Russo R A G, Katsicas M M, Zelazko M
Service of Immunology, Hospital de Pediatría Prof. Dr. Juan P. Garrahan, Pichincha 1890, 1245 Buenos Aires, Argentina.
Clin Exp Rheumatol. 2002 Sep-Oct;20(5):723-6.
To evaluate the effectiveness of etanercept in patients with systemic juvenile idiopathic arthritis (SJIA) refractory to methotrexate (MTX) therapy in a pediatric rheumatology practice.
Fifteen patients with SJIA with active polyarthritis refractory to higher dose MTX (> or = 20 mg/m2/week) for at least 3 months were included. Patients received etanercept 0.4 mg/Kg twice weekly concomitantly with MTX. Observed period of treatment ranged from 5 to 12 months (median 9 months).
Improvement of ESR, swollen and limited joint counts, functional capacity, and general wellbeing was achieved by 14/15 patients. The most significant impact on these variables was observed 3 to 5 months after treatment onset. Mean time to improvement was 2 months. In the 4 patients who presented fever and rash, these signs disappeared after the beginning of etanercept treatment and reappeared during flares. Three patients showed sustained clinical and biochemical remission on low dose MTX (< or = 5 mg/m2/week). Thirteen relapses were observed in 9 (60%) patients at a mean of 7.6 months after therapy was begun. Etanercept was discontinued due to lack of efficacy in 7 patients, only after higher dose (1 mg/kg/dose) was used. MTX and corticosteroid doses were decreased during the observation period. No serious side effects were observed.
Etanercept, in combination with MTX, demonstrated benefit soon after initiation of treatment in patients with refractory SJIA, but flares and progressive loss of effectiveness were observed with continued treatment in most patients. Sharp decreases in the dose of MTX and corticosteroids may have contributed to subsequent occurrence of flares. Changes in MTX and corticosteroids doses should probably need to be made gradually, and it is possible that patients on SJIA should continue on therapeutic doses of MTX while being on etanercept in order to maintain therapeutic benefit.
在儿科风湿病诊疗实践中,评估依那西普对甲氨蝶呤(MTX)治疗无效的全身型幼年特发性关节炎(SJIA)患者的疗效。
纳入15例患有活动性多关节炎且对高剂量MTX(≥20mg/m²/周)治疗至少3个月无效的SJIA患者。患者在接受MTX治疗的同时,每周两次皮下注射依那西普0.4mg/kg。观察期为5至12个月(中位数为9个月)。
14/15例患者的红细胞沉降率(ESR)、肿胀和受限关节计数、功能能力及总体健康状况均得到改善。治疗开始后3至5个月对这些变量的影响最为显著。平均改善时间为2个月。4例出现发热和皮疹的患者,这些症状在依那西普治疗开始后消失,并在病情复发时再次出现。3例患者在低剂量MTX(≤5mg/m²/周)治疗下实现了持续的临床和生化缓解。9例(60%)患者在治疗开始后平均7.6个月出现了13次病情复发。7例患者因疗效不佳停用依那西普,仅在使用更高剂量(1mg/kg/剂量)后才出现这种情况。在观察期内MTX和皮质类固醇剂量降低。未观察到严重副作用。
依那西普联合MTX在难治性SJIA患者治疗开始后不久即显示出疗效,但在大多数患者持续治疗过程中出现了病情复发和疗效逐渐丧失的情况。MTX和皮质类固醇剂量的急剧降低可能导致了随后病情复发的发生。MTX和皮质类固醇剂量的调整可能需要逐步进行,并且SJIA患者在使用依那西普治疗时可能应继续使用治疗剂量的MTX以维持治疗效果。