FRI0497 The Interleukin-1 Inhibitor Canakinumab for Familial Mediterranean Fever: Long-Term Beneficial Effect in A Cohort of 14 Patients
| Autor: | K. Laskari, L. Settas, P.P. Sfikakis, Alexandros Garyfallos, D. Karokis, E. Tsitsami, D. Pikazis, George N. Dalekos, G. Skarantavos, Panagiota Boura |
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| Rok vydání: | 2016 |
| Předmět: |
0301 basic medicine
medicine.medical_specialty medicine.drug_class Urinary system Immunology Familial Mediterranean fever 030105 genetics & heredity General Biochemistry Genetics and Molecular Biology 03 medical and health sciences 0302 clinical medicine Rheumatology Refractory Internal medicine medicine Immunology and Allergy Anakinra business.industry medicine.disease Surgery Canakinumab Concomitant Cohort Corticosteroid business 030217 neurology & neurosurgery medicine.drug |
| Zdroj: | Annals of the Rheumatic Diseases. 75:618.3-619 |
| ISSN: | 1468-2060 0003-4967 |
| DOI: | 10.1136/annrheumdis-2016-eular.4205 |
| Popis: | Background Interleukin-1 (IL-1) is a major mediator of the inflammatory cascade in Familial Mediterranean Fever (FMF) and an established therapeutic target (1). Objectives To assess the efficacy and safety of the IL-1 inhibitor Canakinumab in adult and adolescent patients with refractory FMF. Methods Fourteen patients (7 men) with genetically confirmed FMF, fulfilling the Tel Hashomer criteria, aged 38.5 years (median, range 13–70), with median disease duration of 14 years and active disease despite colchicine (n=9) or both colchicine and anakinra (n=5), received Canakinumab 150mg subcutaneously (sc) every 4 (n=7) or 6 (n=2) or 8 weeks (n=5) for a median of 18 months (range 7–53). Canakinumab was given as monotherapy in 8; 6 patients received concomitant treatment with colchicine and/or corticosteroids. Results Eleven out of 14 patients (79%) achieved complete clinical remission (median time 2 months), while normalization of all laboratory parameters associated with inflammation occurred in 92% of patients (median time 3 months). The remaining patients achieved partial responses. Response was maintained until the last visit in all but 4 patients. Reducing the Canakimumab administration interval led to suppression of disease activity in three cases, whereas in another two patients drug administration intervals could be increased without disease exacerbation. The corticosteroid dose was significantly reduced during follow up. The FMF50 score (2) was achieved by 50% and 86% of patients at 1 and 12 months, respectively. Canakinumab was well tolerated; one patient experienced an urinary tract infection and another one a viral gastroenteritis. Conclusions The rapid and sustained response to Canakinumab in the majority of our patients, together with the favorable safety profile, encourages its further use in FMF. References Ter Haar N et al. Ann Rheum Dis. 2013;72(5):678–85. Ozen S et al. Ann Rheum Dis. 2014;73(5):897–901. Disclosure of Interest None declared |
| Databáze: | OpenAIRE |
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