Evidence map›Paper›PMID 31428522›Full record

ArticleOncoimmunology

A multivariate Th17 metagene for prognostic stratification in T cell non-inflamed triple negative breast cancer.

L Faucheux, M Grandclaudon, M Perrot-Dockès, P Sirven, F Berger, A S Hamy, V Fourchotte, A Vincent-Salomon, F Mechta-Grigoriou, F Reyal and 3 more

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.7field-weighted citation impact, top 14% 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

26 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Review
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    Article
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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

13 authors at 2 institutions in 1 country.

L FaucheuxInstitut Curie, PSL Research University, Paris, France.
M GrandclaudonInstitut Curie, PSL Research University, Paris, France.
M Perrot-DockèsInstitut Curie, PSL Research University, Paris, France.
P SirvenInstitut Curie, PSL Research University, Paris, France.
F BergerInstitut Curie, PSL Research University, Paris, France.ORCID 0000-0002-3251-4060
A S HamyInstitut Curie, PSL Research University, Paris, France.ORCID 0000-0003-4430-3022
V FourchotteDepartement of Surgical Oncology, Institut Curie, Paris, France.
A Vincent-SalomonDiagnostic and Theranostic medicine division, Institut Curie, Paris, France.
F Mechta-GrigoriouInstitut Curie, PSL Research University, Paris, France.
F ReyalInstitut Curie, PSL Research University, Paris, France.ORCID 0000-0002-2318-3589
A Scholer-DahirelInstitut Curie, PSL Research University, Paris, France.
M Guillot-DelostInstitut Curie, PSL Research University, Paris, France.
V SoumelisInstitut Curie, PSL Research University, Paris, France.
Inserm · FRInstitut Curie · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A diversity of T helper (Th) subsets (Th1, Th2, Th17) has been identified in the human tumor microenvironment. In breast cancer, the role of Th subsets remains controversial, and a systematic study integrating Th subset diversity, T cell inflammation, breast cancer molecular subtypes, and patient prognosis, is lacking. In primary untreated breast cancer samples, we analyzed 19 Th cytokines at the protein level. Eight were T cell-specific, and subsequently measured in 106 prospectively-collected untreated samples. The dominant Th cytokines across all breast cancer samples were IFN-γ and IL-2. Th2 cytokines (IL-4, IL-5, IL-13) were expressed at low levels and not associated with any breast cancer subtype. Th17 cytokines (IL-17A and IL-17F) were up-regulated in triple negative breast cancer (TNBC), specifically in T cell non-inflamed tumors. In order to get insight into prognosis, we exploited the METABRIC transcriptomic dataset. We derived Th1, Th2, and Th17 metagenes based on manually curated Th signatures, and found that a high Th17 metagene was of good prognosis in T cell non-inflamed TNBC. Multivariate Cox modeling selected the Nottingham Prognostic Index (NPI), Th2 and Th17 metagenes as additive predictors of breast cancer-specific survival, which defined novel and highly distinct prognostic groups within TNBC. Our results reveal that Th17 is a novel prognostic composite biomarker in T cell non-inflamed TNBC. Integrating immune cell and tumor molecular diversity is an efficient strategy for prognostic stratification of cancer patients.

Indexed as

Breast cancerprognostic stratificationT cellsTh17tumor microenvironment

Identifiers

PMID31428522
PMCPMC6685521
OpenAlexW2954858405

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.