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Background Patients with RA who are at a higher risk for progressive and destructive arthritis could be identified using anti-cyclic citrullinated peptide (anti-CCP) levels. 1 Treatment guidelines recommend the use of non-biologic DMARDs as initial treatment in RA; but, if warranted, biologic (b)DMARDs could be considered in early treatment of RA. 2 Real-world data describing treatment patterns based on anti-CCP designations are limited. Objectives This study evaluated treatment patterns of patients with RA who are anti-CCP positive (+) or negative (–). Methods This retrospective study was based on electronic medical record (EMR) data with a supplemental chart review from a large integrated delivery system. Patients newly diagnosed with RA (International Classification of Diseases, Ninth Revision, Clinical Modification diagnosis code 714.0x) were identified between 1 January 2009 and 31 December 2014. The first RA diagnosis date was designated as the index date. Patients were required to have 12 months of continuous activity in the EMR (6 months pre- and 6 months post-index). Based on the baseline anti-CCP test results, patients were categorized as anti-CCP+ (≥7.0 U) or anti-CCP– ( Results Overall, 217 anti-CCP+ and 191 anti-CCP– patients with RA were included in this study. A higher proportion of anti-CCP+ (153, 70.5%) than anti-CCP– patients (44, 23.0%; p Conclusions After diagnosis of RA, patients who are anti-CCP+ were more likely to start therapy, indicating that physicians were more aggressive in treating this cohort. Patients were treated according to guidelines with non-biologic DMARDs, predominantly MTX. Patterns of treatment change differed between the cohorts; however, treatment response was similar with a complete response rate of 20%. References Singh JA, et al. Arthritis Rheumatol 2016;68:1–26. Niewold TB, et al. QJM 2007;100:193–201. Disclosure of Interest K. Price Employee of: Bristol-Myers Squibb, Y. Doleh Employee of: Bristol-Myers Squibb, M. Eaddy Consultant for: Xcenda, A. Ogbonnaya Employee of: Xcenda, H.-C. Shih Employee of: Xcenda, H. Ahmad Shareholder of: Bristol-Myers Squibb, Employee of: Bristol-Myers Squibb, L. Lamerato Grant/research support from: Centers for Disease Control, National Cancer Institute, Policy Analysis, Inc, Outcomes Research Solutions, Xcenda, eMAXHealth, Merck Pharmaceuticals, Pfizer Pharmaceuticals, Reagan Udall Foundation, AstraZeneca, Employee of: Henry Ford Health System, University of Michigan-Dearborn, A. Szymialis Shareholder of: Bristol-Myers Squibb, Employee of: Bristol-Myers Squibb |
