Evidence map›Paper›PMID 29285237›Full record

ArticleOncotarget2017

Outcome of EGFR-mutated NSCLC patients with MET-driven resistance to EGFR tyrosine kinase inhibitors.

Simon Baldacci, Julien Mazieres, Pascale Tomasini, Nicolas Girard, Florian Guisier, Clarisse Audigier-Valette, Isabelle Monnet, Marie Wislez, Maurice Pérol, Pascal Dô and 8 more

Abstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

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

  1. Non-small cell lung cancer withFrontiers in oncology · 2023
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  15. cfDNA changes for monitoring of targeted therapy in a primaryTranslational lung cancer research · 2020
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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.

Simon BaldacciCHU Lille, Thoracic Oncology Department, Univ. Lille, Siric ONCOLille, Lille, France.
Julien MazieresToulouse University Hospital, Université Paul Sabatier, Toulouse, France.
Pascale TomasiniAix-Marseille University, Assistance Publique Hôpitaux de Marseille, Multidisciplinary Oncology & Therapeutic Innovations Department, Marseille, France.
Nicolas GirardLouis Pradel Hospital, Hospices Civils de Lyon, Lyon, France.
Florian GuisierRouen University Hospital, Thoracic oncology unit & Normandy University, IRIB, LITIS Lab, EA 4103 QuantIF team, Rouen, France.
Clarisse Audigier-ValetteService de Pneumologie, Centre Hospitalier Sainte Musse, Toulon, France.
Isabelle MonnetCentre Hospitalier Intercommunal de Créteil, Créteil, France.
Marie WislezAPHP Hôpital Tenon, Paris, France.
Maurice PérolDepartment of Medical Oncology, Centre Léon Bérard, Lyon, France.
Pascal DôCentre Régional de Lutte Contre le Cancer François Baclesse, Caen, France.
Eric DansinCentre Oscar Lambret, Lille, France.
Charlotte LeducCHU Strasbourg, Strasbourg, France.
Etienne Giroux LeprieurAPHP - Hôpital Ambroise Paré, Boulogne-Billancourt, France.
Denis Moro-SibilotUnité d'Oncologie Thoracique, Service de Pneumologie, CHU Grenoble-Alpes, La Tronche, France.
David TulasneUniv. Lille, CNRS, Institut Pasteur de Lille, UMR 8161, M3T, Mechanisms of Tumorigenesis and Targeted Therapies, Lille, France.
Zoulika KherroucheCHU Lille, Thoracic Oncology Department, Univ. Lille, Siric ONCOLille, Lille, France.
Julien LabreucheEA 2694 University of Lille, Lille, France.
Alexis B CortotCHU Lille, Thoracic Oncology Department, Univ. Lille, Siric ONCOLille, Lille, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Several mechanisms of acquired resistance to EGFR tyrosine kinase inhibitors (TKIs) in EGFR-mutated NSCLC have been described including the T790M mutation and Methods: Patients with metastatic EGFR-mutated NSCLC displaying high MET overexpression or Results: Forty two patients were included. The median overall survival (OS), and the median post EGFR TKI progression overall survival (PPOS) were 36.2 months [95%CI 27.3-66.5] and 18.5 months [95%CI 10.6-27.4] respectively. Nineteen out of 36 tumors tested for MET FISH had Conclusion: MET-driven resistance to EGFR TKI defines a specific pattern of resistance characterized by low objective response rate to MET inhibitors given alone and overlapping with T790M mutations. Further studies are warranted to define adequate therapeutic strategies for MET-driven resistance to EGFR TKI.

Indexed as

EGFRMETnon small cell lung cancerresistancetyrosine kinase inhibitors

Identifiers

PMID29285237
PMCPMC5739624

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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.