Evidence map›Paper›PMID 34283048›Full record

ArticleCancers2021

The Immune Microenvironment of Chordomas: An Immunohistochemical Analysis.

Maroa Dridi, Lila Krebs-Drouot, David Meyronet, Jean Marc Dumollard, François Vassal, Emmanuel Jouanneau, Timothée Jacquesson, Cédric Barrey, Sylvain Grange, Jean Boutonnat and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
5.4field-weighted citation impact, top 3% 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

18 citing papers in PubMed, 32 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

12 authors at 3 institutions in 1 country.

Maroa DridiPathology Department, University Hospital of Saint-Etienne, 42055 Saint-Etienne, France.
Lila Krebs-DrouotPathology Department, University Hospital of Grenoble, 38700 Grenoble, France.
David MeyronetEast Pathology Institute, Hospices Civils de Lyon, 69677 Lyon, France.
Jean Marc DumollardPathology Department, University Hospital of Saint-Etienne, 42055 Saint-Etienne, France.
François VassalNeurosurgery Department, University Hospital of Saint-Etienne, 42055 Saint-Etienne, France.
Emmanuel JouanneauClaude Bernard University, Lyon 1, 69100 Lyon, France.
Timothée JacquessonDepartment of Neurosurgery B, Neurological Hospital Pierre Wertheimer, 69500 Lyon, France.ORCID 0000-0001-9985-3617
Cédric BarreyClaude Bernard University, Lyon 1, 69100 Lyon, France.
Sylvain GrangeRadiology Department, University Hospital of Saint-Etienne, 42055 Saint-Etienne, France.
Jean BoutonnatPathology Department, University Hospital of Grenoble, 38700 Grenoble, France.ORCID 0000-0003-2360-4379
Michel Péoc'hPathology Department, University Hospital of Saint-Etienne, 42055 Saint-Etienne, France.ORCID 0000-0001-5453-0021
Georgia KarpathiouPathology Department, University Hospital of Saint-Etienne, 42055 Saint-Etienne, France.
Centre Hospitalier Universitaire de Saint-Étienne · FRUniversité Claude Bernard Lyon 1 · FRCentre Hospitalier Universitaire de Grenoble · FR

Funding

Direction des Affaires Medicales et de la Recherche, Hopital Universitaire de Saint-Etienne NA
6 · The paper itself

Abstract

Chordomas are rare sarcomas that are usually treated by surgery and/or radiotherapy since these are chemo-resistant tumors, but immunotherapy could be a possible option for chordoma patients. However, few reports investigating the composition of the chordoma immune microenvironment exist. We immunohistochemically studied 81 chordomas regarding their immune microenvironment factors and compared them with clinicopathological data. Macrophages and CD4 cells were the most prominent inflammatory cell populations, followed by CD8 T cells, while CD20 B cells and high endothelial venules (MECA-79+) were less frequently found. PD-L1 (22C3) expression by inflammatory cells was found in 21 (26%) tumors and was associated with a larger tumor size. None of the cases showed the expression of PD-L1 by tumor cells. Survival analysis showed that younger patients had a better overall survival. Considering the immunohistochemical factors studied, higher CD8, the presence of PD-L1+ immune cells, and higher vascular density were adverse prognostic factors, but in multivariate analysis, only PD-L1+ immune cells retained prognostic significance. To conclude, chordoma tumor cells do not express PD-L1, but PD-L1+ immune cells seem to play a negative prognostic role, supporting the need for further studies in this field and the possible beneficial role of immunotherapy in these patients.

Indexed as

CD20CD4CD8immunohistochemistrymacrophagesMECA-79PD-L1prognosisvascular density

Identifiers

PMID34283048
PMCPMC8268246
OpenAlexW3175788354

What OpenQuestion holds

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LicenceCC BY
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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.