Abstract
Results At baseline, 7 patients were treated with the initial dosage of 2 mg/kg (or 150 mg, if > 40 Kg) every 8 weeks. In 5 patients (2 MWS/CINCA overlap, 5 CINCA) the dosage was 4 mg/kg (or 300 mg) every 8 weeks. During the following 12 months modification of dosage of frequency was performed in 7/12 patients. The 5 patients at higher dosage during the CACZ885D2306 study needed to increase the frequency of administration with a mean frequency of 6 weeks (range 4-8). The mean reason was the presence of mild clinical manifestation and/or persistent elevation of acute phase reactants. In one of these patients the therapy was subsequently discontinued due to persistent disease activity. An increased frequency (6 and 7 weeks) was also performed in 1 MWS and 1 CINCA patient, respectively. In 5 patients the treatment was not modified being effective in the control of the disease.
Highlights
No clear information on the optimal dosage of Canakinumab in cryopyrin-associated periodic syndromes (CAPS) is available
Aim To analyse the modification of dosage schedule of Canakinumab in CAPS in 12 months of routinely clinical practice
Patients were previously enrolled in the CACZ885D2306 trial and studied for the following 12 months
Summary
No clear information on the optimal dosage of Canakinumab in CAPS is available. Canakinumab in the routinary clinical practice in cryopyrin-associated periodic syndromes (CAPS): one year of follow-up R Caorsi1*, L Lepore2, F Zulian3, M Alessio4, A Stabile5, M Finetti1, A Martini1, M Gattorno1 From 18th Pediatric Rheumatology European Society (PReS) Congress Bruges, Belgium.
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