Evidence map›Paper›PMID 29278885›Full record

ArticleCancer biomarkers : section A of Disease markers2018

EGFR and AKT1 overexpression are mutually exclusive and associated with a poor survival in resected gastric adenocarcinomas.

Iacopo Petrini, Monica Lencioni, Enrico Vasile, Lorenzo Fornaro, Lorenzo Belluomini, Giulia Pasquini, Laura Ginocchi, Chiara Caparello, Gianna Musettini, Caterina Vivaldi and 8 more

Abstract read
In one paragraph

Article in Cancer biomarkers : section A of Disease markers, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 17% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 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

18 authors at 1 institution in 1 country.

Iacopo PetriniMedical Oncology, University Hospital of Pisa, 56126 Pisa, Italy.
Monica LencioniMedical Oncology, University Hospital of Pisa, 56126 Pisa, Italy.
Enrico VasileMedical Oncology, University Hospital of Pisa, 56126 Pisa, Italy.
Lorenzo FornaroMedical Oncology, University Hospital of Pisa, 56126 Pisa, Italy.
Lorenzo BelluominiMedical Oncology, University Hospital of Pisa, 56126 Pisa, Italy.
Giulia PasquiniMedical Oncology, University Hospital of Pisa, 56126 Pisa, Italy.
Laura GinocchiMedical Oncology, University Hospital of Pisa, 56126 Pisa, Italy.
Chiara CaparelloMedical Oncology, University Hospital of Pisa, 56126 Pisa, Italy.
Gianna MusettiniMedical Oncology, University Hospital of Pisa, 56126 Pisa, Italy.
Caterina VivaldiMedical Oncology, University Hospital of Pisa, 56126 Pisa, Italy.
Sara CaponiMedical Oncology, University Hospital of Pisa, 56126 Pisa, Italy.
Sergio RicciMedical Oncology, University Hospital of Pisa, 56126 Pisa, Italy.
Agenese ProiettiSurgical Pathology, Unit 3, University Hospital of Pisa, 56126 Pisa, Italy.
Gabriella FontaniniSurgical Pathology, Unit 3, University Hospital of Pisa, 56126 Pisa, Italy.
Antonio Giuseppe NaccaratoSurgical Pathology, Unit 1, University Hospital of Pisa, 56126 Pisa, Italy.
Vincenzo NardiniSurgical Pathology, Unit 2, University Hospital of Pisa, 56126 Pisa, Italy.
Stefano SantiEsophageal Surgery, University Hospital of Pisa, 56126 Pisa, Italy.
Alfredo FalconeMedical Oncology, University Hospital of Pisa, 56126 Pisa, Italy.
Azienda Ospedaliera Universitaria Pisana · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe evaluation of molecular targets in gastric cancer has demonstrated the predictive role of HER2 amplification for trastuzumab treatment in metastatic gastric cancer. Besides HER2, other molecular targets are under evaluation in metastatic gastric tumors. However, very little is known about their role in resected tumors. We evaluated the expression of HER2, EGFR, MET, AKT1 and phospho-mTOR in resected stage II-III adenocarcinomas.

methodsNinety-two patients with resected stomach (63%) or gastro-esophageal adenocarcinomas (27%) were evaluated. Antibodies anti-HER2, EGFR, MET, AKT1 and phospho-mTOR were used for immunostaining of formalin-fixed paraffin-embedded slides. Using FISH, HER2 amplification was evaluated in cases with an intermediate (+2) staining.

resultsEGFR overexpression (11%) was a poor prognostic factor for overall survival (3-year OS: 47% vs 77%; Log-Rank p= 0.033). MET overexpression (36%) was associated with a trend for a worse survival (3-year OS: 65% vs 77%; Log-Rank p= 0.084). HER2 amplification/overexpression and mTOR hyper-phosphorylation were observed in 13% and 48% of tumors, respectively. AKT1 overexpression (8%) was not a prognostic factor by itself (p= 0.234). AKT1 and EGFR overexpression was mutually exclusive and patients with EGFR or AKT1 overexpression experienced a poor prognosis (3-year OS: 52% vs. 79%, Log-Rank p= 0.005).

conclusionsEGFR is confirmed a poor prognostic factor in resected gastric cancers. We firstly describe a mutually exclusive overexpression of EGFR and AKT1 with potential prognostic implications, suggesting the relevance of this pathway for the growth of gastric cancers.

Indexed as

AdenocarcinomaAdultAgedAged, 80 and overBiomarkers, TumorCombined Modality TherapyErbB ReceptorsFemaleHumansImmunohistochemistryIn Situ Hybridization, FluorescenceKaplan-Meier EstimateMaleMiddle AgedNeoplasm GradingNeoplasm MetastasisAKT1 protein, humanBiomarkers, TumorErbB ReceptorsProto-Oncogene Proteins c-aktAKT1EGFRGastric cancergastro-esophageal junction cancerMET

Identifiers

PMID29278885
PMCPMC13078293
OpenAlexW2779160250

What OpenQuestion holds

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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.