Division of Orthopaedic Surgery, Department of Regenerative and Transplant Medicine, Niigata University Graduate School of Medical and Dental Sciences.
Tohoku J Exp Med. 2020 May;251(1):9-18. doi: 10.1620/tjem.251.9.
Rheumatoid arthritis (RA) is an autoimmune disease characterized by systemic articular and bone manifestations and its pathogenesis is driven by a complex network of proinflammatory cytokines, including tumor necrosis factor and interleukin (IL)-6. Treatment of rheumatoid arthritis (RA) has been standardized by the introduction of a treat-to-target approach. Subcutaneous tocilizumab (TCZ-SC) is a humanized anti-IL-6 receptor monoclonal antibody, and is widely used for refractory RA patients in the clinical settings. However, it remains unknown whether TCZ-SC shows effectiveness for elderly onset RA. The study was aimed to assess the effectiveness and safety of TCZ-SC in elderly-onset rheumatoid arthritis (EORA) patients in daily practice. Fifty-five RA patients were divided into two age groups upon TCZ-SC administration: young (Y) group (< 65 years old, n = 30) and elderly-onset (EO) group (> 65 years old, n = 25). Disease activity score-28 (DAS28) upon TCZ-SC administration (4.84 in EO group vs. 4.41 in Y group) was significantly decreased to 1.94 vs. 1.93 at 3 months and 1.61 vs. 1.75 at 12 months after administration. The clinical remission (DAS28 < 2.6) rate was 75% in EO group vs. 83% in Y group at 3 months and 90% vs. 85% at 12 months. The retention rate at 12 months was 88% in EO group and 92% in Y group without significant difference. The cessation cases of adverse events were two in each group. In conclusion, TCZ-SC showed good clinical effectiveness and safety in EORA patients. TCZ-SC is a useful agent for patients with EORA.
类风湿关节炎(RA)是一种以全身关节和骨骼表现为特征的自身免疫性疾病,其发病机制是由肿瘤坏死因子和白细胞介素(IL)-6 等促炎细胞因子的复杂网络驱动的。引入靶向治疗方法已经使类风湿关节炎(RA)的治疗标准化。皮下注射托珠单抗(TCZ-SC)是一种人源化抗 IL-6 受体单克隆抗体,在临床环境中广泛用于治疗难治性 RA 患者。然而,TCZ-SC 对老年起病的 RA 是否有效尚不清楚。本研究旨在评估 TCZ-SC 在日常实践中对老年起病类风湿关节炎(EORA)患者的疗效和安全性。55 例 RA 患者在接受 TCZ-SC 治疗后按年龄分为两组:年轻(Y)组(<65 岁,n=30)和老年起病(EO)组(>65 岁,n=25)。接受 TCZ-SC 治疗后,DAS28 评分(EO 组 4.84,Y 组 4.41)显著降低,治疗后 3 个月分别降至 1.94 和 1.93,治疗后 12 个月分别降至 1.61 和 1.75。EO 组在治疗后 3 个月和 12 个月时的临床缓解率(DAS28<2.6)分别为 75%和 90%,Y 组分别为 83%和 85%。EO 组和 Y 组的 12 个月保留率分别为 88%和 92%,差异无统计学意义。两组各有 2 例因不良事件停药。结论:TCZ-SC 对 EORA 患者具有良好的临床疗效和安全性。TCZ-SC 是治疗 EORA 患者的有效药物。