Evidence map›Paper›PMID 39583866›Full record

ArticleJACC. Advances2024

Elevations of Cardiac Troponin in Patients Receiving Immune Checkpoint Inhibitors: Data From a Prospective Study.

Pieter F van den Berg, Valentina Bracun, Michel Noordman, Peter van der Meer, Canxia Shi, Sjoukje F Oosting, Joseph Pierre Aboumsallem, Sanne de Wit, Wouter C Meijers, Mathilde Jalving and 2 more

Abstract read
In one paragraph

Article in JACC. Advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Review
  4. Role of Troponins in CardioOncology.Current treatment options in oncology · 2026
    Review
  5. Article
  6. TIM-3 in Cardiovascular Disease.Current heart failure reports · 2026
    Review
  7. Observational
  8. Article
  9. Article
  10. Review
  11. Review
  12. Review
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  14. Article
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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

12 authors.

Pieter F van den BergDepartment of Cardiology, University Medical Center Groningen, Groningen, the Netherlands.
Valentina BracunDepartment of Cardiology, University Medical Center Groningen, Groningen, the Netherlands.
Michel NoordmanDepartment of Medical Oncology, University Medical Center Groningen, Groningen, the Netherlands.
Peter van der MeerDepartment of Cardiology, University Medical Center Groningen, Groningen, the Netherlands.
Canxia ShiErasmus Medical Center, Cardiovascular Institute, Thorax Center, Department of Cardiology, Rotterdam, the Netherlands.
Sjoukje F OostingDepartment of Medical Oncology, University Medical Center Groningen, Groningen, the Netherlands.
Joseph Pierre AboumsallemDepartment of Cardiology, University Medical Center Groningen, Groningen, the Netherlands.
Sanne de WitDepartment of Cardiology, University Medical Center Groningen, Groningen, the Netherlands.
Wouter C MeijersDepartment of Cardiology, University Medical Center Groningen, Groningen, the Netherlands.
Mathilde JalvingDepartment of Medical Oncology, University Medical Center Groningen, Groningen, the Netherlands.
Michel van KruchtenDepartment of Medical Oncology, University Medical Center Groningen, Groningen, the Netherlands.
Rudolf A de BoerErasmus Medical Center, Cardiovascular Institute, Thorax Center, Department of Cardiology, Rotterdam, the Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Immune checkpoint inhibitors (ICIs) are increasingly used in the treatment of cancer. However, immune-related adverse events are prevalent in patients receiving ICI therapy. A serious immune-related adverse event is ICI-myocarditis, which is complex to diagnose given that the significance of early symptoms and biomarker trajectories, such as high-sensitivity troponin T (hs-TnT) are unclear. Objectives: The purpose of the study was to evaluate kinetics of hs-TnT in cancer patients receiving ICI and to identify patients at risk of developing ICI-myocarditis. Methods: This prospective, observational, single-center study included 164 patients receiving ICI therapy. Patients' history, demographics, and clinical characteristics, as well as survival statistics, were collected from electronic patient records and used to analyze associations between elevated hs-TnT (≥14 ng/L) and a significant rise in hs-TnT (100% rise from baseline, with an absolute value ≥2x upper limit of normal (ie, ≥28 ng/L) with ICI-myocarditis. Results: We included 164 patients with a mean follow-up time of 1.60 ± 0.91 years. Melanoma was the most common type of cancer in the patient population, and most patients received treatment with programmed cell death protein 1 (PD-1). Twenty-six patients (16%) exhibited significant hs-TnT elevations, while 8 patients (5%) developed ICI-myocarditis. In 18 of 26 (69%) patients, ICI-myocarditis could not be diagnosed with certainty, while 10 of 26 (38%) patients had no other signs of symptoms of cardiac damage. All 8 myocarditis cases were preceded by significantly higher hs-TnT elevations than asymptomatic patients. Despite a high ICI-myocarditis incidence in our study population, cardiac mortality remained low (4%). Conclusions: Significant hs-TnT elevations occur more often than previously reported, are often asymptomatic, and do not always lead to myocarditis diagnosis.

Indexed as

cardiac biomarkershs-TnThypertroponinemiaICIimmunotherapymyocarditis

Identifiers

PMID39583866
PMCPMC11584941

What Socratic holds

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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 Socratic graph.