Nishimoto Norihiro, Hashimoto Jun, Miyasaka Nobuyuki, Yamamoto Kazuhiko, Kawai Shinichi, Takeuchi Tsutomu, Murata Norikazu, van der Heijde Désirée, Kishimoto Tadamitsu
Laboratory of Immune Regulation, Graduate School of Frontier Biosciences, Osaka University 1-3, Yamada-oka, Suita, Osaka, 565-0871, Japan.
Ann Rheum Dis. 2007 Sep;66(9):1162-7. doi: 10.1136/ard.2006.068064. Epub 2007 May 7.
To evaluate the ability of tocilizumab (a humanised anti-IL-6 receptor antibody) monotherapy to inhibit progression of structural joint damage in patients with RA.
In a multi-centre, x ray reader-blinded, randomised, controlled trial, 306 patients with active RA of <5 years' duration were allocated to receive either tocilizumab monotherapy at 8 mg/kg intravenously every 4 weeks or conventional disease-modifying antirheumatic drugs (DMARDs) for 52 weeks. Radiographs of hands and forefeet were scored by the van der Heijde modified Sharp method.
Patients had a mean disease duration of 2.3 years and a disease activity score in 28 joints of 6.5 at baseline. Mean total modified Sharp score (TSS) was 29.4, which was very high despite the relatively short disease duration. At week 52, the tocilizumab group showed statistically significantly less radiographic change in TSS (mean 2.3; 95% CI 1.5 to 3.2) than the DMARD group (mean 6.1; 95% CI 4.2 to 8.0; p<0.01). Tocilizumab monotherapy also improved signs and symptoms. The overall incidences of AEs were 89% and 82% (serious AEs: 18% and 13%; serious infections: 7.6% and 4.1%) in the tocilizumab and DMARD groups, respectively.
Tocilizumab monotherapy was generally well tolerated and provided radiographic benefit in patients with RA.
评估托珠单抗(一种人源化抗白细胞介素-6受体抗体)单药治疗对类风湿关节炎(RA)患者关节结构损伤进展的抑制能力。
在一项多中心、X线阅片者盲法、随机对照试验中,306例病程小于5年的活动性RA患者被随机分配,分别接受每4周一次静脉注射8mg/kg托珠单抗单药治疗或传统改善病情抗风湿药物(DMARDs)治疗,疗程为52周。采用van der Heijde改良Sharp法对手和前足的X线片进行评分。
患者基线时平均病程为2.3年,28个关节的疾病活动评分为6.5。尽管病程相对较短,但平均总改良Sharp评分(TSS)为29.4,仍非常高。在第52周时,托珠单抗组的TSS影像学改变(平均2.3;95%置信区间1.5至3.2)在统计学上显著低于DMARD组(平均6.1;95%置信区间4.2至8.0;p<0.01)。托珠单抗单药治疗还改善了体征和症状。托珠单抗组和DMARD组不良事件的总发生率分别为89%和82%(严重不良事件:18%和13%;严重感染:7.6%和4.1%)。
托珠单抗单药治疗总体耐受性良好,可为RA患者带来影像学益处。