Real-life data on tapering or discontinuation of canakinumab therapy in patients with familial Mediterranean fever

被引:0
作者
Yusuf Karabulut
Halise Hande Gezer
Nuran Öz
İrfan Esen
Mehmet Tuncay Duruöz
机构
[1] Yıldırım Doruk Hospital,Department of Internal Medicine, Division of Rheumatology
[2] Ümraniye Training and Research Hospital,Department of Rheumatology
[3] Marmara University School of Medicine,Department of Physical Medicine and Rehabilitation, Division of Rheumatology
[4] Ankara Şehir Hospital,Department of Internal Medicine, Division of Oncology Ankara
来源
Rheumatology International | 2022年 / 42卷
关键词
Familial Mediterranean fever; Colchicine-resistant; Dose optimisation; Anakinra; Canakinumab;
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摘要
This study aimed to investigate the disease characteristics of familial Mediterranean fever (FMF) patients undergoing dose optimisation and discontinuation of canakinumab therapy. A total of 61 patients diagnosed with FMF and using canakinumab for the resistant disease were enrolled on this retrospective study. Patients’ characteristics, disease activity, treatment response, dose optimisation, dose intervals, attack-free periods, drug-free periods and side effects were noted. Dose intervals were extended in patients who achieved remission without being bound by any protocol at the discretion of the rheumatology physician who followed up with the patients in the outpatient clinic. The drug was discontinued in some patients whose dose intervals were 2 months or longer and remained in remission for 6 months or longer. A total of 57 patients (56% female, median age 32.4 years) were included. The mean attack frequency before canakinumab was 3.4/6 months, while it was 1.2 at the last post-treatment visit (p < 0.001). The median duration of canakinumab use was 46 months. After the first 6 months, the dosing interval was extended in 22 patients, and then treatment was discontinued in 12 of them who did not have an attack in the last 6 months. Three of the 12 patients whose treatment was discontinued started monthly treatment again after their attacks recurred. In the remaining ten patients, dose intervals were extended to 8–12 weeks after 6 months of monthly treatment. Nine patients are still being followed up without attacks and receive only colchicine therapy. Canakinumab is a safe and effective treatment, dose intervals may be extended, and follow-up without medication may be possible for eligible patients. However, there is a need for a consensus on dose optimisation or tapering.
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页码:2211 / 2219
页数:8
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