Cognitive Impairment in Patients with Breast Cancer before Surgery: Results from a CANTO Cohort Subgroup.


Journal

Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology
ISSN: 1538-7755
Titre abrégé: Cancer Epidemiol Biomarkers Prev
Pays: United States
ID NLM: 9200608

Informations de publication

Date de publication:
09 2020
Historique:
received: 04 03 2020
revised: 27 04 2020
accepted: 24 06 2020
pubmed: 3 7 2020
medline: 22 12 2021
entrez: 3 7 2020
Statut: ppublish

Résumé

Twenty to 30% of patients with breast cancer have cognitive impairment after surgery and before adjuvant treatment, but very few studies have focused on cognition before any treatment. This study used a subgroup of women with newly diagnosed breast cancer from the French cancer and toxicities (CANTO) cohort to describe cognition before any treatment in comparison with a group of healthy controls (HC). Cognitive assessment was performed before any breast cancer treatment (surgery or neoadjuvant treatment) on women with newly diagnosed invasive stage I-III breast cancer and HCs. Objective cognitive performance, cognitive complaints, anxiety, depression, and fatigue were assessed. Objective cognitive impairment was defined according to International Cognition and Cancer Task Force recommendations. Of the 264 included patients with breast cancer (54 ± 11 years) and 132 age-matched HCs (53 ± 9 years), overall objective cognitive impairment was observed in 28% of patients with breast cancer and 8% of HCs ( In this prospective study, compared with HCs, patients with localized breast cancer had more objective cognitive impairment before any treatment. Cognitive complaints were mostly related to fatigue. Baseline assessment before treatment is important to assess the impact of each cancer treatment on cognition.

Sections du résumé

BACKGROUND
Twenty to 30% of patients with breast cancer have cognitive impairment after surgery and before adjuvant treatment, but very few studies have focused on cognition before any treatment. This study used a subgroup of women with newly diagnosed breast cancer from the French cancer and toxicities (CANTO) cohort to describe cognition before any treatment in comparison with a group of healthy controls (HC).
METHODS
Cognitive assessment was performed before any breast cancer treatment (surgery or neoadjuvant treatment) on women with newly diagnosed invasive stage I-III breast cancer and HCs. Objective cognitive performance, cognitive complaints, anxiety, depression, and fatigue were assessed. Objective cognitive impairment was defined according to International Cognition and Cancer Task Force recommendations.
RESULTS
Of the 264 included patients with breast cancer (54 ± 11 years) and 132 age-matched HCs (53 ± 9 years), overall objective cognitive impairment was observed in 28% of patients with breast cancer and 8% of HCs (
CONCLUSIONS
In this prospective study, compared with HCs, patients with localized breast cancer had more objective cognitive impairment before any treatment. Cognitive complaints were mostly related to fatigue.
IMPACT
Baseline assessment before treatment is important to assess the impact of each cancer treatment on cognition.

Identifiants

pubmed: 32611581
pii: 1055-9965.EPI-20-0346
doi: 10.1158/1055-9965.EPI-20-0346
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1759-1766

Commentaires et corrections

Type : ErratumIn

Informations de copyright

©2020 American Association for Cancer Research.

Auteurs

Marie Lange (M)

Clinical Research Department, Centre François Baclesse, Caen, France.
Normandie Univ, UNICAEN, INSERM, ANTICIPE, Caen, France.
Cancer & Cognition Platform, Ligue Contre le Cancer, Caen, France.

Isabelle Hardy-Léger (I)

Gustave Roussy, Villejuif, France.
CHU Bicetre, Kremlin Bicetre, France.

Idlir Licaj (I)

Clinical Research Department, Centre François Baclesse, Caen, France.
Normandie Univ, UNICAEN, INSERM, ANTICIPE, Caen, France.
Cancer & Cognition Platform, Ligue Contre le Cancer, Caen, France.
Department of Community Medicine, Faculty of Health Sciences, The UiT Arctic University of Norway, Tromsø, Norway.

Barbara Pistilli (B)

Gustave Roussy, Villejuif, France.

Olivier Rigal (O)

Care Support Department, Centre Henri Becquerel, Rouen, France.
Medical Oncology Department, Centre Henri Becquerel, Rouen, France.

Johan Le Fel (J)

Care Support Department, Centre Henri Becquerel, Rouen, France.

Christelle Lévy (C)

Breast Committee, Centre François Baclesse, Caen, France.

Aurélie Capel (A)

Clinical Research Department, Centre François Baclesse, Caen, France.

Charles Coutant (C)

Centre Georges François Leclerc, Dijon, France.

Jonathan Meyer (J)

Centre Georges François Leclerc, Dijon, France.

Florence Lerebours (F)

Institut Curie, Saint Cloud, France.

Jean Petrucci (J)

Institut Curie, Saint Cloud, France.

Laurence Vanlemmens (L)

Centre Oscar Lambret, Lille, France.

Marine Brion (M)

Centre Oscar Lambret, Lille, France.

Mario Campone (M)

Institut de Cancérologie de l'Ouest, Nantes/Angers, France.

Patrick Soulié (P)

Institut de Cancérologie de l'Ouest, Nantes/Angers, France.

Maxime Blain (M)

Institut de Cancérologie de l'Ouest, Nantes/Angers, France.

Ines Vaz-Luis (I)

UNIT 981, INSERM, Gustave Roussy, Villejuif, Île-de-France, France.

Bénédicte Giffard (B)

Cancer & Cognition Platform, Ligue Contre le Cancer, Caen, France.
Normandie Univ, UNICAEN, PSL University, EPHE, INSERM, U1077, CHU de Caen, Neuropsychologie et Imagerie de la Mémoire Humaine, Caen, France.

Sibille Everhard (S)

UNICANCER, Paris, France.

Fabrice André (F)

Gustave Roussy, Villejuif, France.

Sarah Dauchy (S)

Gustave Roussy, Villejuif, France.

Florence Joly (F)

Clinical Research Department, Centre François Baclesse, Caen, France. f.joly@baclesse.unicancer.fr.
Normandie Univ, UNICAEN, INSERM, ANTICIPE, Caen, France.
Cancer & Cognition Platform, Ligue Contre le Cancer, Caen, France.
CHU de Caen, Medical Oncology Department, Caen, France.

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