Evidence map›Paper›PMID 41165708›Full record

Observational studyJAMA network open2025

Postdiagnosis Statin Use and Breast Cancer Mortality.

Sixten Harborg, Lars Pedersen, Henrik T Sørensen, Thomas P Ahern, Deirdre Cronin-Fenton, Signe Borgquist

Abstract readObservational Study
In one paragraph

Observational study in JAMA network open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. 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

6 authors.

Sixten HarborgDepartment of Oncology, Aarhus University Hospital/Aarhus University, Aarhus, Denmark.
Lars PedersenDepartment of Clinical Epidemiology, Aarhus University/Aarhus University Hospital, Aarhus N, Denmark.
Henrik T SørensenDepartment of Clinical Epidemiology, Aarhus University/Aarhus University Hospital, Aarhus N, Denmark.
Thomas P AhernDepartment of Oncology, Aarhus University Hospital/Aarhus University, Aarhus, Denmark.
Deirdre Cronin-FentonDepartment of Clinical Epidemiology, Aarhus University/Aarhus University Hospital, Aarhus N, Denmark.
Signe BorgquistDepartment of Oncology, Aarhus University Hospital/Aarhus University, Aarhus, Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: Emerging evidence suggests that cholesterol plays a role in breast cancer (BC) metabolism, raising the possibility that cholesterol-lowering medications, such as statins, may improve BC prognosis. Objective: To evaluate the association between postdiagnosis statin initiation and BC mortality using an emulated target trial approach. Design, Setting, and Participants: This observational cohort study using a target trial framework included 96 924 women diagnosed with stage I to III BC from 2000 to 2021 from Nationwide Danish registries, including the Danish Breast Cancer Group's clinical database and the Danish National Prescription Registry. Women with prior invasive BC or prediagnosis use of cholesterol-lowering medication were excluded. Eligible patients were duplicated into a cloned cohort and assigned to 1 of 2 treatment strategies: statin initiation within 36 months postdiagnosis or no statin initiation. Patients were followed up until deviation from the assigned strategy, emigration, death, 10 years of follow-up, or October 5, 2022. Exposures: Initiation of any statin within 36 months after BC diagnosis. Main Outcomes and Measures: The primary outcome was BC mortality. Secondary outcomes included all-cause mortality. Hazard ratios (HRs) and 95% CIs were estimated using inverse probability of censoring weighted (IPCW) Cox regression models with a robust variance estimator. Results: A total of 66 952 patients with BC were enrolled in the emulated target trial (17 152 [27.6%] were aged 50-59 years); 4851 (7.2%) initiated statins within 36 months after diagnosis. Over 606 266 person-years of follow-up, 9130 patients died from BC and 19 679 from any cause. The 10-year risk of breast cancer mortality was 11.8% among statin initiators and 13.5% among noninitiators, corresponding to a risk difference of 1.7% (95% CI, 0.5% to 3.0%). A similar difference was observed for all-cause mortality (23.3% vs 24.5%; risk difference, 1.2%; 95% CI, -0.1% to 2.5%). IPCW analysis yielded an HR of 0.90 (95% CI, 0.85 to 0.95) for BC mortality and 0.92 (95% CI, 0.85 to 1.00) for all-cause mortality among statin initiators vs noninitiators. Conclusions and Relevance: In this cohort study, among 66 952 women with early BC, postdiagnosis statin initiation was associated with a modest reduction in BC and all-cause mortality. These findings support further investigation into the potential role of statins as an adjunct to standard adjuvant BC treatment.

Indexed as

Breast NeoplasmsHydroxymethylglutaryl-CoA Reductase InhibitorsAgedCohort StudiesDenmarkFemaleHumansMiddle AgedRegistriesHydroxymethylglutaryl-CoA Reductase Inhibitors

Identifiers

PMID41165708
PMCPMC12576488

What OpenQuestion holds

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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.