Evidence map›Paper›PMID 31187890›Full record

ReviewComprehensive Physiology2019

Doxorubicin-Induced Cardiomyopathy in Children.

Trevi R Mancilla, Brian Iskra, Gregory J Aune

Open access · greenAbstract readReview
In one paragraph

Review in Comprehensive Physiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing 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

48 citing papers in PubMed, 108 citations in OpenAlex.

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  20. Doxorubicin-induced cardiotoxicity and risk factors.International journal of cardiology. Heart & vasculature · 2024
    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

3 authors at 1 institution in 1 country.

Trevi R MancillaUniversity of Texas Health Science Center San Antonio, San Antonio, Texas, USA.
Brian IskraUniversity of Texas Health Science Center San Antonio, San Antonio, Texas, USA.
Gregory J AuneUniversity of Texas Health Science Center San Antonio, San Antonio, Texas, USA.
The University of Texas Health Science Center at San Antonio · US

Funding

South Texas Medical Scientist Training Program (STX-MSTP)T32GM113896 · NIGMS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CAVAZOS, JOSE E · 2018 to 2022
$1.1M
Targeting Doxorubicin-Induced Mitochondrial Failure in Mesenchymal Stem Cells with MetforminF30AG057213 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI ISKRA, BRIAN · 2017 to 2021
$188k
NIA NIH HHS F30 AG057213NIGMS NIH HHS T32 GM113896
6 · The paper itself

Abstract

Doxorubicin-induced cardiotoxicity in childhood cancer survivors is a growing problem. The population of patients at risk for cardiovascular disease is steadily increasing, as five-year survival rates for all types of childhood cancers continue to improve. Doxorubicin affects the developing heart differently from the adult heart and in a subset of exposed patients, childhood exposure leads to late, irreversible cardiomyopathy. Notably, the prevalence of late-onset toxicity is increasing in parallel with improved survival. By the year 2020, it is estimated that there will be 500,000 childhood cancer survivors and over 50,000 of them will suffer from doxorubicin-induced cardiotoxicity. The majority of the research to-date, concentrated on childhood cancer survivors, has focused mostly on clinical outcomes through well-designed epidemiological and retrospective cohort studies. Preclinical studies have elucidated many of the cellular mechanisms that elicit acute toxicity in cardiomyocytes. However, more research is needed in the areas of early- and late-onset cardiotoxicity and more importantly improving the scientific understanding of how other cells present in the cardiac milieu are impacted by doxorubicin exposure. The overall goal of this review is to succinctly summarize the major clinical and preclinical studies focused on doxorubicin-induced cardiotoxicity. As the prevalence of patients affected by doxorubicin exposure continues to increase, it is imperative that the major gaps in existing research are identified and subsequently utilized to develop appropriate research priorities for the coming years. Well-designed preclinical research models will enhance our understanding of the pathophysiology of doxorubicin-induced cardiotoxicity and directly lead to better diagnosis, treatment, and prevention. © 2019 American Physiological Society. Compr Physiol 9:905-931, 2019.

Indexed as

Age FactorsAntibiotics, AntineoplasticCardiotoxicityChildDNA DamageDoxorubicinEndothelium, VascularErbB ReceptorsHumansMitochondria, HeartMyocytes, CardiacNeuregulinsReactive Oxygen SpeciesAntibiotics, AntineoplasticDoxorubicinEGFR protein, humanErbB ReceptorsNeuregulinsReactive Oxygen Species

Identifiers

PMID31187890
PMCPMC7000168
OpenAlexW2953223155

What OpenQuestion holds

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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.