Katip Celebi University Hospital, Izmir, Turkey.
Dumlupinar University Evliya Celebi Hospital, Kutahya, Turkey.
Arthritis Care Res (Hoboken). 2018 Jul;70(7):1090-1094. doi: 10.1002/acr.23446. Epub 2018 Apr 24.
Approximately 30-45% of patients with familial Mediterranean fever (FMF) have been reported to have attacks despite colchicine treatment. Currently, data on the treatment of colchicine-unresponsive or colchicine-intolerant FMF patients are limited; the most promising alternatives seem to be anti-interleukin-1 (anti-IL-1) agents. Here we report our experience with the off-label use of anti-IL-1 agents in a large group of FMF patients.
In all, 21 centers from different geographical regions of Turkey were included in the current study. The medical records of all FMF patients who had used anti-IL-1 treatment for at least 6 months were reviewed.
In total, 172 FMF patients (83 [48%] female, mean age 36.2 years [range 18-68]) were included in the analysis; mean age at symptom onset was 12.6 years (range 1-48), and the mean colchicine dose was 1.7 mg/day (range 0.5-4.0). Of these patients, 151 were treated with anakinra and 21 with canakinumab. Anti-IL-1 treatment was used because of colchicine-resistant disease in 84% and amyloidosis in 12% of subjects. During the mean 19.6 months of treatment (range 6-98), the yearly attack frequency was significantly reduced (from 16.8 to 2.4; P < 0.001), and 42.1% of colchicine-resistant FMF patients were attack free. Serum levels of C-reactive protein, erythrocyte sedimentation rate, and 24-hour urinary protein excretion (5,458.7 mg/24 hours before and 3,557.3 mg/24 hours after) were significantly reduced.
Anti-IL-1 treatment is an effective alternative for controlling attacks and decreasing proteinuria in colchicine-resistant FMF patients.
据报道,约有 30-45%的家族性地中海热(FMF)患者尽管接受秋水仙碱治疗仍会发作。目前,关于秋水仙碱无反应或不耐受 FMF 患者的治疗数据有限;最有前途的替代方法似乎是抗白细胞介素-1(anti-IL-1)药物。在此,我们报告了在一大群 FMF 患者中使用抗 IL-1 药物的经验。
共有来自土耳其不同地理区域的 21 个中心参与了本研究。回顾了所有接受抗 IL-1 治疗至少 6 个月的 FMF 患者的病历。
共纳入 172 例 FMF 患者(83 例[48%]为女性,平均年龄 36.2 岁[范围 18-68]);症状发作的平均年龄为 12.6 岁(范围 1-48),秋水仙碱的平均剂量为 1.7 毫克/天(范围 0.5-4.0)。这些患者中,151 例接受了阿那白滞素治疗,21 例接受了卡那单抗治疗。84%的患者因秋水仙碱耐药性疾病,12%的患者因淀粉样变性而使用抗 IL-1 治疗。在平均 19.6 个月的治疗期间(范围 6-98),年发作频率显著降低(从 16.8 次减少至 2.4 次;P<0.001),42.1%的秋水仙碱耐药性 FMF 患者无发作。血清 C 反应蛋白、红细胞沉降率和 24 小时尿蛋白排泄量(治疗前为 5458.7 毫克/24 小时,治疗后为 3557.3 毫克/24 小时)显著降低。
抗 IL-1 治疗是控制秋水仙碱耐药性 FMF 患者发作和减少蛋白尿的有效替代方法。