LUNX mRNA-positive cells at different time points predict prognosis in patients with surgically resected nonsmall cell lung cancer
- PMID: 24120632
- DOI: 10.1016/j.trsl.2013.09.010
LUNX mRNA-positive cells at different time points predict prognosis in patients with surgically resected nonsmall cell lung cancer
Abstract
LUNX is a lung-specific gene whose messenger ribonucleic acid (mRNA) expression is strictly limited to normal lung tissue and nonsmall cell lung cancer (NSCLC) tissue. The aim of this study was to investigate whether the detection of LUNX mRNA-positive circulating tumor cells (CTC)s in peripheral blood at different time points is useful for predicting disease recurrence, disease-free survival (DFS), and overall survival (OS) in NSCLC patients undergoing surgery. Serial blood samples from 68 patients with stage I-IIIA NSCLC were examined by real-time quantitative polymerase chain reaction assay targeting LUNX mRNA before (T0) and after surgery (T1) and after the completion of adjuvant chemotherapy (T2). Results showed that LUNX mRNA-positive CTCs were detected in 40 of 68 NSCLC patients (58.8%) before surgery; the detection rates of LUNX mRNA-positive CTCs at T1 and T2 time points were 32.4% (22/68) and 33.3% (20/60), respectively. The detection of LUNX mRNA-positive CTC at 3 time points was associated with lymph node status and pathologic stage. During the follow-up period, patients with LUXN mRNA-positive CTC at 3 time points had a higher relapse rate and a shorter DFS and OS than those without. Multivariate analysis revealed that presence of LUNX mRNA-positive CTC at T1 and T2 time points was an independent unfavorable factor for DFS and OS. In conclusion, detection of LUNX mRNA-positive CTC after surgery and the completion of adjuvant chemotherapy in patients with stage I-IIIA NSCLC are highly predictive for DFS and OS. This technique could aid in the prediction of prognosis and design of tailored treatment.
Keywords: BLD; CTC; Ct; DFS; NSCLC; OS; PBMC; PCR; RTQ-PCR; benign lung disease; circulating tumor cell; disease-free survival; mRNA; messenger ribonucleic acid; non-small cell lung cancer; overall survival; peripheral blood mononuclear cell; polymerase chain reaction; real-time quantitative- PCR; threshold cycle.
Copyright © 2014 Mosby, Inc. All rights reserved.
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