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Predictive and prognostic value of circulating endothelial cells in non-small cell lung cancer patients treated with standard chemotherapy

Purpose Monitoring circulating endothelial cells (CECs) count reflects the tumor vasculature in cancer patients and might be a predictor of response to chemotherapy. We therefore investigated the clinical significance of changes in CECs count after three cycles of platinum-based chemotherapy in pati...

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Published in:Journal of cancer research and clinical oncology 2015-01, Vol.141 (1), p.119-125
Main Authors: Najjar, Fadi, Alammar, Moosheer, Bachour, Marroan, Almalla, Nissreen, Altahan, Moaz, Alali, Ali, Al-Massarani, Ghassan
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container_title Journal of cancer research and clinical oncology
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creator Najjar, Fadi
Alammar, Moosheer
Bachour, Marroan
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Altahan, Moaz
Alali, Ali
Al-Massarani, Ghassan
description Purpose Monitoring circulating endothelial cells (CECs) count reflects the tumor vasculature in cancer patients and might be a predictor of response to chemotherapy. We therefore investigated the clinical significance of changes in CECs count after three cycles of platinum-based chemotherapy in patients with advanced non-small cell lung cancer (NSCLC). Methods Peripheral blood samples were collected from 89 naive NSCLC patients at diagnosis and after chemotherapy. The CECs were quantified by an immuno-magnetic technique and fluorescent microscopy. After chemotherapy, patients were assessed according to the response evaluation criteria in solid tumors as partial response (PR), stable disease (SD) or progression disease (PD). Results Baseline CECs levels were significantly higher in PR patients ( n  = 62) than those in patients with SD/PD ( n  = 27) ( p  = 0.0007). Although there was no significant correlation between baseline CECs levels and progression-free survival (PFS) ( p  = 0.287), patients with high percentage change in CECs count after chemotherapy had significantly longer PFS than those with low percentage change ( p  = 0.048). Regarding treatment efficacy, CECs count significantly decreased after chemotherapy in comparison with CECs count at baseline in patients with PR ( p  
doi_str_mv 10.1007/s00432-014-1778-0
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We therefore investigated the clinical significance of changes in CECs count after three cycles of platinum-based chemotherapy in patients with advanced non-small cell lung cancer (NSCLC). Methods Peripheral blood samples were collected from 89 naive NSCLC patients at diagnosis and after chemotherapy. The CECs were quantified by an immuno-magnetic technique and fluorescent microscopy. After chemotherapy, patients were assessed according to the response evaluation criteria in solid tumors as partial response (PR), stable disease (SD) or progression disease (PD). Results Baseline CECs levels were significantly higher in PR patients ( n  = 62) than those in patients with SD/PD ( n  = 27) ( p  = 0.0007). Although there was no significant correlation between baseline CECs levels and progression-free survival (PFS) ( p  = 0.287), patients with high percentage change in CECs count after chemotherapy had significantly longer PFS than those with low percentage change ( p  = 0.048). Regarding treatment efficacy, CECs count significantly decreased after chemotherapy in comparison with CECs count at baseline in patients with PR ( p  &lt; 0.0001). By contrast, CECs levels after chemotherapy were significantly higher than those at diagnosis in patients with PD ( p  = 0.002). Moreover, there was no significant change between pre- and post-treatment CECs amount in patients with SD ( p  = 0.681). Conclusions Baseline CECs levels might be an early predictive biomarker for treatment efficacy in advanced NSCLC patients. Our results suggest the change in CECs count after chemotherapy as a prognostic factor for tumor response and PFS in NSCLC.