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Abstract Number: 2452

Clinical and Functional Outcomes in Patients with Polyarticular Juvenile Idiopathic Arthritis Following Treatment with Adalimumab

Daniel J. Kingsbury1, Pierre Quartier2, G Horneff3, Kirsten Minden4, Mary Toth5, Nupun A. Varothai6, Anabela Cardoso7 and Jasmina Kalabic6, 1Randall Children's Hospital at Legacy Emanuel, Portland, OR, 2Hopital Necker-Enfants Malades, Paris, France, 3Asklepios Klinik Sankt Augustin, Sankt Augustin, Germany, 4Kinderklinik der Charite, Otto-Heubner Centrum, Berlin, Germany, 5Akron Children's Hospital, Akron, OH, 6AbbVie, North Chicago, IL, 7AbbVie, Amadora, Portugal

Meeting: 2015 ACR/ARHP Annual Meeting

Date of first publication: September 29, 2015

Keywords: Adalimumab and juvenile idiopathic arthritis (JIA)

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Session Information

Date: Tuesday, November 10, 2015

Title: Pediatric Rheumatology - Clinical and Therapeutic Aspects Posters (ACR): Imaging and Novel Clinical Interventions

Session Type: ACR Poster Session C

Session Time: 9:00AM-11:00AM

Background/Purpose: The Juvenile Arthritis Disease Activity Score (JADAS) is increasingly accepted for defining a treat-to-target strategy in patients (pts) with juvenile idiopathic arthritis (JIA)1 The purpose of this study is to use JADAS to evaluate clinical disease activity/control, with or without functional control, in pts with polyarticular or polyarticular-course  JIA (pJIA), following the initiation of adalimumab (ADA) ± concurrent methotrexate (MTX) treatment. To assess the feasibility of JADAS definition of remission (REM) and minimal disease activity (MDA) as part of a treat-to-target strategy.

Methods: Data for this post hoc analysis originated from M10-444, an open-label study in pJIA pts 2 to <4 yrs old or ≥4 yrs weighing <15 kg with moderately to severely active pJIA, in the US and EU (in the EU pts had to previously fail, have an insufficient response, or intolerance to MTX). Pts received subcutaneous ADA (24 mg/m2 body surface area, up to 20 mg/dose), every other week (wk), for ≥24 wks, or until pts reached 4 yrs and weight ≥15 kg (in the EU, pts could continue for up to 1 additional yr ). Disease activity was determined by JADAS based on C-reactive protein (CRP, normalization from 0-10), for 10 or 27 joints (JADAS10/27); functional impairment was determined by the Disability Index- Childhood Health Assessment questionnaire (DI-CHAQ). At wks 12 and 24, the proportion of pts achieving physician-assessed REM (JADAS≤2) or MDA (JADAS≤3.8), and the proportion of pts who achieved both MDA/REM and DI-CHAQ<0.5, was determined using observed cases.

Results: Out of 32 pts, 25 (78%) had received prior MTX and 27/32 (84%) received concomitant MTX during the study. At baseline, pts had a mean JADAS10 of 18.8, JADAS27 of 19.0, and DI-CHAQ of 1.2. After 12 wks on open-label ADA, improvements were observed in clinical and functional outcomes. At wks 12 and 24, the mean JADAS10 was 6.2 and 5.3; mean JADAS27 was 6.4 and 5.6; mean DI-CHAQ was 0.7 and 0.7, respectively. No pts were in REM/MDA at baseline; however after 12 and 24 wks, a sizeable proportion achieved disease control (table). After 12 and 24 wks of ADA treatment, the proportions of pts achieving both, disease control and DI-CHAQ<0.5 also increased from baseline.

Conclusion: Addition of open-label ADA treatment resulted in clinically important improvements in clinical and functional outcomes in pts with pJIA. JADAS 10 and -27 gave comparable results. JADAS REM and MDA are achievable targets with ADA treatment.

 

Table: Numbers of patients who achieved disease control with/without DI-CHAQ<0.5, n/N (%)

 

JADAS27 Disease control

JADAS27 Disease control + DI-CHAQ<0.5

JADAS10 Disease control

JADAS10 Disease control + DI-CHAQ<0.5

Week

REM

MDA

REM

MDA,

REM

MDA

REM

MDA, 

0

0/31 (0.0)

0/31 (0)

0/30 (0)

0/30 (0)

0/31 (0)

0/31 (0)

0/30 (0)

0/30 (0)

12

12/29 (41.4)

14/29 (48.3)

5/22 (22.7)

5/22 (22.7)

12/29 (41.4)

13/29 (44.8)

5/22 (22.7)

5/22 (22.7)

24

10/28 (35.7)

16/28 (57.1)

2/20 (10)

4/20 (20)

9/28 (32.1)

15/28 (53.6)

2/20 (10)

3/20 (15)

REM: JADAS ≤2; MDA:  JADAS ≤3.8

References:

1. Consolaro et al, Arth & Rheum. 2012.


Disclosure: D. J. Kingsbury, AbbVie, 2; P. Quartier, AbbVie, Novartis, Pfizer, BMS, Chugai-Roche, Medimmune, Servier, and Swedish Orphan Biovitrum., 9; G. Horneff, AbbVie, Pfizer, and Roche, 2,AbbVie, Novartis, Pfizer, and Roche, 8; K. Minden, Pfizer and Abbvie, 2,Pfizer, Abbvie, Roche and Pharm-Allergan, 5; M. Toth, None; N. A. Varothai, AbbVie, 1,AbbVie, 3; A. Cardoso, AbbVie, 9; J. Kalabic, AbbVie, 9.

To cite this abstract in AMA style:

Kingsbury DJ, Quartier P, Horneff G, Minden K, Toth M, Varothai NA, Cardoso A, Kalabic J. Clinical and Functional Outcomes in Patients with Polyarticular Juvenile Idiopathic Arthritis Following Treatment with Adalimumab [abstract]. Arthritis Rheumatol. 2015; 67 (suppl 10). https://acrabstracts.org/abstract/clinical-and-functional-outcomes-in-patients-with-polyarticular-juvenile-idiopathic-arthritis-following-treatment-with-adalimumab/. Accessed .
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