Evidence map›Paper›PMID 39703718›Full record

ArticleAdvances in radiation oncology2025

Effect of External Beam Radiation Therapy and Brachytherapy on Circulating Myeloid-Derived Suppressor Cell Populations in Patients Treated Definitively for Cervical Cancer.

Kelsey M Wanhainen, Matthew Berkseth, Nicole Sando, Lydia Golden, Amy Techam, Jennifer Wieworka, Kyra M Boorsma Bergerud, Peter Argenta, Andrea O'Shea, Britt K Erickson and 8 more

Abstract read
In one paragraph

Article in Advances in radiation oncology, 2025. 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

18 authors.

Kelsey M WanhainenUniversity of Minnesota Medical School, Minneapolis, Minnesota.
Matthew BerksethDepartment of Radiation Oncology, University of Minnesota, Minneapolis, Minnesota.
Nicole SandoDepartment of Radiation Oncology, University of Minnesota, Minneapolis, Minnesota.
Lydia GoldenDepartment of Radiation Oncology, University of Minnesota, Minneapolis, Minnesota.
Amy TechamM Health Fairview, Minneapolis, Minnesota.
Jennifer WieworkaM Health Fairview, Minneapolis, Minnesota.
Kyra M Boorsma BergerudDepartment of Radiation Oncology, University of Minnesota, Minneapolis, Minnesota.
Peter ArgentaUniversity of Minnesota Medical School, Minneapolis, Minnesota.
Andrea O'SheaUniversity of Minnesota Medical School, Minneapolis, Minnesota.
Britt K EricksonUniversity of Minnesota Medical School, Minneapolis, Minnesota.
Sally MullanyUniversity of Minnesota Medical School, Minneapolis, Minnesota.
Colleen RivardUniversity of Minnesota Medical School, Minneapolis, Minnesota.
Rahel GhebreUniversity of Minnesota Medical School, Minneapolis, Minnesota.
Deanna TeohUniversity of Minnesota Medical School, Minneapolis, Minnesota.
Margaret ReynoldsUniversity of Minnesota Medical School, Minneapolis, Minnesota.
Stephanie TerezakisUniversity of Minnesota Medical School, Minneapolis, Minnesota.
Jianling YuanUniversity of Minnesota Medical School, Minneapolis, Minnesota.
Lindsey SloanUniversity of Minnesota Medical School, Minneapolis, Minnesota.

Funding

Project 3P01CA254849 · NCI · UNIVERSITY OF MINNESOTA · PI ODDE, DAVID J. · 2021 to 2025
$9.4M
TECH CoreU54CA268069 · NCI · UNIVERSITY OF MINNESOTA · PI David J. Odde · 2022 to 2026
$8.2M
NCI NIH HHS P01 CA254849NCI NIH HHS U54 CA268069
6 · The paper itself

Abstract

Purpose: The immunosuppressive function of myeloid-derived suppressor cells (MDSCs) has been implicated in the regulation of immune responses against cancer and is associated with poor prognosis. Radiation treatment is known to alter immune cell populations within the tumor; however, whether this results in the recruitment of immunosuppressive MDSC populations is not well understood. Here we evaluate the response of circulating MDSC populations in patients treated per standard-of-care cisplatin chemoradiation therapy (CRT) for locally invasive cervical cancer. Methods and Materials: Newly diagnosed, treatment-naïve patients with locally advanced cervical cancer were enrolled. Blood samples were collected from patients prior to starting CRT (T Results: Most patients in our study were Caucasian nonsmokers with human papillomavirus-associated squamous cell carcinoma of the cervix. We saw a trend for increased MDSC frequency in patients with more advanced-stage disease at the time of initiating treatment. MDSCs increase in response to CRT and peak after brachytherapy (T Conclusion: Our study confirms other reports that circulating MDSCs in patients with cervical cancer increase in response to CRT and are associated with more advanced stages. Additionally, we show that MDSC expansion is driven by the g-MDSC subset. We did not see any correlation between MDSC expansion and treatment response, though this may be because of the limited sample size for this study.

Identifiers

PMID39703718
PMCPMC11653128

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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.