Evidence map›Paper›PMID 27105879›Full record

ArticlePathology oncology research : POR2016

The Frequency of EGFR Mutation in Lung Adenocarcinoma and the Efficacy of Tyrosine Kinase Inhibitor Therapy in a Hungarian Cohort of Patients.

Veronika Sárosi, Zoltán Balikó, Gábor Smuk, Terézia László, Mariann Szabó, István Ruzsics, Emese Mezősi

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Article in Pathology oncology research : POR, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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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

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Veronika SárosiDivision of Pulmonology, 1st Department of Medicine, University of Pecs, School of Medicine, 13 Ifjusag, Pecs, H-7624, Hungary.
Zoltán BalikóDivision of Pulmonology, 1st Department of Medicine, University of Pecs, School of Medicine, 13 Ifjusag, Pecs, H-7624, Hungary.
Gábor SmukDepartment of Pathology, University of Pecs, School of Medicine, Pecs, Hungary.
Terézia LászlóDepartment of Pathology, University of Pecs, School of Medicine, Pecs, Hungary.
Mariann SzabóDivision of Pulmonology, 1st Department of Medicine, University of Pecs, School of Medicine, 13 Ifjusag, Pecs, H-7624, Hungary.
István RuzsicsDivision of Pulmonology, 1st Department of Medicine, University of Pecs, School of Medicine, 13 Ifjusag, Pecs, H-7624, Hungary.
Emese MezősiDivision of Pulmonology, 1st Department of Medicine, University of Pecs, School of Medicine, 13 Ifjusag, Pecs, H-7624, Hungary. mezosi.emese@pte.hu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the last decades new therapeutic drugs have been developed for the treatment of non-small cell lung cancer (NSCLC) patients. Tyrosine kinase inhibitors (TKIs) significantly increase the progression free survival (PFS) of patients with NSCLC carrying epidermal growth factor receptor (EGFR) mutations. This type of lung cancer occurs mainly among non-smoking women and Asian origin. However, the new ESMO guideline recommends EGFR mutation analysis in every patient with NSCLC, because in patients with activating EGFR mutation, TKIs should be considered as first line therapy. In our recent work, we analyzed data of patients with EGFR-mutant adenocarcinoma from January 2009. The number of patients investigated was 446, among them 44 cases were positive for EGFR mutation. The ratio of positive cases was 9.86 % that is lower than the average mutation rate in Europe and much lower than that found in Asia. The exon 19 deletion was detected in 61.4 % of the patients, while L858R point mutation in exon 21 was observed in 34.1 % of them. In one subject, both exon 19 and 21 mutations were present simultaneously. A rare mutation located in exon 21 was found in another patient. TKI therapy was conducted in 38 patients. The disease control rate by TKI therapy was 85.7 %; primary resistance was documented in five subjects. Non-smoking patients with EGFR mutant adenocarcinoma had the highest benefit from TKI treatment. Our data support the recommendation that EGFR mutation status should be defined in all cases of locally advanced or metastatic lung adenocarcinoma.

Indexed as

AdenocarcinomaAdenocarcinoma of LungAgedAntineoplastic AgentsErbB ReceptorsExonsFemaleHumansHungaryLung NeoplasmsMaleMiddle AgedMutationProtein Kinase InhibitorsProtein-Tyrosine KinasesAntineoplastic AgentsEGFR protein, humanErbB ReceptorsProtein Kinase InhibitorsProtein-Tyrosine KinasesAdenocarcinomaEGFR mutationNSCLCTKI

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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.