Functional impairment, symptom severity, and overall quality of life in patients with advanced lung or colorectal cancer in six European countries: baseline findings from the ACTION study.

Advanced cancer Colorectal cancer Functional status Lung cancer Palliative care Quality of life Symptoms

Journal

Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer
ISSN: 1433-7339
Titre abrégé: Support Care Cancer
Pays: Germany
ID NLM: 9302957

Informations de publication

Date de publication:
Oct 2021
Historique:
received: 22 12 2020
accepted: 11 03 2021
pubmed: 21 3 2021
medline: 16 10 2021
entrez: 20 3 2021
Statut: ppublish

Résumé

People with advanced cancer often suffer from various symptoms, which can arise from the cancer itself and its treatment, the illness experience, and/or co-morbid conditions. Important patient-reported outcomes such as functional status, symptom severity, and quality of life (QoL) might differ between countries, as countries vary with regard to contextual factors such as their healthcare system. To assess self-reported emotional functioning, physical functioning, symptoms, and overall QoL in patients with advanced lung or colorectal cancer from six European countries, particularly in relation to their country of residence. We used baseline patient data from the ACTION trial, including socio-demographic and clinical data as well as patient-reported data regarding functioning, symptoms, and overall QoL (EORTC QLQ-C15-PAL). Data from 1117 patients (55% lung cancer stage III/IV, 45% colorectal cancer stage IV) were used. The highest (worst) average symptom score was found for fatigue. We found similarities but also important differences in the outcomes across countries. The best scores (the highest for emotional functioning and QoL, the lowest for symptoms) were reported by Dutch and Danish patients. Belgian patients reported relatively low emotional functioning. The optimization of functioning, symptom relief, and overall QoL should be important objectives of healthcare professionals who take care of patients with advanced cancer. There are similarities, but also substantial differences across countries in functional status, symptoms, and overall QoL. Policymakers should take these differences into account and invest in offering health care catered to the needs of their population.

Sections du résumé

BACKGROUND BACKGROUND
People with advanced cancer often suffer from various symptoms, which can arise from the cancer itself and its treatment, the illness experience, and/or co-morbid conditions. Important patient-reported outcomes such as functional status, symptom severity, and quality of life (QoL) might differ between countries, as countries vary with regard to contextual factors such as their healthcare system.
PURPOSE OBJECTIVE
To assess self-reported emotional functioning, physical functioning, symptoms, and overall QoL in patients with advanced lung or colorectal cancer from six European countries, particularly in relation to their country of residence.
METHODS METHODS
We used baseline patient data from the ACTION trial, including socio-demographic and clinical data as well as patient-reported data regarding functioning, symptoms, and overall QoL (EORTC QLQ-C15-PAL).
RESULTS RESULTS
Data from 1117 patients (55% lung cancer stage III/IV, 45% colorectal cancer stage IV) were used. The highest (worst) average symptom score was found for fatigue. We found similarities but also important differences in the outcomes across countries. The best scores (the highest for emotional functioning and QoL, the lowest for symptoms) were reported by Dutch and Danish patients. Belgian patients reported relatively low emotional functioning.
CONCLUSION CONCLUSIONS
The optimization of functioning, symptom relief, and overall QoL should be important objectives of healthcare professionals who take care of patients with advanced cancer. There are similarities, but also substantial differences across countries in functional status, symptoms, and overall QoL. Policymakers should take these differences into account and invest in offering health care catered to the needs of their population.

Identifiants

pubmed: 33742242
doi: 10.1007/s00520-021-06150-8
pii: 10.1007/s00520-021-06150-8
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

5797-5810

Subventions

Organisme : European Union's Seventh Framework Programme for Research and Technological Development (FP7)
ID : 6025410-2

Informations de copyright

© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

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Auteurs

Mariëtte N Verkissen (MN)

Vrije Universiteit Brussel (VUB) & Ghent University, End-of-Life Care Research Group, Brussels, Belgium. mariette.verkissen@vub.be.
Vrije Universiteit Brussel (VUB), Department of Family Medicine and Chronic Care, Brussels, Belgium. mariette.verkissen@vub.be.

Aline De Vleminck (A)

Vrije Universiteit Brussel (VUB) & Ghent University, End-of-Life Care Research Group, Brussels, Belgium.
Vrije Universiteit Brussel (VUB), Department of Family Medicine and Chronic Care, Brussels, Belgium.

Mogens Groenvold (M)

University of Copenhagen, Department of Geriatrics and Palliative Medicine, Bispebjerg and Frederiksberg Hospital, Copenhagen, Denmark.
University of Copenhagen, Department of Public Health, Copenhagen, Denmark.

Lea J Jabbarian (LJ)

Erasmus University Medical Center, Department of Public Health, Rotterdam, Netherlands.

Francesco Bulli (F)

Oncological Network, Prevention and Research Institute (ISPRO), Clinical Epidemiology, Florence, Italy.

Wilfried Cools (W)

Vrije Universiteit Brussel (VUB), Interfaculty Center Data Processing and Statistics, Brussels, Belgium.

Johannes J M van Delden (JJM)

University Medical Center Utrecht, Julius Center for Health Sciences and Primary Care, Utrecht, Netherlands.

Urška Lunder (U)

University Clinic of Respiratory and Allergic Diseases Golnik, Golnik, Slovenia.

Guido Miccinesi (G)

Oncological Network, Prevention and Research Institute (ISPRO), Clinical Epidemiology, Florence, Italy.

Sheila A Payne (SA)

Lancaster University, International Observatory on End of Life Care, Division of Health Research, Lancaster, United Kingdom.

Kristian Pollock (K)

University of Nottingham, School of Health Sciences, Nottingham, United Kingdom.

Judith A C Rietjens (JAC)

Erasmus University Medical Center, Department of Public Health, Rotterdam, Netherlands.

Luc Deliens (L)

Vrije Universiteit Brussel (VUB) & Ghent University, End-of-Life Care Research Group, Brussels, Belgium.
Vrije Universiteit Brussel (VUB), Department of Family Medicine and Chronic Care, Brussels, Belgium.
Ghent University, Department of Public Health and Primary Care, Ghent, Belgium.

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