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A comparison of three treatment strategies in recent onset non-systemic Juvenile Idiopathic Arthritis: initial 3-months results of the BeSt for Kids-study

BACKGROUND: Combination therapy with prednisone or etanercept may induce earlier and/or more improvement in disease activity in Disease Modifying Anti Rheumatic Drug (DMARD) naïve non-systemic Juvenile Idiopathic Arthritis (JIA) patients. Here we present three months clinical outcome of initial trea...

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Autores principales: Hissink Muller, P. C. E., Brinkman, D. M. C., Schonenberg, D., Koopman-Keemink, Y., Brederije, I. C. J., Bekkering, W. P., Kuijpers, T. W., van Rossum, M. A. J., van Suijlekom-Smit, L. W. A., van den Berg, J. M., Allaart, C. F., ten Cate, R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5294738/
https://www.ncbi.nlm.nih.gov/pubmed/28166785
http://dx.doi.org/10.1186/s12969-017-0138-4
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author Hissink Muller, P. C. E.
Brinkman, D. M. C.
Schonenberg, D.
Koopman-Keemink, Y.
Brederije, I. C. J.
Bekkering, W. P.
Kuijpers, T. W.
van Rossum, M. A. J.
van Suijlekom-Smit, L. W. A.
van den Berg, J. M.
Allaart, C. F.
ten Cate, R.
author_facet Hissink Muller, P. C. E.
Brinkman, D. M. C.
Schonenberg, D.
Koopman-Keemink, Y.
Brederije, I. C. J.
Bekkering, W. P.
Kuijpers, T. W.
van Rossum, M. A. J.
van Suijlekom-Smit, L. W. A.
van den Berg, J. M.
Allaart, C. F.
ten Cate, R.
author_sort Hissink Muller, P. C. E.
collection PubMed
description BACKGROUND: Combination therapy with prednisone or etanercept may induce earlier and/or more improvement in disease activity in Disease Modifying Anti Rheumatic Drug (DMARD) naïve non-systemic Juvenile Idiopathic Arthritis (JIA) patients. Here we present three months clinical outcome of initial treatments of the BeSt-for-Kids study. METHODS: Included patients were randomized to either: 1. initial DMARD-monotherapy (sulfasalazine (SSZ) or methotrexate (MTX)), 2. Initial MTX / prednisolone-bridging, 3. Initial combination MTX/etanercept. Percentage inactive disease, adjusted (a) ACR Pedi30, 50 and 70 and JADAS after 6 and 12 weeks of treatment (intention to treat analysis) and side effects are reported. RESULTS: 94 patients (67% girls, 32 (arm 1), 32 (arm 2) and 30 (arm 3) with median (InterQuartileRange) age of 9.1 (4.7-12.9) years were included. 38% were ANA positive, 10 had oligo-articular disease, 68 polyarticular JIA and 16 psoriatic arthritis. Baseline median (IQR) ACRpedi-scores: VAS physician 49 (40-58) mm, VAS patient 54 (37-70) mm, ESR 6.5 (2-14.8)mm/hr, active joint count 8 (5-12), limited joint count 3 (1-5), CHAQ score 0.88 (0.63-1.5). In arm 1, 17 started with MTX, 15 with SSZ. After 3 months, aACR Pedi 50 was reached by 10/32 (31%), 12/32(38%) and 16/30 (53%) (p = 0.19) and aACR Pedi 70 was reached by 8/32 (25%), 6/32(19%) and 14/30(47%) in arms 1-3 (p = 0.04). Toxicity was similar. Few serious adverse events were reported. CONCLUSION: After 3 months of treatment in a randomized trial, patients with recent-onset JIA achieved significantly more clinical improvement (aACRPedi70) on initial combination therapy with MTX / etanercept than on initial MTX or SSZ monotherapy. TRIAL REGISTRATION: NTR1574. Registered 3 December 2008.
