Evidence map›Paper›PMID 41322405›Full record

ArticleFrontiers in immunology2025

Immune cell profiling of peripheral blood in long-term testicular germ cell tumor survivors.

Kristina Kilikova, Andrea Mlcakova, Zuzana Sestakova, Katarina Kalavska, Kristyna Adamikova, Jana Obertova, Patrik Palacka, Katarina Rejlekova, Zuzana Sycova-Mila, Valentina De Angelis and 7 more

Abstract read
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Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

17 authors.

Kristina KilikovaDepartment of Oncology, Faculty Hospital, Trnava, Slovakia.
Andrea MlcakovaDepartment of Medical Oncology, National Cancer Institute, Bratislava, Slovakia.
Zuzana SestakovaFlow cytometry Laboratory, Department of Laboratory Medicine, National Institute of Children's Diseases, Bratislava, Slovakia.
Katarina Kalavska2nd Department of Oncology, Faculty of Medicine, Comenius University & National Cancer Institute, Bratislava, Slovakia.
Kristyna Adamikova2nd Department of Oncology, Faculty of Medicine, Comenius University & National Cancer Institute, Bratislava, Slovakia.
Jana ObertovaDepartment of Medical Oncology, National Cancer Institute, Bratislava, Slovakia.
Patrik PalackaDepartment of Medical Oncology, National Cancer Institute, Bratislava, Slovakia.
Katarina RejlekovaDepartment of Medical Oncology, National Cancer Institute, Bratislava, Slovakia.
Zuzana Sycova-MilaDepartment of Medical Oncology, National Cancer Institute, Bratislava, Slovakia.
Valentina De AngelisDepartment of Medical Oncology, National Cancer Institute, Bratislava, Slovakia.
Zuzana OrszaghovaDepartment of Medical Oncology, National Cancer Institute, Bratislava, Slovakia.
Peter Lesko2nd Department of Oncology, Faculty of Medicine, Comenius University & National Cancer Institute, Bratislava, Slovakia.
Daniela Svetlovska2nd Department of Oncology, Faculty of Medicine, Comenius University & National Cancer Institute, Bratislava, Slovakia.
Beata MladosievicovaInstitute of Pathological Physiology, Faculty of Medicine, Comenius University, Bratislava, Slovakia.
Liang ChengDepartment of Pathology and Laboratory Medicine Brown University Warren Alpert Medical School, the Legorreta Cancer Center at Brown University, and Brown University Health, Providence, RI, United States.
Michal MegoDepartment of Medical Oncology, National Cancer Institute, Bratislava, Slovakia.
Michal ChovanecDepartment of Medical Oncology, National Cancer Institute, Bratislava, Slovakia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: This study addresses changes in peripheral blood immune cell composition and possible late effects of curative treatment in testicular germ cell tumors (GCT) survivors. Methods: We analyzed the immunophenotype in peripheral blood obtained from 202 survivors treated at the National Cancer Institute in Bratislava by flow cytometry. The median long-term follow-up was 13 years (1-35). We divided the survivors into groups as follows: CT-chemotherapy (N = 141), RT-radiotherapy (N = 16), CTRT - chemotherapy + radiotherapy (N = 13), and the control group of patients under active surveillance - AS (N = 32). Results: Survivors treated with AS had a lower number of B-cells (mean ± standard deviation (SD) = 10.3 ± 3.5 vs 11.9 ± 4.2, p=0.04) compared to the CT group. Survivors treated with AS vs RT had a higher number of total lymphocytes (29.8 ± 7.7 vs 25.2 ± 6.3, p=0.04). In AS vs CTRT group B-cells (10.3 ± 3.5 vs 13.7 ± 5, p=0.01) and conventional dendritic cells (cDCs) (74.3 ± 11.8 vs 82.5 ± 6.7, p=0.04) showed lower numbers. Survivors treated with AS vs. ≤ 400 mg/m2 cumulative dose of cisplatin had fewer eosinophils (2.29 ± 1.5 vs 2.99 ± 1.7, p=0.03) and double-negative T-cells (DNT cells) (4.7 ± 3.4 vs 6.6 ± 6.6, p=0.04). In AS vs. ≥ 400 mg/m2, B cells counts were lower in the control group (10.96 ± 5.3 vs 12.3 ± 4.8, p=0.03); treatment with ≤ 400 mg/m2 vs. ≥ 400 mg/m2 resulted in higher counts of eosinophils (3.0 ± 1.7 vs 2.1 ± 1.7, p=0.00025) and DNT cells (6.7 ± 6.7 vs 4.9 ± 3.6, p=0.02). Conclusions: Our study demonstrates an association between both cisplatin-based chemotherapy and radiotherapy with specific immune cell populations, suggesting that these treatment modalities may exert long-term immunomodulatory effects.

Indexed as

Cancer SurvivorsNeoplasms, Germ Cell and EmbryonalTesticular NeoplasmsAdolescentAdultHumansImmunophenotypingMaleMiddle AgedYoung Adultflow cytometryimmune systemimmunophenotypelate toxicitytesticular germ cell tumors

Identifiers

PMID41322405
PMCPMC12657365

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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.