Evidence map›Paper›PMID 41423663›Full record

ArticleCancer medicine2025

Cardiovascular Safety Landscape of ADT in Prostate Cancer Treatment Based on Real-World Analysis.

Wei Wang, Zirui Dong, Baoan Hong, Xin Guan, Yuxuan Wang, Zhipeng Sun, Qi Miao, Ning Zhang

Abstract read
In one paragraph

Article in Cancer medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

8 authors.

Wei WangDepartment of Urology, Beijing Anzhen Hospital, Capital Medical University, Beijing, P. R. China.
Zirui DongDepartment of Urology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, P. R. China.
Baoan HongDepartment of Urology, Beijing Anzhen Hospital, Capital Medical University, Beijing, P. R. China.
Xin GuanDepartment of Nuclear Medicine, First Hospital of Shanxi Medical University, Shanxi Medical University, Taiyuan, Shanxi, P. R. China.
Yuxuan WangDepartment of Urology, Beijing Anzhen Hospital, Capital Medical University, Beijing, P. R. China.
Zhipeng SunDepartment of Urology, Beijing Anzhen Hospital, Capital Medical University, Beijing, P. R. China.
Qi MiaoDepartment of Urology, Beijing Anzhen Hospital, Capital Medical University, Beijing, P. R. China.
Ning ZhangDepartment of Urology, Beijing Anzhen Hospital, Capital Medical University, Beijing, P. R. China.ORCID https://orcid.org/0009-0009-8108-6910

Funding

Beijing Anzhen Hospital High Level Research Funding 2024AZC3001Beijing Anzhen Hospital Science and Technology Development Funding AZYZR202304Beijing Bethune Charitable Foundation mnzl202003Beijing Hospitals Authority Youth Programme QML20231105
6 · The paper itself

Abstract

backgroundProstate cancer is among the most prevalent malignancies worldwide, and cardiovascular disease (CVD) is a major non-cancer cause of death in affected patients. Androgen deprivation therapy (ADT), a mainstay treatment, has raised concerns about cardiotoxicity, yet the CVD risks of individual ADT agents remain unclear.

objectivesTo assess cardiovascular adverse events (AEs) associated with specific ADT drugs using data from the U.S. FDA Adverse Event Reporting System (FAERS).

methodsAE reports related to ADT drugs were extracted from FAERS (Q1 2004-Q3 2024). Disproportionality analyses-including Reporting Odds Ratio (ROR) and Proportional Reporting Ratio (PRR)-were conducted to identify significant cardiovascular safety signals.

resultsDifferent ADT agents exhibited distinct cardiovascular AE profiles. Some drugs were linked to a broader range of CVD-related AEs, while others had more limited associations.

conclusionsADT agents demonstrate heterogeneous cardiotoxicity profiles. These findings emphasize the need for individualized treatment strategies, particularly in patients with pre-existing CVD risks, and may aid clinicians in balancing cancer control with cardiovascular safety.

Indexed as

Androgen AntagonistsAntineoplastic Agents, HormonalCardiotoxicityCardiovascular DiseasesProstatic NeoplasmsAdverse Drug Reaction Reporting SystemsAgedHumansMaleMiddle AgedUnited StatesAndrogen AntagonistsAntineoplastic Agents, HormonalADTcardiovascular toxicityprostate cancer

Identifiers

PMID41423663
PMCPMC12719240

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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.