Clinicopathological implications of MET exon 14 mutations in non-small cell lung cancer - A systematic review and meta-analysis. [Review] (Record no. 3646)

MARC details
000 -LEADER
fixed length control field 02671nam a22003377a 4500
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fixed length control field 180818s20182018 xxu||||| |||| 00| 0 eng d
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 0169-5002
024 ## - OTHER STANDARD IDENTIFIER
Standard number or code 10.1016/j.lungcan.2018.07.006 [doi]
024 ## - OTHER STANDARD IDENTIFIER
Standard number or code S0169-5002(18)30464-1 [pii]
040 ## - CATALOGING SOURCE
Original cataloging agency Ovid MEDLINE(R)
099 ## - LOCAL FREE-TEXT CALL NUMBER (OCLC)
PMID 30089599
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Title Clinicopathological implications of MET exon 14 mutations in non-small cell lung cancer - A systematic review and meta-analysis. [Review]
251 ## - Source
Source Lung Cancer. 123:76-82, 2018 Sep.
252 ## - Abbreviated Source
Abbreviated source Lung Cancer. 123:76-82, 2018 Sep.
253 ## - Journal Name
Journal name Lung cancer (Amsterdam, Netherlands)
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Year 2018
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Manufacturer FY2019
266 ## - Date added to catalog
Date added to catalog 2018-08-16
520 ## - SUMMARY, ETC.
Abstract Copyright (c) 2018 Elsevier B.V. All rights reserved.
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Abstract MET exon 14 mutation is an uncommon genomic alteration in non-small cell lung cancer (NSCLC). This meta-analysis aimed at investigating the clinicopathological and prognostic features of NSCLCs with MET exon 14 mutation in comparison with other genetic events. We performed a search in four electronic databases including PubMed, Web of Science, Scopus, and Virtual Health Library from inception to February 2018. Relevant data were extracted and pooled into odds ratio (OR), mean differences (MD), and corresponding 95% confidence intervals (CI) using the random-effect model. From 168 studies, we included 12 studies comprising of 18,464 NSCLCs for final analyses. Overall, the prevalence of MET exon 14 mutation in NSCLC was 3% (95% CI=2-3), with being most commonly found in pulmonary sarcomatoid carcinoma (13%; 95% CI=4-21). The mutation was more likely to occur in females (OR=0.55; 95% CI=0.33 - 0.90), patients with advanced age (MD=7.48; 95% CI=3.99-10.98), non-smoker (OR=0.48; 95% CI=0.28 - 0.83), and was associated with a worse prognosis (HR=1.82; 95% CI=1.04-3.19). Patients with MET exon 14 mutation had a distinct clinicopathological profile compared to other NSCLC genetic events. To summarize, MET exon 14 is a rare mutation in NSCLC and might be associated with a dismal survival. Patients harboring MET exon 14 skipping are eligible for targeted therapy with c-MET inhibitors, thus emphasizing the need to screen for this mutation in advanced NSCLCs.
546 ## - LANGUAGE NOTE
Language note English
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element IN PROCESS -- NOT YET INDEXED
651 ## - SUBJECT ADDED ENTRY--GEOGRAPHIC NAME
Institution MedStar Union Memorial Hospital
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Department Medicine
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Medline publication type Journal Article
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Medline publication type Review
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Local Authors Ho, An Thi Nhat
790 ## - Authors
All authors Altibi AMA, Ho ATN, Katoh R, Kondo T, Nakazawa T, Vuong HG
856 ## - ELECTRONIC LOCATION AND ACCESS
DOI <a href="https://dx.doi.org/10.1016/j.lungcan.2018.07.006">https://dx.doi.org/10.1016/j.lungcan.2018.07.006</a>
Public note https://dx.doi.org/10.1016/j.lungcan.2018.07.006
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Koha item type Journal Article
Item type description Article
Holdings
Withdrawn status Lost status Damaged status Not for loan Collection Home library Current library Date acquired Total Checkouts Full call number Barcode Date last seen Price effective from Koha item type
          MedStar Authors Catalog MedStar Authors Catalog 08/16/2018   30089599 30089599 08/16/2018 08/16/2018 Journal Article

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