A Conceptual Framework for Use of Increased Endurance Time During Constant Work Rate Cycle Ergometry as a Patient-Focused Meaningful Outcome in COPD Clinical Trials.

clinical outcome assessment copd drug development exercise endurance physical functioning

Journal

Chronic obstructive pulmonary diseases (Miami, Fla.)
ISSN: 2372-952X
Titre abrégé: Chronic Obstr Pulm Dis
Pays: United States
ID NLM: 101635411

Informations de publication

Date de publication:
29 Apr 2022
Historique:
pubmed: 13 1 2022
medline: 13 1 2022
entrez: 12 1 2022
Statut: ppublish

Résumé

The Chronic Lung Disease Biomarker and Clinical Outcome Assessment Qualification Consortium (CBQC) evaluates the potential of biomarkers and outcome measures as drug development tools. Exercise endurance is an objective indicator of treatment benefit, closely related to daily physical function. Therefore, it is an ideal candidate for an outcome for drug development trials. Unfortunately, no exercise endurance measure is qualified by regulatory authorities for use in trials of chronic obstructive pulmonary disease (COPD) and no approved COPD therapies have claims of improving exercise endurance. Consequently, it has been challenging for developers to consider this outcome when designing clinical trials for new therapies. Endurance time during constant work rate cycle ergometry (CWRCE), performed on an electronically braked stationary cycle ergometer, provides an exercise endurance measure under standardized conditions. Baseline individualized work rate for each participant is set using an incremental test. During CWRCE the patient is encouraged to continue exercising for as long as possible. Although not required, physiological and sensory responses (e.g., pulmonary ventilation, heart rate, dyspnea ratings) are frequently collected to support interpretation of endurance time changes. Exercise tolerance limit is reached when the individual is limited by symptoms, unable to maintain pedaling cadence or unable to continue safely. At exercise cessation, exercise duration is recorded. An CWRCE endurance time increase from the pre-treatment baseline is proposed as a key efficacy endpoint in clinical trials. In COPD, improved exercise endurance has a direct relationship to the experience of physical functioning in daily life, which is a patient-centered, meaningful benefit.

Identifiants

pubmed: 35018752
doi: 10.15326/jcopdf.2021.0258
pmc: PMC9166337
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

252-265

Subventions

Organisme : AstraZeneca
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL151452
Pays : United States
Organisme : GlaxoSmithKline
Pays : United States
Organisme : Chiesi
Pays : United States
Organisme : Boehringer Ingelheim
Pays : United States
Organisme : Novartis
Pays : United States
Organisme : NICHD NIH HHS
ID : P50 HD098593
Pays : United States

Informations de copyright

JCOPDF © 2021.

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Auteurs

Richard Casaburi (R)

Rehabilitation Clinical Trials Center, Lundquist Institute for Biomedical Innovation at Harbor- UCLA Medical Center, Torrance, California, United States.

Debora D Merrill (DD)

COPD Foundation, Washington, DC, United States.

Gale Harding (G)

Evidera, Bethesda, Maryland, United States.

Nancy K Leidy (NK)

Evidera, Bethesda, Maryland, United States.

Harry B Rossiter (HB)

Rehabilitation Clinical Trials Center, Lundquist Institute for Biomedical Innovation at Harbor- UCLA Medical Center, Torrance, California, United States.

Ruth Tal-Singer (R)

COPD Foundation, Washington, DC, United States.

Alan Hamilton (A)

Medical Department, Boehringer Ingelheim, Burlington, Ontario, Canada.

Classifications MeSH