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Abstract Number: 2735

Regional Variability of Minimal Disease Activity Among Psoriatic Arthritis Patients in Canada: An Analysis from a Prospective, Observational Registry

Proton Rahman1, Dalton Sholter2, Michelle Teo3, Regan Arendse4, Denis Choquette5, Mary Bell6, Angeliki Karellis7, Eliofotisti Psaradellis8, Francois Nantel9, Allen J Lehman10, Cathy Tkaczyk11, Karina Maslova10 and Brendan Osborne11, 1Rheumatology, St Claires Mercy Hospital, St Johns, NF, Canada, 2University of Alberta, Edmonton, AB, Canada, 3Balfour Medical Clinic, Penticton, BC, Canada, 4University of Saskatchewan, Saskatoon, ON, Canada, 5Rheumatology, Institut de Recherche en Rhumatologie de Montréal (IRRM), Montréal, QC, Canada, 6University of Toronto, Toronto, ON, Canada, 7Department of Surgery, McGill University, Montreal, QC, Canada, 8JSS Medical Research, Montreal, QC, Canada, 919 Green belt Dr, Janssen Inc., Toronto, ON, Canada, 10Janssen Inc., Toronto, ON, Canada, 11Medical Affairs, Janssen Inc., Toronto, ON, Canada

Meeting: 2016 ACR/ARHP Annual Meeting

Date of first publication: September 28, 2016

Keywords: Biologics, psoriatic arthritis and treatment

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Session Information

Date: Tuesday, November 15, 2016

Title: Spondylarthropathies and Psoriatic Arthritis – Clinical Aspects and Treatment - Poster III

Session Type: ACR Poster Session C

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

Background/Purpose:  Although remission remains the ultimate treatment goal in psoriatic arthritis (PsA) management, minimal disease activity (MDA), which encompasses remission and low disease activity, constitutes an attainable goal. Given that variability may exist across Canadian provinces both in regard to patient characteristics at anti-TNF initiation and in PsA management in routine clinical practice, the aim of the current analysis was to assess the regional variability in MDA achievement among Canadian patients initiating treatment with anti-TNF in real-world.

Methods:  BioTRAC is an ongoing, prospective registry of patients initiating treatment for PsA, ankylosing spondylitis, or rheumatoid arthritis with infliximab or golimumab. PsA patients who were enrolled during 2002-2015, had ≥1 follow-up assessment and MDA data available were included. MDA was defined as the fulfillment of ≥5 of the following criteria: TJC28≤1, SJC28≤1, PASI≤1 or BSA≤3, Pain (VAS) ≤15mm, PtGA (VAS) ≤20 mm, HAQ≤0.5, tender entheseal points ≤1. Provinces were regrouped by region: Western (Alberta, British Columbia, and Saskatchewan), Ontario, Quebec and Maritimes. Continuous and categorical variables were assessed with the non-parametric Kruskal-Wallis test and the Chi-square test, respectively.

Results:  223 PsA patients (51.4% male) were included in the analysis. The mean (SD) age was 49.8 (11.1) years, and disease duration was 5.8 (6.6) years. The proportion of patients in BioTRAC by Canadian region was 6.4%, 50.5%, 29.7% and 13.4% for the Western region, Ontario, Quebec and the Maritime region, respectively. The mean (SD) disease duration was significantly different among regions with [Western: 5.00 (5.48), Ontario: 5.76 (6.51), Quebec: 7.47 (7.60), Maritimes: 1.8 (1.9) years; p=0.027]. Baseline disease parameters for TJC, SJC, pain, PtGA, and HAQ-DI were statistically comparable at baseline among Canadian regions. However, significant between-group differences were observed at baseline for mean (SD) enthesitis count [Western: 7.00 (4.21), Ontario: 1.14 (2.90), Quebec: 1.33 (2.14), Maritime: 3.16 (3.88); p<0.001], and PASI [Western: 4.76 (4.98), Ontario: 3.71 (5.51), Quebec: 1.45 (2.94), Maritime: 1.18 (1.32); p=0.001]. At baseline, 6 and 12 months of treatment, 11.7%, 43.5%, and 44.8% of patients achieved MDA, respectively. A statistical trend was observed between regions with respect to MDA achievement at 6 or 12 months of treatment (p=0.127). Ontario and Quebec patients had the highest MDA rates (55.9% and 52.1%), while 44.4% and 18.2% of patients in Maritime and Western provinces presented with MDA, respectively.

Conclusion:  MDA achievement rates vary across Canada which could be attributed to differences in the patient profile and in disease duration at anti-TNF initiation.


Disclosure: P. Rahman, Janssen Inc., 5; D. Sholter, Janssen Inc., 5; M. Teo, None; R. Arendse, None; D. Choquette, None; M. Bell, Paid Consultant of Janssen Inc., Canada, 5; A. Karellis, Employee of JSS Research, 3; E. Psaradellis, employee of JSS Medical Research, 3; F. Nantel, Employee of Janssen Inc., 3; A. J. Lehman, Employee of Janssen Inc., 3; C. Tkaczyk, Employee of Janssen Inc., 3; K. Maslova, Employee of Janssen Inc., 3; B. Osborne, Employee of Janssen Inc., 3.

To cite this abstract in AMA style:

Rahman P, Sholter D, Teo M, Arendse R, Choquette D, Bell M, Karellis A, Psaradellis E, Nantel F, Lehman AJ, Tkaczyk C, Maslova K, Osborne B. Regional Variability of Minimal Disease Activity Among Psoriatic Arthritis Patients in Canada: An Analysis from a Prospective, Observational Registry [abstract]. Arthritis Rheumatol. 2016; 68 (suppl 10). https://acrabstracts.org/abstract/regional-variability-of-minimal-disease-activity-among-psoriatic-arthritis-patients-in-canada-an-analysis-from-a-prospective-observational-registry/. Accessed .
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