Evidence map›Paper›PMID 24790795›Full record

ArticleOncoimmunology2014

Immune-related gene signatures predict the outcome of neoadjuvant chemotherapy.

Gautier Stoll, David Enot, Bernhard Mlecnik, Jérôme Galon, Laurence Zitvogel, Guido Kroemer

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed, 2 pooled it
10.1field-weighted citation impact, top 1% 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

61 citing papers in PubMed, 2 syntheses or guidelines pooled it, 82 citations in OpenAlex.

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1 more citing papers are in PubMed but not listed here.

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

6 authors at 5 institutions in 1 country.

Gautier StollUniversité Paris Descartes/Paris V, Sorbonne Paris Cité; Paris, France ; Equipe 11 labellisée Ligue Nationale contre le Cancer ; Cordeliers Research Center; INSERM U1138; Paris, France.
David EnotMetabolomics and Cell Biology Platforms; Gustave Roussy Cancer Campus; Villejuif, France.
Bernhard MlecnikUniversité Paris Descartes/Paris V, Sorbonne Paris Cité; Paris, France ; Laboratory of Integrative Cancer Immunology; INSERM U1138; Paris, France ; Cordeliers Research Center; Université Pierre et Marie Curie Paris 6; Paris, France.
Jérôme GalonUniversité Paris Descartes/Paris V, Sorbonne Paris Cité; Paris, France ; Laboratory of Integrative Cancer Immunology; INSERM U1138; Paris, France ; Cordeliers Research Center; Université Pierre et Marie Curie Paris 6; Paris, France.
Laurence ZitvogelINSERM U1015; Villejuif, France ; Faculté de Médecine; Université Paris Sud; Le Kremlin Bicêtre, France ; Center of Clinical Investigations in Biotherapies of Cancer (CICBT) 507; Villejuif, France.
Guido KroemerUniversité Paris Descartes/Paris V, Sorbonne Paris Cité; Paris, France ; Equipe 11 labellisée Ligue Nationale contre le Cancer ; Cordeliers Research Center; INSERM U1138; Paris, France ; Metabolomics and Cell Biology Platforms; Gustave Roussy Cancer Campus; Villejuif, France ; INSERM, U848; Villejuif, France ; Pôle de Biologie; Hôpital Européen Georges Pompidou, AP-HP; Paris, France.
Inserm · FRCentre de Recherche des Cordeliers · FRDélégation Paris 5 · FRInstitut Gustave Roussy · FRUniversité Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is ample evidence that neoadjuvant chemotherapy of breast carcinoma is particularly efficient if the tumor presents signs of either a pre-existent or therapy-induced anticancer immune response. Antineoplastic chemotherapies are particularly beneficial if they succeed in inducing immunogenic cell death, hence converting the tumor into its own therapeutic vaccine. Immunogenic cell death is characterized by a pre-mortem stress response including endoplasmic reticulum stress and autophagy. Based on these premises, we attempted to identify metagenes that reflect an intratumoral immune response or local stress responses in the transcriptomes of breast cancer patients. No consistent correlations between immune- and stress-related metagenes could be identified across several cohorts of patients, representing a total of 1045 mammary carcinomas. Moreover, few if any, of the stress-relevant metagenes influenced the probability of pathological complete response to chemotherapy. In contrast, several immune-relevant metagenes had a significant positive impact on response rates. This applies in particular to a CXCL13-centered, highly reproducible metagene signature reflecting the intratumoral presence of interferon-γ-producing T cells.

Indexed as

autophagybreast cancercolorectal cancerendoplasmic stressimmunogenic cell deathtumor-infiltrating lymphocytes

Identifiers

PMID24790795
PMCPMC4004621
OpenAlexW2069350359

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.