Department of Pediatric Rheumatology, Kanuni Sultan Süleyman Research and Training Hospital, University of Health Science, No: 46/1 Kucukcekmece, Istanbul, 34303, Turkey.
Department of Pediatric Rheumatology, Şanlıurfa Research and Training Hospital, Şanlıurfa, Turkey.
Rheumatol Int. 2019 Sep;39(9):1615-1619. doi: 10.1007/s00296-019-04385-7. Epub 2019 Jul 20.
Juvenile idiopathic arthritis is the most common chronic rheumatic disease of childhood resulting in disability in untreated cases. Disease modifying anti-rheumatic drugs form the first-line treatment in JIA. However, the data about leflunomide (LFN) in treatment of JIA is limited. We reviewed the medical files of JIA patients who were followed-up regularly and had received LFN. A total of 38 patients were included to the study. Among them, 24 had oligoarticular JIA, eleven had polyarticular JIA, two had ERA and one had psoriatic arthritis. 36 were initially treated with methotrexate and two patients diagnosed with ERA were treated with sulfasalazine. Sulfasalazine treatment was switched to LFN due to inadequate response at the 3rd month of therapy. Methotrexate was ceased due to gastrointestinal intolerance in 36 patients. Of these 36 patients, 19 patients had either low disease activity (n = 13) or remission (n = 6). LFN was administered to 13 patients with low disease activity. During the follow-up of the six patients in remission, relapse ensued and LFN treatment was started. The remaining 17 patients had moderate (n = 10) or high (n = 7) disease activity requiring biologic agents. But due to inadequate response to biologic agents, LFN was added to the therapy. All of the patients were clinically inactive at the last visit. Only two adverse events resolving within 2 weeks were noted (Lymphopenia = 1, elevated liver enzymes = 1). LFN may be an alternative therapy in case of MTX intolerance or toxicity.
幼年特发性关节炎是儿童中最常见的慢性风湿性疾病,如果未经治疗,可导致残疾。改善病情的抗风湿药物是幼年特发性关节炎的一线治疗药物。然而,关于来氟米特(LFN)治疗幼年特发性关节炎的数据有限。我们回顾了定期随访并接受 LFN 治疗的幼年特发性关节炎患者的病历。共有 38 名患者纳入本研究。其中,24 名患者为寡关节型幼年特发性关节炎,11 名患者为多关节型幼年特发性关节炎,2 名患者为幼年型类风湿关节炎,1 名患者为银屑病关节炎。36 名患者最初接受甲氨蝶呤治疗,2 名幼年型类风湿关节炎患者因治疗 3 个月后反应不佳而改用柳氮磺胺吡啶治疗。由于胃肠道不耐受,36 名患者停止使用甲氨蝶呤。在这 36 名患者中,19 名患者的疾病活动度较低(n=13)或缓解(n=6)。13 名疾病活动度较低的患者接受 LFN 治疗。在缓解期的 6 名患者中,有 1 名出现复发,开始使用 LFN 治疗。其余 17 名患者疾病活动度为中度(n=10)或高度(n=7),需要使用生物制剂。但由于生物制剂反应不佳,开始添加 LFN 治疗。所有患者在最后一次就诊时均无临床症状。仅注意到 2 例不良事件(淋巴细胞减少症 1 例,肝酶升高 1 例)在 2 周内得到解决。LFN 可能是甲氨蝶呤不耐受或毒性的替代治疗。