Evidence map›Paper›PMID 34127811›Full record

ArticleBritish journal of cancer2021

T-regulatory cells predict clinical outcome in soft tissue sarcoma patients: a clinico-pathological study.

Maria A Smolle, Laurin Herbsthofer, Barbara Granegger, Mark Goda, Iva Brcic, Marko Bergovec, Susanne Scheipl, Barbara Prietl, Martin Pichler, Armin Gerger and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in British journal of cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.6field-weighted citation impact, top 13% of its field
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

22 citing papers in PubMed, 28 citations in OpenAlex.

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  15. Genomic Profiling of Radiation-Induced Sarcomas Reveals the Immunologic Characteristics and Its Response to Immune Checkpoint Blockade.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
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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 at 2 institutions in 1 country.

Maria A SmolleDepartment of Orthopaedics and Trauma, Medical University of Graz, Graz, Austria.
Laurin HerbsthoferCenter for Biomarker Research in Medicine (CBmed), Graz, Austria.
Barbara GraneggerDepartment of Orthopaedics and Trauma, Medical University of Graz, Graz, Austria.
Mark GodaDepartment of Orthopaedics and Trauma, Medical University of Graz, Graz, Austria.
Iva BrcicDiagnostic and Research Institute of Pathology, Medical University of Graz, Graz, Austria.
Marko BergovecDepartment of Orthopaedics and Trauma, Medical University of Graz, Graz, Austria.
Susanne ScheiplDepartment of Orthopaedics and Trauma, Medical University of Graz, Graz, Austria.
Barbara PrietlCenter for Biomarker Research in Medicine (CBmed), Graz, Austria.
Martin PichlerDivision of Clinical Oncology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Armin GergerDivision of Clinical Oncology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Christopher RossmannDivision of Clinical Oncology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Jakob RiedlDivision of Clinical Oncology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Martina TombergerCenter for Biomarker Research in Medicine (CBmed), Graz, Austria.
Pablo López-GarcíaCenter for Biomarker Research in Medicine (CBmed), Graz, Austria.ORCID http://orcid.org/0000-0001-5419-7337
Amin El-HeliebiCenter for Biomarker Research in Medicine (CBmed), Graz, Austria.
Andreas LeithnerDepartment of Orthopaedics and Trauma, Medical University of Graz, Graz, Austria.
Bernadette Liegl-AtzwangerDiagnostic and Research Institute of Pathology, Medical University of Graz, Graz, Austria.
Joanna SzkanderaDivision of Clinical Oncology, Department of Internal Medicine, Medical University of Graz, Graz, Austria. Joanna.szkandera@medunigraz.at.ORCID http://orcid.org/0000-0002-2217-893X
Medical University of Graz · ATCenter For Biomarker Research In Medicine · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSoft tissue sarcomas (STS) are generally considered non-immunogenic, although specific subtypes respond to immunotherapy. Antitumour response within the tumour microenvironment relies on a balance between inhibitory and activating signals for tumour-infiltrating lymphocytes (TILs). This study analysed TILs and immune checkpoint molecules in STS, and assessed their prognostic impact regarding local recurrence (LR), distant metastasis (DM), and overall survival (OS).

methodsOne-hundred and ninety-two surgically treated STS patients (median age: 63.5 years; 103 males [53.6%]) were retrospectively included. Tissue microarrays were constructed, immunohistochemistry for PD-1, PD-L1, FOXP3, CD3, CD4, and CD8 performed, and staining assessed with multispectral imaging. TIL phenotype abundance and immune checkpoint markers were correlated with clinical and outcome parameters (LR, DM, and OS).

resultsSignificant differences between histology and all immune checkpoint markers except for FOXP3+ and CD3-PD-L1+ cell subpopulations were found. Higher levels of PD-L1, PD-1, and any TIL phenotype were found in myxofibrosarcoma as compared to leiomyosarcoma (all p < 0.05). The presence of regulatory T cells (Tregs) was associated with increased LR risk (p = 0.006), irrespective of margins. Other TILs or immune checkpoint markers had no significant impact on outcome parameters.

conclusionsTIL and immune checkpoint marker levels are most abundant in myxofibrosarcoma. High Treg levels are independently associated with increased LR risk, irrespective of margins.

Indexed as

AgedB7-H1 AntigenBiomarkers, TumorCD3 ComplexCD4 AntigensCD8 AntigensFemaleFibrosarcomaForkhead Transcription FactorsHumansLeiomyosarcomaMaleMiddle AgedMyxosarcomaProgrammed Cell Death 1 ReceptorRetrospective StudiesB7-H1 AntigenBiomarkers, TumorCD274 protein, humanCD3 ComplexCD4 AntigensCD8 AntigensForkhead Transcription FactorsFOXP3 protein, humanPDCD1 protein, humanProgrammed Cell Death 1 Receptor

Identifiers

PMID34127811
PMCPMC8405702
OpenAlexW3170978106

What OpenQuestion holds

Textmetadata
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.