Department of Rheumatology and Clinical Immunology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Department of Clinical Immunology, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan.
Rheumatology (Oxford). 2024 Feb 1;63(2):349-357. doi: 10.1093/rheumatology/kead299.
Anaemia, a common comorbidity of RA, is related to high disease activity and poor prognosis. It is unknown which biologic/targeted synthetic (b/ts)-DMARDs are optimal for patients with anaemia and RA in regulating anaemia and controlling disease activity.
We investigated the change in haemoglobin (Hb) levels, drug retention rates and disease activities after the administration of b/ts-DMARDs with different modes of action [TNF inhibitors (TNFis), immunoglobulin fused with cytotoxic T-lymphocyte antigen (CTLA-4-Ig), IL-6 receptor inhibitors (IL-6Ris) and Janus kinase inhibitors (JAKis)] in patients with RA stratified by baseline Hb levels using the multicentre observational registry for patients with RA in Japan (ANSWER cohort).
A total of 2093 patients with RA were classified into three groups based on tertiles of the baseline Hb levels (Hblow, anaemic; Hbint, intermediate; Hbhigh, non-anaemic). IL-6Ri increased Hb levels in all groups (the mean change at 12 months in Hblow was +1.5 g/dl, Hbint +0.7 g/dl and Hbhigh +0.1 g/dl). JAKis increased the Hb level in patients with anaemia and RA and retained or decreased the Hb level in non-anaemic patients (the mean change at 12 months in Hblow was +0.6 g/dl, Hbint 0 g/dl and Hbhigh -0.3 g/dl). In patients with anaemia and RA, overall adjusted 3-year drug retention rates were higher in JAKi followed by IL-6Ri, CTLA4-Ig and TNFi (78.6%, 67.9%, 61.8% and 50.8%, respectively). Change of disease activity at 12 months was not different among different b/ts-DMARDs treatments.
IL-6Ri and JAKi can effectively treat patients with anaemia and RA in a real-world setting.
贫血是 RA 的常见合并症,与疾病高活动度和预后不良有关。目前尚不清楚哪种生物/靶向合成(b/ts)-DMARD 药物最适合贫血和 RA 患者,既能调节贫血又能控制疾病活动度。
我们使用日本 RA 多中心观察性登记研究(ANSWER 队列),根据基线血红蛋白(Hb)水平将接受不同作用机制的 b/ts-DMARD 治疗的 RA 患者(TNF 抑制剂(TNFis)、与细胞毒性 T 淋巴细胞抗原融合的免疫球蛋白(CTLA-4-Ig)、IL-6 受体抑制剂(IL-6Ris)和 Janus 激酶抑制剂(JAKis))分为三组。
共 2093 例 RA 患者根据基线 Hb 水平的三分位数分为三组(Hb 低值,贫血;Hb 中值,中间;Hb 高值,非贫血)。所有组的 IL-6Ri 均增加 Hb 水平(Hb 低值组 12 个月时的平均变化为+1.5g/dl,Hb 中值组为+0.7g/dl,Hb 高值组为+0.1g/dl)。JAKi 增加了贫血和 RA 患者的 Hb 水平,并保留或降低了非贫血患者的 Hb 水平(Hb 低值组 12 个月时的平均变化为+0.6g/dl,Hb 中值组为 0g/dl,Hb 高值组为-0.3g/dl)。在贫血和 RA 患者中,JAKi 后 3 年的药物保留率总体调整后较高,随后是 IL-6Ri、CTLA4-Ig 和 TNFis(分别为 78.6%、67.9%、61.8%和 50.8%)。不同 b/ts-DMARD 治疗 12 个月时疾病活动度的变化无差异。
在真实环境中,IL-6Ri 和 JAKi 可以有效治疗贫血和 RA 患者。