Evidence map›Paper›PMID 40681529›Full record

ArticleScientific reports2025

Breast cancer survival and mortality among women with type 2 diabetes: a retrospective cohort study.

Alison J Sears, Sarah H Wild, Ines Mesa-Eguiagaray, Peter S Hall, Jonine D Figueroa

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

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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

1 citing paper in PubMed.

  1. Article
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

5 authors.

Alison J SearsUsher Institute, University of Edinburgh, Edinburgh, UK.ORCID https://orcid.org/0009-0003-0181-4460
Sarah H WildUsher Institute, University of Edinburgh, Edinburgh, UK.ORCID https://orcid.org/0000-0001-7824-2569
Ines Mesa-EguiagarayUsher Institute, University of Edinburgh, Edinburgh, UK.ORCID https://orcid.org/0000-0002-6784-2419
Peter S HallUsher Institute, University of Edinburgh, Edinburgh, UK.ORCID https://orcid.org/0000-0001-6015-7841
Jonine D FigueroaUsher Institute, University of Edinburgh, Edinburgh, UK. jonine.figueroa@nih.gov.ORCID https://orcid.org/0000-0002-5100-623X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Type 2 diabetes (T2DM) is estimated to affect over 200 million women globally and over 2 million women are estimated to be diagnosed with breast cancer each year. This study aimed to determine the association between breast cancer molecular subtypes and survival in a cohort of women with T2DM. A retrospective cohort study was conducted using linked Scottish population-based data for 3,042 women diagnosed with T2DM prior to their diagnosis of invasive breast cancer between 2010 and 2019 that had complete data available. The women in the cohort were aged 50 to 84 years at the time of breast cancer diagnosis. Univariate analyses were performed using non-parametric ten-year Kaplan Meier (KM) estimates for breast cancer survival by molecular subtype. Hazard ratios (HR) for breast cancer mortality within three years were estimated using Cox proportional hazard models, adjusting for age at breast cancer diagnosis, year of diagnosis, Scottish region, mode of detection, treatment, area-based socioeconomic status, and T2DM duration were conducted. Multiple imputation was performed as a sensitivity analysis. The distribution of molecular subtype based on St Gallen's criteria was luminal A (58%), luminal B (HER2-) (19.2%), triple negative (9.9%), luminal B (HER2 +) (8.5%), and HER2-enriched (4.4%). There were 286 breast cancer deaths in total within three years. KM estimates showed women with HER2-enriched tumours had the worst survival at ages 50 to 69, while those with triple-negative tumours had the worst survival at ages 70 to 84. Adjusted HRs (95% confidence intervals) for mortality over 3 years compared to luminal A were 2.04 (1.43, 2.90) for luminal B (HER2-), 5.68 (3.40, 9.50) for triple negative, 2.22 (1.46, 3.38) for luminal B (HER2 +), and 2.93 (1.63, 5.27) for HER2-enriched. The imputed cohort adjusted HRs were attenuated, particularly for HER2-enriched (HR = 1.71 (1.01, 2.89)) and triple negative (HR = 2.74 (1.72, 4.37)). Like the general population, triple negative and HER2-enriched tumors had worse prognosis compared to luminal A tumors and their association with breast cancer mortality are similar in women with type 2 diabetes and the general population. However, our findings revealed differences in the survival ranking of HER2-enriched and triple-negative subtypes for breast cancer diagnosed in the 50-69 age group between women with type 2 diabetes and the general population, warranting further exploration.

Indexed as

Breast NeoplasmsDiabetes Mellitus, Type 2AgedAged, 80 and overFemaleHumansKaplan-Meier EstimateMiddle AgedPrognosisProportional Hazards ModelsRetrospective StudiesScotlandTriple Negative Breast NeoplasmsBreast cancerCox proportional hazard modelsMolecular subtypeSurvivalType 2 diabetes

Identifiers

PMID40681529
PMCPMC12274475

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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.