Evidence map›Paper›PMID 42086620›Full record

ArticleNature communications2026

A retrospective pharmacovigilance analysis based on the FAERS database reveals sex-associated differences in toxicities of CAR T-cell therapy.

Yuan Liu, Jingwen Yang, Madiha Iqbal, Mehmet Uyanik, Mei Luo, Liqi Yang, Yanyan Lou, Lixia Diao, Olalekan O Oluwole, Javid J Moslehi and 2 more

Abstract read
In one paragraph

Article in Nature communications, 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

12 authors.

Yuan Liu *Department of Biostatistics and Health Data Science, Indiana University School of Medicine, Indianapolis, IN, USA. yl218@iu.edu.ORCID http://orcid.org/0000-0003-2030-1153
Jingwen Yang *Department of Biostatistics and Health Data Science, Indiana University School of Medicine, Indianapolis, IN, USA.
Madiha IqbalDivision of Hematology-Oncology, Department of Medicine, Mayo Clinic, Jacksonville, FL, USA.
Mehmet UyanikDivision of Hematology-Oncology, Department of Medicine, Mayo Clinic, Jacksonville, FL, USA.
Mei LuoDepartment of Biostatistics and Health Data Science, Indiana University School of Medicine, Indianapolis, IN, USA.ORCID http://orcid.org/0000-0002-0183-2373
Liqi YangDepartment of Biostatistics and Health Data Science, Indiana University School of Medicine, Indianapolis, IN, USA.
Yanyan LouDivision of Hematology-Oncology, Department of Medicine, Mayo Clinic, Jacksonville, FL, USA.
Lixia DiaoDepartment of Bioinformatics and Computational Biology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.ORCID http://orcid.org/0000-0001-6995-4492
Olalekan O OluwoleDivision of Hematology and Oncology, Vanderbilt University Medical Center, Nashville, TN, USA.
Javid J MoslehiSection of Cardio-Oncology & Immunology; Cardiovascular Research Institute (CVRI), University of California San Francisco, School of Medicine, San Francisco, CA, USA.
Douglas B JohnsonDivision of Hematology and Oncology, Vanderbilt University Medical Center, Nashville, TN, USA. douglas.b.johnson@vumc.org.ORCID http://orcid.org/0000-0002-6390-773X
Leng HanDepartment of Biostatistics and Health Data Science, Indiana University School of Medicine, Indianapolis, IN, USA. lenghan@iu.edu.ORCID http://orcid.org/0000-0002-7380-2640

Funding

MolQTL: A comprehensive resource for molecular quantitative trait loci inhuman cancer.R01HG011633 · NHGRI · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI HAN, LENG · 2021 to 2025
$1.9M
U.S. Department of Health & Human Services | NIH | National Human Genome Research Institute (NHGRI) R01HG011633
6 · The paper itself

Abstract

Chimeric antigen receptor (CAR) T-cell therapy has significantly advanced treatment outcomes for hematological malignancies; however, therapy-associated toxicities are often severe and sex-related differences in toxicity remain under-investigated. Here, we extract data from FDA Adverse Event Reporting System (FAERS) to evaluate sex-associated differences in CAR T-cell therapy toxicities. Among 7700 cases, females show higher reporting odds of cytokine release syndrome (CRS), with a reporting odds ratio (ROR) of 1.10 and a confidence interval (CI) of [1.00, 1.20], as well as leukemias (ROR = 1.34; CI [1.05, 1.70]). Elevated reporting odds in females are observed across multiple organ systems. Comparisons across cancer treatments indicate that sex-associated reporting patterns in CAR T-cell therapy cannot be attributed to baseline sex differences across cancer therapies. Stratified analyses further identify heterogeneity by cancer type and CAR T product. These results highlight distinct sex-associated toxicity patterns and may support incorporating sex into toxicity management.

Indexed as

Immunotherapy, AdoptivePharmacovigilanceReceptors, Chimeric AntigenAdverse Drug Reaction Reporting SystemsCytokine Release SyndromeDatabases, FactualFemaleHumansLeukemiaMaleRetrospective StudiesSex FactorsUnited StatesUnited States Food and Drug AdministrationReceptors, Chimeric Antigen

Identifiers

PMID42086620
PMCPMC13347020

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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.