Evidence map›Paper›PMID 21317458›Full record

ArticleOncotarget2010

Beta-blocker drug therapy reduces secondary cancer formation in breast cancer and improves cancer specific survival.

Desmond G Powe, Melanie J Voss, Kurt S Zänker, Hany O Habashy, Andrew R Green, Ian O Ellis, Frank Entschladen

Open access · hybridAbstract readComparative StudyEvaluation Study
In one paragraph

Article in Oncotarget, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 264 papers, 10 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
264citing papers in PubMed, 10 pooled it
17.0field-weighted citation impact, top 1% of its field
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

264 citing papers in PubMed, 10 syntheses or guidelines pooled it, 439 citations in OpenAlex.

  1. Pooled it
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  4. Beta-blocker use and breast cancer outcomes: a meta-analysis.Breast cancer research and treatment · 2024
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  11. Trial
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  14. Perioperative COX-2 and β-Adrenergic Blockade Improves Metastatic Biomarkers in Breast Cancer Patients in a Phase-II Randomized Trial.Clinical cancer research : an official journal of the American Association for Cancer Research · 2017
    Trial
  15. Selective regulation of βMedical oncology (Northwood, London, England) · 2026
    Article
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  20. Molecular mechanisms and therapeutic targets in lung cancer-nerve crosstalk.Chinese medical journal pulmonary and critical care medicine · 2026
    Review

204 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 2 countries.

Desmond G PoweDepartment of Cellular Pathology, Queen's Medical Centre, Nottingham University Hospitals NHS Trust, Nottingham, NG7 2UH, UK and The John van Geest Cancer Research Centre School of Science and Technology, Nottingham Trent University, Clifton Lane, Nottingham NG11 8NS UK.
Melanie J VossInstitute of Immunology, University of Witten/Herdecke, DE-58448, Witten, Germany.
Kurt S ZänkerInstitute of Immunology, University of Witten/Herdecke, DE-58448, Witten, Germany.
Hany O HabashySchool of Molecular Medical Sciences, University of Nottingham, Nottingham, NG7 2UH, UK.
Andrew R GreenSchool of Molecular Medical Sciences, University of Nottingham, Nottingham, NG7 2UH, UK.
Ian O EllisSchool of Molecular Medical Sciences, University of Nottingham, Nottingham, NG7 2UH, UK.
Frank EntschladenInstitute of Immunology, University of Witten/Herdecke, DE-58448, Witten, Germany.
University of Nottingham · GBWitten/Herdecke University · DEQueen's Medical Centre · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Laboratory models show that the beta-blocker, propranolol, can inhibit norepinephrine-induced breast cancer cell migration. We hypothesised that breast cancer patients receiving beta-blockers for hypertension would show reduced metastasis and improved clinical outcome. Three patient subgroups were identified from the medical records of 466 consecutive female patients (median age 57, range 28-71) with operable breast cancer and follow-up (>10 years). Two subgroups comprised 43 and 49 hypertensive patients treated with beta-blockers or other antihypertensives respectively, prior to cancer diagnosis. 374 patients formed a non-hypertensive control group. Metastasis development, disease free interval, tumour recurrence and hazards risk were statistically compared between groups. Kaplan-Meier plots were used to model survival and DM. Beta-blocker treated patients showed a significant reduction in metastasis development (p=0.026), tumour recurrence (p=0.001), and longer disease free interval (p=0.01). In addition, there was a 57% reduced risk of metastasis (Hazards ratio=0.430; 95% CI=0.200-0.926, p=0.031), and a 71% reduction in breast cancer mortality after 10 years (Hazards ratio=0.291; 95% CI=0.119-0.715, p=0.007). This proof-of-principle study showed beta-blocker therapy significantly reduces distant metastases, cancer recurrence, and cancer-specific mortality in breast cancer patients suggesting a novel role for beta-blocker therapy. A larger epidemiological study leading to randomised clinical trials is needed for breast and other cancer types including colon, prostate and ovary.

Indexed as

Adrenergic beta-AntagonistsAdultAgedBreast NeoplasmsCarcinomaDisease-Free SurvivalDown-RegulationFemaleFollow-Up StudiesHumansHypertensionMiddle AgedNeoplasm MetastasisNeoplasm Recurrence, LocalSurvival AnalysisTreatment OutcomeAdrenergic beta-Antagonists

Identifiers

PMID21317458
PMCPMC3248123
OpenAlexW2150740158

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.