Evidence map›Paper›PMID 40940394›Full record

Observational studyScientific reports2025

Macrophage polarization is associated with postoperative seroma development in breast cancer in the SerMa pilot cohort.

Felicitas Magdalena Schneider, Nicole Pochert, Fritzi Schittek, Melitta Beatrice Köpke, Carl Mathis Wild, Johanna Marie Veh, Natalie Renate Rohrmoser, Christina Kuhn, Birgit Urban, Klaus-Henning Kahl and 12 more

Abstract readObservational Study
In one paragraph

Observational study in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

22 authors.

Felicitas Magdalena SchneiderGynecology, Obstetrics and Senology, Faculty of Medicine, University of Augsburg, Stenglinstraße 2, 86156, Augsburg, Germany.
Nicole PochertGynecology, Obstetrics and Senology, Faculty of Medicine, University of Augsburg, Stenglinstraße 2, 86156, Augsburg, Germany.
Fritzi SchittekGynecology, Obstetrics and Senology, Faculty of Medicine, University of Augsburg, Stenglinstraße 2, 86156, Augsburg, Germany.
Melitta Beatrice KöpkeGynecology, Obstetrics and Senology, Faculty of Medicine, University of Augsburg, Stenglinstraße 2, 86156, Augsburg, Germany.
Carl Mathis WildGynecology, Obstetrics and Senology, Faculty of Medicine, University of Augsburg, Stenglinstraße 2, 86156, Augsburg, Germany.
Johanna Marie VehGynecology, Obstetrics and Senology, Faculty of Medicine, University of Augsburg, Stenglinstraße 2, 86156, Augsburg, Germany.
Natalie Renate RohrmoserGynecology, Obstetrics and Senology, Faculty of Medicine, University of Augsburg, Stenglinstraße 2, 86156, Augsburg, Germany.
Christina KuhnGynecology, Obstetrics and Senology, Faculty of Medicine, University of Augsburg, Stenglinstraße 2, 86156, Augsburg, Germany.
Birgit UrbanGynecology, Obstetrics and Senology, Faculty of Medicine, University of Augsburg, Stenglinstraße 2, 86156, Augsburg, Germany.
Klaus-Henning KahlBavarian Center for Cancer Research (BKFZ), Partner Site Augsburg, Augsburg, Germany.
Mariella SchneiderGynecology, Obstetrics and Senology, Faculty of Medicine, University of Augsburg, Stenglinstraße 2, 86156, Augsburg, Germany.
Angelika MattmerGynecology, Obstetrics and Senology, Faculty of Medicine, University of Augsburg, Stenglinstraße 2, 86156, Augsburg, Germany.
Ludwig Christian HinskeDigital Medicine, University Hospital of Augsburg, Stenglinstraße 2, 86156, Augsburg, Germany.
Regina FluhrerBiochemistry and Molecular Biology, Institute of Theoretical Medicine, Faculty of Medicine, University of Augsburg, Universitätsstrasse 2, 86159, Augsburg, Germany.
Monika M GolasHuman Genetics, Faculty of Medicine, University of Augsburg, Stenglinstraße 2, 86156, Augsburg, Germany.
Michael UntchDepartment of Gynecology and Obstetrics, Breast Cancer Center, Helios Klinikum Berlin Buch, Berlin, Germany.
Thorsten KuehnDepartment of Gynecology and Obstetrics, University Hospital Ulm, Ulm, Germany.
Maggie Banys-PaluchowskiDepartment of Gynecology and Obstetrics, University Hospital Schleswig-Holstein, Lübeck, Germany.
Udo JeschkeGynecology, Obstetrics and Senology, Faculty of Medicine, University of Augsburg, Stenglinstraße 2, 86156, Augsburg, Germany. udo.jeschke@med.uni-augsburg.de.
Claudia Traidl-HoffmannHelmholtz Center Munich, Institute of Environmental Medicine, German Research Center for Environmental Health, Neuherberg, Germany.
Christian DanneckerGynecology, Obstetrics and Senology, Faculty of Medicine, University of Augsburg, Stenglinstraße 2, 86156, Augsburg, Germany.
Nina DitschGynecology, Obstetrics and Senology, Faculty of Medicine, University of Augsburg, Stenglinstraße 2, 86156, Augsburg, Germany. nina.ditsch@uk-augsburg.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Seroma formation is a frequent complication following mastectomy in the surgical treatment of breast cancer with profound consequences for the patients including possibly quality of life impairing implant complications. The pathogenesis remains unknown, leading to a lack of efficient preventive and curative strategies. The study's objective was to determine whether the macrophage infiltration of the tumor microenvironment and surrounding adipose tissue at the time of primary surgery is associated with postoperative seroma development. The observational monocentric SerMa pilot study was conducted from 12/2019 to 12/2022. We included 91 breast cancer and 9 carcinoma in situ cases treated with mastectomy at the University Hospital Augsburg, Germany. Patients with previous malignancies, metastatic disease and known immunodeficiency were excluded. The patients underwent different mastectomy procedures with or without implant- or expander-based breast reconstruction. The study's main outcome was seroma formation up to six months post-surgery, determined by clinical examination and fine needle aspiration of the seroma fluid if clinically necessary. Macrophage markers (CD68 and CD163) were immunohistochemically determined in formalin fixed paraffin-embedded slides containing the primary tumor and surrounding adipose tissue. Two groups were then formed as independent variables: cases with (seroma +) and without postoperative seroma formation (seroma-). Since all parameters in this study were not normally distributed, the non-parametric Mann-Whitney-U-test was used. A p-value < 0.05 was considered statistically significant. CD68 + cells (cases with seroma (seroma +): median = 90.7 cells, IQR = 62.5-130.5; cases without seroma (seroma-): median = 64.3 cells, IQR = 47.0-115-0, p = 0.036) and CD163 + cells (seroma + : median = 58.3 cells, IQR = 33.0-91.4; seroma-: median = 40.7 cells, IQR = 28.3-55.3, p = 0.027) in the tumor microenvironment and in the surrounding adipose tissue (CD68 + cells (seroma + : median = 8.0 cells, IQR = 5.3-11.0; seroma-: median = 4.7 cells, IQR = 3.0-10.0, p = 0.013), CD163 + cells (seroma + : median = 11.0 cells, IQR = 6.7-15.0; seroma-: median = 6.7 cells, IQR = 3.0-9.7, p = 0.016)) were significantly higher in cases with postoperative seroma formation compared to cases without. In the SerMa pilot study macrophage polarization within the primary tumor and surrounding adipose tissue was associated with post-operative seroma formation in breast cancer patients. This might be a suitable biomarker for predicting a higher risk of seroma formation.

Indexed as

Breast NeoplasmsMacrophagesMastectomyPostoperative ComplicationsSeromaAdultAgedAntigens, CDAntigens, Differentiation, MyelomonocyticCD163 AntigenCD68 MoleculeFemaleHumansMammaplastyMiddle AgedPilot ProjectsAntigens, CDAntigens, Differentiation, MyelomonocyticCD163 AntigenCD68 antigen, humanCD68 MoleculeCD163CD68MacrophagesMastectomyPPARγSeromaTumor microenvironment

Identifiers

PMID40940394
PMCPMC12432247

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Registered trials

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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.