Evidence map›Paper›PMID 39388649›Full record

ArticleJCO oncology practice2025

Real-World Immune-Related Adverse Events in Patients With Early Triple-Negative Breast Cancer Who Received Pembrolizumab.

Athira Jayan, Jasmine S Sukumar, Benjamin Fangman, Tejal Patel, Akshara Singareeka Raghavendra, Diane Liu, Sarah Pasyar, Ronald Rauch, Karen Basen-Engquist, Debasish Tripathy and 3 more

Abstract read
In one paragraph

Article in JCO oncology practice, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

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

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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

13 authors.

Athira JayanDepartment of Breast Medical Oncology, MD Anderson Cancer Center, Houston, TX.ORCID 0000-0001-8926-3306
Jasmine S SukumarDepartment of Breast Medical Oncology, MD Anderson Cancer Center, Houston, TX.ORCID 0000-0001-6994-8527
Benjamin FangmanDepartment of General Oncology, MD Anderson Cancer Center, Houston, TX.ORCID 0000-0003-2437-0738
Tejal PatelDepartment of Breast Medical Oncology, MD Anderson Cancer Center, Houston, TX.ORCID 0000-0003-1676-8439
Akshara Singareeka RaghavendraDepartment of Breast Medical Oncology, MD Anderson Cancer Center, Houston, TX.ORCID 0000-0002-6425-4400
Diane LiuDepartment of Health Disparities Research, MD Anderson Cancer Center, Houston, TX.
Sarah PasyarDepartment of Health Disparities Research, MD Anderson Cancer Center, Houston, TX.
Ronald RauchDepartment of Breast Medical Oncology, MD Anderson Cancer Center, Houston, TX.ORCID 0009-0003-1005-3587
Karen Basen-EngquistDepartment of Cancer Medicine, MD Anderson Cancer Center, Houston, TX.ORCID 0000-0001-7299-0646
Debasish TripathyDepartment of Breast Medical Oncology, MD Anderson Cancer Center, Houston, TX.ORCID 0000-0002-5711-2404
Yinghong WangDepartment of Gastroenterology, Hepatology & Nutrition, MD Anderson Cancer Center, Houston, TX.ORCID 0000-0002-5148-6130
Sonya S KhanDepartment of Endocrine Neoplasia and HD, MD Anderson Cancer Center, Houston, TX.ORCID 0009-0009-4456-6739
Carlos H BarcenasDepartment of Breast Medical Oncology, MD Anderson Cancer Center, Houston, TX.ORCID 0000-0001-5377-9167

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI DIANE BODURKA · 1985 to 2026
$290.8M
NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

purposeThe addition of pembrolizumab to chemotherapy in high-risk early triple-negative breast cancer (TNBC) improves cancer outcomes. However, pembrolizumab induces varied immune-related adverse events (irAEs) where some can be severe or lifelong. This retrospective study describes real-world patterns of irAEs in patients with TNBC who received pembrolizumab.

methodsWe evaluated irAEs in patients with TNBC from a comprehensive cancer center and a community hospital who received pembrolizumab with chemotherapy between 2021 and 2023, excluding those enrolled in clinical trials. We used national guidelines to grade toxicities. Logistic regression assessed the effect of clinicopathologic variables on irAEs adjusting for covariates.

resultsWe identified 233 patients with a median age of 51 years, 62% had stage II TNBC, 35% had stage III TNBC, 25% were Hispanic, 21% were Black, and 42% were White. Eighty patients (34%) developed 100 separate irAEs. The most common irAEs were endocrinopathies (52%) and GI (23%); there were 26 grade ≥3 irAEs, which all resulted in hospitalization, the most common being GI (13 instances); 45 required systemic steroids, 16 required additional immunosuppressive therapy, and 32 patients discontinued pembrolizumab because of irAEs. Two patients who developed colitis eventually died due to complications. Most (67 instances) irAEs were unresolved at the time of last follow-up, but 55% (37/67) had improved to grade 1. No clinicopathologic factors were associated with the development or severity of irAEs.

conclusionIn this real-world diverse population, we observed rates of irAEs comparable with KEYNOTE-522, where endocrinopathies were the most prevalent, but GI irAEs were also prevalent and severe. This emphasizes a critical issue as pembrolizumab is increasingly being used in early TNBC and could have long-term survivorship implications.

Indexed as

Antibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalDrug-Related Side Effects and Adverse ReactionsTriple Negative Breast NeoplasmsAdultAgedFemaleHumansMiddle AgedRetrospective StudiesAntibodies, Monoclonal, HumanizedAntineoplastic Agents, Immunologicalpembrolizumab

Identifiers

PMID39388649
PMCPMC12208142

What OpenQuestion 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 OpenQuestion graph.