Changes in the Use of Comprehensive Geriatric Assessment in Clinical Trials for Older Patients with Cancer over Time

Author:

Le Saux Olivia12,Falandry Claire34,Gan Hui K.567,You Benoit12,Freyer Gilles12,Péron Julien189

Affiliation:

1. Medical Oncology Department, Hospices Civils de Lyon (IC-HCL), Pierre-Bénite, France

2. Lyon 1 University, EMR 3738, Faculté de Médecine Lyon-Sud, Oullins, France

3. Geriatric Unit, Centre Hospitalier Lyon Sud, Pierre-Bénite, France

4. CarMen biomedical research laboratory (Cardiovascular diseases, Metabolism, diabetology and Nutrition) INSERM UMR 1060, Université de Lyon, Oullins, France

5. Olivia Newton-John Cancer Research Institute, Heidelberg, Australia

6. School of Cancer Medicine, La Trobe University, Heidelberg, Australia

7. Department of Medicine, Melbourne University, Melbourne, Australia

8. Statistics unit, Hospices Civils de Lyon (IC-HCL), Pierre-Bénite, France

9. CNRS, UMR 5558 Biometry and Evolutionary Biology laboratory Université Lyon 1, Villeurbanne, France

Abstract

Abstract Background The objective of this study was to describe the implementation of comprehensive geriatric assessment (CGA) in clinical trials dedicated to older patients before and after the creation of the International Society of Geriatric Oncology in the early 2000s. Subjects, Materials, and Methods All phase I, II, and III trials dedicated to the treatment of cancer among older patients published between 2001 and 2004 and between 2011 and 2014 were reviewed. We considered that a CGA was performed when the authors indicated an intention to do so in the Methods section of the article. We collected each geriatric domain assessed using a validated tool even in the absence of a clear CGA, including nutritional, functional, cognitive, and psychological status, comorbidity, comedication, overmedication, social status and support, and geriatric syndromes. Results A total of 260 clinical trials dedicated to older patients were identified over the two time periods: 27 phase I, 193 phase II, and 40 phase III trials. CGA was used in 9% and 8% of phase II and III trials, respectively; it was never used in phase I trials. Performance status was reported in 67%, 79%, and 75% of phase I, II, and III trials, respectively. Functional assessment was reported in 4%, 11%, and 13% of phase I, II, and III trials, respectively. Between the two time periods, use of CGA increased from 1% to 11% (p = .0051) and assessment of functional status increased from 3% to 14% (p = .0094). Conclusion The use of CGA in trials dedicated to older patients increased significantly but remained insufficient.

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

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