Evidence map›Paper›PMID 39619775›Full record

ArticleJTO clinical and research reports2025

Racial Differences in Systemic Immune Parameters in Individuals With Lung Cancer.

Mitchell S von Itzstein, Jialiang Liu, Hong Mu-Mosley, Farjana Fattah, Jason Y Park, Jeffrey A SoRelle, J David Farrar, Mary E Gwin, David Hsiehchen, Yvonne Gloria-McCutchen and 12 more

Abstract read
In one paragraph

Article in JTO clinical and research reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

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

  1. Pooled it
  2. Metabolic syndrome and immune-related adverse events.Cancer immunology, immunotherapy : CII · 2026
    Article
  3. Genetic haplotypes inJournal for immunotherapy of cancer · 2025
    Article
  4. Review
  5. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors.

Mitchell S von ItzsteinDepartment of Internal Medicine (Division of Hematology-Oncology), University of Texas Southwestern Medical Center, Dallas, Texas.
Jialiang LiuQuantitative Biomedical Research Center, University of Texas Southwestern Medical Center, Dallas, Texas.
Hong Mu-MosleyHarold C. Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, Texas.
Farjana FattahHarold C. Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, Texas.
Jason Y ParkDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, Texas.
Jeffrey A SoRelleDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, Texas.
J David FarrarDepartment of Immunology, University of Texas Southwestern Medical Center. Dallas, Texas.
Mary E GwinDepartment of Internal Medicine (Division of Hematology-Oncology), University of Texas Southwestern Medical Center, Dallas, Texas.
David HsiehchenDepartment of Internal Medicine (Division of Hematology-Oncology), University of Texas Southwestern Medical Center, Dallas, Texas.
Yvonne Gloria-McCutchenHarold C. Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, Texas.
Edward K WakelandDepartment of Immunology, University of Texas Southwestern Medical Center. Dallas, Texas.
Suzanne ColeDepartment of Internal Medicine (Division of Hematology-Oncology), University of Texas Southwestern Medical Center, Dallas, Texas.
Sheena BhallaDepartment of Internal Medicine (Division of Hematology-Oncology), University of Texas Southwestern Medical Center, Dallas, Texas.
Radhika KainthlaDepartment of Internal Medicine (Division of Hematology-Oncology), University of Texas Southwestern Medical Center, Dallas, Texas.
Igor PuzanovRoswell Park Comprehensive Cancer Center, Buffalo, New York.
Benjamin SwitzerRoswell Park Comprehensive Cancer Center, Buffalo, New York.
Gregory A DanielsMoores Cancer Center, University of California San Diego Health, San Diego, California.
Yousef ZakhariaUniversity of Iowa Hospitals and Clinics, Iowa City, Iowa.
Montaser ShaheenUniversity of Texas Health Science Center, San Antonio, Texas.
Jianjun ZhangMD Anderson Cancer Center, Houston, Texas.
Yang XieQuantitative Biomedical Research Center, University of Texas Southwestern Medical Center, Dallas, Texas.
David E GerberDepartment of Internal Medicine (Division of Hematology-Oncology), University of Texas Southwestern Medical Center, Dallas, Texas.

Funding

UNIVERSITY OF TEXAS--SPORE IN LUNG CANCERP50CA070907 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI HEYMACH, JOHN V. · 1996 to 2024
$57.4M
UT Southwestern Medical Center Simmons Comprehensive Cancer CenterP30CA142543 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI Kathryn Ann O'Donnell · 2010 to 2026
$53.7M
Finding the optimal balance of immunotherapy efficacy and toxicity.U01AI156189 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI GERBER, DAVID ERIC, WAKELAND, EDWARD K. · 2020 to 2024
$3.1M
University of Texas Southwestern - Stimulating Access to Research in Residency (UT-StARR) ProgramR38HL150214 · NHLBI · UT SOUTHWESTERN MEDICAL CENTER · PI Anand Kumar Rohatgi · 2021 to 2026
$1.8M
NCI NIH HHS P30 CA142543NCI NIH HHS P50 CA070907NHLBI NIH HHS R38 HL150214NIAID NIH HHS U01 AI156189
6 · The paper itself

Abstract

Introduction: Racial and ethnic disparities in the presentation and outcomes of lung cancer are widely known. To evaluate potential factors contributing to these observations, we measured systemic immune parameters in Black and White patients with lung cancer. Methods: Patients scheduled to receive cancer immunotherapy were enrolled in a multi-institutional prospective biospecimen collection registry. Clinical and demographic information were obtained from electronic medical records. Pretreatment peripheral blood samples were collected and analyzed for cytokines using a multiplex panel and for immune cell populations using mass cytometry. Differences between Black and White patients were determined and corrected for multiple comparisons. Results: A total of 187 patients with NSCLC (Black, 19; White, 168) were included in the analysis. Compared with White patients, Black patients had greater comorbidity (median Charlson Comorbidity Index 5 versus 3; Conclusions: Black and White patients with lung cancer exhibit several differences in immune parameters, with Black patients exhibiting greater levels of numerous proinflammatory cytokines and cell populations. The etiology and clinical significance of these differences warrant further evaluation.

Indexed as

CytokinesDisparitiesImmune cellsImmunotherapyLung cancerRace

Identifiers

PMID39619775
PMCPMC11605181

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.