, Martini, Alberto, Giannini, Edward H.
Format Journal Article
LanguageEnglish
Published Hoboken, USA John Wiley & Sons, Inc 01.11.2010
Subjects
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ISSN2151-464X
2151-4658
2151-4658
DOI10.1002/acr.20283

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Summary:Objective To assess health‐related quality of life (HRQOL) in abatacept‐treated children/adolescents with juvenile idiopathic arthritis (JIA). Methods In this phase III, double‐blind, placebo‐controlled trial, subjects with active polyarticular course JIA and an inadequate response/intolerance to ≥1 disease‐modifying antirheumatic drug (including biologics) received abatacept 10 mg/kg plus methotrexate (MTX) during the 4‐month open‐label period (period A). Subjects achieving the American College of Rheumatology Pediatric 30 criteria for improvement (defined “responders”) were randomized to abatacept or placebo (plus MTX) in the 6‐month double‐blind withdrawal period (period B). HRQOL assessments included 15 Child Health Questionnaire (CHQ) health concepts plus the physical (PhS) and psychosocial summary scores (PsS), pain (100‐mm visual analog scale), the Children's Sleep Habits Questionnaire, and a daily activity participation questionnaire. Results A total of 190 subjects from period A and 122 from period B were eligible for analysis. In period A, there were substantial improvements across all of the CHQ domains (greatest improvement was in pain/discomfort) and the PhS (8.3 units) and PsS (4.3 units) with abatacept. At the end of period B, abatacept‐treated subjects had greater improvements versus placebo in all domains (except behavior) and both summary scores. Similar improvement patterns were seen with pain and sleep. For participation in daily activities, an additional 2.6 school days/month and 2.3 parents' usual activity days/month were gained in period A responders with abatacept, and further gains were made in period B (1.9 versus 0.9 [P = 0.033] and 0.2 versus −1.3 [P = 0.109] school days/month and parents' usual activity days/month, respectively, in abatacept‐ versus placebo‐treated subjects). Conclusion Improvements in HRQOL were observed with abatacept, providing real‐life tangible benefits to children with JIA and their parents/caregivers.
Bibliography:ClinicalTrials.gov
Dr. Ruperto has received consultant fees, speaking fees, and/or honoraria (less than $10,000 each) from Bristol‐Myers Squibb, Roche, and Novartis.
Dr. Hashkes has received honoraria (less than $10,000) from Novartis.
identifier: NCT00095173.
Dr. Quartier has received consultant fees, speaking fees, and/or honoraria (less than $10,000) from Bristol‐Myers Squibb.
Dr. Martini has received consultant fees, speaking fees, and/or honoraria (less than $10,000 each) from Bristol‐Myers Squibb and Novartis.
Dr. Lovell has received consultant fees, speaking fees, and/or honoraria (less than $10,000 each) from AstraZeneca, Forest Research, Abbott, Centocor, Wyeth Pharmaceuticals, Amgen, Bristol‐Myers Squibb, Novartis, UBC, Xoma, Regeneron, Hoffman‐La Roche, and Pfizer.
Drs. Sigal and Block and Ms Covucci own stock and/or hold stock options in Bristol‐Myers Squibb.
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ISSN:2151-464X
2151-4658
2151-4658
DOI:10.1002/acr.20283