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spelling pubmed-52947382017-02-09 A comparison of three treatment strategies in recent onset non-systemic Juvenile Idiopathic Arthritis: initial 3-months results of the BeSt for Kids-study Hissink Muller, P. C. E. Brinkman, D. M. C. Schonenberg, D. Koopman-Keemink, Y. Brederije, I. C. J. Bekkering, W. P. Kuijpers, T. W. van Rossum, M. A. J. van Suijlekom-Smit, L. W. A. van den Berg, J. M. Allaart, C. F. ten Cate, R. Pediatr Rheumatol Online J Short Report BACKGROUND: Combination therapy with prednisone or etanercept may induce earlier and/or more improvement in disease activity in Disease Modifying Anti Rheumatic Drug (DMARD) naïve non-systemic Juvenile Idiopathic Arthritis (JIA) patients. Here we present three months clinical outcome of initial treatments of the BeSt-for-Kids study. METHODS: Included patients were randomized to either: 1. initial DMARD-monotherapy (sulfasalazine (SSZ) or methotrexate (MTX)), 2. Initial MTX / prednisolone-bridging, 3. Initial combination MTX/etanercept. Percentage inactive disease, adjusted (a) ACR Pedi30, 50 and 70 and JADAS after 6 and 12 weeks of treatment (intention to treat analysis) and side effects are reported. RESULTS: 94 patients (67% girls, 32 (arm 1), 32 (arm 2) and 30 (arm 3) with median (InterQuartileRange) age of 9.1 (4.7-12.9) years were included. 38% were ANA positive, 10 had oligo-articular disease, 68 polyarticular JIA and 16 psoriatic arthritis. Baseline median (IQR) ACRpedi-scores: VAS physician 49 (40-58) mm, VAS patient 54 (37-70) mm, ESR 6.5 (2-14.8)mm/hr, active joint count 8 (5-12), limited joint count 3 (1-5), CHAQ score 0.88 (0.63-1.5). In arm 1, 17 started with MTX, 15 with SSZ. After 3 months, aACR Pedi 50 was reached by 10/32 (31%), 12/32(38%) and 16/30 (53%) (p = 0.19) and aACR Pedi 70 was reached by 8/32 (25%), 6/32(19%) and 14/30(47%) in arms 1-3 (p = 0.04). Toxicity was similar. Few serious adverse events were reported. CONCLUSION: After 3 months of treatment in a randomized trial, patients with recent-onset JIA achieved significantly more clinical improvement (aACRPedi70) on initial combination therapy with MTX / etanercept than on initial MTX or SSZ monotherapy. TRIAL REGISTRATION: NTR1574. Registered 3 December 2008. BioMed Central 2017-02-06 /pmc/articles/PMC5294738/ /pubmed/28166785 http://dx.doi.org/10.1186/s12969-017-0138-4 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Short Report
Hissink Muller, P. C. E.
Brinkman, D. M. C.
Schonenberg, D.
Koopman-Keemink, Y.
Brederije, I. C. J.
Bekkering, W. P.
Kuijpers, T. W.
van Rossum, M. A. J.
van Suijlekom-Smit, L. W. A.
van den Berg, J. M.
Allaart, C. F.
ten Cate, R.
A comparison of three treatment strategies in recent onset non-systemic Juvenile Idiopathic Arthritis: initial 3-months results of the BeSt for Kids-study
title A comparison of three treatment strategies in recent onset non-systemic Juvenile Idiopathic Arthritis: initial 3-months results of the BeSt for Kids-study
title_full A comparison of three treatment strategies in recent onset non-systemic Juvenile Idiopathic Arthritis: initial 3-months results of the BeSt for Kids-study
title_fullStr A comparison of three treatment strategies in recent onset non-systemic Juvenile Idiopathic Arthritis: initial 3-months results of the BeSt for Kids-study
title_full_unstemmed A comparison of three treatment strategies in recent onset non-systemic Juvenile Idiopathic Arthritis: initial 3-months results of the BeSt for Kids-study
title_short A comparison of three treatment strategies in recent onset non-systemic Juvenile Idiopathic Arthritis: initial 3-months results of the BeSt for Kids-study
title_sort comparison of three treatment strategies in recent onset non-systemic juvenile idiopathic arthritis: initial 3-months results of the best for kids-study
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5294738/
https://www.ncbi.nlm.nih.gov/pubmed/28166785
http://dx.doi.org/10.1186/s12969-017-0138-4
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