Evidence map›Paper›PMID 25176972›Full record

ReviewEuropean respiratory review : an official journal of the European Respiratory Society2014

Molecular mechanisms of resistance in epidermal growth factor receptor-mutant lung adenocarcinomas.

Alexis B Cortot, Pasi A Jänne

Registry-linked trialOpen access · diamondAbstract readReview
In one paragraph

Review in European respiratory review : an official journal of the European Respiratory Society, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04640870 (An Observational Study to Assess the Molecular Epidemiology of Epidermal Growth Factor Receptor), which is not on this map. Cited by 87 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
87citing papers in PubMed, 1 pooled it
12.3field-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.

NCT04640870 completednot on this mapstarted 2015, after this paper: background citation

An Observational Study to Assess the Molecular Epidemiology of Epidermal Growth Factor Receptor (EGFR) Mutations in Patients With Advanced EGFR Mutation-positive Non-small Cell Lung Cancer Treated With Afatinib in Real-world Clinical Set-tings in Greece

TypeobservationalSponsorHellenic Cooperative Oncology GroupRan2015 to 2020Enrolled59ConditionsNon Small Cell Lung Cancer, EGF-R Positive Non-Small Cell Lung Cancer, EGFR Gene MutationArmsAfatinib
3 · Its place in the literature

Who cites it

87 citing papers in PubMed, 1 synthesis or guideline pooled it, 152 citations in OpenAlex.

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

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

2 authors at 1 institution in 1 country.

Alexis B CortotThoracic Oncology Dept, Hopital Calmette, Lille University Hospital, Université Lille Nord de France, Lille, France. UMR8161, Institut de Biologie de Lille, Siric OncoLille, Universités Lille 1, Lille, France. Lowe Center for Thoracic Oncology, Dana Farber Cancer Institute, Boston, MA, USA. Thoracic Oncology Dept, Hopital Calmette, Lille University Hospital, Université Lille Nord de France, Lille, France. UMR8161, Institut de Biologie de Lille, Siric OncoLille, Universités Lille 1, Lille, France. Lowe Center for Thoracic Oncology, Dana Farber Cancer Institute, Boston, MA, USA. alexis.cortot@chru-lille.fr.
Pasi A JänneThoracic Oncology Dept, Hopital Calmette, Lille University Hospital, Université Lille Nord de France, Lille, France. UMR8161, Institut de Biologie de Lille, Siric OncoLille, Universités Lille 1, Lille, France. Lowe Center for Thoracic Oncology, Dana Farber Cancer Institute, Boston, MA, USA.
Harvard University Press · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The discovery of epidermal growth factor receptor (EGFR) mutations in nonsmall cell lung cancer (NSCLC) has allowed the identification of a subset of patients whose tumours are exquisitely sensitive to EGFR tyrosine kinase inhibitors (TKIs). Despite the efficacy and superiority of EGFR TKIs over chemotherapy as first-line therapy, all patients will ultimately develop progressive disease, with a median of 9-13 months progression-free survival. A better understanding of the molecular mechanisms underlying resistance to EGFR TKIs can help design new drugs and therapeutic strategies to overcome resistance. This has been illustrated by the new generation TKIs that are effective on the T790M mutation, which is the most frequent mechanism of acquired resistance to EGFR TKIs. In this article, we will address the main molecular mechanisms of primary and acquired resistance to EGFR TKIs in EGFR-mutant NSCLC.

Indexed as

Carcinoma, Non-Small-Cell LungDrug Resistance, NeoplasmErbB ReceptorsHumansLung NeoplasmsMutationPhenotypePhosphotransferasesSmokingErbB ReceptorsPhosphotransferases

Identifiers

PMID25176972
PMCPMC9487318
OpenAlexW1983159571

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

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.