Evidence map›Paper›PMID 26369701›Full record

ArticleOncotarget2015

Negative prognostic impact of regulatory T cell infiltration in surgically resected esophageal cancer post-radiochemotherapy.

Erika Vacchelli, Michaela Semeraro, David P Enot, Kariman Chaba, Vichnou Poirier Colame, Peggy Dartigues, Aurelie Perier, Irene Villa, Sylvie Rusakiewicz, Caroline Gronnier and 4 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 9% 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

40 citing papers in PubMed, 1 synthesis or guideline pooled it, 57 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 6 institutions in 1 country.

Erika VacchelliGustave Roussy Cancer Campus, Villejuif, France.
Michaela SemeraroGustave Roussy Cancer Campus, Villejuif, France.
David P EnotGustave Roussy Cancer Campus, Villejuif, France.
Kariman ChabaGustave Roussy Cancer Campus, Villejuif, France.
Vichnou Poirier ColameGustave Roussy Cancer Campus, Villejuif, France.
Peggy DartiguesDepartment of Pathology, Gustave Roussy Cancer Campus, Villejuif, France.
Aurelie PerierGustave Roussy Cancer Campus, Villejuif, France.
Irene VillaDigital Pathology, Departement of Pathology, Gustave Roussy Cancer Campus, Villejuif, France.
Sylvie RusakiewiczGustave Roussy Cancer Campus, Villejuif, France.
Caroline GronnierDepartment of Digestive and Oncological Surgery, Claude Huriez University Hospital, Lille, France.
Diane GoéréGustave Roussy Cancer Campus, Villejuif, France.
Christophe MarietteDepartment of Digestive and Oncological Surgery, Claude Huriez University Hospital, Lille, France.
Laurence ZitvogelGustave Roussy Cancer Campus, Villejuif, France.
Guido KroemerGustave Roussy Cancer Campus, Villejuif, France.
Inserm · FRInstitut Gustave Roussy · FRHôpital Claude Huriez · FRCentre de Recherche des Cordeliers · FRUniversité Paris Cité · FRUniversité Paris-Sud · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ever accumulating evidence indicates that the long-term effects of radiotherapy and chemotherapy largely depend on the induction (or restoration) of an anticancer immune response. Here, we investigated this paradigm in the context of esophageal carcinomas treated by neo-adjuvant radiochemotherapy, in a cohort encompassing 196 patients. We found that the density of the FOXP3+ regulatory T cell (Treg) infiltrate present in the residual tumor (or its scar) correlated with the pathological response (the less Tregs the more pronounced was the histological response) and predicted cancer-specific survival. In contrast, there was no significant clinical impact of the frequency of CD8+ cytotoxic T cells. At difference with breast or colorectal cancer, a loss-of-function allele of toll like receptor 4 (TLR4) improved cancer-specific survival of patients with esophageal cancer. While a loss-of-function allele of purinergic receptor P2X, ligand-gated ion channel, 7 (P2RX7) failed to affect cancer-specific survival, its presence did correlate with an increase in Treg infiltration. Altogether, these results corroborate the notion that the immunosurveillance seals the fate of patients with esophageal carcinomas treated with conventional radiochemotherapy.

Indexed as

AllelesApoptosisCD8-Positive T-LymphocytesChemoradiotherapyCohort StudiesEsophageal NeoplasmsFemaleForkhead Transcription FactorsGene Expression Regulation, NeoplasticGenotypeHumansImmunohistochemistryLymphocytes, Tumor-InfiltratingMalePrognosisReceptors, Purinergic P2X7Forkhead Transcription FactorsFOXP3 protein, humanP2RX7 protein, humanReceptors, Purinergic P2X7TLR4 protein, humanToll-Like Receptor 4apoptosisATG16L1autophagyimmunogenic cell deathpattern recognition receptor

Identifiers

PMID26369701
PMCPMC4673233
OpenAlexW1481423378

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.