Home LiteratureArticle Details
PMID: 21422424 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Evaluation and prognostic significance of circulating tumor cells in patients with non-small-cell lung cancer.

Krebs MG, Sloane R, Priest L, Lancashire L, Hou JM, Greystoke A, Ward TH, Ferraldeschi R, Hughes A, Clack G, Ranson M, Dive C, Blackhall FH

Abstract

Lung cancer is the leading cause of cancer-related death worldwide. Non-small-cell lung cancer (NSCLC) lacks validated biomarkers to predict treatment response. This study investigated whether circulating tumor cells (CTCs) are detectable in patients with NSCLC and what their ability might be to provide prognostic information and/or early indication of patient response to conventional therapy. In this single-center prospective study, blood samples for CTC analysis were obtained from 101 patients with previously untreated, stage III or IV NSCLC both before and after administration of one cycle of standard chemotherapy. CTCs were measured using a semiautomated, epithelial cell adhesion molecule-based immunomagnetic technique. The number of CTCs in 7.5 mL of blood was higher in patients with stage IV NSCLC (n = 60; range, 0 to 146) compared with patients with stage IIIB (n = 27; range, 0 to 3) or IIIA disease (n = 14; no CTCs detected). In univariate analysis, progression-free survival was 6.8 v 2.4 months with P < .001, and overall survival (OS) was 8.1 v 4.3 months with P < .001 for patients with fewer than five CTCs compared with five or more CTCs before chemotherapy, respectively. In multivariate analysis, CTC number was the strongest predictor of OS (hazard ratio [HR], 7.92; 95% CI, 2.85 to 22.01; P < .001), and the point estimate of the HR was increased with incorporation of a second CTC sample that was taken after one cycle of chemotherapy (HR, 15.65; 95% CI, 3.63 to 67.53; P < .001). CTCs are detectable in patients with stage IV NSCLC and are a novel prognostic factor for this disease. Further validation is warranted before routine clinical application.

MeSH Terms
Adult Aged Aged, 80 and over Antineoplastic Combined Chemotherapy Protocols/therapeutic use Biomarkers, Tumor/analysis Carcinoma, Non-Small-Cell Lung/drug therapy,immunology,pathology Cell Adhesion Molecules/analysis Disease-Free Survival England Female Humans Immunomagnetic Separation Kaplan-Meier Estimate Lung Neoplasms/drug therapy,immunology,pathology Male Middle Aged Neoplasm Staging Neoplastic Cells, Circulating/drug effects,immunology,pathology Predictive Value of Tests Proportional Hazards Models Prospective Studies Risk Assessment Risk Factors Time Factors Treatment Outcome
Chemicals
Biomarkers, Tumor Cell Adhesion Molecules
Authors & Affiliations
13 authors, click to expand affiliations / ORCID
Krebs Matthew G
Clinical and Experimental Pharmacology Group, Paterson Institute for Cancer Research, Manchester, United Kingdom.
Sloane Robert
Priest Lynsey
Lancashire Lee
Hou Jian-Mei
Greystoke Alastair
Ward Tim H
Ferraldeschi Roberta
Hughes Andrew
Clack Glen
Ranson Malcolm
Dive Caroline
Blackhall Fiona H
Article Info
Journal
Journal of clinical oncology : official journal of the American Society of Clinical Oncology
Abbr.
J Clin Oncol
ISSN
1527-7755
Published
2011-04-20
Epub
2011-00-21
Pages
1556-63
Language
English
Region
United States
NLM ID
8309333
Subset
IM
Grants
Cancer Research UK · United Kingdom
Corrections
CommentIn
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com