THU0536 Efficacy and Post-Vaccination Antibody Titer Data in Children with Caps Aged 28 Days to 4 Years Treated with Canakinumab

• Published in: Annals of the rheumatic diseases Vol. 74; no. Suppl 2; p. 394
• Main Authors: Uziel, Y., Brogan, P., Hofer, M., Kuemmerle-Deschner, J., Lauwerys, B., Speziale, A., Abrams, K., Leon, K., Wei, X., Laxer, R., Lachmann, H.
• Format: Journal Article
• Language: English
• Published: London BMJ Publishing Group LTD 01.06.2015
• ISSN: 0003-4967; 1468-2060
• DOI: 10.1136/annrheumdis-2015-eular.4434

BackgroundCanakinumab (CAN) has proven efficacy in patients with CAPS aged ≥2 years1. However, patients can require treatment in infancy where CAN has not yet been studied. IL-1 inhibition has not affected antibody production after vaccination in healthy volunteers2, but no data in CAPS patients receiving standard childhood vaccines are available.ObjectivesTo evaluate the efficacy and safety of CAN, including post-vaccination antibody production, in children with CAPS ≤4 yrs of age.MethodsCAN-naïve patients with confirmed CAPS aged 28 days to 4 yrs received open-label CAN dosed 2-12 mg/kg every 4 or 8 weeks for 56 weeks. Efficacy was evaluated by complete response (clinical response and normal CRP) and subsequent relapse. Safety was evaluated by adverse event (AE) reporting and vaccination response evaluated by post-vaccine antibody titers measured at 28 and 57 days post vaccination. Vaccines evaluated included DTP; H. Flu; N. Men.; influenza; Hep B; and Strep. Pneum.ResultsSeventeen patients, 6 less than 24 months old (44 days-5 months), were enrolled. The phenotypic distribution was: FCAS (n=1), MWS (n=12), and NOMID (n=4). All 17 patients achieved a clinical response and 16 achieved a complete response. Seven patients required dose escalation to achieve and/or maintain their responses. The patient who did not achieve a complete response was a 1 yr old with persistently elevated CRP. Of the 16 with a complete response, 4 (2 with MWS and 2 with NOMID) subsequently relapsed, but all regained complete response; 2 (1 MWS; 1 NOMID) with and 2 (1 MWS; 1 NOMID) without dose escalation. No CAPS flares were reported with vaccination and a rise in post-vaccination antibody titers was observed for all vaccines evaluated. The most common type of AE reported was an infection, typically involving the upper respiratory tract. Four patients experienced a serious AE (SAE), with no SAE occurring more than once. No patient discontinued due to an AE.ConclusionsCanakinumab is a highly effective treatment for patients with CAPS aged as young as 44 days old. The safety profile was acceptable and similar to that observed for older patients. Canakinumab appears to have no effect on the ability to produce antibodies against standard childhood non-live vaccines.ReferencesLachmann H, et al. N Engl J Med. 2009;60:2416-25.Chioato A, et al. Clin Vaccine Immunol. 2010;17:1952-1957.Disclosure of InterestY. Uziel Consultant for: Novartis, Speakers bureau: Novartis, P. Brogan Grant/research support from: Institutional grant support to undertake the study described in this abstract, Consultant for: SOBI, Roche, M. Hofer Consultant for: Novartis, J. Kuemmerle-Deschner Grant/research support from: Novartis, Consultant for: Novartis, B. Lauwerys: None declared, A. Speziale Employee of: Novartis, K. Abrams Shareholder of: Novartis, Employee of: Novartis, K. Leon Employee of: Novartis, X. Wei Employee of: Novartis, R. Laxer Grant/research support from: Database funding from Novartis, Consultant for: Participant in Ad Board for Novartis, H. Lachmann Consultant for: Novartis, Speakers bureau: Novartis