Evidence map›Paper›PMID 40634318›Full record

ArticleScientific reports2025

Real-world FDA database analysis unveiling cardiovascular adverse events associated with bispecific T cell engagers in multip myeloma.

Chang Shan, Yanli Zhang, Xinxin Zhang, Lu Li, Yanwei Chen, Ying Liu

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Review
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  6. 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

6 authors.

Chang Shan *Department of Cardiology, The First Affiliated Hospital of Dalian Medical University, 222 Zhongshan Road, Dalian, Liaoning Province, China.
Yanli Zhang *Department of Cardiology, The First Affiliated Hospital of Dalian Medical University, 222 Zhongshan Road, Dalian, Liaoning Province, China.
Xinxin ZhangDepartment of Cardiology, The First Affiliated Hospital of Dalian Medical University, 222 Zhongshan Road, Dalian, Liaoning Province, China.
Lu LiDepartment of Pharmacy, First Afffliated Hospital of Dalian Medical University, 222 Zhongshan Road, Dalian, 116011, Liaoning Province, China. lilu12312007@163.com.
Yanwei ChenDepartment of Pharmacy, First Afffliated Hospital of Dalian Medical University, 222 Zhongshan Road, Dalian, 116011, Liaoning Province, China. chenyanweile@163.com.
Ying LiuDepartment of Cardiology, The First Affiliated Hospital of Dalian Medical University, 222 Zhongshan Road, Dalian, Liaoning Province, China. yingliu.med@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Our study aimed to analyze the reported cardiovascular AEs (CVAEs) associated with approved bispecific T-cell engagers (BiTEs) for multiple myeloma (MM), providing insights that could guide safer clinical use of BiTEs. Data were obtained from the FDA Adverse Event Reporting System (FAERS) database for the period from the fourth quarter of 2022 to the first quarter of 2024. A total of 1336 adverse events were reported, of which 112 were CVAEs, accounting for 8.4%. Reporting odds ratio (ROR) and information components (ICs) were extracted from the disproportionality analysis. At standardized MedDRA querie (SMQ) level, arrhythmias (n = 41, ROR025 = 1.49), noninfectious myocarditis/pericarditis (n = 184, ROR025 = 3.11), cardiomyopathy (n = 33, ROR025 = 1.52), shock (n = 23, ROR025 = 4.13) and cardiac failure (n = 16, ROR025 = 1.17) exhibited the positive signal strengths in ROR. And logistic regression analysis reveals that critical risk factors for BiTE-associated CVAEs include older age, male sex, weight loss, cytokine release syndrome, and respiratory failure. In the time-to-onset analysis, majority of CVAEs occurred within the first month (60.9%) and had early-failure type characteristics. It also should be emphasized that CVAEs were commonly associated with serious outcomes, with the most frequently reported being death (34%) Findings above suggest BiTE therapy in MM patients is significantly associated with an increased risk of CVAEs in clinic, and those who develop CVAEs have poorer prognosis. The study may provide important evidence for the precise management and mitigation of cardiovascular risks during BiTE therapy in MM patients, ensuring better clinical outcomes.

Indexed as

Antibodies, BispecificCardiovascular DiseasesMultiple MyelomaT-LymphocytesAdultAdverse Drug Reaction Reporting SystemsAgedDatabases, FactualFemaleHumansMaleMiddle AgedRisk FactorsUnited StatesUnited States Food and Drug AdministrationAntibodies, BispecificBispecific T-cell engagersCardio-oncologyCardiovascular adverse eventsFaers databasesRecurrent or refractory multiple myeloma

Identifiers

PMID40634318
PMCPMC12241570

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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.