International Journal of COPD (Jul 2020)

Patient-Reported Outcomes (PROs) in COPD Clinical Trials: Trends and Gaps

  • Afroz N,
  • Gutzwiller FS,
  • Mackay AJ,
  • Naujoks C,
  • Patalano F,
  • Kostikas K

Journal volume & issue
Vol. Volume 15
pp. 1789 – 1800

Abstract

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Nuzhat Afroz,1 Florian S Gutzwiller,2 Alex J Mackay,3,4 Christel Naujoks,2 Francesco Patalano,5 Konstantinos Kostikas6,7 1Patient Access Services, Novartis Healthcare Private Limited, Hyderabad, India; 2Global Patient Access, Novartis Pharma AG, Basel, Switzerland; 3National Heart and Lung Institute, Imperial College London, London, UK; 4Global Medical Affairs and Drug Development, Novartis Pharma AG, Basel, Switzerland; 5Clinical Development and Analytic, Global Drug Development, Novartis Pharma AG, Basel, Switzerland; 6Respiratory Medicine Department, University of Ioannina, Ioannina, Greece; 7Global Medical Affairs, Respiratory, Novartis Pharma AG, Basel, SwitzerlandCorrespondence: Nuzhat AfrozNovartis Healthcare Private Limited, Hyderabad 500032, IndiaTel +91 40675841975Email [email protected]: Key characteristics of chronic obstructive pulmonary disease (COPD) that significantly affect health-related quality of life (HRQoL) include chest symptoms, dyspnea, cough, sputum production, and exacerbations. Additional areas of impact are sleep, fatigue, emotional well-being, social functioning, and coping. Patient-reported outcomes (PROs) are essential to evaluate symptoms, impact of symptoms on activities of daily living, and treatment response. This review summarizes COPD-specific PRO endpoints from randomized controlled trials of approved and commonly used COPD drugs. A search conducted in “ClinicalTrials.gov” to identify COPD clinical trials (only completed Phase III and IV) incorporating PRO endpoints yielded a total of 104 clinical trials for inclusion in this analysis. Both symptom-based and HRQoL-specific PRO measures were reported. Several COPD-specific PRO measures are available; however, the St. George’s Respiratory Questionnaire (SGRQ) and the Baseline and Transition Dyspnea Indexes (BDI/TDI) were reported in the majority of the studies. Results reflected a gap in terms of full coverage of key impacted areas from a patient’s perspective. Methodological issues identified in this review related to scoring of instruments require careful consideration, as these challenges may limit the complete assessment of drug benefits. Selection of PRO measures aligned with the expected treatment benefit of a drug in a clinical trial should reflect patients’ perspective holistically.Keywords: chronic obstructive pulmonary disease, patient-reported outcomes, clinical trials, endpoints, Patient-Focused Drug Development, randomized controlled trials

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