TY - JOUR
T1 - Treatable traits in the NOVELTY study
AU - for the NOVELTY Study Investigators
AU - Agustí, Alvar
AU - Rapsomaniki, Eleni
AU - Beasley, Richard
AU - Hughes, Rod
AU - Müllerová, Hana
AU - Papi, Alberto
AU - Pavord, Ian D.
AU - van den Berge, Maarten
AU - Faner, Rosa
AU - Benhabib, Gabriel
AU - Ruiz, Xavier Bocca
AU - del Olmo, Ricardo
AU - Lisanti, Raul Eduardo
AU - Marino, Gustavo
AU - Mattarucco, Walter
AU - Nogueira, Juan
AU - Parody, Maria
AU - Pascale, Pablo
AU - Rodriguez, Pablo
AU - Silva, Damian
AU - Svetliza, Graciela
AU - Victorio, Carlos F.
AU - Rolon, Roxana Willigs
AU - Yañez, Anahi
AU - Anderson, Gary
AU - Baines, Stuart
AU - Bowler, Simon
AU - Bremner, Peter
AU - Bull, Sheetal
AU - Carroll, Patrick
AU - Chaalan, Mariam
AU - Farah, Claude
AU - Hammerschlag, Gary
AU - Hancock, Kerry
AU - Harrington, Zinta
AU - Katsoulotos, Gregory
AU - Kim, Joshua
AU - Langton, David
AU - Lee, Donald
AU - Peters, Matthew
AU - Prassad, Lakshman
AU - Reddel, Helen
AU - Sajkov, Dimitar
AU - Santiago, Francis
AU - Simpson, Frederick Graham
AU - Tai, Sze
AU - Thomas, Paul
AU - Wark, Peter
AU - Cançado, José Eduardo Delfini
AU - Hudes, Golda
N1 - Funding Information:
The authors thank participants in the NOVELTY study for their willingness to contribute to medical research, and all field investigators for the quality of their work. Editorial support, under the direction of the authors, was provided by Richard Knight, PhD, CMC Connect, McCann Health Medical Communications, and was funded by AstraZeneca, Cambridge, UK, in accordance with Good Publication Practice (GPP3) guidelines. The NOVELTY study is funded by AstraZeneca.
Funding Information:
Alvar Agustí has received payments in his role as a member of the scientific committee of NOVELTY; received research grants from AstraZeneca, Chiesi, GSK, Menarini, MSD and Zambon; consulting fees from AstraZeneca, Chiesi, GSK, Menarini, MSD and Zambon; and payment or honoraria from AstraZeneca, Chiesi, GSK, Menarini, MSD and Zambon. Eleni Rapsomaniki and Rod Hughes are employees of AstraZeneca. Hana Müllerová is an employee and shareholder of AstraZeneca. Richard Beasley received research grants from AstraZeneca, Cure Kids (NZ), Genentech, GSK and HRC (NZ); consulting fees from AstraZeneca, Avillion and Theravance; payment or honoraria from AstraZeneca, Cipla and Asthma and Respiratory Foundation NZ; support for attending meetings from AstraZeneca and Theravance; and is the Chair of the adult asthma guidelines group for the Asthma and Respiratory Foundation of NZ. Alberto Papi received research grants from AstraZeneca, Boehringer Ingelheim, Chiesi, GSK, Pfizer, Sanofi and Teva; consulting fees from AstraZeneca, Avillion, Chiesi, Elpen Pharmaceuticals, GSK, IQVIA, Novartis and Sanofi; and payment or honoraria from AstraZeneca, Avillion, Boehringer Ingelheim, Chiesi, Edmond Pharma, Elpen Pharmaceuticals, GSK, IQVIA, Menarini, MSD, Mundipharma, Novartis, Sanofi, Teva and Zambon. Ian D. Pavord received research grants from Chiesi; consulting fees from Almirall, AstraZeneca, Boehringer Ingelheim, Chiesi, Circassia, Dey Pharma, Genentech, GSK, Knopp Biosciences, Merck, MSD, Napp Pharmaceuticals, Novartis, Regeneron Pharmaceuticals Inc., Respivert, Schering‐Plough and Teva; payment or honoraria from Aerocrine, Almirall, AstraZeneca, Boehringer Ingelheim, Chiesi, GSK, Novartis, Regeneron Pharmaceuticals Inc., Sanofi and Teva; support for attending meetings from AstraZeneca, Chiesi, GSK, Regeneron Pharmaceuticals Inc., Sanofi, Teva and Napp Pharmaceuticals; and other financial or non‐financial interests from AstraZeneca, Boehringer Ingelheim, GSK, Regeneron Pharmaceuticals Inc., Sanofi and Teva. Maarten van den Berge received research grants from Genentech, GSK, Novartis, Roche and Sanofi. Rosa Faner received research grants from AstraZeneca, GSK, Instituto de Salud Carlos III—Spanish National Health Service and Menarini; consulting fees from GSK; and payment or honoraria from Chiesi.
