FRI0396 CHARACTERIZATION OF PATIENTS WITH INFLAMMATORY BOWEL DISEASE IN THE ANKYLOSING SPONDYLITIS COHORT PRIOR AND DURING ADALIMUMAB TREATMENT: DATA FROM A LARGE GERMAN NON-INTERVENTIONAL STUDY. (June 2019)

• Record Type: Journal Article
• Authors: Köhm, Michaela; Schmalzing, Marc; Schwaneck, Eva Christina; Gnann, Holger; Tony, Hans-Peter; Greger, Gerd; Boas, Annika; Burkhardt, Harald; Behrens, Frank
• Is Part Of: Annals of the rheumatic diseases. Volume 78(2019)Supplement 2
• Page Start: 883
• Page End: 883
• Publication Date: 2019-06
• Subjects: Rheumatism -- Periodicals; 616.723005
• DOI: 10.1136/annrheumdis-2019-eular.5464
• Languages: English
• ISSNs: 0003-4967

Abstract

Abstract : Background: Spondylarthritidies (SpA) are characterized by different disease manifestations such as arthritis, enthesitis, dactylitis and associated to concomitant diseases like Inflammatory bowel diseases (IBD) including ulcerative colitis (UC) and crohn's disease (CD). IBD might have a specific role to SpA due to common pathophysiological pathways. Characteristics of the rheumatic disease and response to treatment may differ within the phenotypic manifestation and with and without associated diseases. Adalimumab (ADA) is a monoclonal antibody inhibiting TNF alpha which has demonstrated efficacy in both, nraxSpA and ankylosing spondylitis (AS) as well as for UC and CD. Objectives: To evaluate patient baseline characteristics prior to and treatment response on different disease manifestations in a cohort of AS patients with IBD compared to an AS without IBD during ADA treatment. Methods: Data from a large German multicenter prospective observational non-interventional study (n=3.756) of patients with active AS who initiated ADA therapy during routine clinical care were analyzed with focus on specific patient groups: (1) patients with AS and IBD at baseline (n=166) and (2) patients with AS without IBD at baseline (n= 3.590). Patient characteristics and data of efficacy on different disease manifestations and prevalence of concomitant IBD over 24 months were analyzed. Results: Of 3.756 patients in the main analysis set, 166 (4.4%) were identified to suffer from concomitant IBD at baseline. Baseline characteristics showed differences in gender distribution, proportion of patients with enthesitis, psoriasis and uveitis showing a higher proportion of each for the IBD group (Table). After 24 months of ADA treatment, both groups had similar decreases for BASDAI, BASMI, BASFI and dactylitis improvement. The IBD group had a fast decrease in BASDAI at M6 to its maximum improvement (delta of 1.9) which was kept stable until M24. For clearance of enthesitis, ADA had its largest therapeutic effect at M6 in the IBD group (clearance in 15.3% of the patients) while the AS without IBD group had the largest decrease of 10.2% at month 24. Resolving of uveitis with ADA therapy was more often seen in the IBD group compared to the AS without IBD (delta of 6% at M12 compared to delta of 2.6% at M12, respectively). The prevalence of IBD in AS in patients treated with ADA changed from 4.4% at baseline to 1.9% at M24. Conclusion: Within the cohort of AS, patients' characteristics of manifestations are associated to different treatment responses: Patients identified to have IBD at baseline respond better for resolving of enthesitis and show a faster response in BASDAI compared to the group without IBD. Overall a significant reduction in the prevalence of clinically relevant IBD was seen earliest at month 3 after ADA initiation. Acknowledgement: This study was sponsored by AbbVie Deutschland GmbH & Co KG. AbbVie contributed to the study design, data analysis, and in the writing, revision, and approval of the abstract. Medical writing services were provided by CIRI, Frankfurt am Main, Germany, under contract with AbbVie for medical writing services. Disclosure of Interests: Michaela Köhm Grant/research support from: BMS, Pfizer, Janssen, Consultant for: BMS, Pfizer, Janssen; AbbVie, Speakers bureau: BMS, Pfizer, Janssen, AbbVie, Marc Schmalzing Grant/research support from: Pfizer, Chugai, MSD, Janssen-Cilag, BMS, Celgene, UCB, Consultant for: Abbvie, Chugai, Genzyme, Hexal/Sandoz, MSD, Novartis, Roche, Sanofi Pasteur, Speakers bureau: Actelion, Baxalta/Shire, BMS, Celgene, Chugai, Janssen-Cilag, MSD, Novartis, Pfizer, Roche, UCB, Eva Christina Schwaneck: None declared, Holger Gnann: None declared, Hans-Peter Tony Consultant for: Eli Lilly and Company, Speakers bureau: Eli Lilly and Company, Gerd Greger : None declared, Annika Boas Shareholder of: AbbVie, Harald Burkhardt Grant/research support from: BMS, Pfizer, Janssen, Consultant for: AbbVie, BMS, Pfizer, Janssen, Roche, Chugai, Speakers bureau: AbbVie, BMS, Pfizer, Janssen, Roche, Chugai, Frank Behrens Grant/research support from: AbbVie, Pfizer, Roche, Chugai, Prophylix, Bioline, Novartis, Consultant for: AbbVie, Pfizer, Roche, Chugai, UCB, Bristol-Myers Squibb, Celgene, MSD, Novartis, Biotest, Janssen, Genzyme, Eli Lilly, Speakers bureau: Ad board: AbbVie, Pfizer, Roche, Chugai, UCB, Bristol-Myers Squibb, Celgene, Novartis, Biotest, Janssen, Genzyme, Eli Lilly