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Association between LKB1 expression and prognosis of patients with solid tumours: an updated systematic review and meta-analysis

Authors :
Qiu Qin Li
Jue Ling Wei
Xin-Hua Zhao
Rong Rui Huo
Juan Tang
Han Yue Mo
Feng Juan Zhao
Yun Hong Ren
Rong Rong Jia
Xue Mei You
Source :
BMJ Open, Vol 9, Iss 8 (2019), BMJ Open
Publication Year :
2019
Publisher :
BMJ Publishing Group, 2019.

Abstract

ObjectivesLiver kinase B1 (LKB1) is considered a tumour suppressor that can control cell growth and metabolism. Whether LKB1 expression levels are related to clinicopathology and prognosis is controversial. This review aimed to quantitatively examine the latest evidence on this question.DesignAn updated systematic review and meta-analysis on the association between LKB1 expression and prognosis of patients with solid tumours were performed.Data sourcesEligible studies were identified through literature searches from database establishment until 15 June 2018 in the following databases: Embase, PubMed, Web of Science, Cochrane Library, China National Knowledge Infrastructure and Wan Fang databases.Eligibility criteriaThe association between LKB1 expression and clinicopathological characteristics, overall survival (OS), disease-free survival (DFS) and relapse-free survival (RFS) of patients with solid tumours were reported. Sufficient data were available to calculate the OR or HR and 95% CI.Data extraction and synthesisRelevant data were meta-analysed for OS, DFS, RFS and various clinical parameters.ResultsThe systematic review included 25 studies containing 6012 patients with solid tumours. Compared with patients with high LKB1 expression, patients with low expression showed significantly shorter OS in univariate analysis (HR=1.63, 95% CI 1.35 to 1.97, pConclusionLow LKB1 expression predicts shorter OS, worse tumour differentiation, larger tumours, earlier lymph node metastasis and more advanced TNM stage. Low LKB1 expression may be a useful biomarker of poor clinicopathology and prognosis.

Details

Language :
English
ISSN :
20446055
Volume :
9
Issue :
8
Database :
OpenAIRE
Journal :
BMJ Open
Accession number :
edsair.doi.dedup.....11cfb357bcd32e842983de09278af85e