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Developing a fit-for-purpose composite symptom score as a symptom burden endpoint for clinical trials in patients with malignant pleural mesothelioma.
Cleeland, Charles S; Keating, Karen N; Cuffel, Brian; Elbi, Cem; Siegel, Jonathan M; Gerlinger, Christoph; Symonds, Tara; Sloan, Jeff A; Dueck, Amylou C; Bottomley, Andrew; Wang, Xin Shelley; Williams, Loretta A; Mendoza, Tito R.
  • Cleeland CS; Department of Symptom Research, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
  • Keating KN; Symptom Assessment Systems, 1416 Marconi St, Houston, TX, USA.
  • Cuffel B; Bayer HealthCare Pharmaceuticals, Whippany, NJ, USA.
  • Elbi C; Bayer HealthCare Pharmaceuticals, Whippany, NJ, USA.
  • Siegel JM; Bayer HealthCare Pharmaceuticals, Whippany, NJ, USA.
  • Gerlinger C; Bayer HealthCare Pharmaceuticals, Whippany, NJ, USA.
  • Symonds T; Bayer AG, Berlin, Germany.
  • Sloan JA; Gynecology, Obstetrics and Reproductive Medicine, University Medical School of Saarland, Homburg/Saar, Germany.
  • Dueck AC; Clinical Outcomes Solutions, Folkestone, Kent, UK.
  • Bottomley A; Division of Biomedical Statistics and Informatics, Department of Health Sciences Research, Mayo Clinic, Rochester, MN, USA.
  • Wang XS; Section of Biostatistics, Division of Health Sciences Research, Mayo Clinic, Phoenix, AZ, USA.
  • Williams LA; Quality of Life Department, European Organisation for Research and Treatment of Cancer, Brussels, Belgium.
  • Mendoza TR; Bottomley Consulting Group, Brussels, Belgium.
Sci Rep ; 14(1): 14839, 2024 06 27.
Article en En | MEDLINE | ID: mdl-38937473
ABSTRACT
We developed a composite symptom score (CSS) representing disease-related symptom burden over time in patients with malignant pleural mesothelioma (MPM). Longitudinal data were collected from an open-label Phase IIB study in which 239 patients completed the validated MD Anderson Symptom Inventory for MPM (MDASI-MPM). A blinded, independent review committee of external patient-reported outcomes experts advised on MDASI-MPM symptoms to include in the CSS. Through iterative analyses of potential symptom-item combinations, 5 MPM symptoms (pain, fatigue, shortness of breath, muscle weakness, coughing) were selected. The CSS correlated strongly with the full MDASI-MPM symptom set (0.92-0.94) and the Lung Cancer Symptom Scale-Mesothelioma (0.79-0.87) at each co-administration of the scales. The CSS also had good sensitivity to worsening disease and global quality-of-life ratings. The MDASI-MPM CSS can be used as an outcome in MPM clinical trials, including in responder analyses and at the individual patient level. It is brief enough to administer frequently, including electronically, to better capture symptom trajectories during and after a trial and in clinical practice. As a single score, the CSS addresses multiplicity issues that can arise when several symptoms increase due to worsening disease. Our process can be adapted to produce a CSS for other advanced-cancer trials.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Pleurales / Calidad de Vida / Mesotelioma Maligno Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Pleurales / Calidad de Vida / Mesotelioma Maligno Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Año: 2024 Tipo del documento: Article