Evidence map›Paper›PMID 39972319›Full record

ArticleBreast cancer research : BCR2025

Interaction between APOE Ɛ4 status, chemotherapy and endocrine therapy on cognitive functioning among breast cancer survivors: the CANTO-Cog longitudinal study.

Mylène Duivon, François Christy, Emilie Thomas, Justine Lequesne, Hélène Castel, Catherine Gaudin, Dominique Delmas, Sandrine Boyault, Olivier Rigal, Chayma Bousrih and 8 more

Abstract read
In one paragraph

Article in Breast cancer research : BCR, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors.

Mylène DuivonANTICIPE U1086 INSERM-UCN, Equipe Labellisée Ligue Contre le Cancer, Centre François Baclesse, Normandie Université UNICAEN, 14000, Caen, France.
François ChristyANTICIPE U1086 INSERM-UCN, Equipe Labellisée Ligue Contre le Cancer, Centre François Baclesse, Normandie Université UNICAEN, 14000, Caen, France.
Emilie ThomasPlateforme de Génomique des Cancers, Centre de Recherche en Cancérologie de Lyon CRCL, INSERM U1052, CNRS UMR 5286, Centre Léon Bérard, Université Claude Bernard Lyon 1, 69008, Lyon, France.
Justine LequesneANTICIPE U1086 INSERM-UCN, Equipe Labellisée Ligue Contre le Cancer, Centre François Baclesse, Normandie Université UNICAEN, 14000, Caen, France.
Hélène CastelServices Unit PLATON, Cancer and Cognition Platform, University of Caen Normandy, 14000, Caen, France.
Catherine GaudinUNICANCER, 75654, Paris, France.
Dominique DelmasUNICANCER, 75654, Paris, France.
Sandrine BoyaultPlateforme de Génomique des Cancers, Centre de Recherche en Cancérologie de Lyon CRCL, INSERM U1052, CNRS UMR 5286, Centre Léon Bérard, Université Claude Bernard Lyon 1, 69008, Lyon, France.
Olivier RigalCare Support Department, Centre Henri Becquerel, 76000, Rouen, France.
Chayma BousrihGustave Roussy, 94800, Villejuif, France.
Christelle LévyInstitut Normand du Sein, Centre François Baclesse, 14000, Caen, France.
Florence LereboursMedical Oncology Department, Institut Curie, 92210, Saint Cloud, France.
Antonio Di MeglioCancer Survivorship Group, INSERM U981, Gustave Roussy FR Department for the Organization of Patient Pathways, Gustave Roussy, Villejuif, France.
Patricia A GanzDivision of Hematology Oncology, Department of Medicine, David Geffen School of Medicine, University of California, Los Angeles, CA, USA.
Kathleen Van DykDepartment of Psychiatry and Biobehavioral Sciences, Semel Institute for Neuroscience and Human Behavior, University of California, Los Angeles, Los Angeles, CA, USA.
Ines Vaz LuisCancer Survivorship Group, INSERM U981, Gustave Roussy FR Department for the Organization of Patient Pathways, Gustave Roussy, Villejuif, France.
Marie LangeANTICIPE U1086 INSERM-UCN, Equipe Labellisée Ligue Contre le Cancer, Centre François Baclesse, Normandie Université UNICAEN, 14000, Caen, France. m.lange@baclesse.unicancer.fr.
Florence JolyANTICIPE U1086 INSERM-UCN, Equipe Labellisée Ligue Contre le Cancer, Centre François Baclesse, Normandie Université UNICAEN, 14000, Caen, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundApolipoprotein Ɛ4 genotype (APOE4) has been associated with cancer-related cognitive impairment, but its interaction with treatments remains unclear. This longitudinal study aims to evaluate the association between APOE4 and cognitive impairment in women with breast cancer (BC) undergoing chemotherapy (CT) or endocrine therapy (ET).

findingsPatients with stage I-III breast cancer completed cognitive tests at diagnosis (before surgery), then at year-1, year-2, and year-4 post-diagnosis. APOE4 status (APOE4+ [carriers] vs. APOE4- [non-carriers]) was genotyped from blood sample. Cognitive outcomes included episodic memory, working memory, attention, processing speed, and executive functions. Patients were defined as having overall cognitive impairment if ≥ 2 domains were impaired. We fitted logistic and linear mixed models to assess associations of APOE4 status with cognitive impairment over time and interactions of APOE4 with CT and ET. Among 334 patients, 64 (19%) were APOE4+, 117 (35%) patients were treated with CT, 41 (12%) with ET, and 162 (49%) with CT+ET. There were no significant association between overall cognitive impairment and APOE4, nor interactions with CT or ET. At year-4, APOE4+ patients treated with ET had lower attention performance than APOE4- patients not treated with ET, and APOE4+ patients not treated with ET had lower episodic memory performance than APOE4- patients not treated with ET.

conclusionsThis study suggests APOE4 genotyping is ineffective for detecting cognitive impairment in BC. New genotypes should be identified to predict cognitive decline in BC.

Indexed as

Antineoplastic Agents, HormonalApolipoprotein E4Breast NeoplasmsCancer SurvivorsCognitionCognitive DysfunctionAdultAgedAntineoplastic Combined Chemotherapy ProtocolsFemaleGenotypeHumansLongitudinal StudiesMiddle AgedAntineoplastic Agents, HormonalApolipoprotein E4APOE4Breast cancerCancer-related cognitive impairmentChemotherapyEndocrine therapy

Identifiers

PMID39972319
PMCPMC11841345

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.