Evidence map›Paper›PMID 41854318›Full record

ArticleJACC. Case reports2026

Chemotherapy as Second Hit in Desmoplakin Cardiomyopathy.

Del Castillo Santiago, Blanco Rocío, Fernandez Ferro Germán, Brögger Maria Noel, Bergier Mariano, Falconi Mariano, Pérez de Arenaza Diego, Pizarro Rodolfo

Abstract readCase Reports
In one paragraph

Article in JACC. Case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Del Castillo SantiagoCardio-Oncology Section, Cardiology Department, Hospital Italiano de Buenos Aires, Buenos Aires, Argentina. Electronic address: santiago.delcastillo@hospitalitaliano.org.ar.
Blanco RocíoSection of Inherited and Familial Cardiomyopathies, Cardiology Department, Hospital Italiano de Buenos Aires, Buenos Aires, Argentina.
Fernandez Ferro GermánOberarzt, Electrophysiology Laboratory, Department of Cardiology and Rhythmology, Johannes Gutenberg-Universität Mainz, Mainz, Germany.
Brögger Maria NoelCardiovascular Genetics Specialist, Health in Code, A Coruña, Spain.
Bergier MarianoResidency Program, Hospital Italiano de Buenos Aires, Buenos Aires, Argentina.
Falconi MarianoCardiovascular Imaging Unit, Cardiology Department, Hospital Italiano de Buenos Aires, Buenos Aires, Argentina.
Pérez de Arenaza DiegoCardiovascular Imaging Unit, Cardiology Department, Hospital Italiano de Buenos Aires, Buenos Aires, Argentina.
Pizarro RodolfoCardiology Department, Hospital Italiano de Buenos Aires, Buenos Aires, Argentina.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCancer therapy-related cardiac dysfunction is traditionally considered an acquired cardiomyopathy; however, genetic susceptibility may predispose patients to disproportionate myocardial injury, supporting a second-hit model. CASE SUMMARY: A 37-year-old woman with breast cancer and no cardiovascular history developed left ventricular dysfunction during anthracycline chemotherapy, with further deterioration after anti-human epidermal growth factor receptor 2 therapy. Cardiovascular magnetic resonance demonstrated biventricular dysfunction, ventricular dilatation, and ring-like subepicardial late gadolinium enhancement, atypical for isolated cardiotoxicity. Genetic testing revealed a pathogenic loss-of-function Desmoplakin variant, establishing DSP-related cardiomyopathy. Anti-human epidermal growth factor receptor 2 therapy was discontinued, heart failure therapy optimized, and an implantable cardioverter-defibrillator implanted for primary prevention. DISCUSSION: This case shows how chemotherapy may unmask latent genetic cardiomyopathy, emphasizing the diagnostic value of tissue characterization and genetic testing when ventricular dysfunction is unexpected. TAKE-HOME MESSAGE: Severe ventricular dysfunction during cancer therapy should prompt genetic evaluation, with cardiovascular magnetic resonance and genetic testing playing a key role in guiding diagnosis and risk stratification.

Indexed as

cardiotoxicityDesmoplakin cardiomyopathysecond hit

Identifiers

PMID41854318
PMCPMC13008527

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.