Evidence map›Paper›PMID 22042954›Full record

ArticleJournal of clinical oncology : official journal of the American Society of Clinical Oncology2011

Genetic activation of the MET pathway and prognosis of patients with high-risk, radically resected gastric cancer.

Francesco Graziano, Nadia Galluccio, Paola Lorenzini, Annamaria Ruzzo, Emanuele Canestrari, Silvia D'Emidio, Vincenzo Catalano, Valerio Sisti, Claudia Ligorio, Francesca Andreoni and 7 more

Abstract read
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In one paragraph

Article in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 101 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
101citing papers in PubMed, 3 pooled it
17.7field-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

101 citing papers in PubMed, 3 syntheses or guidelines pooled it, 164 citations in OpenAlex.

  1. Molecular-targeted first-line therapy for advanced gastric cancer.The Cochrane database of systematic reviews · 2016
    Pooled it
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  4. The NanoString-based multigene assay as a novel platform to screen EGFR, HER2, and MET in patients with advanced gastric cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2015
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  6. Randomized phase II trial of Onartuzumab in combination with erlotinib in patients with advanced non-small-cell lung cancer.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2013
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  8. Article
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  16. An Observatory for theCancers · 2023
    Review
  17. TargetingCancers · 2023
    Review
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  19. Review
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 1 institution in 1 country.

Francesco GrazianoAzienda Ospedaliera Ospedali Riuniti Marche Nord 61122, Pesaro, Italy. frada@tin.it
Nadia Galluccio
Paola Lorenzini
Annamaria Ruzzo
Emanuele Canestrari
Silvia D'Emidio
Vincenzo Catalano
Valerio Sisti
Claudia Ligorio
Francesca Andreoni
Eliana Rulli
Enrico Di Oto
Giammaria Fiorentini
Costantino Zingaretti
Michele De Nictolis
Federico Cappuzzo
Mauro Magnani
Ospedali Riuniti Marche Nord · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo investigate whether prognosis of patients with high-risk gastric cancer may depend on MET copy number gain (CNG) or an activating truncation within a deoxyadenosine tract element (DATE) in the promoter region of the MET ligand HGF. PATIENTS AND

methodsA single-institution cohort of 230 patients with stage II/III gastric cancer was studied. Formalin-fixed paraffin-embedded tumor specimens were used for DNA extraction. Quantitative polymerase chain reaction (qPCR) for MET CNG and sequencing for HGF DATE truncation (< 25 deoxyadenosines instead of 30) were used. Results were analyzed for association with disease-free survival (DFS) and overall survival (OS). To assess the reliability of the qPCR measurement, a random sample of cases was reanalyzed using an alternative assay (fluorescent in situ hybridization [FISH]) with calculation of the intracorrelation coefficient (ICC).

resultsIn 216 assessable patients, MET CNG five or more copies and homozygous HGF-truncated DATE occurred in 21 patients (10%) and 30 patients (13%), respectively. Patients with MET CNG five or more copies (MET-positive) showed significantly worse prognosis with multivariate hazard ratio (HR) of 3.02 (95% CI, 1.71 to 5.33; P < .001) for DFS and multivariate HR of 2.91 (95% CI, 1.65 to 5.11; P < .001) for OS. The agreement between qPCR and FISH was high, with ICC = 0.9% (95% CI, 0.81% to 0.95%; the closer the ICC is to 1, the greater is the agreement). HGF-truncated DATE did not show relevant prognostic effect.

conclusionIn this study, qPCR revealed approximately 10% of white patients with gastric cancer harboring MET CNG of five or more copies. This marker was significantly associated with unfavorable prognosis. This information is relevant to the current clinical development of anti-MET compounds.

Indexed as

AdultAgedFemaleGene AmplificationGene DosageHepatocyte Growth FactorHumansIn Situ Hybridization, FluorescenceMaleMiddle AgedPolymerase Chain ReactionPrognosisProto-Oncogene Proteins c-metRiskSignal TransductionStomach NeoplasmsHepatocyte Growth FactorMET protein, humanProto-Oncogene Proteins c-met

Identifiers

PMID22042954
OpenAlexW2152176528

What OpenQuestion holds

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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.