Evidence map›Paper›PMID 41035100›Full record

ArticleCardio-oncology (London, England)2025

Cardiovascular disease and diagnosis of advanced prostate cancer.

Kevin T Nead, Allen M Haas, Jing Zhao, Ting Xiong, Chad Tang, Sharon H Giordan, Nicholas J Leeper

Abstract read
In one paragraph

Article in Cardio-oncology (London, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 2 pooled it
–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

2 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
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

7 authors.

Kevin T NeadDepartment of Epidemiology, University of Texas MD Anderson Cancer Center,, 6900 Fannin Street, Office FHB6.1060, Houston, TX, 77030, USA. ktnead@mdanderson.org.
Allen M HaasDepartment of Health Services Research, University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Jing ZhaoDepartment of Epidemiology, University of Texas MD Anderson Cancer Center,, 6900 Fannin Street, Office FHB6.1060, Houston, TX, 77030, USA.
Ting XiongDivision of Vascular Surgery, Department of Surgery, Stanford University School of Medicine, Stanford, CA, USA.
Chad TangDepartment of Genitourinary Radiation Oncology, University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Sharon H GiordanDepartment of Health Services Research, University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Nicholas J LeeperDivision of Vascular Surgery, Department of Surgery, Stanford University School of Medicine, Stanford, CA, USA.

Funding

Clonal expansion, resistance to efferocytosis and innate immunity in atherosclerosisR35HL144475 · NHLBI · STANFORD UNIVERSITY · PI LEEPER, NICHOLAS JAMES · 2019 to 2024
$5.1M
Impact of clonal hematopoiesis mutations on toxicity and outcomes following oncologic therapyK08CA263313 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI NEAD, KEVIN THOMAS · 2021 to 2025
$1.2M
Cancer Prevention and Research Institute of Texas RR190077NCI NIH HHS K08CA263313NHLBI NIH HHS R35HL144475
6 · The paper itself

Abstract

introductionCardiovascular disease (CVD) and cancer are the two leading causes of death in the US. Preclinical models support a direct effect of cardiovascular disease (CVD) on accelerated cancer growth and spread. Our objective is to test the hypothesis that individuals with prevalent CVD are at an increased risk of presenting with more advanced prostate cancer at diagnosis.

methodsWe conducted a case-control study in the Surveillance, Epidemiology, and End Results (SEER)-Medicare linked databases from 2010-2019. The analysis was undertaken from October 2024 to February 2025. We included male individuals aged ≥ 67 years diagnosed with invasive prostate cancer with at least two healthcare interactions and evidence of PSA screening in the 3 to 24 months prior to cancer diagnosis. Our exposure of interest was CVD in the 3 to 24 months prior to cancer diagnosis. Our a priori hypothesis tested the odds of prevalent CVD in patients with localized (T1-2 and N0 and M0) versus advanced (T3-4 or N + or M +) prostate cancer at diagnosis.

resultsOur analysis included 12,120 matched individuals, with median age 75 years (interquartile range 71-80), of which 88% were white, 8% were black, and 59% had prevalent CVD. Multivariable adjusted models demonstrated that individuals with advanced prostate cancer at diagnosis had a statistically significant 10% increased odds of prevalent CVD (OR, 1.10; 95% CI, 1.00-1.22; p = 0.047). This finding was strongest when examining individuals with regional or distant spread at diagnosis (N + or M + ; OR, 1.19; 95% CI, 1.05-1.34; p = 0.006). Further, individuals with Gleason score ≥ 8 disease at diagnosis, had an increased odds of prevalent CVD (OR, 1.07; 95% CI, 1.01-1.13; p = 0.020).

conclusionWe demonstrate an association between prevalent CVD and advanced prostate cancer at diagnosis. Our results may help guide patients regarding personalized screening decisions, given current guidelines recommending shared decision-making, and can be used to facilitate targeted screening approaches.

Identifiers

PMID41035100
PMCPMC12486819

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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.