Patient disposition of responders to adalimumab+methotrexate at year 2 (OLE entry) from the primary study who were in methotrexate non-use or use groups.

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Presentation transcript:

Patient disposition of responders to adalimumab+methotrexate at year 2 (OLE entry) from the primary study who were in methotrexate non-use or use groups during the OLE. AE, adverse event; ELISA, enzyme-linked immunosorbent assay; LDA, low disease activity; MTX, methotrexate; OLE, open-label extension. *Patients entering the OLE received open-label adalimumab 40 mg every other week and could receive MTX at the investigator’s discretion. †In the MTX non-use group, eight patients discontinued because of AEs (stage III malignant melanoma (n=1); squamous cell carcinoma of the tongue (n=1); mycobacterium marinum skin infection (n=1); mycobacterium avium complex infection (n=1); cholecystitis and gastric adenocarcinoma (n=1); alternations of cardiac rhythm (n=1); psoriasis-like eczema and severe bone marrow puncture due to lymphocytosis (n=1) and anaemia, fever and aortic valve endocarditis (n=1). ‡In the MTX use group, five patients discontinued because of AEs (cognitive impairment and a positive ELISA test (n=1); neutropenia (n=1); dyspnoea on exertion (n=1); nasal ulcer (n=1) and atrial fibrillation, encephalopathia, Gram-negative sepsis, septic shock, multiorgan failure, haemophagocytic syndrome, respiratory insufficiency, melena and Epstein-Barr virus infection (n=1). §Reflects the percentages of year 2 LDA responders who were in MTX non-use or use groups during the OLE and completed OLE year 3 (year 5 of the study). Patient disposition of responders to adalimumab+methotrexate at year 2 (OLE entry) from the primary study who were in methotrexate non-use or use groups during the OLE. AE, adverse event; ELISA, enzyme-linked immunosorbent assay; LDA, low disease activity; MTX, methotrexate; OLE, open-label extension. *Patients entering the OLE received open-label adalimumab 40 mg every other week and could receive MTX at the investigator’s discretion. †In the MTX non-use group, eight patients discontinued because of AEs (stage III malignant melanoma (n=1); squamous cell carcinoma of the tongue (n=1); mycobacterium marinum skin infection (n=1); mycobacterium avium complex infection (n=1); cholecystitis and gastric adenocarcinoma (n=1); alternations of cardiac rhythm (n=1); psoriasis-like eczema and severe bone marrow puncture due to lymphocytosis (n=1) and anaemia, fever and aortic valve endocarditis (n=1). ‡In the MTX use group, five patients discontinued because of AEs (cognitive impairment and a positive ELISA test (n=1); neutropenia (n=1); dyspnoea on exertion (n=1); nasal ulcer (n=1) and atrial fibrillation, encephalopathia, Gram-negative sepsis, septic shock, multiorgan failure, haemophagocytic syndrome, respiratory insufficiency, melena and Epstein-Barr virus infection (n=1). §Reflects the percentages of year 2 LDA responders who were in MTX non-use or use groups during the OLE and completed OLE year 3 (year 5 of the study). Edward C Keystone et al. RMD Open 2018;4:e000637 Copyright © BMJ Publishing Group & EULAR. All rights reserved.