Guselkumab, a Selective Interleukin-23 p19 Subunit Inhibitor, Resolves Dactylitis in Patients With Active Psoriatic Arthritis: Pooled Results Through Week 52 From Two Phase 3 Studies.

Dennis McGonagle, Iain B McInnes, Atul Deodhar, Georg Schett, May Shawi, Soumya D Chakravarty, Alexa P Kollmeier, Xie L Xu, Shihong Sheng, Stephen Xu, Christopher T Ritchlin, Proton Rahman, Phillip J Mease
{"title":"Guselkumab, a Selective Interleukin-23 p19 Subunit Inhibitor, Resolves Dactylitis in Patients With Active Psoriatic Arthritis: Pooled Results Through Week 52 From Two Phase 3 Studies.","authors":"Dennis McGonagle,&nbsp;Iain B McInnes,&nbsp;Atul Deodhar,&nbsp;Georg Schett,&nbsp;May Shawi,&nbsp;Soumya D Chakravarty,&nbsp;Alexa P Kollmeier,&nbsp;Xie L Xu,&nbsp;Shihong Sheng,&nbsp;Stephen Xu,&nbsp;Christopher T Ritchlin,&nbsp;Proton Rahman,&nbsp;Phillip J Mease","doi":"10.1002/acr2.11537","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>Previous analyses of pooled DISCOVER-1 and DISCOVER-2 data through Week 24 showed significantly higher rates of dactylitis resolution in patients treated with guselkumab compared with placebo. Here, we investigate associations between dactylitis resolution and other outcomes through 1 year.</p><p><strong>Methods: </strong>Patients were randomized 1:1:1 to receive subcutaneous injections of guselkumab 100 mg at Week 0, Week 4, and then every 4 or 8 weeks, or placebo with crossover to guselkumab at Week 24. Independent assessors determined dactylitis severity score (DSS; 0-3/digit; total = 0-60). Dactylitis resolution (DSS = 0) (prespecified) and at least 20%, at least 50%, and at least 70% DSS improvement from baseline (post hoc) were determined through Week 52 (nonresponder imputation for treatment failure through Week 24 and for missing data through Week 52). ACR50, tender/swollen joints, low disease activity (LDA) as assessed by composite indices, and radiographic progression (DISCOVER-2 only) were assessed in patients with dactylitis versus without dactylitis resolution at Week 24 and Week 52.</p><p><strong>Results: </strong>Patients with dactylitis at baseline (473 of 1118) had more severe joint and skin disease than those without dactylitis (645 of 1118). At Week 52, approximately 75% of guselkumab-randomized patients with dactylitis at baseline had complete resolution; approximately 80% had at least 70% DSS improvement. Through Week 52, new-onset dactylitis (DSS ≥1) was uncommon among patients with a DSS of 0 at baseline. Guselkumab-randomized patients with dactylitis resolution were more likely to achieve ACR50, at least 50% reduction in tender and swollen joints, and LDA at Week 24 and Week 52 than those without resolution. At Week 52, patients with dactylitis resolution had numerically less radiographic progression from baseline (DISCOVER-2).</p><p><strong>Conclusion: </strong>Through 1 year, approximately 75% of guselkumab-randomized patients had complete resolution of dactylitis; patients exhibiting resolution were more likely to achieve other important clinical outcomes. Given the high burden of dactylitis, resolution may be associated with better long-term patient outcomes.</p>","PeriodicalId":7084,"journal":{"name":"ACR Open Rheumatology","volume":"5 4","pages":"227-240"},"PeriodicalIF":0.0000,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/e7/31/ACR2-5-227.PMC10100698.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACR Open Rheumatology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/acr2.11537","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Objective: Previous analyses of pooled DISCOVER-1 and DISCOVER-2 data through Week 24 showed significantly higher rates of dactylitis resolution in patients treated with guselkumab compared with placebo. Here, we investigate associations between dactylitis resolution and other outcomes through 1 year.

