Evidence map›Paper›PMID 31358539›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2019

Characterization and Comparison of GITR Expression in Solid Tumors.

Luis Vence, Samantha L Bucktrout, Irina Fernandez Curbelo, Jorge Blando, Bevin M Smith, Ashley E Mahne, John C Lin, Terrence Park, Edward Pascua, Tao Sai and 10 more

Open access · hybridAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
5.0field-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, 1 synthesis or guideline pooled it, 60 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

20 authors at 2 institutions in 1 country.

Luis Vence *The Immunotherapy Platform, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Samantha L Bucktrout *Cancer Immunology Discovery Unit, South San Francisco, California.
Irina Fernandez CurbeloThe Immunotherapy Platform, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Jorge BlandoThe Immunotherapy Platform, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Bevin M SmithCancer Immunology Discovery Unit, South San Francisco, California.
Ashley E MahneCancer Immunology Discovery Unit, South San Francisco, California.
John C LinCancer Immunology Discovery Unit, South San Francisco, California.
Terrence ParkCancer Immunology Discovery Unit, South San Francisco, California.
Edward PascuaCancer Immunology Discovery Unit, South San Francisco, California.
Tao SaiCancer Immunology Discovery Unit, South San Francisco, California.
Javier Chaparro-RiggersCancer Immunology Discovery Unit, South San Francisco, California.
Sumit K SubudhiDepartment of Genitourinary Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Jorge B ScuttiThe Immunotherapy Platform, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Maria G HigaThe Immunotherapy Platform, The University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0003-2045-6112
Hao ZhaoThe Immunotherapy Platform, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Shalini S YadavThe Immunotherapy Platform, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Anirban MaitraDepartment of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Ignacio I WistubaDepartment of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
James P AllisonThe Immunotherapy Platform, The University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0001-8980-5697
Padmanee SharmaThe Immunotherapy Platform, The University of Texas MD Anderson Cancer Center, Houston, Texas. PadSharma@mdanderson.org.
The University of Texas MD Anderson Cancer Center · USDiscovery Institute · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

purposeDetermine the differential effect of a FcγR-binding, mIgG2a anti-GITR antibody in mouse tumor models, and characterize the tumor microenvironment for the frequency of GITR expression in T-cell subsets from seven different human solid tumors.

resultsThe therapeutic benefit of 21B6 was greatest in CT26 followed by MC38, and was least in the B16 tumor model. The frequency of CD8 T cells and effector CD4 T cells within the immune infiltrate correlated with response to treatment with GITR antibody. Analysis of clinical tumor samples showed that NSCLC, renal cell carcinoma, and melanoma had the highest proportions of GITR-expressing cells and highest per-cell density of GITR expression on CD4

conclusionsHuman tumor data suggest that NSCLC, renal cell carcinoma, and melanoma should be the tumor subtypes prioritized for anti-GITR therapy development.

Indexed as

AnimalsAntibodies, Anti-IdiotypicCell Line, TumorCell ProliferationFlow CytometryForkhead Transcription FactorsGlucocorticoid-Induced TNFR-Related ProteinHumansMelanoma, ExperimentalMiceReceptors, IgGT-Lymphocyte SubsetsTumor MicroenvironmentAntibodies, Anti-IdiotypicFCGR1A protein, humanForkhead Transcription FactorsFoxp3 protein, mouseGlucocorticoid-Induced TNFR-Related ProteinReceptors, IgGTnfrsf18 protein, mouse

Identifiers

PMID31358539
PMCPMC6825542
OpenAlexW2964432225

What OpenQuestion holds

Textmetadata
LicenceTDM
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.