Evidence map›Paper›PMID 39759436›Full record

ArticleJACC. Advances2025

Multimodal Fusion Artificial Intelligence Model to Predict Risk for MACE and Myocarditis in Cancer Patients Receiving Immune Checkpoint Inhibitor Therapy.

Chadi Ayoub, Lalith Appari, Milagros Pereyra, Juan M Farina, Chieh-Ju Chao, Isabel G Scalia, Ahmed K Mahmoud, Mohammed Tiseer Abbas, Nima Ali Baba, Jiwoong Jeong and 4 more

Abstract read
In one paragraph

Article in JACC. Advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 3 pooled it
–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

16 citing papers in PubMed, 3 syntheses or guidelines pooled it.

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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

14 authors.

Chadi AyoubDepartment of Cardiovascular Medicine, Mayo Clinic, Phoenix, Arizona, USA.
Lalith AppariDepartment of Radiology, Mayo Clinic, Phoenix, Arizona, USA.
Milagros PereyraDepartment of Cardiovascular Medicine, Mayo Clinic, Phoenix, Arizona, USA.
Juan M FarinaDepartment of Cardiovascular Medicine, Mayo Clinic, Phoenix, Arizona, USA.
Chieh-Ju ChaoDepartment of Cardiovascular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Isabel G ScaliaDepartment of Cardiovascular Medicine, Mayo Clinic, Phoenix, Arizona, USA.
Ahmed K MahmoudDepartment of Cardiovascular Medicine, Mayo Clinic, Phoenix, Arizona, USA.
Mohammed Tiseer AbbasDepartment of Cardiovascular Medicine, Mayo Clinic, Phoenix, Arizona, USA.
Nima Ali BabaDepartment of Cardiovascular Medicine, Mayo Clinic, Phoenix, Arizona, USA.
Jiwoong JeongDepartment of Cardiovascular Medicine, Mayo Clinic, Phoenix, Arizona, USA.
Steven J LesterDepartment of Cardiovascular Medicine, Mayo Clinic, Phoenix, Arizona, USA.
Bhavik N PatelDepartment of Radiology, Mayo Clinic, Phoenix, Arizona, USA.
Reza ArsanjaniDepartment of Cardiovascular Medicine, Mayo Clinic, Phoenix, Arizona, USA.
Imon BanerjeeDepartment of Radiology, Mayo Clinic, Phoenix, Arizona, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Immune checkpoint inhibitor (ICI) therapy has dramatically improved the prognosis for some cancers but can be associated with myocarditis, adverse cardiovascular events, and mortality. Objectives: The aim of this study was to develop an artificial intelligence (AI) model to predict the increased likelihood for the development of ICI-related myocarditis and adverse cardiovascular events. Methods: Cancer patients treated with ICI at a tertiary institution from 2011 to 2022 were reviewed. Baseline characteristics, laboratory values, electrocardiograms, and cardiovascular clinical outcomes were extracted. A composite outcome of ICI-related myocarditis and major adverse cardiovascular events (transient ischemic attack/stroke, new diagnosis of heart failure, myocardial infarction, and cardiac death) was used to develop a multimodal joint fusion AI model by combining baseline tabular data with electrocardiogram (ECG) in a single end-to-end model. ECG data were parsed using 1-D convolution and tubular data using multilayer perceptron. Results: Of 2,258 cancer patients who had ICI therapy and troponin measurement (mean age 68.5 ± 11.5 years, 59.7% male), the composite of cardiovascular clinical adverse events, including ICI-related myocarditis and major adverse cardiovascular events, occurred in 264 (11.7%) unique patients, with 428 events overall (including 59 [3%] ICI-related myocarditis events and 59 [3%] cardiac deaths). The proposed joint fusion model outperformed individual ECG and baseline electronic medical record data and laboratory value models with an area under the operating characteristics curve of 0.72 (0.64 true positive rate and 0.98 negative predictive value). Conclusion: A multimodal fusion AI model to predict myocarditis and adverse cardiovascular events in cancer patients starting ICI therapy had good prognostic performance. It may have clinical utility in identifying at-risk patients who may benefit from closer surveillance.

Indexed as

artificial intelligencecardiovascular eventsimmune checkpoint inhibitormyocarditis

Identifiers

PMID39759436
PMCPMC11699614

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.