Evidence map›Paper›PMID 40613977›Full record

ArticleBreast cancer research and treatment2025

Adverse events in patients treated with neoadjuvant chemo/immunotherapy for triple negative breast cancer: results from seven academic medical centers.

Jessica Mezzanotte-Sharpe, Chih-Yuan Hsu, David Choi, Hollie Sheffield, Sara Zelinskas, Ekaterina Proskuriakova, Mateo Montalvo, Danelle S Lee, Jennifer G Whisenant, Keaton Gaffney and 9 more

Abstract readMulticenter Study
In one paragraph

Article in Breast cancer research and treatment, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

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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

19 authors.

Jessica Mezzanotte-SharpeDivision of Hematology and Oncology, Vanderbilt University Medical Center, 2200 Pierce Avenue, 777 PRB, Nashville, TN, 37232-6307, USA.
Chih-Yuan HsuDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, TN, USA.
David ChoiJohns Hopkins Sidney Kimmel Comprehensive Cancer Center, Baltimore, MD, USA.
Hollie SheffieldDivision of Hematology/Oncology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Sara ZelinskasDivision of Medical Oncology, The Ohio State University Comprehensive Cancer Center, Columbus, OH, USA.
Ekaterina ProskuriakovaDepartment of Medicine, University of Illinois Chicago, Chicago, IL, USA.
Mateo MontalvoSection of Medical Oncology, Yale School of Medicine, New Haven, CT, USA.
Danelle S LeeSection of Medical Oncology, Yale School of Medicine, New Haven, CT, USA.
Jennifer G WhisenantDivision of Hematology and Oncology, Vanderbilt University Medical Center, 2200 Pierce Avenue, 777 PRB, Nashville, TN, 37232-6307, USA.
Keaton GaffneyClinical Pharmacy, Vanderbilt University Medical Center, Nashville, TN, USA.
Michael S ThompsonClinical Pharmacy, Vanderbilt University Medical Center, Nashville, TN, USA.
Kim BlenmanSection of Medical Oncology, Yale School of Medicine, New Haven, CT, USA.
Karine TawagiDepartment of Medicine, University of Illinois Chicago, Chicago, IL, USA.
Lynn SymondsDepartment of Medicine, University of Washington School of Medicine, Seattle, WA, USA.
Cesar Santa-MariaJohns Hopkins Sidney Kimmel Comprehensive Cancer Center, Baltimore, MD, USA.
Nisha UnniDivision of Hematology/Oncology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Dionisia QuirogaDivision of Medical Oncology, The Ohio State University Comprehensive Cancer Center, Columbus, OH, USA.
Yu ShyrDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, TN, USA.
Laura C KennedyDivision of Hematology and Oncology, Vanderbilt University Medical Center, 2200 Pierce Avenue, 777 PRB, Nashville, TN, 37232-6307, USA. laura.kennedy@vumc.org.

Funding

Vanderbilt Clinical Oncology Research Career Development ProgramK12CA090625 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Debra L. Friedman, Paula Jill Hurley · 2001 to 2026
$16.9M
VOLT (Vanderbilt Oncology Training Program)T32CA217834 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Debra L. Friedman, Douglas B Johnson · 2018 to 2026
$2.7M
NCI NIH HHS K12 CA090625NCI NIH HHS T32 CA217834VOLT T32 2T32CA217834-07
6 · The paper itself

Abstract

purposeThe standard-of-care neoadjuvant treatment for early-stage or locally advanced triple negative breast cancer (TNBC) is the KEYNOTE-522 regimen that combines pembrolizumab and chemotherapy. Although this approach has superior response and survival rates, high-grade adverse events (AEs) are common. Real-world data from a diverse patient population is needed to better understand practice patterns and the impact of immunotherapy in TNBC patients.

methodsMedical records from TNBC patients were retrospectively reviewed during neoadjuvant and adjuvant treatment with pembrolizumab and chemotherapy. CTCAE version 5.0 was used to grade AEs. Variables were reported with descriptive statistics, and AE, pCR and hospitalization rates were estimated with 95% confidence intervals.

resultsWe identified 415 patients from seven academic medical centers; 60% identified as White and 21% as Black. pCR rate was 52%. 88% of patients experienced an AE, 38% experienced a grade 3+ AE, and 31% stopped pembrolizumab early. Hospitalization rate was 26%. There were no statistically significant differences in AE, pCR or hospitalization rates between White and Black patients. Obese patients had a statistically significant higher hospitalization rate (p = 0.014). There were 18 deaths during treatment, mainly from progressive TNBC.

conclusionThis is one of the largest real-world, diverse patient cohorts for TNBC patients treated with chemotherapy and pembrolizumab. pCR rate was lower than that reported in the KEYNOTE-522 study and in smaller real-world studies, potentially due to high rates of pembrolizumab and chemotherapy discontinuation. AEs and hospitalizations were common, with obese patients more likely to be hospitalized than patients with a normal BMI.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsImmunotherapyNeoadjuvant TherapyTriple Negative Breast NeoplasmsAcademic Medical CentersAdultAgedAntibodies, Monoclonal, HumanizedChemotherapy, AdjuvantFemaleHumansMiddle AgedRetrospective StudiesTreatment OutcomeAntibodies, Monoclonal, HumanizedpembrolizumabImmune-related adverse eventsPembrolizumabTriple negative breast cancer

Identifiers

PMID40613977
PMCPMC12259778

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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.