Connective tissue disease related interstitial lung diseases and idiopathic pulmonary fibrosis: Provisional core sets of domains and instruments for use in clinical trials

Lesley Ann Saketkoo, Shikha Mittoo, Dörte Huscher, Dinesh Khanna, Paul F. Dellaripa, Oliver Distler, Kevin R. Flaherty, Sid Frankel, Chester V. Oddis, Christopher P. Denton, Aryeh Fischer, Otylia M. Kowal-Bielecka, Daphne Lesage, Peter A. Merkel, Kristine Phillips, David Pittrow, Jeffrey Swigris, Katerina Antoniou, Robert P. Baughman, Flavia V. CastelinoRomy B. Christmann, Lisa Christopher-Stine, Harold R. Collard, Vincent Cottin, Sonye Danoff, Kristin B. Highland, Laura Hummers, Ami A. Shah, Dong Soon Kim, David A. Lynch, Frederick W. Miller, Susanna M. Proudman, Luca Richeldi, Jay H. Ryu, Nora Sandorfi, Catherine Sarver, Athol U. Wells, Vibeke Strand, Eric L. Matteson, Kevin K. Brown, James R. Seibold

Research output: Contribution to journalArticle

Abstract

Rationale: Clinical trial design in interstitial lung diseases (ILDs) has been hampered by lack of consensus on appropriate outcome measures for reliably assessing treatment response. In the setting of connective tissue diseases (CTDs), some measures of ILD disease activity and severity may be confounded by non-pulmonary comorbidities. Methods: The Connective Tissue Disease associated Interstitial Lung Disease (CTD-ILD) working group of Outcome Measures in Rheumatology-a non-profit international organisation dedicated to consensus methodology in identification of outcome measures-conducted a series of investigations which included a Delphi process including >248 ILD medical experts as well as patient focus groups culminating in a nominal group panel of ILD experts and patients. The goal was to define and develop a consensus on the status of outcome measure candidates for use in randomised controlled trials in CTD-ILD and idiopathic pulmonary fibrosis (IPF). Results: A core set comprising specific measures in the domains of lung physiology, lung imaging, survival, dyspnoea, cough and health-related quality of life is proposed as appropriate for consideration for use in a hypothetical 1-year multicentre clinical trial for either CTD-ILD or IPF. As many widely used instruments were found to lack full validation, an agenda for future research is proposed. Conclusion: Identification of consensus preliminary domains and instruments to measure them was attained and is a major advance anticipated to facilitate multicentre RCTs in the field.

Original languageEnglish (US)
Pages (from-to)428-436
Number of pages9
JournalThorax
Volume69
Issue number5
DOIs
StatePublished - May 2014

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ASJC Scopus subject areas

  • Pulmonary and Respiratory Medicine

Cite this

Saketkoo, L. A., Mittoo, S., Huscher, D., Khanna, D., Dellaripa, P. F., Distler, O., Flaherty, K. R., Frankel, S., Oddis, C. V., Denton, C. P., Fischer, A., Kowal-Bielecka, O. M., Lesage, D., Merkel, P. A., Phillips, K., Pittrow, D., Swigris, J., Antoniou, K., Baughman, R. P., ... Seibold, J. R. (2014). Connective tissue disease related interstitial lung diseases and idiopathic pulmonary fibrosis: Provisional core sets of domains and instruments for use in clinical trials. Thorax, 69(5), 428-436. https://doi.org/10.1136/thoraxjnl-2013-204202