Evidence map›Paper›PMID 39272903›Full record

ArticleCancers2024

Immune-Related Adverse Events of Genitourinary Cancer Patients, a Retrospective Cohort Study.

John C Hunting, Logan Deyo, Eric Olson, Andrew T Faucheux, Sarah N Price, Thomas W Lycan

Abstract read
In one paragraph

Article in Cancers, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
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.

John C HuntingDepartment of Internal Medicine, Wake Forest School of Medicine, Wake Forest University, Winston-Salem, NC 27157, USA.
Logan DeyoDepartment of Internal Medicine, Wake Forest School of Medicine, Wake Forest University, Winston-Salem, NC 27157, USA.ORCID 0009-0008-5271-4845
Eric OlsonDepartment of Hematology & Oncology, Wake Forest School of Medicine, Wake Forest University, Winston-Salem, NC 27157, USA.
Andrew T FaucheuxDepartment of Hematology & Oncology, Wake Forest School of Medicine, Wake Forest University, Winston-Salem, NC 27157, USA.ORCID 0000-0003-1176-6282
Sarah N PriceDepartment of Social Sciences and Health Policy, Wake Forest School of Medicine, Wake Forest University, Winston-Salem, NC 27157, USA.ORCID 0000-0002-1622-1700
Thomas W LycanDepartment of Hematology & Oncology, Wake Forest School of Medicine, Wake Forest University, Winston-Salem, NC 27157, USA.ORCID 0000-0001-9475-1558

Funding

CTSA K12 Program at Wake ForestK12TR004931 · NCATS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Nicholette D. Allred · 2024 to 2026
$2.3M
NCATS NIH HHS K12 TR004931
6 · The paper itself

Abstract

backgroundImmune checkpoint inhibitors (ICIs) have become common lines of therapy for genitourinary cancers (GUcs). Given their widespread use, understanding the risk factors, comparative profiles, and timing of immune-related adverse events (irAEs) is essential.

methodsWe created an IRB-approved retrospective registry of all patients who received at least one dose of an ICI for any indication between 1 February 2011 and 7 April 2022 at a comprehensive cancer center and its outreach clinics. Dichotomous outcomes were modeled using multivariable logistic regression. Survival outcomes were compared using multivariable Cox regression.

resultsAmong 3101 patients, 196 had renal cell carcinoma (RCC) and 170 had urothelial tumors. RCC patients were more likely to experience irAEs (OR 1.78; 95% CI 1.32-2.39), whereas urothelial carcinoma patients were not (OR 1.22; 95% CI 0.88-1.67). RCC patients were more prone to dermatitis, thyroiditis, acute kidney injury, and myocarditis, compared to other tumors, while urothelial carcinoma patients were not. The impact of irAEs on survival was not significantly different for GUcs compared to other tumors.

conclusionsRCC primaries have a significantly different irAE profile than most tumors, as opposed to urothelial primaries. Further, RCC was more likely to experience any irAEs. Heterogeneity of survival benefits by irAEs was not seen.

Indexed as

adverse eventsand survivalgenitourinary cancerimmunotherapyoutcomes

Identifiers

PMID39272903
PMCPMC11394475

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.