Evidence map›Paper›PMID 26680641›Full record

ArticleBMC cancer2015

High EGFR protein expression and exon 9 PIK3CA mutations are independent prognostic factors in triple negative breast cancers.

William Jacot, Caroline Mollevi, Frédéric Fina, Evelyne Lopez-Crapez, Pierre-Marie Martin, Pierre-Emmanuel Colombo, Frédéric Bibeau, Gilles Romieu, Pierre-Jean Lamy

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

18 citing papers in PubMed, 24 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

9 authors at 4 institutions in 1 country.

William JacotDepartment of Medical Oncology, Montpellier Cancer Institute Val d'Aurelle, 208, rue des Apothicaires, Montpellier, F-34298, France. william.jacot@icm.unicancer.fr.
Caroline MolleviBiostatistical Research Unit, Montpellier Cancer Institute Val d'Aurelle, 208, rue des Apothicaires, Montpellier, F-34298, France. Caroline.Mollevi@icm.unicancer.fr.
Frédéric FinaDepartment of Oncobiology, Assistance Publique - Hôpitaux de Marseille, Boulevard Pierre Dramard, Marseille, F-13916, France. frederic.fina@ap-hm.fr.
Evelyne Lopez-CrapezTranslationnal Research Unit, Montpellier Cancer Institute Val d'Aurelle, 208, rue des Apothicaires, Montpellier, F-34298, France. evelyne.crapez@icm.unicancer.fr.
Pierre-Marie MartinDepartment of Oncobiology, Assistance Publique - Hôpitaux de Marseille, Boulevard Pierre Dramard, Marseille, F-13916, France. martin@chauvet.org.
Pierre-Emmanuel ColomboDepartment of Surgical Oncology, Montpellier Cancer Institute Val d'Aurelle, 208, rue des Apothicaires, Montpellier, F-34298, France. Pierre-Emmanuel.Colombo@icm.unicancer.fr.
Frédéric BibeauDepartment of Pathology, Montpellier Cancer Institute Val d'Aurelle, 208, rue des Apothicaires, Montpellier, F-34298, France. frederic.bibeau@icm.unicancer.fr.
Gilles RomieuDepartment of Medical Oncology, Montpellier Cancer Institute Val d'Aurelle, 208, rue des Apothicaires, Montpellier, F-34298, France. Gilles.Romieu@icm.unicancer.fr.
Pierre-Jean LamyDepartment of Oncogenetics, Montpellier Cancer Institute Val d'Aurelle, 208, rue des Apothicaires, Montpellier, F-34298, France. pierre-jean.lamy@icm.unicancer.fr.
Inserm · FRInstitut de Recherche en Cancérologie de Montpellier · FRAix-Marseille Université · FRUniversité de Bretagne Occidentale · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTriple negative breast cancers (TNBC) are a more aggressive subset of breast cancer. A better understanding of its biology could allow the rational development of targeted therapies.

methodsWe extensively analyzed the EGFR/PI3K/PTEN axis in a large, homogeneous population of TNBC to help defining the putative role of anti-EGFR and -PI3K targeted therapies in this setting. EGFR gene amplification, EGFR protein expression, PIK3CA and PTEN gene alterations (two members of EGFR downstream pathways) and their clinicopathological and prognostic implications were analyzed in 204 TNBC samples from European patients.

resultsEGFR amplification was detected in 18 of the 204 TNBC specimens (8.9 %) and was significantly associated with higher EGFR protein levels. Fourteen PIK3CA mutations were identified in exon 9 (6.7 %), and 17 in exon 20 (8.3 %). PIK3CA mutations, especially in exon 9, were significantly associated with grade I-II tumors. PTEN deletions were detected in 43 samples (21.50 %) and were significantly associated with grade III tumors (p < 0.001). Univariate analysis showed a significant association between relapse-free survival (RFS), T and N stage and exon 9 PIK3CA mutations. Overall survival was significantly associated with T stage, N stage and adjuvant chemotherapy, which was administered to 70.3 % of patients. In multivariate analyses, T stage, N stage, presence of exon 9 PIK3CA mutations and high EGFR protein level were independent poor prognostic factors for RFS, while adjuvant chemotherapy was associated with a better outcome.

conclusionsHigh EGFR protein expression and exon 9 PIK3CA activating mutations are independent prognostic factors in TNBC. The efficacy of anti-PI3K targeted therapies needs to be evaluated in this setting.

Indexed as

AdultAgedAged, 80 and overClass I Phosphatidylinositol 3-KinasesErbB ReceptorsExonsFemaleGene AmplificationGene Expression Regulation, NeoplasticHumansMiddle AgedMutationPhosphatidylinositol 3-KinasesPrognosisPTEN PhosphohydrolaseTriple Negative Breast NeoplasmsClass I Phosphatidylinositol 3-KinasesEGFR protein, humanErbB ReceptorsPhosphatidylinositol 3-KinasesPIK3CA protein, humanPTEN PhosphohydrolasePTEN protein, human

Identifiers

PMID26680641
PMCPMC4683760
OpenAlexW2209515009

What OpenQuestion holds

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LicenceCC BY
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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.