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Abstract Number: 1205

Real-World Remission Outcomes in the First Year Following RA Diagnosis Vary Considerably with the Disease Activity Index Used and a Sizable Proportion Have Persistent Active Disease Across All Measures: Results from the Canadian Early Arthritis Cohort (CATCH)

Orit Schieir1, Susan J. Bartlett 2, Marie-France Valois 3, Louis Bessette 4, Gilles Boire 5, Glen Hazlewood 6, Carol Hitchon 7, Edward Keystone 8, Janet Pope 9, Carter Thorne 10, Diane Tin 11, Vivian Bykerk 12 and Canadian Early Arthritis Cohort (CATCH) Investigators 13, 1University of Toronto, Montreal, Canada, 2McGill University, Montreal, QC, Canada, 3McGill University, Montreal, Canada, 4Laval University, Quebec City, QC, Canada, 5Sherbrooke University, Sherbrooke, QC, Canada, 6University of Calgary, Calgary, Canada, 7University of Manitoba, Winnipeg, Canada, 8Mount Sinai Hospital and University of Toronto, Toronto, ON, Canada, 9Western University, London, ON, Canada, 10Southlake Regional Health Centre, Newmarket, ON, Canada, 11Southlake Regional Health Centre, Newmarket, Canada, 12Hospital for Special Surgery, New York City, NY, 13Canadian Early Arthritis Cohort (CATCH) Study, Toronto, Canada

Meeting: 2019 ACR/ARP Annual Meeting

Keywords: Early Rheumatoid Arthritis, remission and outcome measures

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Session Information

Date: Monday, November 11, 2019

Title: Measures Of Healthcare Quality Poster II: Improving Care

Session Type: Poster Session (Monday)

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

Background/Purpose: Early RA diagnosis and initiation of DMARDs following a treat-to -target approach is recommended to optimize remission outcomes. Several RA disease activity indices are commonly used in research and practice. The choice of index however, may impact treatment decisions and quality improvement (QI) program evaluations. Study objectives were to: 1) compare remission outcomes in the first year across 4 commonly used clinical disease activity indices; 2) estimate changes in remission over time across indices coinciding with release of RA best practice recommendations, and 3) identify predictors of persistent active disease across all measures.

Methods: Data were from patients with early RA (symptoms < 1 year, 100% Met ACR/EULAR RA criteria) enrolled in a prospective national ERA cohort study between Jan- 2007 and Mar-2018.  Study participants had active disease at enrollment, were treated with DMARDs, and completed clinical evaluations, laboratory assessments and patient-reported outcomes every 3-months for the first 12-months of follow up. T-tests and chi-squared tests were used to compare patient characteristics, early treatment strategies, and remission outcomes using 4 commonly used clinical indices (DAS28< 2.6 OR DAS28CRP < 2.5, CDAI ≤ 2.8, SDAI≤ 3.3, and ACR/EULAR Boolean remission – SJC28, TJC28, CRP, PGA all ≦ 1). Logistic regression was used to identify predictors of persistent active disease across all measures by 12-months among baseline sociodemographic, RA clinical characteristics and patient-reported outcomes.

Results: Among 1202 adults eligible for this analysis, 877 (73%) were women, mean (sd) age was 55 (14), average disease activity was high across measures (DAS28 5.1 (1.4); CDAI 27 (14); SDAI 29 (15)) and majority (98%) were treated with csDMARDs +/- MTX. Remission by 12-months varied considerably across indices ranging from 33% to 62%, though improvement in remission before and after implementation of best practice recommendations was similar across all indices (~+15%)  (Figure 1).  378 (31%) did not achieve remission across all indices. In adjusted logistic regression models, persistent active disease across indices was associated with baseline older age, female sex, longer symptom duration, positive serology, obesity, tender joints and higher pain (Table 1). In stratified analyses by sex,  persistent active disease was more strongly associated with obesity and more tender joints in women, and positive serology and smoking in men.

Conclusion: The choice of index had a sizable impact on remission classification with important implications for decision-making surrounding treatment intensification in clinical practice.  However all indices showed similar levels of improvement in remission before and after implementation of best practice recommendations suggesting that choice of index may be less important when evaluating QI programs. In the interim, in the absence of a single  “best measure” that also takes in to account the patient’s perspective, study results looking across measures point to unmet needs for achieving remission in approximately 1 in 3 ERA patients.

