Evidence map›Paper›PMID 31239476›Full record

ArticleScientific reports2019

CD163+ immune cell infiltrates and presence of CD54+ microvessels are prognostic markers for patients with embryonal rhabdomyosarcoma.

Jakob Nikolas Kather, Christian Hörner, Cleo-Aron Weis, Thiha Aung, Christian Vokuhl, Christel Weiss, Monika Scheer, Alexander Marx, Katja Simon-Keller

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

33 citing papers in PubMed, 49 citations in OpenAlex.

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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

9 authors at 6 institutions in 1 country.

Jakob Nikolas KatherApplied Tumor Immunity, German Cancer Research Center, Heidelberg, Germany.
Christian HörnerInstitute of Pathology, University Medical Center Mannheim, Mannheim, Germany.
Cleo-Aron WeisInstitute of Pathology, University Medical Center Mannheim, Mannheim, Germany.
Thiha AungCenter of Plastic-, Hand- and Reconstructive Surgery, University of Regensburg, Regensburg, Germany.
Christian VokuhlInstitute of Pathology, Paidopathology, University Medical Center Kiel, Kiel, Germany.
Christel WeissDepartment of Medical Statistics and Biomathematics, University Medical Centre Mannheim, Mannheim, Germany.
Monika ScheerPediatrics 5 (Oncology, Hematology, Immunology), Olgahospital, Klinikum Stuttgart, Stuttgart, Germany.
Alexander MarxInstitute of Pathology, University Medical Center Mannheim, Mannheim, Germany.ORCID http://orcid.org/0000-0001-9722-2483
Katja Simon-KellerInstitute of Pathology, University Medical Center Mannheim, Mannheim, Germany. katja.simon-keller@medma.uni-heidelberg.de.ORCID http://orcid.org/0000-0003-2340-8765
Heidelberg University · DEGerman Cancer Research Center · DEOlgahospital · DEUniversity Hospital Schleswig-Holstein · DEUniversity Medical Centre Mannheim · DEUniversity of Regensburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rhabdomyosarcomas (RMS) are rare and often lethal diseases. It is assumed that the tumor microenvironment (TME) of RMS exerts an immunosuppressive function, but there is currently no systematic analysis of the immune cells infiltrating sarcoma tissue. Focusing on two common types of RMS (alveolar [RMA] and embryonal [RME]), we performed a comprehensive immunohistochemical analysis of tumor-infiltrating immune cells in the TME. We performed a qualitative estimation of infiltrating immune cells in the tumor microenvironment by an experienced pathologist as well as a quantitative digital pathology analysis. We found that (1) manual and automatic quantification of tumor-infiltrating immune cells were consistent; (2) RME tumors showed a higher degree of immune cell infiltration than RMA tumors but (3) the number of tumor infiltrating lymphocytes was low compared to other solid tumor types; (4) microvascular density correlated with immune cell infiltration and (5) CD163 positive macrophages as well as CD54 positive microvessels were more often detected in RME than in RMA and correlated with patient overall and event free survival. Our systematic analysis provides a comprehensive view of the immune landscape of RMS which needs to be taken into account for developing immunotherapies for this rare type of cancer.

Indexed as

Antigens, CDAntigens, Differentiation, MyelomonocyticB7-H1 AntigenBiomarkers, TumorBiopsyB-LymphocytesCD163 AntigenHumansMicrovesselsPrognosisProgrammed Cell Death 1 ReceptorReceptors, Cell SurfaceRhabdomyosarcoma, EmbryonalAntigens, CDAntigens, Differentiation, MyelomonocyticB7-H1 AntigenBiomarkers, TumorCD163 AntigenCD274 protein, humanPDCD1 protein, humanProgrammed Cell Death 1 ReceptorReceptors, Cell Surface

Identifiers

PMID31239476
PMCPMC6592899
OpenAlexW2954460587

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.