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Authors Sun WW, Xu ZH, Lian P, Gao BL, Hu JA
Received 13 December 2016
Accepted for publication 21 February 2017
Published 4 May 2017 Volume 2017:10 Pages 2413—2424
DOI https://doi.org/10.2147/OTT.S130087
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Manfred Beleut
Peer reviewer comments 3
Editor who approved publication: Dr Carlos Vigil Gonzales
Abstract: Circulating tumor cells (CTCs) possess profound influence on tumor
metastases and disease progression. This study aimed to investigate the
correlation of CTCs with clinical characteristics and T-cell immunity, and to
explore whether CTCs and the subpopulations can serve as an independent
prognostic factor in advanced non-small cell lung cancer (NSCLC). A prospective
study was conducted in late stages of NSCLC patients. The levels of overall
CTCs and the three subpopulation CTCs were enumerated using the CanPatrol™ CTC
enrichment system. The information about the patients which included the
clinical characteristics, survival status at the 200th day postdiagnosis, and
the levels of T cells was collected. Mann–Whitney U test,
Kruskal–Wallis H test, Cox regression, and Spearman’s
rank correlation coefficient were the statistical methods used in this study.
We detected CTCs in 27 of the 31 eligible patients; the level of epithelial–mesenchymal
circulating tumor cells (EMCTCs) was higher than that of epithelial circulating
tumor cells and that of mesenchymal circulating tumor cells (MCTCs) in the
majority of NSCLC patients. Organ metastases were positively associated with
the levels of overall CTCs, EMCTCs, and MCTCs (P <0.05).
EMCTCs and MCTCs were associated with worse clinical outcomes. Additionally,
the levels of EMCTCs were negatively associated with the levels of CD3+ T
cells (P =0.01) and CD8+ T
cells (P =0.04). In conclusion, the levels
of CTCs were positively associated with organ metastases, particularly bone
metastases, but were negatively associated with T-cell levels. The levels of
EMCTCs and MCTCs had negative prognostic value.
Keywords: clinical trial, non-small cell lung cancer,
circulating tumor cells, organ metastases, prognosis, lymphocyte T immune
system
