Evidence map›Paper›PMID 40107671›Full record

ArticleJournal for immunotherapy of cancer2025

Cardiac MRI study of adverse events in patients treated with immune checkpoint inhibitors: a prospective cohort study of cardiac adverse events.

Agnese Losurdo, Cristina Panico, Chiara Catalano, Simone Serio, Laura Giordano, Lorenzo Monti, Federica Catapano, Stefano Figliozzi, Carla D'Andrea, Angelo Dipasquale and 13 more

Abstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
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

23 authors.

Agnese Losurdo *Department of Biomedical Sciences, Humanitas University, Pieve Emanuele (MI), Italy.
Cristina Panico *Department of Biomedical Sciences, Humanitas University, Pieve Emanuele (MI), Italy.
Chiara Catalano *Department of Biomedical Sciences, Humanitas University, Pieve Emanuele (MI), Italy.
Simone SerioCardiology Unit, IRCCS Humanitas Research Hospital, Rozzano (MI), Italy.
Laura GiordanoBiostatistics Unit, IRCCS Humanitas Research Hospital, Rozzano, Italy.
Lorenzo MontiDepartment of Biomedical Sciences, Humanitas University, Pieve Emanuele (MI), Italy.
Federica CatapanoDepartment of Biomedical Sciences, Humanitas University, Pieve Emanuele (MI), Italy.
Stefano FigliozziDepartment of Biomedical Sciences, Humanitas University, Pieve Emanuele (MI), Italy.
Carla D'AndreaCardiology Unit, IRCCS Humanitas Research Hospital, Rozzano (MI), Italy.ORCID http://orcid.org/0000-0003-1101-9789
Angelo DipasqualeMedical Oncology and Hematology Unit, IRCCS Humanitas Research Hospital, Rozzano (MI), Italy.
Pasquale PersicoMedical Oncology and Hematology Unit, IRCCS Humanitas Research Hospital, Rozzano (MI), Italy.
Antonio Di MuzioDepartment of Biomedical Sciences, Humanitas University, Pieve Emanuele (MI), Italy.
Marco CremonesiAdaptive Immunity Laboratory, IRCCS Humanitas Research Hospital, Rozzano (MI), Italy.
Alessandro MarcheseCardiology Unit, IRCCS Humanitas Research Hospital, Rozzano (MI), Italy.
Maria Chiara TronconiMedical Oncology and Hematology Unit, IRCCS Humanitas Research Hospital, Rozzano (MI), Italy.
Matteo PerrinoMedical Oncology and Hematology Unit, IRCCS Humanitas Research Hospital, Rozzano (MI), Italy.
Giovanna FinocchiaroMedical Oncology and Hematology Unit, IRCCS Humanitas Research Hospital, Rozzano (MI), Italy.
Enrico LugliLaboratory of Translational Immunology, IRCCS Humanitas Research Hospital, Rozzano (MI), Italy.
Marco FranconeDepartment of Biomedical Sciences, Humanitas University, Pieve Emanuele (MI), Italy.
Armando SantoroDepartment of Biomedical Sciences, Humanitas University, Pieve Emanuele (MI), Italy.
Gianluigi Condorelli *Department of Biomedical Sciences, Humanitas University, Pieve Emanuele (MI), Italy marinos.kallikourdis@humanitasresearch.it gianluigi.condorelli@hunimed.eu matteo.simonelli@hunimed.eu.
Matteo Simonelli *Department of Biomedical Sciences, Humanitas University, Pieve Emanuele (MI), Italy marinos.kallikourdis@humanitasresearch.it gianluigi.condorelli@hunimed.eu matteo.simonelli@hunimed.eu.ORCID http://orcid.org/0000-0002-5264-1251
Marinos Kallikourdis *Department of Biomedical Sciences, Humanitas University, Pieve Emanuele (MI), Italy marinos.kallikourdis@humanitasresearch.it gianluigi.condorelli@hunimed.eu matteo.simonelli@hunimed.eu.ORCID http://orcid.org/0000-0001-9318-3368

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune checkpoint inhibitors (ICIs) revolutionized cancer therapy, yet require management of immune-related adverse events (irAEs). Fulminant myocarditis is a rare irAE, but lower-severity cardiac events are being reported more frequently, leading to an unmet need for irAE prevention, early diagnosis, and treatment, especially for long-life-expectancy patients. We recruited 57 patients, stratified according to therapy regime (monotherapy (30%) or combination (33%) cohort) or history of cardiac disease or presence of at least two cardiovascular risk factors other than prior or active smoking (cardiovascular cohort (37%)). We performed a complete cardiological assessment with clinical visit, 12-lead ECG, multiparametric cardiac MRI as well as peripheral blood mononuclear cell immunophenotyping, prior to ICI initiation and around 2 months later. ICI treatment was associated with a significant left ventricular ejection function (LVEF) reduction pre-ICI versus post-ICI treatment (60.1±8% to 58.1±8%, p=0.002, paired t-test) and more than 3% LVEF loss in a substantial proportion of patients (18; 32%). These patients also showed significantly higher T2 values (p=0.037, unpaired t-test), putative sign of cardiac edema. The loss of cardiac function did not differ among patients with different tumor types, therapy regimes or history of cardiac disease. Immunophenotyping analyses showed a reduction of programmed cell death protein 1 staining on both CD4

Indexed as

Heart DiseasesImmune Checkpoint InhibitorsMagnetic Resonance ImagingNeoplasmsAgedFemaleHumansMaleMiddle AgedProspective StudiesImmune Checkpoint InhibitorsCardiotoxicityImmune Checkpoint InhibitorsImmune related adverse event - irAE

Identifiers

PMID40107671
PMCPMC11927457

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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.