Juvenile Myositis Pathogenesis and Therapeutics Unit, National Institute of Arthritis Musculoskeletal and Skin Diseases, National Institutes of Health (NIH), Bethesda, MD, USA.
Section of Rheumatology, Department of Medicine, University of Chicago, Chicago, IL, USA.
Rheumatology (Oxford). 2023 Nov 2;62(11):3680-3689. doi: 10.1093/rheumatology/kead111.
The 2016 ACR-EULAR Response Criteria for JDM was developed as a composite measure with differential weights of six core set measures (CSMs) to calculate a Total Improvement Score (TIS). We assessed the contribution of each CSM, representation of muscle-related and patient-reported CSMs towards improvement, and frequency of CSM worsening across myositis response criteria (MRC) categories in validation of MRC.
Data from JDM patients in the Rituximab in Myositis trial (n = 48), PRINTO JDM trial (n = 139), and consensus patient profiles (n = 273) were included. Observed vs expected CSM contributions were compared using Sign test. Characteristics of MRC categories were compared by Wilcoxon tests with Bonferroni adjustment. Spearman correlation of changes in TIS and individual CSMs were examined. Agreement between physician-assessed change and MRC categories was evaluated by weighted Cohen's kappa.
Of 457 JDM patients with IMACS CSMs and 380 with PRINTO CSMs, 9-13% had minimal, 19-23% had moderate and 41-50% had major improvement. The number of improved and absolute percentage change of CSMs increased by MRC improvement level. Patients with minimal improvement by MRC had a median of 0-1 CSM worsened, and those with moderate/major improvement had a median of zero worsening CSMs. Of patients improved by MRC, 94-95% had improvement in muscle strength and 93-95% had improvement in ≥1 patient-reported CSM. IMACS and PRINTO CSMs performed similarly. Physician-rated change and MRC improvement categories had moderate-to-substantial agreement (Kappa 0.5-0.7).
The ACR-EULAR MRC perform consistently across multiple studies, supporting its further use as an efficacy end point in JDM trials.
2016 年 ACR-EULAR JDM 缓解标准是作为一个综合指标制定的,对 6 项核心标准测量指标(CSM)进行了差异化权重计算,得出总改善评分(TIS)。我们评估了每项 CSM 的贡献,肌肉相关和患者报告的 CSM 对改善的代表性,以及在 MRC 验证中肌炎缓解标准(MRC)各类别中 CSM 恶化的频率。
纳入了 Rituximab in Myositis 试验(n=48)、PRINTO JDM 试验(n=139)和共识患者特征(n=273)中的 JDM 患者数据。采用符号检验比较观察到的与预期的 CSM 贡献。采用 Wilcoxon 检验和 Bonferroni 校正比较 MRC 类别的特征。检查 TIS 和个体 CSM 变化之间的 Spearman 相关性。采用加权 Cohen's kappa 评估医生评估的变化与 MRC 类别的一致性。
457 例具有 IMACS CSM 的 JDM 患者和 380 例具有 PRINTO CSM 的 JDM 患者中,9-13%有微小改善,19-23%有中度改善,41-50%有主要改善。MRC 改善水平的提高与 CSM 改善的数量和绝对百分比变化相关。根据 MRC 评估为微小改善的患者中,有中位数为 0-1 项 CSM 恶化,而中度/主要改善的患者中,有中位数为零项 CSM 恶化。根据 MRC 改善的患者中,94-95%的肌肉力量改善,93-95%的患者至少有 1 项患者报告的 CSM 改善。IMACS 和 PRINTO CSM 的表现相似。医生评估的变化和 MRC 改善类别具有中等至较大的一致性(Kappa 值为 0.5-0.7)。
ACR-EULAR MRC 在多项研究中表现一致,支持其进一步作为 JDM 试验的疗效终点使用。