Evidence map›Paper›PMID 42453165›Full record

ArticleEcancermedicalscience2026

Safety of immune checkpoint inhibitors in a diverse patient population: a single-institution experience.

Grace M Ferri, John F Murphy, Akash Oza, Alexander J B Bulteel, Wafaa Abbasi, Rachel Anderson, Mehmed Taha Dinc, Eva Gaufberg, Kayra Cengiz, Sainikhil Sontha and 5 more

Abstract read
In one paragraph

Article in Ecancermedicalscience, 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

15 authors.

Grace M FerriSection of General Internal Medicine, Department of Medicine, Boston Medical Center, Boston, MA 02215, USA.
John F MurphySection of General Internal Medicine, Department of Medicine, Boston Medical Center, Boston, MA 02215, USA.
Akash OzaSection of General Internal Medicine, Department of Medicine, Boston Medical Center, Boston, MA 02215, USA.
Alexander J B BulteelSection of General Internal Medicine, Department of Medicine, Boston Medical Center, Boston, MA 02215, USA.
Wafaa AbbasiBoston University Chobanian and Avedisian School of Medicine, Boston, MA 02215, USA.
Rachel AndersonSection of General Internal Medicine, Department of Medicine, Boston Medical Center, Boston, MA 02215, USA.
Mehmed Taha DincSection of General Internal Medicine, Department of Medicine, Boston Medical Center, Boston, MA 02215, USA.
Eva GaufbergBoston University Chobanian and Avedisian School of Medicine, Boston, MA 02215, USA.
Kayra CengizBoston University Chobanian and Avedisian School of Medicine, Boston, MA 02215, USA.
Sainikhil SonthaBoston University Chobanian and Avedisian School of Medicine, Boston, MA 02215, USA.
Janice WeinbergDepartment of Biostatistics, Boston University School of Public Health, Boston, MA 02215, USA.
Patrick KurpaskaSection of Hematology and Oncology, Boston University Chobanian and Avedisian School of Medicine and Boston Medical Center, Boston, MA 02215, USA.
Yashvin Onkarappa MangalaSection of Hematology and Oncology, Boston University Chobanian and Avedisian School of Medicine and Boston Medical Center, Boston, MA 02215, USA.
Matthew KulkeSection of Hematology and Oncology, Boston University Chobanian and Avedisian School of Medicine and Boston Medical Center, Boston, MA 02215, USA.
Umit TapanSection of Hematology and Oncology, Boston University Chobanian and Avedisian School of Medicine and Boston Medical Center, Boston, MA 02215, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Among racial and socioeconomic minorities not appropriately represented by trial populations, rates of immune-related adverse events (irAEs) are unclear. Objective: We sought to characterise factors associated with irAEs in adult cancer patients at Boston Medical Center, a safety-net hospital serving a diverse patient population, including racial and ethnic minorities. Methods: We performed a retrospective study on all adult cancer patients at Boston Medical Center treated with first-line immune checkpoint inhibitors (ICIs) between 7/1/15 and 6/30/22. Baseline demographic (including socioeconomic) and oncologic variables were collected. Results: From the overall cohort (n = 469), 34 patients (n = 34, 7%) on first-line ICI without prior chemotherapy developed at least one ICI toxicity. Toxicity was experienced in 10% of White patients, 5% of Black patients, 7% of Hispanic patients, 7% of non-Hispanic patients, 9% of public insurance recipients and 7% of private insurance recipients. When comparing those who sustained irAEs (n = 34) relative to their counterparts (n = 435), Fisher's exact test did not indicate any significant association between incidence of irAEs and gender (p = 0.853), race (p = 0.352), ethnicity (p = 1.00), language (p = 0.827), insurance (p = 1.00), education (p = 0.267) or smoking (p = 0.695). Conclusion: We did not identify disproportionate rates of toxicity among patients of racial and ethnic minorities or with public insurance. These findings suggest that management decisions and toxicity risk assessment should not be based solely on race or socioeconomic status. Future studies featuring diverse patient populations must be conducted to formulate clinical algorithms for irAE management.

Indexed as

antineoplastic agentsdiversitydrug-induced abnormalitiesequityimmunotherapyinclusionmedical oncology

Identifiers

PMID42453165
PMCPMC13365962

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.