Ustekinumab improves health‐related quality of life in patients with moderate‐to‐severe Crohn's disease: Results up to Week 104 of the STARDUST trial

Author:

Panés Julian1ORCID,Vermeire Séverine2ORCID,D'Haens Geert R.3,Danese Silvio4,Magro Fernando56,Nazar Maciej7,Le Bars Manuela8,Lahaye Marjolein9,Ni Lioudmila10,Bravatà Ivana11,Gaya Daniel R.12,Peyrin‐Biroulet Laurent1314ORCID,Dignass Axel15ORCID,

Affiliation:

1. Department of Gastroenterology Hospital Clinic of Barcelona IDIBAPS, CIBERehd Barcelona Spain

2. Department of Gastroenterology & Hepatology University Hospitals Leuven Leuven Belgium

3. Amsterdam University Medical Center University of Amsterdam Amsterdam The Netherlands

4. Gastroenterology and Endoscopy IRCCS Ospedale San Raffaele and University Vita‐Salute San Raffaele Milan Italy

5. Department of Pharmacology & Therapeutics Institute for Molecular and Cell Biology Faculty of Medicine University of Porto Porto Portugal

6. Department of Gastroenterology Hospital de São João Porto Portugal

7. Janssen‐Cilag Polska Sp. z o.o. Warsaw Poland

8. Janssen‐Cilag Issy‐les‐Moulineaux France

9. Janssen‐Cilag BV Breda The Netherlands

10. Janssen Cilag Russia Moscow Russian Federation

11. Janssen‐Cilag Milan Italy

12. Department of Gastroenterology Glasgow Royal Infirmary Glasgow UK

13. University of Lorraine INSERM NGERE Nancy France

14. Groupe Hospitalier Privé Ambroise Paré ‐ Hartmann Paris IBD Center Neuilly sur Seine France

15. Department of Medicine I Agaplesion Markus Hospital Frankfurt/Main Germany

Abstract

AbstractBackgroundSTARDUST is a phase 3b randomized controlled trial comparing two ustekinumab treatment strategies in patients with Crohn's disease (CD): treat‐to‐target (T2T) versus standard of care (SoC).ObjectiveWe investigated the effect of a T2T or SoC ustekinumab treatment strategy on health‐related quality of life (HRQoL) and work productivity and activity impairment (WPAI) over a 2‐year follow‐up period.MethodsAt Week 16, adult patients with moderate‐to‐severe active CD were randomized 1:1 to either T2T or SoC treatment groups. We assessed changes from baseline in HRQoL measures (Inflammatory Bowel Disease Questionnaire [IBDQ], EuroQoL 5‐dimension 5‐level [visual analogue scale and index], Functional Assessment of Chronic Illness Therapy‐Fatigue, Hospital Anxiety and Depression Scale‐Anxiety and ‐Depression) and the WPAI questionnaire in two patient populations: randomized analysis set (RAS, patients randomized to either T2T or SoC at Week 16 and completed Week 48) and modified RAS (mRAS, patients who entered the long‐term extension [LTE] period at Week 48).ResultsAt Week 16, 440 patients were randomized to T2T (n = 219) or SoC (n = 221) arms; 366 patients completed Week 48. Of these, 323 patients entered the LTE and 258 patients completed 104 weeks of treatment. In the RAS population, percentages of patients achieving IBDQ response and remission were not significantly different between treatment arms at Weeks 16 and 48. In the overall mRAS population, IBDQ response and remission increased over time from Weeks 16–104. In both populations, improvements from baseline in all HRQoL measurements were observed at Week 16 and maintained until either Week 48 or Week 104, respectively. In both populations, improvements from baseline in T2T and SoC arms at Weeks 16, 48 or 104 in WPAI domains were observed.ConclusionIndependent of treatment strategy (T2T or SoC), ustekinumab was effective in improving HRQoL measurements and WPAI over a period of 2 years.

Funder

Janssen Pharmaceuticals

Publisher

Wiley

Subject

Gastroenterology,Oncology

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3