A prospective study examining cachexia predictors in patients with incurable cancer.


Journal

BMC palliative care
ISSN: 1472-684X
Titre abrégé: BMC Palliat Care
Pays: England
ID NLM: 101088685

Informations de publication

Date de publication:
04 Jun 2019
Historique:
received: 31 08 2018
accepted: 20 05 2019
entrez: 6 6 2019
pubmed: 6 6 2019
medline: 20 12 2019
Statut: epublish

Résumé

Early intervention against cachexia necessitates a predictive model. The aims of this study were to identify predictors of cachexia development and to create and evaluate accuracy of a predictive model based on these predictors. A secondary analysis of a prospective, observational, multicentre study was conducted. Patients, who attended a palliative care programme, had incurable cancer and did not have cachexia at baseline, were amenable to the analysis. Cachexia was defined as weight loss (WL) > 5% (6 months) or WL > 2% and body mass index< 20 kg/m Six-hundred-twenty-eight patients were included in the analysis. Median age was 65 years (IQR 17), 359(57%) were female and median Karnofsky performance status was 70(IQR 10). Median follow-up was 109 days (IQR 108), and 159 (25%) patients developed cachexia. Initial WL, cancer type, appetite and chronic obstructive pulmonary disease were significant predictors (p ≤ 0.04). A five-level model was created with each level carrying an increasing risk of cachexia development. For Risk-level 1-patients (WL < 3%, breast or hematologic cancer and no or little appetite loss), median time to cachexia development was not reached, while Risk-level 5-patients (WL 3-5%) had a median time to cachexia development of 51 days. Accuracy of cachexia predictions at 3 months was 76%. Important predictors of cachexia have been identified and used to construct a predictive model of cancer cachexia. ClinicalTrials.gov Identifier: NCT01362816 .

Sections du résumé

BACKGROUND BACKGROUND
Early intervention against cachexia necessitates a predictive model. The aims of this study were to identify predictors of cachexia development and to create and evaluate accuracy of a predictive model based on these predictors.
METHODS METHODS
A secondary analysis of a prospective, observational, multicentre study was conducted. Patients, who attended a palliative care programme, had incurable cancer and did not have cachexia at baseline, were amenable to the analysis. Cachexia was defined as weight loss (WL) > 5% (6 months) or WL > 2% and body mass index< 20 kg/m
RESULTS RESULTS
Six-hundred-twenty-eight patients were included in the analysis. Median age was 65 years (IQR 17), 359(57%) were female and median Karnofsky performance status was 70(IQR 10). Median follow-up was 109 days (IQR 108), and 159 (25%) patients developed cachexia. Initial WL, cancer type, appetite and chronic obstructive pulmonary disease were significant predictors (p ≤ 0.04). A five-level model was created with each level carrying an increasing risk of cachexia development. For Risk-level 1-patients (WL < 3%, breast or hematologic cancer and no or little appetite loss), median time to cachexia development was not reached, while Risk-level 5-patients (WL 3-5%) had a median time to cachexia development of 51 days. Accuracy of cachexia predictions at 3 months was 76%.
CONCLUSION CONCLUSIONS
Important predictors of cachexia have been identified and used to construct a predictive model of cancer cachexia.
TRIAL REGISTRATION BACKGROUND
ClinicalTrials.gov Identifier: NCT01362816 .

Identifiants

pubmed: 31164115
doi: 10.1186/s12904-019-0429-2
pii: 10.1186/s12904-019-0429-2
pmc: PMC6549342
doi:

Banques de données

ClinicalTrials.gov
['NCT01362816']

Types de publication

Journal Article Multicenter Study Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

46

Subventions

Organisme : Marie Curie
ID : MCCC-RP-16-A20997
Pays : United Kingdom
Organisme : Helsinn
ID : NA
Organisme : Kreftforeningen
ID : NA
Organisme : Helse Midt-Norge
ID : 6070

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Auteurs

Ola Magne Vagnildhaug (OM)

Department of Clinical and Molecular Medicine, Faculty of Medicine and Health Sciences, NTNU - Norwegian University of Science and Technology, Postbox 8905 MTFS, NO-7491, Trondheim, Norway. ola.m.vagnildhaug@ntnu.no.
Cancer Clinic, St. Olav's Hospital, Trondheim University Hospital, Postboks 3250 Sluppen, NO-7006, Trondheim, Norway. ola.m.vagnildhaug@ntnu.no.

Cinzia Brunelli (C)

Palliative Care, Pain Therapy and Rehabilitation Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, via Giacomo Venezian 1, 20133, Milan, Italy.
European Palliative Care Research Centre (PRC), Department of Oncology, Oslo University Hospital, and Institute of Clinical Medicine, University of Oslo, Box 4956, Nydalen, 0424, Oslo, Norway.

Marianne J Hjermstad (MJ)

European Palliative Care Research Centre (PRC), Department of Oncology, Oslo University Hospital, and Institute of Clinical Medicine, University of Oslo, Box 4956, Nydalen, 0424, Oslo, Norway.

Florian Strasser (F)

Department of Internal Medicine and Palliative Care Centre, Cantonal Hospital, Oncological Palliative Medicine, Section Oncology, Rorschacher Strasse 95, CH-9007, St. Gallen, Switzerland.

Vickie Baracos (V)

Division of Palliative Care Medicine, Department of Oncology, University of Alberta, Cross Cancer Institute 11560 University Avenue, Edmonton, Alberta, T6G 1Z2, Canada.

Andrew Wilcock (A)

Nottingham University Hospitals NHS Trust, Hucknall Road, Nottingham, NG5 1PB, UK.

Maria Nabal (M)

Hospital Universitari Arnau de Vilanova and Universidad de Lleida, Av. Alcalde Rovira Roure 80, 25198, Lleida, Spain.

Stein Kaasa (S)

European Palliative Care Research Centre (PRC), Department of Oncology, Oslo University Hospital, and Institute of Clinical Medicine, University of Oslo, Box 4956, Nydalen, 0424, Oslo, Norway.

Barry Laird (B)

Edinburgh Cancer Research UK Centre, University of Edinburgh, Western General Hospital, Crewe Road South, Edinburgh, EH4 2XR, UK.

Tora S Solheim (TS)

Department of Clinical and Molecular Medicine, Faculty of Medicine and Health Sciences, NTNU - Norwegian University of Science and Technology, Postbox 8905 MTFS, NO-7491, Trondheim, Norway.
Cancer Clinic, St. Olav's Hospital, Trondheim University Hospital, Postboks 3250 Sluppen, NO-7006, Trondheim, Norway.

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Classifications MeSH