Figure 1 Prevalence and Improvement in Remission Outcomes by 12-Months Across 4 Commonly used Clinical Remission Indices


Disclosure: O. Schieir, None; S. Bartlett, Abbie, 2, Abbvie, 2, 5, Bayer, 5, International Society of QOL Research, 6, Janssen, 5, 8, Lilly, 5, Merck, 5, 8, Novartis, 5, 8, Pfizer, 5, Pfizer Inc, 8, PROMIS International, 6, UCB, 5, 8; M. Valois, None; L. Bessette, AbbVie, 2, 5, 8, Abbvie, 2, 5, 8, Amgen, 2, 5, 8, Amgen, BMS, Janssen, Roche, UCB Pharma, AbbVie Inc, Pfizer, Merck, Celgene, Sanofi, Eli Lilly, and Novartis., 2, 5, 8, BMS, 2, 5, 8, Bristol-Myers Squibb, 2, 5, 8, Bristol-Myers-Squibb, 2, 5, 8, Celgene, 2, 5, 8, Eli Lilly, 2, 5, 8, Eli Lilly and Company, 2, 5, 8, Janssen, 2, 5, 8, Lilly, 2, 5, 8, Merck, 2, 5, 8, Novartis, 2, 5, 8, Pfizer, 2, 5, 8, Pfizer Inc, 2, 5, Roche, 2, 5, 8, Sanofi, 2, 5, 8, UCB, 2, 5, 8, UCB Pharma, 2, 5; G. Boire, Abbvie, 2, Amgen, 2, 5, BMS, 2, 5, 8, Bristol-Myers Squibb, 2, 5, 8, Celgene, 5, Eli Lilly, 2, 5, Lilly, 2, 5, Merck, 2, 8, Novartis, 2, Pfizer, 2, 5, 8; G. Hazlewood, None; C. Hitchon, Pfizer, 2, UCB, 2, UCB Canada, 2; E. Keystone, Abbvie, 2, 5, 8, Amgen, 2, 5, 8, AstraZeneca, 5, Astra-Zeneca, 5, Biotest, 5, BMS, 2, 5, 8, Celltrion, 5, Crescendo, 5, Crescendo Bioscience, 5, F. Hoffmann-La Roche Inc, 2, 5, 8, Genentech, 5, Genentech Inc., 5, Genzyme, 5, Gilead, 2, 5, Gilead Sciences, Inc., 5, Janssen, 2, 5, 8, Lilly, 2, 5, 8, Merck, 5, 8, Pfizer, 2, 5, 8, Pfizer Pharmaceuticals, 2, 5, 8, Roche, 2, 5, 8, Sandoz, 5, Sanofi, 2, 5, 8, Sanofi-Aventis, 2, 8, UCB, 5, 8; J. Pope, AbbVie, 5, Abbvie, 5, Actelion, 5, Actellion, 5, Amgen, 2, 5, AstraZeneca, 2, Astra-Zeneca, 2, Bayer, 2, 5, BMS, 2, 5, Eicos Sciences, 5, Eli Lilly & Company, 5, Eli Lilly and Company, 5, EMERALD, 5, Emerald, 5, Genzyme, 5, Janssen, 5, Lilly, 5, Merck, 2, 5, Novartis, 5, Pfizer, 2, 5, Roche, 2, 5, Sandoz, 5, Sanofi, 5, Seattle Genetics, 2, UCB, 2, 5, 8; C. Thorne, Abbvie, 2, 5, Amgen, 2, 5, CaREBiodam, 2, Celgene, 2, 5, Centocor, 5, Janssen, 5, Lilly, 5, Medexus/Medac, 5, 8, Merck, 5, Novartis, 2, 5, Pfizer, 2, 5, Sandoz, 5, Sanofi, 5; D. Tin, None; V. Bykerk, AbbVie, 5, Amgen, 1, 2, 3, 5, 8, Brainstorm Therapeutics, 1, 2, 3, 5, 8, Bristol-Myers Squibb, 5, Genentech, 5, Gilead, 5, NIH, 2, Pfizer, 1, 2, 3, 5, 8, Regeneron, 5, Regeneron Pharmaceuticals, Inc, 5, Sanofi, 5, Sanofi/Genzyme-Regeneron, 5, Sanofi-Genzyme/Regeneron, 1, 2, 3, 5, 8, Scipher, 1, 2, 3, 5, 8, The Cedar Hill Foundation, 9, UCB, 1, 2, 3, 5, 8, UCB Pharma, 5; C. (CATCH) Investigators, Amgen, 2, Pfizer Canada, 2, AbbVie Corporation, 2, Medexus Inc., 2, Eli Lilly Canada, 2, Merck Canada, 2, Sandoz Canada Biopharmaceuticals, 2.

To cite this abstract in AMA style:

Schieir O, Bartlett S, Valois M, Bessette L, Boire G, Hazlewood G, Hitchon C, Keystone E, Pope J, Thorne C, Tin D, Bykerk V, (CATCH) Investigators C. Real-World Remission Outcomes in the First Year Following RA Diagnosis Vary Considerably with the Disease Activity Index Used and a Sizable Proportion Have Persistent Active Disease Across All Measures: Results from the Canadian Early Arthritis Cohort (CATCH) [abstract]. Arthritis Rheumatol. 2019; 71 (suppl 10). https://acrabstracts.org/abstract/real-world-remission-outcomes-in-the-first-year-following-ra-diagnosis-vary-considerably-with-the-disease-activity-index-used-and-a-sizable-proportion-have-persistent-active-disease-across-all-measure/. Accessed .
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