Residual Disease Activity in Canadian Patients With Psoriatic Arthritis Treated With Advanced Therapies: Results From a Multiregistry Analysis (UNISON-PsA)

Author:

Gladman Dafna D.ORCID,Chandran VinodORCID,Rosen Cheryl F.ORCID,Rohekar SherryORCID,Boyd TristanORCID,Eder LihiORCID,Rahman ProtonORCID,Dutz JanORCID,Chan Jonathan,Haydey Richard P.,Barac Snezana,Laliberté Marie-ClaudeORCID,Girard Tanya,Fournier Pierre-André,Sutton Mitchell,Pereira Daniel,Chim Tina,Coupal LouisORCID,Choquette DenisORCID

Abstract

ObjectiveAlthough patient outcomes in psoriatic arthritis (PsA) have improved with the advent of advanced therapies, there remains a high unmet need to treat residual disease activity. The objective of the current study was to quantify residual disease activity and burden of disease in Canadian patients with PsA.MethodsThis was a multiregion, observational, retrospective analysis of patient data extracted from the Rhumadata and the International Psoriasis and Arthritis Research Team (IPART) registries, analyzing deidentified data from patients who had initiated advanced therapy for the treatment of PsA between January 2010 and December 2019. The primary endpoint was the proportion of patients failing to achieve minimal disease activity (MDA) within 6 months; secondary endpoints included clinical and patient-reported burden of disease. Descriptive statistics included summaries by region, treatment class, and number of prior advanced therapies.ResultsOne thousand five hundred ninety-six patients were included. The proportions of patients who failed to achieve MDA within 6 months of an advanced therapy were 64.8% in Ontario, 68.3% in Western Canada, 74.8% in Quebec, and 75% in the Atlantic/East region. Failure to achieve MDA was higher among patients receiving an IL-17i compared with a TNFi in all regions except the Atlantic/East. Between 73.2% and 78.6% of patients reported pain at 6 months, and continuing functional impairment varied from 24% in the West to 83.3% in the Atlantic/East.ConclusionThere is substantial burden and unmet need for improved therapies for Canadians with PsA. There is a wide regional variation in outcomes that requires further assessment.

Publisher

The Journal of Rheumatology

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