Evidence map›Paper›PMID 42199067›Full record

ArticleEuropean heart journal2026

Chimeric antigen receptor T-cell therapy and cardiovascular outcomes in US Medicare beneficiaries.

Raja Zaghlol, Elena Deych, Daniel A Ladin, David A Russler-Germain, Walter Schiffer, Nischit Baral, R J Waken, Bonnie Ky, Karen E Joynt Maddox, Joshua D Mitchell

Abstract read
In one paragraph

Article in European heart journal, 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

10 authors.

Raja ZaghlolDivision of Cardiovascular Disease, Washington University School of Medicine, 660 South Euclid Avenue, Campus Box 8086, St.Louis, MO 63110, USA.
Elena DeychDivision of Cardiovascular Disease, Washington University School of Medicine, 660 South Euclid Avenue, Campus Box 8086, St.Louis, MO 63110, USA.ORCID 0000-0002-6083-3579
Daniel A LadinDivision of Cardiovascular Disease, Washington University School of Medicine, 660 South Euclid Avenue, Campus Box 8086, St.Louis, MO 63110, USA.
David A Russler-GermainDivision of Oncology, Department of Medicine, Washington University School of Medicine, St.Louis, MO, USA.ORCID 0000-0003-1009-2247
Walter SchifferDivision of Cardiovascular Disease, Washington University School of Medicine, 660 South Euclid Avenue, Campus Box 8086, St.Louis, MO 63110, USA.
Nischit BaralCardiovascular Division, Columbia University, Mount Sinai Medical Center, Miami, FL, USA.
R J WakenDivision of Biostatistics, Washington University School of Medicine, St.Louis, MO, USA.ORCID 0000-0001-6678-7764
Bonnie KyDivision of Cardiology, Department of Medicine, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.ORCID 0000-0002-6628-9981
Karen E Joynt MaddoxDivision of Cardiovascular Disease, Washington University School of Medicine, 660 South Euclid Avenue, Campus Box 8086, St.Louis, MO 63110, USA.ORCID 0000-0003-3779-8653
Joshua D MitchellDivision of Cardiovascular Disease, Washington University School of Medicine, 660 South Euclid Avenue, Campus Box 8086, St.Louis, MO 63110, USA.ORCID 0000-0001-7371-5742

Funding

Rural-Urban Disparities In Spillover Effects of COVID-19U01NR020555 · NINR · WASHINGTON UNIVERSITY · PI JOYNT MADDOX, KAREN ELLEN · 2022 to 2024
$1.5M
MENTORING IN PATIENT-ORIENTED RESEARCH IN DEEP PHENOTYPING IN CARDIO-ONCOLOGYK24HL167127 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI Bonnie Ky · 2023 to 2026
$496k
NHLBI NIH HHS K24 HL167127NIH HHS 1U01NR020555NINR NIH HHSNINR NIH HHS U01 NR020555
6 · The paper itself

Abstract

BACKGROUND AND

aimsChimeric antigen receptor T-cell (CAR-T) therapies are cellular immunotherapies that improve survival in patients with relapsed haematologic malignancies. However, their association with major adverse cardiovascular events (MACE) has received limited study, particularly in older adults. This study investigated the incidence of MACE, associated risk factors, and their impact on survival among older patients undergoing CAR-T in the USA.

methodsMedicare fee-for-service beneficiaries over 65 who received inpatient CAR-T therapy between 2018 and 2023 were included. Baseline characteristics were assessed during the 12 months preceding CAR-T. MACE were defined as a composite of acute heart failure (HF), cardiogenic shock, myocardial infarction, cardiac tamponade, ventricular arrhythmia, complete heart block, or stroke. Multivariable models were adjusted for demographics, malignancy type, and baseline cardiovascular comorbidities.

resultsAmong 3292 patients receiving CAR-T, 191 (5.8%) had MACE. Most common events were acute HF (3.1%), followed by ischaemic (1.3%) and haemorrhagic stroke (1%). Pre-treatment atrial fibrillation/flutter [adjusted odds ratio (aOR) 1.52 (1.08-2.16)], cardiomyopathy [aOR 2.49 (1.75-3.54)], and cerebrovascular disease [aOR 2.40 (1.30-4.43)] were independently associated with MACE. In 2021-23, MACE were also associated with immune effector cell-associated neurotoxicity syndrome and higher-grade cytokine release syndrome. MACE were associated with higher in-hospital mortality [aOR 16.9 (11.0-26.1)] and 1-year mortality after discharge [adjusted hazard ratio 1.91 (1.46-2.49)].

conclusionsIn the largest national sample of older adults receiving CAR-T, MACE occurred in 5.8% of patients and were associated with increased in-hospital and 1-year mortality. Further investigation into preventive and mitigating measures is needed.

Indexed as

Cardiovascular DiseasesImmunotherapy, AdoptiveReceptors, Chimeric AntigenAgedAged, 80 and overFemaleHumansMaleMedicareRetrospective StudiesRisk FactorsUnited StatesReceptors, Chimeric AntigenCardio-oncologyCAR-TChimeric antigen receptorMACEMajor adverse cardiovascular eventMedicare

Identifiers

PMID42199067
PMCPMC13380970

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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.