Publisher Copyright:
© 2022 The Authors. Respirology published by John Wiley & Sons Australia, Ltd on behalf of Asian Pacific Society of Respirology.
PY - 2022/11
Y1 - 2022/11
N2 - Background and objective: Asthma and chronic obstructive pulmonary disease (COPD) are two prevalent and complex diseases that require personalized management. Although a strategy based on treatable traits (TTs) has been proposed, the prevalence and relationship of TTs to the diagnostic label and disease severity established by the attending physician in a real-world setting are unknown. We assessed how the presence/absence of specific TTs relate to the diagnosis and severity of ‘asthma’, ‘COPD’ or ‘asthma + COPD’. Methods: The authors selected 30 frequently occurring TTs from the NOVELTY study cohort (NOVEL observational longiTudinal studY; NCT02760329), a large (n = 11,226), global study that systematically collects data in a real-world setting, both in primary care clinics and specialized centres, for patients with ‘asthma’ (n = 5932, 52.8%), ‘COPD’ (n = 3898, 34.7%) or both (‘asthma + COPD’; n = 1396, 12.4%). Results: The results indicate that (1) the prevalence of the 30 TTs evaluated varied widely, with a mean ± SD of 4.6 ± 2.6, 5.4 ± 2.6 and 6.4 ± 2.8 TTs/patient in those with ‘asthma’, ‘COPD’ and ‘asthma + COPD’, respectively (p < 0.0001); (2) there were no large global geographical variations, but the prevalence of TTs was different in primary versus specialized clinics; (3) several TTs were specific to the diagnosis and severity of disease, but many were not; and (4) both the presence and absence of TTs formed a pattern that is recognized by clinicians to establish a diagnosis and grade its severity. Conclusion: These results provide the largest and most granular characterization of TTs in patients with airway diseases in a real-world setting to date.
AB - Background and objective: Asthma and chronic obstructive pulmonary disease (COPD) are two prevalent and complex diseases that require personalized management. Although a strategy based on treatable traits (TTs) has been proposed, the prevalence and relationship of TTs to the diagnostic label and disease severity established by the attending physician in a real-world setting are unknown. We assessed how the presence/absence of specific TTs relate to the diagnosis and severity of ‘asthma’, ‘COPD’ or ‘asthma + COPD’. Methods: The authors selected 30 frequently occurring TTs from the NOVELTY study cohort (NOVEL observational longiTudinal studY; NCT02760329), a large (n = 11,226), global study that systematically collects data in a real-world setting, both in primary care clinics and specialized centres, for patients with ‘asthma’ (n = 5932, 52.8%), ‘COPD’ (n = 3898, 34.7%) or both (‘asthma + COPD’; n = 1396, 12.4%). Results: The results indicate that (1) the prevalence of the 30 TTs evaluated varied widely, with a mean ± SD of 4.6 ± 2.6, 5.4 ± 2.6 and 6.4 ± 2.8 TTs/patient in those with ‘asthma’, ‘COPD’ and ‘asthma + COPD’, respectively (p < 0.0001); (2) there were no large global geographical variations, but the prevalence of TTs was different in primary versus specialized clinics; (3) several TTs were specific to the diagnosis and severity of disease, but many were not; and (4) both the presence and absence of TTs formed a pattern that is recognized by clinicians to establish a diagnosis and grade its severity. Conclusion: These results provide the largest and most granular characterization of TTs in patients with airway diseases in a real-world setting to date.
KW - COPD
KW - airways
KW - allergy
KW - asthma
KW - bronchitis
KW - chronic obstructive pulmonary disease
KW - emphysema
KW - smoking
UR - http://www.scopus.com/inward/record.url?scp=85134514840&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85134514840&partnerID=8YFLogxK
U2 - 10.1111/resp.14325
DO - 10.1111/resp.14325
M3 - Article
C2 - 35861464
AN - SCOPUS:85134514840
SN - 1323-7799
VL - 27
SP - 929
EP - 940
JO - Respirology
JF - Respirology
IS - 11
ER -