Cognitive Changes After Adjuvant Treatment in Older Adults with Early-Stage Breast Cancer.


Journal

The oncologist
ISSN: 1549-490X
Titre abrégé: Oncologist
Pays: England
ID NLM: 9607837

Informations de publication

Date de publication:
01 2019
Historique:
received: 30 10 2017
accepted: 17 04 2018
pubmed: 24 6 2018
medline: 25 3 2020
entrez: 24 6 2018
Statut: ppublish

Résumé

Group-based trajectory modeling is particularly important to identify subgroups of patients with pathological cognitive changes after cancer treatment. To date, only one study has explored cognitive trajectories in older patients with cancer. The present article describes objective cognitive changes before to after adjuvant treatment in older adults with early-stage breast cancer (EBC) after adjuvant treatment compared with healthy controls. Participants were patients ≥65 years of age with newly diagnosed EBC and healthy controls (age-, sex-, and education-matched). The pretreatment assessment was conducted before adjuvant therapy, and the post-treatment assessment after the end of the first adjuvant treatment. Objective cognitive changes before to after treatment were evaluated based on the Reliable Change Index for cognitive decline accounting for cognitive impairment status. The sample consisted of women newly diagnosed with EBC ( This study described for the first time objective cognitive changes before to after treatment of older adults with EBC immediately after the end of adjuvant treatment. A longer-term remote follow-up of adjuvant treatment is needed to better understand the cognitive trajectories of older patients with EBC. After the end of adjuvant treatment, 31% of older adults with early-stage breast cancer without initial objective cognitive impairment developed impairment, and 6% experienced accelerated cognitive decline. Initial cognitive functioning should be included in the balance of benefits and harms of systemic therapy for patients who are likely to be at highest risk for cognitive decline after cancer treatments. Regular cognitive follow-up of patients who had cognitive impairment before cancer treatment should monitor symptoms suggestive of neurodegenerative disease and avert the effect of cognitive disorders on patients' autonomy.

Sections du résumé

BACKGROUND
Group-based trajectory modeling is particularly important to identify subgroups of patients with pathological cognitive changes after cancer treatment. To date, only one study has explored cognitive trajectories in older patients with cancer. The present article describes objective cognitive changes before to after adjuvant treatment in older adults with early-stage breast cancer (EBC) after adjuvant treatment compared with healthy controls.
PATIENTS AND METHODS
Participants were patients ≥65 years of age with newly diagnosed EBC and healthy controls (age-, sex-, and education-matched). The pretreatment assessment was conducted before adjuvant therapy, and the post-treatment assessment after the end of the first adjuvant treatment. Objective cognitive changes before to after treatment were evaluated based on the Reliable Change Index for cognitive decline accounting for cognitive impairment status.
RESULTS
The sample consisted of women newly diagnosed with EBC (
CONCLUSION
This study described for the first time objective cognitive changes before to after treatment of older adults with EBC immediately after the end of adjuvant treatment. A longer-term remote follow-up of adjuvant treatment is needed to better understand the cognitive trajectories of older patients with EBC.
IMPLICATIONS FOR PRACTICE
After the end of adjuvant treatment, 31% of older adults with early-stage breast cancer without initial objective cognitive impairment developed impairment, and 6% experienced accelerated cognitive decline. Initial cognitive functioning should be included in the balance of benefits and harms of systemic therapy for patients who are likely to be at highest risk for cognitive decline after cancer treatments. Regular cognitive follow-up of patients who had cognitive impairment before cancer treatment should monitor symptoms suggestive of neurodegenerative disease and avert the effect of cognitive disorders on patients' autonomy.

Identifiants

pubmed: 29934409
pii: theoncologist.2017-0570
doi: 10.1634/theoncologist.2017-0570
pmc: PMC6324624
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

62-68

Informations de copyright

© AlphaMed Press 2018.

Déclaration de conflit d'intérêts

Disclosures of potential conflicts of interest may be found at the end of this article.

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Auteurs

Marie Lange (M)

INSERM, U1086, ANTICIPE, Caen, France.
Clinical Research Department, Caen, France.
Cancer & Cognition, Platform, Ligue Contre le Cancer, CHU de Caen, Caen, France.

Natacha Heutte (N)

Clinical Research Department, Caen, France.
Cancer & Cognition, Platform, Ligue Contre le Cancer, CHU de Caen, Caen, France.

Sabine Noal (S)

Breast Committee Department, Centre François Baclesse, Caen, France.

Olivier Rigal (O)

Cancer & Cognition, Platform, Ligue Contre le Cancer, CHU de Caen, Caen, France.
Departments of Care Support, Centre Henri-Becquerel, Rouen, France.
Medical Oncology, Centre Henri-Becquerel, Rouen, France.

Jean-Emmanuel Kurtz (JE)

Oncology-Hematology Department, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.

Christelle Lévy (C)

Breast Committee Department, Centre François Baclesse, Caen, France.

Djelila Allouache (D)

Breast Committee Department, Centre François Baclesse, Caen, France.

Chantal Rieux (C)

Clinical Research Department, Caen, France.

Johan Lefel (J)

Departments of Care Support, Centre Henri-Becquerel, Rouen, France.

Bénédicte Clarisse (B)

Clinical Research Department, Caen, France.

Alexandra Leconte (A)

Clinical Research Department, Caen, France.

Corinne Veyret (C)

Medical Oncology, Centre Henri-Becquerel, Rouen, France.

Philippe Barthélémy (P)

Oncology-Hematology Department, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.

Nadine Longato (N)

Oncology-Hematology Department, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.

Laure Tron (L)

INSERM, U1086, ANTICIPE, Caen, France.
Cancer & Cognition, Platform, Ligue Contre le Cancer, CHU de Caen, Caen, France.
kCHU de Caen, Caen, France.

Hélène Castel (H)

INSERM U982, Laboratory of Neuronal and Neuroendocrine Differentiation and Communication, Rouen University, Mont-Saint-Aignan, France.

Francis Eustache (F)

Normandie University, UNICAEN, PSL Research University, EPHE, INSERM, U1077, CHU de Caen, Neuropsychologie et Imagerie de la Mémoire Humaine Department, Caen, France.

Bénédicte Giffard (B)

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

Florence Joly (F)

INSERM, U1086, ANTICIPE, Caen, France f.joly@baclesse.fr.
Clinical Research Department, Caen, France.
Cancer & Cognition, Platform, Ligue Contre le Cancer, CHU de Caen, Caen, France.
Medical Oncology Department, CHU de Caen, Caen, France.

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