The added value of health-related quality of life as a prognostic indicator of overall survival and progression-free survival in glioma patients: a meta-analysis based on individual patient data from randomised controlled trials.


Journal

European journal of cancer (Oxford, England : 1990)
ISSN: 1879-0852
Titre abrégé: Eur J Cancer
Pays: England
ID NLM: 9005373

Informations de publication

Date de publication:
07 2019
Historique:
received: 10 04 2019
revised: 13 05 2019
accepted: 13 05 2019
pubmed: 17 6 2019
medline: 2 6 2020
entrez: 17 6 2019
Statut: ppublish

Résumé

Prognostic value of health-related quality of life (HRQoL) data may be important to inform patients in clinical practice and to guide clinical decision-making. Our study investigated the added prognostic value of HRQoL for overall survival (OS) and progression-free survival (PFS) in a large heterogeneous sample of glioma patients, besides known prognostic factors. We included individual baseline data from previously published randomised controlled trials (RCTs) in glioma patients in which HRQoL was assessed through the European Organisation for Research and Treatment of Cancer QLQ-C30 and QLQ-BN20 questionnaires. Multivariable Cox regression models (stratified for newly diagnosed versus recurrent disease) were constructed, first with clinical variables (age, sex, tumour type, performance status, allocated treatment and extent of resection) only and subsequently with HRQoL variables added, separately for OS and PFS. The added prognostic value of HRQoL was calculated using C-indices. Baseline HRQoL and clinical data from 15 RCTs were included, comprising 5217 patients. In the model including both clinical and HRQoL variables, better cognitive and role functioning and less motor dysfunction were independently associated with longer OS, whereas better role and cognitive functioning, less nausea and vomiting and more appetite loss were independently associated with prolonged PFS. However, C-indices indicated only a small prognostic improvement of the models for OS and PFS when adding HRQoL to the clinical prognostic variables (+1.1% for OS and +.7% for PFS). Our findings demonstrate that several baseline HRQoL variables are independently prognostic for OS and PFS, yet the added value of HRQoL to the known clinical prognostic variables was small.

Identifiants

pubmed: 31203194
pii: S0959-8049(19)30315-6
doi: 10.1016/j.ejca.2019.05.012
pii:
doi:

Types de publication

Journal Article Meta-Analysis Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

190-198

Informations de copyright

Copyright © 2019 Elsevier Ltd. All rights reserved.

Auteurs

Marijke Coomans (M)

Department of Neurology, Leiden University Medical Center, Leiden, the Netherlands. Electronic address: m.b.coomans@lumc.nl.

Linda Dirven (L)

Department of Neurology, Leiden University Medical Center, Leiden, the Netherlands; Department of Neurology, Haaglanden Medical Center, Den Haag, the Netherlands.

Neil K Aaronson (N)

Division of Psychosocial Research and Epidemiology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.

Brigitta G Baumert (BG)

Department of Radiation-oncology, University Hospital Bonn, Germany; Department of Radiation Oncology (MAASTRO Clinic), and GROW (School for Oncology and Developmental Biology), Maastricht University Medical Center, Maastricht, the Netherlands.

Martin van den Bent (M)

The Brain Tumor Center, Erasmus MC Cancer Institute, Rotterdam, the Netherlands.

Andrew Bottomley (A)

Quality of Life Department, European Organisation for Research and Treatment of Cancer, Brussels, Belgium.

Alba A Brandes (AA)

Department of Medical Oncology, Azienda USL-IRCCS Institute of Neurological Sciences, Bologna, Italy.

Olivier Chinot (O)

Aix-Marseille Univ, APHM, CNRS, INP, Inst Neurophysiopathol, CHU Timone, Service de Neuro-Oncologie, Marseille, France.

Corneel Coens (C)

Quality of Life Department, European Organisation for Research and Treatment of Cancer, Brussels, Belgium.

Thierry Gorlia (T)

European Organization for Research and Treatment of Cancer Headquarters, Brussels, Belgium.

Ulrich Herrlinger (U)

Division of Clinical Neurooncology, Department of Neurology and Center of Integrated Oncology (CIO), University of Bonn, Bonn, Germany.

Florence Keime-Guibert (F)

Groupe Hôpital Pitié-Salpetrière, Paris, France.

Annika Malmström (A)

Department of Advanced Home Care and Department of Clinical and Experimental Medicine, Linköping University, Linköping, Sweden.

Francesca Martinelli (F)

Quality of Life Department, European Organisation for Research and Treatment of Cancer, Brussels, Belgium.

Roger Stupp (R)

Northwestern University, Feinberg School of Medicine, Chicago, IL, USA.

Andrea Talacchi (A)

Department of Neurosciences, Azienda Ospedaliera San Giovanni Addolorata, Roma, Italy.

Michael Weller (M)

Department of Neurology, University Hospital and University of Zurich, Zurich, Switzerland.

Wolfgang Wick (W)

Neurology Clinic and National Centre for Tumour Diseases, University Hospital Heidelberg, Heidelberg, Germany; German Consortium of Translational Cancer Research (DKTK), Clinical Cooperation Unit Neurooncology, German Cancer Research Center, Heidelberg, Germany.

Jaap C Reijneveld (JC)

Department of Neurology and Brain Tumour Center Amsterdam, Amsterdam University Medical Center, Amsterdam, the Netherlands.

Martin J B Taphoorn (MJB)

Department of Neurology, Leiden University Medical Center, Leiden, the Netherlands; Department of Neurology, Haaglanden Medical Center, Den Haag, the Netherlands.

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