Interpreting Evaluating Respiratory Symptoms™ in COPD Diary Scores in Clinical Trials: Terminology, Methods, and Recommendations

被引:3
作者
Leidy, Nancy Kline [1 ,3 ]
Bushnell, Donald M. [1 ]
Thach, Chau [2 ]
Hache, Carolina [2 ]
Gutzwiller, Florian S. [2 ]
机构
[1] Evidera, Bethesda, MD USA
[2] Novartis Pharm AG, Basel, Switzerland
[3] 7101 Wisconsin Ave Suite 1400, Bethesda, MD 20814 USA
来源
CHRONIC OBSTRUCTIVE PULMONARY DISEASES-JOURNAL OF THE COPD FOUNDATION | 2022年 / 9卷 / 04期
关键词
Evaluating Respiratory Symptoms (TM) in Chronic Obstructive Pulmonary Disease; patient-reported outcome measure; symptomatic relief; interpretation recommendations for PRO measures; PROs and clinical trials; QUALITY-OF-LIFE; EXACERBATIONS; RELIABILITY; VALIDITY;
D O I
10.15326/jcopdf.2022.0307
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Accurately interpreting scores on patient-reported outcome (PRO) measures is essential to understanding and communicating treatment benefit. Over the years, terminology and methods for developing recommendations for PRO score interpretation in clinical trials have evolved, leading to some confusion in the field. The phrase "minimal clinically important difference (MCID)" has been simplified to "minimal important difference (MID)" and use of responder thresholds to interpret statistically significant treatment effects has increased. Anchor-based derivation methods continue to be the standard, with specific variations preferred by regulatory authorities for drug development programs. In the midst of these changes, the Evaluating Respiratory Symptoms (TM) in COPD (E-RS:COPD) was developed and qualified for use as an endpoint in chronic obstructive pulmonary disease (COPD) drug development programs. This paper summarizes the evolution of terminology and method preferences for the development of recommendations for interpreting scores from PRO measures used in clinical trials, and how these changes are reflected in the E-RS:COPD recommendations. The intent is to add clarity to discussions around PRO endpoints and facilitate use of the E-RS:COPD as a key efficacy endpoint in clinical trials of COPD.
引用
收藏
页码:576 / 590
页数:15
相关论文
共 35 条
  • [1] [Anonymous], 2020, Global Strategy for the Diagnosis, Management and Prevention of Chronic Obstructive Pulmonary Disease: 2020 Report
  • [2] Evaluation of a respiratory symptom diary for clinical studies of idiopathic pulmonary fibrosis
    Bacci, Elizabeth Dansie
    O'Quinn, Sean
    Leidy, Nancy Kline
    Murray, Lindsey
    Vernon, Margaret
    [J]. RESPIRATORY MEDICINE, 2018, 134 : 130 - 138
  • [3] Use of the Evaluating Respiratory SymptomsTM in COPD as an Outcome Measure in Clinical Trials: A Rapid Systematic Review
    Bushnell, Donald M.
    Wilson, Rozanne
    Gutzwiller, Florian S.
    Leidy, Nancy K.
    Hache, Carolina
    Thach, Chau
    Vogelmeier, Claus F.
    [J]. CHRONIC OBSTRUCTIVE PULMONARY DISEASES-JOURNAL OF THE COPD FOUNDATION, 2021, 8 (04): : 551 - 571
  • [4] Clinical COPD Questionnaire in patients with chronic respiratory disease
    Canavan, Jane L.
    Dilaver, Deniz
    Clark, Amy L.
    Jones, Sarah E.
    Nolan, Claire M.
    Kon, Samantha S. C.
    Man, William D. -C.
    [J]. RESPIROLOGY, 2014, 19 (07) : 1006 - 1012
  • [5] Cohen J., 1988, STAT POWER ANAL BEHA, P75
  • [6] Donohue James F, 2005, COPD, V2, P111
  • [7] EMA, 2014, ANNEX SUMMARY PRODUC
  • [8] European Medicines Agency (EMA), 2014, DUAK GEN
  • [9] European Medicines Agency (EMA), 2015, DRAFT QUALIFICATION
  • [10] Food and Drug Administration (FDA), 2014, ATTACHMENT GUIDANCE