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Longterm beneficial effect of canakinumab in colchicine-resistant familial mediterranean fever

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Autore
Laskari K., Boura P., Dalekos G.N., Garyfallos A., Karokis D., Pikazis D., Settas L., Skarantavos G., Tsitsami E., Sfikakis P.P.
Data
2017
Language
en
DOI
10.3899/jrheum.160518
Soggetto
anakinra
azathioprine
canakinumab
colchicine
corticosteroid derivative
infliximab
methotrexate
methylprednisolone
antiinflammatory agent
canakinumab
colchicine
interleukin 1 receptor blocking agent
monoclonal antibody
adolescent
adult
age distribution
aged
Article
clinical article
clinical examination
controlled study
diarrhea
disease activity
disease duration
disease registry
drug efficacy
drug safety
drug tolerability
drug withdrawal
familial Mediterranean fever
female
follow up
Greece
human
laboratory test
leukopenia
longitudinal study
male
monotherapy
myalgia
off label drug use
priority journal
recurrent disease
remission
retrospective study
sex difference
treatment response
urinary tract infection
viral gastroenteritis
familial Mediterranean fever
middle aged
retreatment
treatment failure
treatment outcome
young adult
Adolescent
Adult
Aged
Anti-Inflammatory Agents
Antibodies, Monoclonal
Colchicine
Familial Mediterranean Fever
Female
Humans
Interleukin 1 Receptor Antagonist Protein
Male
Middle Aged
Off-Label Use
Remission Induction
Retreatment
Retrospective Studies
Treatment Failure
Treatment Outcome
Young Adult
Journal of Rheumatology
Mostra tutti i dati dell'item
Abstract
Objective. To assess the efficacy and safety of the interleukin-1β (IL-1β) inhibitor canakinumab in all adolescent and adult patients with familial Mediterranean fever (FMF) identified from the Greek National Registry for off-label drug use between 2010 and 2015. Methods. In this retrospective longitudinal outcome study, clinical and laboratory data were collected from 14 patients (7 men) aged median 38.5 years (range 13-70), with median disease duration of 14 years, and active FMF despite colchicine (n = 9) or both colchicine and anakinra (n = 5). Results.All patients continued to receive canakinumab at last visit (median of 18 mos, range 13-53), which was initially given as monotherapy (n = 8) or in combination with colchicine and/or corticosteroids, every 4 (n = 7), 6 (n = 2), or 8 weeks (n = 5). Eleven patients (79%), including 6 receiving monotherapy, achieved complete clinical remission within 2 months (median), while normalization of all laboratory variables denoting inflammation occurred in 92% at 3 months (median). The remaining 3 patients achieved partial responses. Responses were sustained in all but 4 patients, who relapsed. Reducing the canakinumab administration interval from 8 or 6 weeks to 4 weeks led to suppression of disease activity in the relapsing patients. On the other hand, drug administration interval could be safely increased in 2 patients in remission. Corticosteroid doses were significantly reduced during followup. Canakinumab was well tolerated; 1 patient experienced a urinary tract infection and another one a viral gastroenteritis. Conclusion. Treatment with canakinumab in an individualized dosing scheme results in rapid and sustained remission in colchicine-resistant FMF. © 2016 Journal of Rheumatology.
URI
http://hdl.handle.net/11615/75695
Collections
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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