Prognostic value of comorbidities in older patients with cancer: the ELCAPA cohort study.


Journal

ESMO open
ISSN: 2059-7029
Titre abrégé: ESMO Open
Pays: England
ID NLM: 101690685

Informations de publication

Date de publication:
10 2023
Historique:
received: 12 06 2023
revised: 31 08 2023
accepted: 04 09 2023
medline: 30 10 2023
pubmed: 14 10 2023
entrez: 13 10 2023
Statut: ppublish

Résumé

In older patients, comorbidities competed with cancer for mortality risk. We assessed the prognostic value of comorbidities in older patients with cancer. We analysed all patients >70 years of age with colorectal, breast, prostate, or lung cancer included in the prospective ELCAPA cohort. The Cumulative Illness Rating Scale-Geriatrics (CIRS-G) score was used to assess comorbidities. The primary endpoint was overall survival (OS) at 3, 12, and 36 months. The adjusted difference in the restricted mean survival time (RMST) was used to assess the strength of the relationship between comorbidities and survival. Of the 1551 patients included (median age 82 years; interquartile range 78-86 years), 502 (32%), 575 (38%), 283 (18%), and 191 (12%) had colorectal, breast, prostate, and lung cancer, respectively, and 50% had metastatic disease. Hypertension, kidney failure, and cognitive impairment were the most common comorbidities (67%, 38%, and 29% of the patients, respectively). A CIRS-G score >17, two or more severe comorbidities, more than seven comorbidities, heart failure, and cognitive impairment were independently associated with shorter OS. The greatest effect size was observed for CIRS-G >17 (versus CIRS-G <11): at 36 months, the adjusted differences in the RMST (95% confidence interval) were -6.0 months (-9.3 to -2.6 months) for colorectal cancer, -9.1 months (-13.2 to -4.9 months) for breast cancer, -8.3 months (-12.8 to -3.9 months) for prostate cancer, and -5.5 months (-9.9 to -1.1 months) for lung cancer (P < 0.05 for all). Comorbidities' type, number, and severity were independently associated with shorter OS. A 17-point cut-off over 56 for the total CIRS-G score could be considered in clinical practice.

Sections du résumé

BACKGROUND
In older patients, comorbidities competed with cancer for mortality risk. We assessed the prognostic value of comorbidities in older patients with cancer.
PATIENTS AND METHODS
We analysed all patients >70 years of age with colorectal, breast, prostate, or lung cancer included in the prospective ELCAPA cohort. The Cumulative Illness Rating Scale-Geriatrics (CIRS-G) score was used to assess comorbidities. The primary endpoint was overall survival (OS) at 3, 12, and 36 months. The adjusted difference in the restricted mean survival time (RMST) was used to assess the strength of the relationship between comorbidities and survival.
RESULTS
Of the 1551 patients included (median age 82 years; interquartile range 78-86 years), 502 (32%), 575 (38%), 283 (18%), and 191 (12%) had colorectal, breast, prostate, and lung cancer, respectively, and 50% had metastatic disease. Hypertension, kidney failure, and cognitive impairment were the most common comorbidities (67%, 38%, and 29% of the patients, respectively). A CIRS-G score >17, two or more severe comorbidities, more than seven comorbidities, heart failure, and cognitive impairment were independently associated with shorter OS. The greatest effect size was observed for CIRS-G >17 (versus CIRS-G <11): at 36 months, the adjusted differences in the RMST (95% confidence interval) were -6.0 months (-9.3 to -2.6 months) for colorectal cancer, -9.1 months (-13.2 to -4.9 months) for breast cancer, -8.3 months (-12.8 to -3.9 months) for prostate cancer, and -5.5 months (-9.9 to -1.1 months) for lung cancer (P < 0.05 for all).
CONCLUSIONS
Comorbidities' type, number, and severity were independently associated with shorter OS. A 17-point cut-off over 56 for the total CIRS-G score could be considered in clinical practice.

Identifiants

pubmed: 37832389
pii: S2059-7029(23)01066-9
doi: 10.1016/j.esmoop.2023.101831
pmc: PMC10594025
pii:
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

101831

Informations de copyright

Copyright © 2023 The Authors. Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Disclosure The authors have declared no conflicts of interest.

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Auteurs

M-A Benderra (MA)

Université Paris-Est Créteil, INSERM, IMRB, Créteil, France; AP-HP, Henri-Mondor Hospital, Public Health Department & Clinical Research Unit (URC Mondor), Créteil, France; Institut Universitaire de Cancérologie (IUC), AP-HP, Sorbonne Université, Paris, France; Department of Medical Oncology, AP-HP, Tenon Hospital, Paris, France. Electronic address: marc-antoine.benderra@aphp.fr.

A G Serrano (AG)

Université Paris-Est Créteil, INSERM, IMRB, Créteil, France; AP-HP, Henri-Mondor Hospital, Public Health Department & Clinical Research Unit (URC Mondor), Créteil, France.

E Paillaud (E)

Université Paris-Est Créteil, INSERM, IMRB, Créteil, France; Department of Geriatrics, AP-HP, HEGP Hospital, Paris, France.

C M Tapia (CM)

Université Paris-Est Créteil, INSERM, IMRB, Créteil, France; AP-HP, Henri-Mondor Hospital, Public Health Department & Clinical Research Unit (URC Mondor), Créteil, France.

T Cudennec (T)

Department of Geriatrics, AP-HP, Ambroise-Paré Hospital, Boulogne-Billancourt, France.

C Chouaïd (C)

Department of Geriatrics, Centre Hospitalier Inter-Communal de Creteil (CHIC), Creteil, France.

E Lorisson (E)

Department of Geriatrics, Centre Hospitalier Inter-Communal de Creteil (CHIC), Creteil, France.

A de la Taille (A)

Department of Urology, AP-HP, Henri-Mondor Hospital, Université de Paris Est, Créteil, France.

M Laurent (M)

Université Paris-Est Créteil, INSERM, IMRB, Créteil, France; Department of Geriatrics, AP-HP, Hopitaux Henri-Mondor/Emile Roux, Limeil-Brevannes, France.

E Brain (E)

Department of Clinical Research & Medical Oncology, Institut Curie (Hôpital René Huguenin), Saint-Cloud, France.

M Bringuier (M)

Department of Medical Oncology, Institut Curie, Saint-Cloud, France; Department of Supportive Care, Institut Curie, Saint-Cloud, France.

J Gligorov (J)

Institut Universitaire de Cancérologie (IUC), AP-HP, Sorbonne Université, Paris, France; Department of Medical Oncology, AP-HP, Tenon Hospital, Paris, France.

P Caillet (P)

Université Paris-Est Créteil, INSERM, IMRB, Créteil, France; Department of Geriatrics, AP-HP, HEGP Hospital, Paris, France.

F Canoui-Poitrïne (F)

Université Paris-Est Créteil, INSERM, IMRB, Créteil, France; AP-HP, Henri-Mondor Hospital, Public Health Department & Clinical Research Unit (URC Mondor), Créteil, France.

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