Evidence map›Paper›PMID 34216282›Full record

ReviewCurrent cardiology reports2021

Cardiovascular Toxicity of Androgen Deprivation Therapy.

Julia Boland, William Choi, Maximillian Lee, Jianqing Lin

Open access · bronzeAbstract readReview
In one paragraph

Review in Current cardiology reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

12 citing papers in PubMed, 32 citations in OpenAlex.

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  11. Targeting Breast Cancer: An Overlook on Current Strategies.International journal of molecular sciences · 2023
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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

4 authors at 1 institution in 1 country.

Julia BolandGeorge Washington University Hospital, Washington, DC, USA.
William ChoiGeorge Washington University Hospital, Washington, DC, USA.
Maximillian LeeGeorge Washington University Hospital, Washington, DC, USA.
Jianqing LinGeorge Washington University Hospital, Washington, DC, USA. Jilin@mfa.gwu.edu.ORCID http://orcid.org/0000-0002-0406-690X
George Washington University Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purpose of reviewAndrogen deprivation therapy (ADT) is the standard of care for the treatment of advanced prostate cancer (PC). ADT, particularly with GnRH agonists, leads to increased risk of cardiovascular disease, including myocardial infarction, hypertension, and stroke. This review discusses the options of ADT, the mechanism of ADT-associated cardiovascular side effects, and potential benefit by using GnRH antagonists. RECENT

findingsGnRH antagonists have relatively less cardiovascular adverse effects compared to GnRH agonists. We highlight on a recently published phase III clinical trial on the oral GnRH antagonist, relugolix, and its comparative benefit to traditional GnRH agonist regarding development of cardiovascular disease. Recent data reinforces that GnRH antagonists have a more favorable cardiovascular outcomes compared to GnRH agonists yet maintain a similar efficacy profile. From the data we reviewed, GnRH antagonists may be the preferred method of ADT for PC, but further data with primary cardiovascular outcomes are warranted.

Indexed as

Cardiovascular DiseasesMyocardial InfarctionProstatic NeoplasmsAndrogen AntagonistsAndrogensGonadotropin-Releasing HormoneHumansMaleAndrogen AntagonistsAndrogensGonadotropin-Releasing HormoneAndrogen deprivation therapyCardio-oncologyCardiovascular toxicityCoronary artery diseaseGnRH antagonistProstate cancer

Identifiers

PMID34216282
PMCPMC8254069
OpenAlexW3174266602

What OpenQuestion holds

Textmetadata
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.