Evidence map›Paper›PMID 41965742›Full record

ArticleCardio-oncology (London, England)2026

Cardiotoxicity prevention trials in the era of contemporary cancer therapies: a systematic review.

Malak Munir, Ahmed Sayed, Sanam Ghazi, Eric H Yang, Avirup Guha, Narendranath Epperla, Daniel Addison

Abstract read
In one paragraph

Article in Cardio-oncology (London, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Malak Munir *Karsh Division of Gastroenterology and Hepatology, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Ahmed Sayed *Houston Methodist DeBakey Heart & Vascular Center, Houston, TX, USA.
Sanam GhaziCardio-Oncology Program, University of Texas Southwestern Medical Center, Texas, USA.
Eric H YangDivision of Cardiology, Department of Medicine, UCLA Cardio-Oncology Program, University of California at Los Angeles, Los Angeles, CA, USA.
Avirup GuhaCardio-Oncology Program, Augusta University Medical Center, Augusta, GA, USA.
Narendranath EpperlaDivision of Hematology and Hematologic Malignancies, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
Daniel AddisonCardio-Oncology Program, University of Texas Southwestern Medical Center, Texas, USA. daniel.addison@utsouthwestern.edu.

Funding

American Heart Association 847740American Heart Association American Heart Association-Robert Wood Johnson Foundation grantNIH HHS P50-CA140158
6 · The paper itself

Abstract

backgroundCardiovascular toxicity is an increasingly important limitation of effective contemporary cancer therapies. Yet, the extent to which trials focus on preventing cardiotoxic events in patients receiving contemporary therapies is unknown.

methodsLeveraging PubMed, CENTRAL, clinicaltrials.gov, and publicly available reviews to identify all randomized controlled trials (RCTs) testing interventions for prevention or management of cardiotoxicity in cancer patients through 2024, we assessed the proportion of cardiotoxicity prevention trials that studied contemporary cancer therapies (biologic, targeted, or immune-based therapies). We included RCTs of interventional therapies/strategies against cardiotoxicity during cancer treatment. Data on trial baseline characteristics, design, funding, and reporting were extracted. Regression models were used to define trial and population factors associated with drug selection, reporting bias, and subsequent translation into guidelines.

resultsOverall, there were 126 trials, evaluating 15 prevention strategies, enrolling 16,111 participants (45.6 ± 13.9 years, 81.3% female, median trial duration of 23 months). Among trials, 17.5% evaluated patients receiving biologic, targeted, and/or immune-based therapies, including 2.4% of trials focused on immune-based therapies (one IL-2 and two immune checkpoint inhibitors). Most trials (109 [86.5%]) used surrogate endpoints. Over time, there was no temporal increase in the proportion of trials assessing biologic, targeted, or immune-based cancer therapies.

conclusionCollectively, these data suggest that among trials focused on preventing cardiotoxicity, contemporary cancer therapies were not frequently evaluated.

Indexed as

Cancer therapiesCardio-oncologyCardiotoxicity prevention trials

Identifiers

PMID41965742
PMCPMC13220620

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.