Division of Rheumatology, Cantonal Hospital, St. Gallen, Switzerland.
University of California, Los Angeles, CA, USA.
Arthritis Res Ther. 2022 Aug 25;24(1):207. doi: 10.1186/s13075-022-02891-x.
Anemia is common in patients with rheumatoid arthritis (RA). Higher hemoglobin (Hb) levels may be associated with better clinical outcomes and patient-reported outcomes (PROs). To assess this hypothesis, we conducted two post hoc analyses in three sarilumab phase III studies: TARGET, MOBILITY, and MONARCH.
Pooled data from combination therapy from placebo-controlled MOBILITY (sarilumab + methotrexate) and TARGET (sarilumab + conventional synthetic disease-modifying antirheumatic drugs [csDMARDs]) and monotherapy data from active-controlled MONARCH (sarilumab vs. adalimumab) studies were included. Associations between Hb levels and clinical measures and PROs were assessed over 24 weeks. The mean changes from baseline in clinical outcomes and PROs (to week 24) and radiographic outcomes (to week 52) were evaluated between low and normal Hb levels (based on the World Health Organization [WHO] criteria).
From TARGET, MOBILITY, and MONARCH, 546, 1197, and 369 patients, respectively, were stratified according to Hb levels (low vs. normal). Over 24 weeks, higher Hb levels were found to be consistently associated with better clinical outcomes and PROs in combination therapy and monotherapy groups and were more pronounced among the patients treated with sarilumab than those treated with placebo and adalimumab. The mean change from baseline to week 24 in clinical efficacy measures and PROs was similar in patients with low vs. normal Hb at baseline. Differences between sarilumab and/or adalimumab, for all outcomes, were larger for low Hb subgroups. In MOBILITY, by week 52, the inhibition of progression of structural damage (assessed via Modified Total Sharp Score [mTSS]) was 84% (sarilumab 200 mg) and 68% (sarilumab 150 mg) vs. placebo in patients with low Hb and 97% (sarilumab 200 mg) and 68% (sarilumab 150 mg) vs. placebo in patients with normal Hb. Similar results were observed for other radiographic outcomes.
In these post hoc analyses, a consistent relationship was observed between higher Hb levels and better clinical outcomes and PROs in patients with RA. Irrespective of the baseline Hb levels, sarilumab treatment was associated with improvements in clinical measures and PROs over 24 weeks (improvements were more pronounced than those with adalimumab treatment) and mitigation of joint damage progression over 52 weeks.
ClinTrials.gov NCT01061736, NCT01709578, and NCT02332590.
贫血在类风湿关节炎(RA)患者中很常见。较高的血红蛋白(Hb)水平可能与更好的临床结局和患者报告的结局(PROs)相关。为了评估这一假设,我们在三项沙利鲁单抗 III 期研究(TARGET、MOBILITY 和 MONARCH)中进行了两项事后分析。
包括联合治疗(安慰剂对照 MOBILITY[沙利鲁单抗+甲氨蝶呤]和 TARGET[沙利鲁单抗+常规合成疾病修饰抗风湿药物(csDMARDs])的组合疗法和活性对照 MONARCH(沙利鲁单抗与阿达木单抗)研究中的单药数据。在 24 周内评估 Hb 水平与临床指标和 PROs 的关联。评估低和正常 Hb 水平(基于世界卫生组织[WHO]标准)之间基线至第 24 周的临床结局和 PROs(至第 24 周)和放射学结局(至第 52 周)的平均变化。
来自 TARGET、MOBILITY 和 MONARCH 的 546、1197 和 369 名患者分别根据 Hb 水平(低与正常)进行分层。在 24 周内,联合治疗和单药治疗组中,较高的 Hb 水平与更好的临床结局和 PROs 持续相关,并且在接受沙利鲁单抗治疗的患者中比接受安慰剂和阿达木单抗治疗的患者更为明显。在基线 Hb 正常的患者中,基线至第 24 周的临床疗效和 PROs 的平均变化相似。对于所有结局,沙利鲁单抗和/或阿达木单抗之间的差异在 Hb 较低的亚组中更大。在 MOBILITY 中,在第 52 周时,结构损伤进展的抑制(通过改良总 Sharp 评分[mTSS]评估)在 Hb 较低的患者中,沙利鲁单抗 200mg 组为 84%,沙利鲁单抗 150mg 组为 68%,而安慰剂组为 97%,沙利鲁单抗 200mg 组为 68%,而安慰剂组为 150mg 组为 68%。在其他放射学结局中也观察到了类似的结果。
在这些事后分析中,观察到较高的 Hb 水平与 RA 患者更好的临床结局和 PROs 之间存在一致的关系。无论基线 Hb 水平如何,沙利鲁单抗治疗均可在 24 周内改善临床指标和 PROs(改善程度大于阿达木单抗治疗),并在 52 周内减轻关节损伤进展。
ClinTrials.gov NCT01061736、NCT01709578 和 NCT02332590。