Health Outcomes for Definite Concurrent Chemoradiation in Locally Advanced Non-Small Cell Lung Cancer: A Prospective Study.


Journal

Respiration; international review of thoracic diseases
ISSN: 1423-0356
Titre abrégé: Respiration
Pays: Switzerland
ID NLM: 0137356

Informations de publication

Date de publication:
Historique:
received: 21 06 2018
accepted: 21 09 2018
pubmed: 23 11 2018
medline: 22 8 2020
entrez: 23 11 2018
Statut: ppublish

Résumé

In patients with locally advanced lung cancer treated with concurrent chemoradiation, outcome measurements have been mostly limited to survival. We aimed to measure outcomes that matter to these patients beyond survival in a general clinical practice. In a prospective single-centre study, consecutive patients with locally advanced non-small cell lung cancer reported their own outcomes using the EORTC Quality of Life Questionnaire Core 30 at baseline, during therapy, at therapy stop and till 1 year after therapy end every 3 months. Survival, complications, quality of death and case-mix variables were measured. There were 32 consecutive patients included prospectively from June 2013 until September 2016. Median overall survival was 24.3 months (95% CI 12.7-35.9). Severe toxicity (grade III-IV) was frequent (haematologic toxicity III-IV in 59%). Patient-reported outcomes (PROs) documented the burden on global health status and on functional domains (physical, role, social, emotional and cognitive functioning). Deterioration was pronounced during and after treatment with drops over 20 up to 40% points from baseline for physical, role and social functioning. Clinically meaningful negative effects did persist up to 6 and 9 months for physical and role functioning. Fifty-six percent of the deceased patients died in hospital. The assault on health-related quality of life during concurrent chemoradiation for locally advanced lung cancer is considerable. Loss of physical and role functioning persists up to 6 and 9 months after therapy end, respectively. Measuring PROs can help to identify issues for improvement of the value of care delivered.

Sections du résumé

BACKGROUND BACKGROUND
In patients with locally advanced lung cancer treated with concurrent chemoradiation, outcome measurements have been mostly limited to survival.
OBJECTIVES OBJECTIVE
We aimed to measure outcomes that matter to these patients beyond survival in a general clinical practice.
METHODS METHODS
In a prospective single-centre study, consecutive patients with locally advanced non-small cell lung cancer reported their own outcomes using the EORTC Quality of Life Questionnaire Core 30 at baseline, during therapy, at therapy stop and till 1 year after therapy end every 3 months. Survival, complications, quality of death and case-mix variables were measured.
RESULTS RESULTS
There were 32 consecutive patients included prospectively from June 2013 until September 2016. Median overall survival was 24.3 months (95% CI 12.7-35.9). Severe toxicity (grade III-IV) was frequent (haematologic toxicity III-IV in 59%). Patient-reported outcomes (PROs) documented the burden on global health status and on functional domains (physical, role, social, emotional and cognitive functioning). Deterioration was pronounced during and after treatment with drops over 20 up to 40% points from baseline for physical, role and social functioning. Clinically meaningful negative effects did persist up to 6 and 9 months for physical and role functioning. Fifty-six percent of the deceased patients died in hospital.
CONCLUSIONS CONCLUSIONS
The assault on health-related quality of life during concurrent chemoradiation for locally advanced lung cancer is considerable. Loss of physical and role functioning persists up to 6 and 9 months after therapy end, respectively. Measuring PROs can help to identify issues for improvement of the value of care delivered.

Identifiants

pubmed: 30466111
pii: 000493984
doi: 10.1159/000493984
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

310-318

Informations de copyright

© 2018 S. Karger AG, Basel.

Auteurs

Pham Anh Hong Nguyen (PAH)

Department of Respiratory Medicine/Thoracic Oncology, Onze-Lieve-Vrouw Ziekenhuis Aalst, Aalst, Belgium.
Department of Respiratory Medicine, University Hospital Gasthuisberg, Leuven, Belgium.

Piet Vercauter (P)

Department of Respiratory Medicine/Thoracic Oncology, Onze-Lieve-Vrouw Ziekenhuis Aalst, Aalst, Belgium.

Luc Verbeke (L)

Department of Radiation Oncology, Onze-Lieve-Vrouw Ziekenhuis Aalst, Aalst, Belgium.

Roel Beelen (R)

Department of Thoracic Surgery, Onze-Lieve-Vrouw Ziekenhuis Aalst, Aalst, Belgium.

Christophe Dooms (C)

Department of Respiratory Medicine, University Hospital Gasthuisberg, Leuven, Belgium.

Kurt G Tournoy (KG)

Department of Respiratory Medicine/Thoracic Oncology, Onze-Lieve-Vrouw Ziekenhuis Aalst, Aalst, Belgium, Kurt.Tournoy@OLVZ-aalst.be.
Faculty of Medicine and Life Sciences, Ghent University, Ghent, Belgium, Kurt.Tournoy@OLVZ-aalst.be.

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