Methods: Patients were randomized 1:1:1 to receive subcutaneous injections of guselkumab 100 mg at Week 0, Week 4, and then every 4 or 8 weeks, or placebo with crossover to guselkumab at Week 24. Independent assessors determined dactylitis severity score (DSS; 0-3/digit; total = 0-60). Dactylitis resolution (DSS = 0) (prespecified) and at least 20%, at least 50%, and at least 70% DSS improvement from baseline (post hoc) were determined through Week 52 (nonresponder imputation for treatment failure through Week 24 and for missing data through Week 52). ACR50, tender/swollen joints, low disease activity (LDA) as assessed by composite indices, and radiographic progression (DISCOVER-2 only) were assessed in patients with dactylitis versus without dactylitis resolution at Week 24 and Week 52.

Results: Patients with dactylitis at baseline (473 of 1118) had more severe joint and skin disease than those without dactylitis (645 of 1118). At Week 52, approximately 75% of guselkumab-randomized patients with dactylitis at baseline had complete resolution; approximately 80% had at least 70% DSS improvement. Through Week 52, new-onset dactylitis (DSS ≥1) was uncommon among patients with a DSS of 0 at baseline. Guselkumab-randomized patients with dactylitis resolution were more likely to achieve ACR50, at least 50% reduction in tender and swollen joints, and LDA at Week 24 and Week 52 than those without resolution. At Week 52, patients with dactylitis resolution had numerically less radiographic progression from baseline (DISCOVER-2).

Conclusion: Through 1 year, approximately 75% of guselkumab-randomized patients had complete resolution of dactylitis; patients exhibiting resolution were more likely to achieve other important clinical outcomes. Given the high burden of dactylitis, resolution may be associated with better long-term patient outcomes.

Abstract Image

Abstract Image

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Guselkumab是一种选择性白介素- 23p19亚单位抑制剂,可缓解活动性银屑病关节炎患者的趾炎:两项3期研究的52周汇总结果
目的:先前对截至第24周的DISCOVER-1和DISCOVER-2数据的汇总分析显示,与安慰剂相比,接受guselkumab治疗的患者的指炎消退率显着更高。在这里,我们调查了1年内指炎消退和其他结果之间的关系。方法:患者以1:1:1的比例随机分组,分别在第0周、第4周、之后每4周或8周皮下注射100 mg的guselkumab,或在第24周接受安慰剂与guselkumab交叉。独立评估人员确定了指炎严重程度评分(DSS;0 - 3 /数字;total = 0-60)。在第52周确定了手指炎消退(DSS = 0)(预先指定)和至少20%、至少50%和至少70%的DSS较基线改善(事后)(第24周治疗失败和第52周缺失数据的无应答归因)。在第24周和第52周分别评估了指炎患者与无指炎患者的ACR50、关节压痛/肿胀、由综合指数评估的低疾病活动性(LDA)和影像学进展(仅DISCOVER-2)。结果:基线时患有指趾炎的患者(473 / 1118)比无指趾炎的患者(645 / 1118)有更严重的关节和皮肤疾病。在第52周时,大约75%的基线时使用固塞库单抗随机化的指炎患者完全消退;大约80%的患者的DSS至少改善了70%。到第52周,在基线DSS为0的患者中,新发指趾炎(DSS≥1)并不常见。与没有缓解的患者相比,使用guselkumab随机分组的指炎缓解患者更有可能在第24周和第52周达到ACR50,关节触痛和肿胀至少减少50%,以及LDA。在第52周,指尖炎消退的患者与基线相比放射学进展较少(DISCOVER-2)。结论:经过1年,大约75%的guselkumab随机患者的指炎完全消退;表现出缓解的患者更有可能达到其他重要的临床结果。鉴于趾炎的高负担,解决可能与更好的长期患者预后相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Redox Pathogenesis in Rheumatic Diseases. Treatment for Rheumatoid Arthritis Associated With Alterations in the Gastrointestinal Microbiota. CD14+ Dendritic-Shaped Cells Functioning as Dendritic Cells in Rheumatoid Arthritis Synovial Tissues. Patient-Led Urate Self-Monitoring to Improve Clinical Outcomes in People With Gout: A Feasibility Study. Detection and Grading of Radiographic Hand Osteoarthritis Using an Automated Machine Learning Platform.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1