Catanoso Maria Grazia, Macchioni Pierluigi, Boiardi Luigi, Pipitone Nicolò, Salvarani Carlo
Arcispedale Santa Maria Nuova, Reggio Emilia, Italy.
Arthritis Rheum. 2007 Dec 15;57(8):1514-9. doi: 10.1002/art.23095.
To investigate whether etanercept has a steroid-sparing effect in the treatment of patients with relapsing polymyalgia rheumatica (PMR).
The study group comprised patients with relapsing PMR who were not able to reduce their prednisone dosage below 7.5-10 mg/day and who had experienced corticosteroid-related side effects. Patients received injections of etanercept 25 mg twice weekly for 24 weeks, and were followed up for 3 additional months after treatment withdrawal. Patients regularly underwent clinical assessment, measurement of erythrocyte sedimentation rate and C-reactive protein level, and ultrasound (US) examination of the shoulders during the 9 months of the followup period.
All 6 enrolled patients responded to etanercept with sustained remission (improvement of at least 70% according to European League Against Rheumatism response criteria for PMR in 4 patients and at least 50% in 2 patients) and were able to significantly reduce their median prednisone daily dosage without experiencing a disease relapse (8.75 mg versus 2.5 mg; P = 0.026) at the end of the 9-month study period. US shoulder examination performed at the end of followup demonstrated a parallel reduction of glenohumeral and periarticular inflammation. A significant reduction in the cumulative prednisone dose 9 months before versus the 9-month study period was observed (mean +/- SD 1,767 +/- 524 mg versus 730 +/- 182 mg; P = 0.028). Three patients developed nonsevere side effects: bacterial cystitis in 2 and influenza in 1.
These results, which should be confirmed in a controlled study, suggest that etanercept may be a safe and useful corticosteroid-sparing agent in relapsing PMR.
探讨依那西普在治疗复发性风湿性多肌痛(PMR)患者时是否具有激素节省效应。
研究组包括复发性PMR患者,这些患者无法将泼尼松剂量降至7.5 - 10毫克/天以下,且出现了与皮质类固醇相关的副作用。患者每周两次接受25毫克依那西普注射,共24周,并在停药后额外随访3个月。在9个月的随访期内,患者定期接受临床评估、红细胞沉降率和C反应蛋白水平测量,以及肩部超声(US)检查。
所有6名入组患者对依那西普有反应,病情持续缓解(根据欧洲抗风湿病联盟PMR反应标准,4名患者改善至少70%,2名患者改善至少50%),并且在9个月研究期结束时能够显著降低泼尼松的每日中位剂量而无疾病复发(8.75毫克对2.5毫克;P = 0.026)。随访结束时进行的肩部超声检查显示盂肱关节和关节周围炎症同时减轻。观察到随访前9个月与9个月研究期相比,累积泼尼松剂量显著降低(平均±标准差1767±524毫克对730±182毫克;P = 0.028)。3名患者出现非严重副作用:2名患者发生细菌性膀胱炎,1名患者发生流感。
这些结果应在对照研究中得到证实,提示依那西普在复发性PMR中可能是一种安全有效的激素节省剂。