Section of Rheumatology at University of Chicago and Division of Rheumatology and Clinical Immunology, Department of Medicine, University of Pittsburgh, Pittsburgh, PA, USA.
Juvenile Myositis Pathogenesis and Therapeutics Unit, National Institute of Arthritis Musculoskeletal and Skin Diseases, National Institutes of Health (NIH), Bethesda, MD, USA.
Rheumatology (Oxford). 2023 Nov 2;62(11):3672-3679. doi: 10.1093/rheumatology/kead110.
The ACR-EULAR Myositis Response Criteria (MRC) were developed as a composite measure using absolute percentage change in six core set measures (CSMs). We aimed to further validate the MRC by assessing the contribution of each CSM, frequency of strength vs extramuscular activity improvement, representation of patient-reported outcome measures (PROM), and frequency of CSM worsening.
Data from adult dermatomyositis/polymyositis patients in the rituximab (n = 147), etanercept (n = 14), and abatacept (n = 19) trials, and consensus patient profiles (n = 232) were evaluated. The Total Improvement Score (TIS), number of improving vs worsening CSMs, frequency of improvement with and without muscle-related CSMs, and contribution of PROM were evaluated by MRC category. Regression analysis was performed to assess contribution of each CSM to the MRC.
Of 412 adults with dermatomyositis/polymyositis, there were 37%, 24%, 25%, and 14% with no, minimal, moderate, and major MRC improvement, respectively. The number of improving CSMs and absolute percentage change in all CSMs increased by improvement category. In minimal-moderate improvement, only physician-reported disease activity contributed significantly more than expected by MRC. Of patients with at least minimal improvement, 95% had improvement in muscle-related measures and a majority (84%) had improvement in PROM. Patients with minimal improvement had worsening in a median of 1 CSM, and most patients with moderate-major improvement had no worsening CSMs. Physician assessment of change generally agreed with MRC improvement categories.
The ACR-EULAR MRC performs consistently across multiple studies, further supporting its use as an efficacy end point in future myositis therapeutic trials.
ACR-EULAR 肌炎缓解标准(MRC)是作为使用六个核心测量指标(CSMs)的绝对百分比变化的综合衡量标准而制定的。我们旨在通过评估每个 CSM 的贡献、力量与肌肉外活动改善的频率、患者报告的结果测量(PROM)的代表性以及 CSM 恶化的频率,进一步验证 MRC。
评估了利妥昔单抗(n=147)、依那西普(n=14)和阿巴西普(n=19)试验中的成年皮肌炎/多发性肌炎患者以及共识患者概况(n=232)的数据。通过 MRC 类别评估总改善评分(TIS)、改善与恶化 CSM 的数量、有无肌肉相关 CSM 改善的频率以及 PROM 的贡献。进行回归分析以评估每个 CSM 对 MRC 的贡献。
在 412 名皮肌炎/多发性肌炎成年患者中,分别有 37%、24%、25%和 14%无、最小、中度和主要 MRC 改善。改善 CSM 的数量和所有 CSM 的绝对百分比变化随着改善类别而增加。在最小中度改善中,只有医生报告的疾病活动比 MRC 预期的贡献更大。在至少有最小改善的患者中,95%的患者肌肉相关测量有改善,大多数患者(84%)的 PROM 有改善。最小改善的患者有中位数 1 个 CSM 恶化,大多数中度-主要改善的患者无 CSM 恶化。医生对变化的评估通常与 MRC 改善类别一致。
ACR-EULAR MRC 在多项研究中表现一致,进一步支持其在未来肌炎治疗试验中作为疗效终点的使用。