Efficacy and NSAID-sparing effect of secukinumab 150 mg in ankylosing spondylitis: results from phase IV ASTRUM study.

IF 3.4 2区 医学 Q2 RHEUMATOLOGY
Therapeutic Advances in Musculoskeletal Disease Pub Date : 2024-06-05 eCollection Date: 2024-01-01 DOI:10.1177/1759720X241255486
Uta Kiltz, Xenofon Baraliakos, Jan Brandt-Jürgens, Ulf Wagner, Sebastian Lieb, Christian Sieder, Christian Mann, Jürgen Braun
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引用次数: 0

Abstract

Background: Radiographic axial spondyloarthritis (r-axSpA), formerly known as ankylosing spondylitis (AS), is a chronic, inflammatory rheumatic disease associated with symptoms such as inflammatory back pain, morning stiffness, and arthritis. First-line recommendations for patients with AS include treatment with nonsteroidal anti-inflammatory drugs (NSAIDs) for reducing pain and stiffness.

Objectives: The objective of our study is to evaluate the efficacy and short-term NSAID-sparing effect of secukinumab in patients with AS currently treated with NSAIDs.

Design: We assessed the clinical Assessment of SpondyloArthritis International Society (ASAS20) response to secukinumab and evaluated the extent to which the use of concomitant NSAID can be reduced between weeks 4 and 12 in r-axSpA patients treated with secukinumab 150 mg compared with placebo.

Methods: ASTRUM was a prospective 24-week randomized controlled trial of adult patients with active r-axSpA [Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) ⩾4] who had a documented inadequate response to ⩾2 NSAIDs. Patients were randomized (1:1:1) to initiate treatment with subcutaneous secukinumab 150 mg from either week 0 (group 1), week 4 (group 2), or week 16 (group 3). From week 4 onward, tapering of NSAIDs was allowed in all groups.

Results: This study included 211 patients (n = 71, 70, and 70 in groups 1, 2, and 3, respectively). ASAS20 response at week 12 for pooled groups 1 and 2 versus group 3 was 51.1% versus 44.3% (p = 0.35). A higher proportion of patients in groups 1 and 2 achieved ASAS40 and BASDAI50 and showed improvements in other secondary clinical outcomes as compared to group 3 at week 16. More patients in groups 1 and 2 versus group 3 stopped their NSAID intake from baseline through week 16.

Conclusion: Treatment with secukinumab improved clinical outcomes and showed a short-term NSAID-sparing effect in patients with r-axSpA, even though the primary endpoint was not met.

Trial registration: ClinicalTrials.gov; NCT02763046, EudraCT 2015-004575-74.

secukinumab 150 毫克对强直性脊柱炎的疗效和非甾体类抗炎药保留效应:ASTRUM IV 期研究结果。
背景:放射性轴性脊柱关节炎(r-axSpA)以前称为强直性脊柱炎(AS),是一种慢性炎症性风湿病,伴有炎性背痛、晨僵和关节炎等症状。对强直性脊柱炎患者的一线治疗建议包括使用非甾体抗炎药(NSAIDs)来减轻疼痛和僵硬:我们的研究旨在评估secukinumab对目前接受非甾体抗炎药治疗的强直性脊柱炎患者的疗效和短期非甾体抗炎药替代效果:我们评估了国际脊柱炎协会(ASAS20)对secukinumab的临床反应,并评估了与安慰剂相比,接受secukinumab 150毫克治疗的r-axSpA患者在第4周和第12周之间减少同时使用NSAID的程度:ASTRUM是一项为期24周的前瞻性随机对照试验,研究对象为患有活动性r-axSpA[巴斯强直性脊柱炎疾病活动指数(BASDAI)⩾4]、对⩾2种非甾体抗炎药反应不足的成年患者。患者被随机分配(1:1:1),从第0周(第1组)、第4周(第2组)或第16周(第3组)开始接受150毫克的皮下注射secukinumab治疗。从第4周开始,所有组别均允许减量服用非甾体抗炎药:本研究共纳入 211 名患者(第 1、第 2 和第 3 组的人数分别为 71、70 和 70)。第 12 周时,第 1 组和第 2 组的 ASAS20 反应率为 51.1%,第 3 组为 44.3%(P = 0.35)。与第 3 组相比,第 1 组和第 2 组有更高比例的患者在第 16 周达到了 ASAS40 和 BASDAI50,其他次要临床结果也有所改善。从基线到第16周,第1组和第2组与第3组相比,有更多的患者停止了非甾体抗炎药的摄入:结论:尽管主要终点未达到,但使用secukinumab治疗可改善r-axSpA患者的临床疗效,并显示出短期节省非甾体抗炎药的效果:试验注册:ClinicalTrials.gov;NCT02763046,EudraCT 2015-004575-74。
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来源期刊
CiteScore
6.80
自引率
4.80%
发文量
132
审稿时长
18 weeks
期刊介绍: Therapeutic Advances in Musculoskeletal Disease delivers the highest quality peer-reviewed articles, reviews, and scholarly comment on pioneering efforts and innovative studies across all areas of musculoskeletal disease.
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