Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, Toho University, 2-22-36 Ohashi, Meguro-ku, Tokyo, 153-8515, Japan.
Sci Rep. 2021 Mar 25;11(1):6865. doi: 10.1038/s41598-021-86335-7.
To elucidate the disease-flare process in rheumatoid arthritis (RA) after discontinuing biological disease-modifying antirheumatic drugs (bDMARDs), we first focused on RA-flare prediction after achieving stringent remission criteria. Patients with RA who maintained a simplified disease activity index ≤ 3.3 for ≥ 3 months during November 2014-January 2018 in our medical centre in Tokyo, Japan, were eligible. The primary endpoint was flare (disease activity score 28-erythrocyte sedimentation rate ≥ 3.2 with increase from baseline > 0.6) within 2 years after bDMARD discontinuation. Comprehensive clinical assessments, ultrasonographic evaluation of 40 joints, and blood sampling for 12 biomarkers were performed every 2-3 months for 2 years unless patients experienced flare. Flare-positive and flare-negative patients were compared using univariate and Kaplan-Meier analyses. Thirty-six patients (80.6% female, median disease duration, 5.2 years; median treatment period with discontinued bDMARD, 2 years; median remission duration, 18 months) were enrolled. Twenty patients (55.6%) experienced RA flare 43-651 (median, 115) days after the first skipped date of bDMARDs. Two patients who withdrew without disease flare were excluded from the comparison. Clinical and ultrasonographic evaluations did not show significant between-group differences; Kaplan-Meier analysis showed that higher baseline soluble tumour necrosis factor receptor 1 (sTNFR1) concentration impacted subsequent disease flare (p = 0.0041); higher baseline interleukin (IL)-2 concentration was exclusively beneficial to patients with lower sTNFR1 (p = 0.0058), resulting in remission maintenance in 83.3% of patients with lower sTNFR1 and higher IL-2. We demonstrated the usefulness of combined biomarker evaluation for predicting sustained remission after bDMARD discontinuation in RA.
为了阐明类风湿关节炎(RA)患者停用生物制剂后疾病复发的过程,我们首先关注的是达到严格缓解标准后疾病复发的预测。符合条件的患者为在日本东京我们的医疗中心,2014 年 11 月至 2018 年 1 月期间,简化疾病活动度指数(DAS28-ESR)≤3.3 且至少 3 个月,且从基线升高≥0.6。主要终点为停用生物制剂后 2 年内疾病复发(DAS28-ESR≥3.2,且与基线相比升高>0.6)。除非患者出现疾病复发,否则每 2-3 个月进行一次全面的临床评估、40 个关节的超声评估和 12 项生物标志物的血液检测。采用单变量和 Kaplan-Meier 分析比较疾病复发阳性和阴性患者。共纳入 36 例患者(80.6%为女性,中位疾病持续时间为 5.2 年;停用的生物制剂中位治疗时间为 2 年;中位缓解时间为 18 个月)。20 例(55.6%)患者在首次漏用生物制剂后的 43-651 天(中位 115 天)出现 RA 复发。有 2 例因未出现疾病复发而退出研究,故未纳入比较。临床和超声评估未显示组间有显著差异;Kaplan-Meier 分析表明,较高的基线可溶性肿瘤坏死因子受体 1(sTNFR1)浓度影响随后的疾病复发(p=0.0041);较高的基线白细胞介素(IL)-2 浓度仅对 sTNFR1 较低的患者有益(p=0.0058),从而使 sTNFR1 较低且 IL-2 较高的患者中 83.3%的患者保持缓解。我们证明了联合生物标志物评估在预测 RA 患者停用生物制剂后持续缓解中的作用。