The First Department of Internal Medicine, School of Medicine, University of Occupational and Environmental Health, Japan, Kitakyushu, Japan.
Medical Department, AbbVie GK, Tokyo, Japan.
Ann Rheum Dis. 2015 Feb;74(2):389-95. doi: 10.1136/annrheumdis-2013-204016. Epub 2013 Nov 28.
To investigate the possibility of discontinuing adalimumab (ADA) for 1 year without flaring (DAS28-erythrocyte sedimentation rate (ESR) ≥3.2), and to identify factors enabling established patients with rheumatoid arthritis (RA) to remain ADA-free.
Of 197 RA patients treated with ADA+methotrexate (MTX), 75 patients who met the ADA-free criteria (steroid-free and sustained DAS28-ESR remission for 6 months with stable MTX doses) were studied for 1 year.
The mean disease duration and DAS28-ESR score in 75 patients was 7.5 years and 5.1 at baseline, respectively. The proportion of patients who sustained DAS28-ESR <2.6 (48%) and DAS28-ESR <3.2 (62%) for 1 year were significantly lower in the ADA discontinuation group than in the ADA continuation group; however, in patients with deep remission (DAS28-ESR ≤1.98) identified by receiver operating characteristics analysis following logistic analysis, these rates increased to 68% and 79%, respectively, with no significant difference between both groups. Remarkably, ADA readministration to patients with flare was effective in returning DAS28-ESR to <3.2 within 6 months in 90% and 9 months in 100% patients; among the patients who sustained DAS28-ESR <3.2 during ADA discontinuation, 100% remained in structural remission and 94% in functional remission.
The possibility of remaining ADA-free for 1 year was demonstrated in established patients with RA with outcomes that ADA can be discontinued without flaring in 79% patients with deep remission, with similar rates in the ADA continuation group, and showed no functional or structural damage in patients with DAS28-ESR <3.2. ADA readministration to patients with flare during ADA discontinuation was effective.
探讨阿达木单抗(ADA)停药 1 年不复发(DAS28-红细胞沉降率(ESR)≥3.2)的可能性,并确定使已确诊的类风湿关节炎(RA)患者能够持续停用 ADA 的因素。
在接受 ADA+甲氨蝶呤(MTX)治疗的 197 例 RA 患者中,对符合 ADA 无治疗标准的 75 例患者(无激素且稳定 MTX 剂量下,DAS28-ESR 缓解持续 6 个月)进行了 1 年的研究。
75 例患者的平均疾病病程和 DAS28-ESR 基线评分分别为 7.5 年和 5.1。在 ADA 停药组中,1 年内持续 DAS28-ESR<2.6(48%)和 DAS28-ESR<3.2(62%)的患者比例显著低于 ADA 继续治疗组;然而,在通过逻辑分析后的受试者工作特征分析中确定的深度缓解(DAS28-ESR≤1.98)患者中,这些比例分别增加至 68%和 79%,两组间无显著差异。值得注意的是,在有复发的患者中重新使用 ADA,90%的患者在 6 个月内、100%的患者在 9 个月内使 DAS28-ESR 恢复至<3.2;在 ADA 停药期间持续 DAS28-ESR<3.2 的患者中,100%保持结构缓解,94%保持功能缓解。
在已确诊的 RA 患者中,ADA 停药 1 年的可能性得到了证实,在深度缓解的患者中,79%的患者可以停用 ADA 而不复发,ADA 继续治疗组的比例相似,且 DAS28-ESR<3.2 的患者没有功能或结构损伤。在 ADA 停药期间,对有复发的患者重新使用 ADA 是有效的。