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Abstract Number: 1831

Predictors of Response, Adverse Events and Treatment Retention in Psoriatic Arthritis Patients Treated with Golimumab in a Prospective, Observational Registry

Proton Rahman1, Isabelle Fortin2, Regan Arendse3, Derek Haaland4, Arthur Karasik5, Maqbool Sheriff6, Emmanouil Rampakakis7, Meagan Rachich8, Francois Nantel9, Allen Lehman8 and Odalis Asin-Milan8, 1Department of Medicine, Eastern Health and Memorial University of Newfoundland, St John's, NL, Canada, 2CREQ, Rimouski, QC, Canada, 3University of Saskatchewan, Saskatoon, SK, Canada, 4McMaster University, Hamilton, Ontario and The Waterside Clinic, Oro Medonte, ON, Canada, 5Arthur Karasik Medicine Professional Corporation, Toronto, ON, Canada, 6Nanaimo Regional Hospital, Nanaimo, BC, Canada, 7JSS Medical Research, Montréal, QC, Canada, 8Janssen Inc., Toronto, ON, Canada, 9., Montréal, QC, Canada

Meeting: ACR Convergence 2021

Keywords: Psoriatic arthritis, registry

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Session Information

Date: Tuesday, November 9, 2021

Title: Spondyloarthritis Including PsA – Treatment Poster III: Psoriatic Arthritis II (1801–1835)

Session Type: Poster Session D

Session Time: 8:30AM-10:30AM

Background/Purpose: The Biologic Treatment Registry Across Canada (BioTRAC) was a prospective, observational registry that enrolled psoriatic arthritis (PsA) patients treated with subcutaneous golimumab (GLM) between 2010 and 2017.

Methods: Patient visits occurred at baseline and every 6 months thereafter. Multivariate logistic regression was used to identify independent predictors of achieving specific efficacy and safety endpoints and included the following covariates: age, gender, disease duration, enrolment period, concomitant medication, smoking and employment.

Results: A total of 281 patients were enrolled and followed for a mean duration of 1.9 years. The proportion of male gender was 46.3% and the mean disease duration at baseline was 6.1 years.

MDA was more likely to be achieved with lower baseline DAS28-CRP [OR (95% CI): 0.62 (0.45–0.84); p=0.002] and in patients who were employed [2.64 (1.22–5.71); p=0.014]. VLDA was more likely to be achieved with lower age [OR (95% CI): 0.96 (0.94–0.99); p=0.005], lower baseline DAS28-CRP [0.63 (0.44–0.89); p=0.009] and in patients who were employed [6.45 (2.30–18.27); p< 0.001], whereas VLDA was less likely to be achieved in patients who smoked [0.30 (0.10–0.92); p=0.035].

DAPSA LDA was more likely to be achieved with lower baseline DAPSA [OR (95% CI): 0.96 (0.94–0.98); p< 0.001]. DAPSA remission was more likely to be achieved with lower age [OR (95% CI): 0.98 (0.95–1.00); p=0.048] and lower baseline DAPSA [0.98 (0.96–1.00); p=0.043], while less likely to be achieved with later enrolment [2016-2017 vs. 2010–2012: 0.30 (0.11–0.78); p=0.014] and in patients who smoked [0.37 (0.15–0.93); p=0.035]. HAQ < 0.5 was more likely to be achieved in male vs. female gender [OR (95%): 2.03 (1.08–3.83); p=0.028] and in patients with lower baseline HAQ scores [0.19 (0.11–0.34); p< 0.001].

AEs were more likely to occur with baseline concomitant DMARD [1.97 (1.07–3.63); p=0.030] or NSAID use [1.88 (1.05–3.37); p=0.033], yet less likely in male vs. female [0.54 (0.30–0.98); p=0.043]. SAEs were more likely to occur with older age [1.04 (1.00–1.07); p=0.041], and less likely in patients enrolled later [2013–2015 vs. 2010–2012: 0.05 (0.01–0.18); p< 0.001 and 2016–2017 vs. 2010–2012: 0.03 (0.01–0.14); p< 0.001]. Being employed at baseline was a significant positive predictor of GLM retention [0.61 (0.38–0.97); p=0.035].

Conclusion: In PsA patients treated with golimumab, young age, employment and lower disease activity at baseline were associated with better treatment outcomes.


Disclosures: P. Rahman, Janssen, 2, 5, 6, Novartis, 2, 5, 6, AbbVie, 2, 6, Amgen, 2, 6, Bristol Myers Squibb, 2, 6, Celgene, 2, 6, Eli Lilly, 2, 6, Pfizer, 2, 6, UCB, 2, 6, Merck, 2, 6; I. Fortin, Janssen Inc., 6; R. Arendse, None; D. Haaland, AbbVie, 2, 5, 6, Adiga Life Sciences, 5, Amgen, 2, 5, 6, Bristol-Myers Squibb, 2, 5, 6, Can-Fite BioPharma, 5, Celgene, 5, Eli Lilly, 5, 6, Gilead, 5, GlaxoSmithKline, 2, 5, 6, Janssen, 2, 5, 6, Novartis, 2, 5, 6, Pfizer, 2, 5, 6, Regeneron, 5, Sanofi, 2, 5, 6, UCB, 2, 5, 6, AstraZeneca, 6, Merck, 6, Takeda, 2, 6, Roche, 2, 6; A. Karasik, Janssen Inc., 6, Janssen Inc., 2, 6; M. Sheriff, None; E. Rampakakis, None; M. Rachich, Janssen, 3, 11; F. Nantel, None; A. Lehman, Janssen Inc., 3; O. Asin-Milan, Janssen, 3.

To cite this abstract in AMA style:

Rahman P, Fortin I, Arendse R, Haaland D, Karasik A, Sheriff M, Rampakakis E, Rachich M, Nantel F, Lehman A, Asin-Milan O. Predictors of Response, Adverse Events and Treatment Retention in Psoriatic Arthritis Patients Treated with Golimumab in a Prospective, Observational Registry [abstract]. Arthritis Rheumatol. 2021; 73 (suppl 9). https://acrabstracts.org/abstract/predictors-of-response-adverse-events-and-treatment-retention-in-psoriatic-arthritis-patients-treated-with-golimumab-in-a-prospective-observational-registry/. Accessed .
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