Evidence map›Paper›PMID 30299157›Full record

ArticleCNS oncology2018

Distribution of tumor-infiltrating immune cells in glioblastoma.

Enrique Orrego, Carlos A Castaneda, Miluska Castillo, Luis A Bernabe, Sandro Casavilca, Arnab Chakravarti, Wei Meng, Pamela Garcia-Corrochano, Maria R Villa-Robles, Rocio Zevallos and 4 more

Open access · goldAbstract read
In one paragraph

Article in CNS oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

50 citing papers in PubMed, 65 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

14 authors at 2 institutions in 2 countries.

Enrique OrregoNeurosurgery Department, Instituto Nacional de Enfermedades Neoplasicas, Lima, 15038, Peru.
Carlos A CastanedaResearch Department, Instituto Nacional de Enfermedades Neoplasicas, Lima, 15038, Peru.
Miluska CastilloResearch Department, Instituto Nacional de Enfermedades Neoplasicas, Lima, 15038, Peru.
Luis A BernabeResearch Department, Instituto Nacional de Enfermedades Neoplasicas, Lima, 15038, Peru.
Sandro CasavilcaPathology Department, Instituto Nacional de Enfermedades Neoplasicas, Lima, 15038, Peru.
Arnab ChakravartiDepartment of Radiation Oncology, The Ohio State University Comprehensive Cancer Center-Arthur G. James Cancer Hospital, Columbus, OH, 43210, USA.
Wei MengDepartment of Radiation Oncology, The Ohio State University Comprehensive Cancer Center-Arthur G. James Cancer Hospital, Columbus, OH, 43210, USA.
Pamela Garcia-CorrochanoNeurosurgery Department, Instituto Nacional de Enfermedades Neoplasicas, Lima, 15038, Peru.
Maria R Villa-RoblesPathology Department, Instituto Nacional de Enfermedades Neoplasicas, Lima, 15038, Peru.
Rocio ZevallosPathology Department, Instituto Nacional de Enfermedades Neoplasicas, Lima, 15038, Peru.
Omar MejiaResearch Department, Instituto Nacional de Enfermedades Neoplasicas, Lima, 15038, Peru.
Pedro DezaNeurosurgery Department, Instituto Nacional de Enfermedades Neoplasicas, Lima, 15038, Peru.
Carolina Belmar-LopezResearch Department, Instituto Nacional de Enfermedades Neoplasicas, Lima, 15038, Peru.
Luis OjedaNeurosurgery Department, Instituto Nacional de Enfermedades Neoplasicas, Lima, 15038, Peru.
Instituto Nacional de Enfermedades Neoplásicas · PEThe Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimEvaluation of features related to infiltrating immune cell level in glioblastoma.

methodsTumor-infiltrating lymphocytes (TILs) through H&E staining, and TILs (CD3, CD4, CD8 and CD20) and macrophage (CD68 and CD163) levels through immunohistochemistry were evaluated through digital analysis.

resultsCD68 (9.1%), CD163 (2.2%), CD3 (1.6%) and CD8 (1.6%) had the highest density. Higher CD4

conclusionMacrophages are more frequent than TILs. Some subsets are associated with clinical features.

Indexed as

AdolescentAdultAgedBiomarkers, TumorBrain NeoplasmsChildCohort StudiesDNA MethylationDNA Modification MethylasesDNA Repair EnzymesFemaleGlioblastomaHumansLymphocytes, Tumor-InfiltratingMacrophagesMaleBiomarkers, TumorDNA Modification MethylasesDNA Repair EnzymesMGMT protein, humanTumor Suppressor ProteinsbiomarkerglioblastomamacrophagesMGMToverall survivalprognosistumor-infiltrating lymphocytes

Identifiers

PMID30299157
PMCPMC6331699
OpenAlexW2897425460

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.