</description><identifier>ISSN: 0171-5216</identifier><identifier>EISSN: 1432-1335</identifier><identifier>DOI: 10.1007/s00432-014-1778-0</identifier><identifier>PMID: 25037116</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject><![CDATA[Adenocarcinoma - drug therapy ; Adenocarcinoma - mortality ; Adenocarcinoma - pathology ; Adult ; Aged ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Biomarkers ; Biomarkers, Tumor - analysis ; Cancer Research ; Carboplatin - administration & dosage ; Carcinoma, Non-Small-Cell Lung - drug therapy ; Carcinoma, Non-Small-Cell Lung - mortality ; Carcinoma, Non-Small-Cell Lung - pathology ; Carcinoma, Squamous Cell - drug therapy ; Carcinoma, Squamous Cell - mortality ; Carcinoma, Squamous Cell - pathology ; Chemotherapy ; Cisplatin - administration & dosage ; Clinical outcomes ; Deoxycytidine - administration & dosage ; Deoxycytidine - analogs & derivatives ; Endothelium ; Endothelium, Vascular - pathology ; Female ; Follow-Up Studies ; Hematology ; Humans ; Internal Medicine ; Lung cancer ; Lung Neoplasms - drug therapy ; Lung Neoplasms - mortality ; Lung Neoplasms - pathology ; Male ; Medicine ; Medicine & Public Health ; Middle Aged ; Neoplasm Staging ; Neoplastic Cells, Circulating - pathology ; Oncology ; Original Article – Clinical Oncology ; Prognosis ; Prospective Studies ; ROC Curve ; Survival Rate ; Taxoids - administration & dosage ; Vinblastine - administration & dosage ; Vinblastine - analogs & derivatives]]></subject><ispartof>Journal of cancer research and clinical oncology, 2015-01, Vol.141 (1), p.119-125</ispartof><rights>Springer-Verlag Berlin Heidelberg 2014</rights><rights>Springer-Verlag Berlin Heidelberg 2015</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c442t-81ae9976973ae9826b19bf615e40970f72cf93953a69f302fce11060fd4184263</citedby><cites>FETCH-LOGICAL-c442t-81ae9976973ae9826b19bf615e40970f72cf93953a69f302fce11060fd4184263</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25037116$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Najjar, Fadi</creatorcontrib><creatorcontrib>Alammar, Moosheer</creatorcontrib><creatorcontrib>Bachour, Marroan</creatorcontrib><creatorcontrib>Almalla, Nissreen</creatorcontrib><creatorcontrib>Altahan, Moaz</creatorcontrib><creatorcontrib>Alali, Ali</creatorcontrib><creatorcontrib>Al-Massarani, Ghassan</creatorcontrib><title>Predictive and prognostic value of circulating endothelial cells in non-small cell lung cancer patients treated with standard chemotherapy</title><title>Journal of cancer research and clinical oncology</title><addtitle>J Cancer Res Clin Oncol</addtitle><addtitle>J Cancer Res Clin Oncol</addtitle><description>Purpose Monitoring circulating endothelial cells (CECs) count reflects the tumor vasculature in cancer patients and might be a predictor of response to chemotherapy. We therefore investigated the clinical significance of changes in CECs count after three cycles of platinum-based chemotherapy in patients with advanced non-small cell lung cancer (NSCLC). Methods Peripheral blood samples were collected from 89 naive NSCLC patients at diagnosis and after chemotherapy. The CECs were quantified by an immuno-magnetic technique and fluorescent microscopy. After chemotherapy, patients were assessed according to the response evaluation criteria in solid tumors as partial response (PR), stable disease (SD) or progression disease (PD). Results Baseline CECs levels were significantly higher in PR patients ( n  = 62) than those in patients with SD/PD ( n  = 27) ( p  = 0.0007). Although there was no significant correlation between baseline CECs levels and progression-free survival (PFS) ( p  = 0.287), patients with high percentage change in CECs count after chemotherapy had significantly longer PFS than those with low percentage change ( p  = 0.048). Regarding treatment efficacy, CECs count significantly decreased after chemotherapy in comparison with CECs count at baseline in patients with PR ( p  &lt; 0.0001). By contrast, CECs levels after chemotherapy were significantly higher than those at diagnosis in patients with PD ( p  = 0.002). Moreover, there was no significant change between pre- and post-treatment CECs amount in patients with SD ( p  = 0.681). Conclusions Baseline CECs levels might be an early predictive biomarker for treatment efficacy in advanced NSCLC patients. Our results suggest the change in CECs count after chemotherapy as a prognostic factor for tumor response and PFS in NSCLC.</description><subject>Adenocarcinoma - drug therapy</subject><subject>Adenocarcinoma - mortality</subject><subject>Adenocarcinoma - pathology</subject><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Biomarkers</subject><subject>Biomarkers, Tumor - analysis</subject><subject>Cancer Research</subject><subject>Carboplatin - administration &amp; dosage</subject><subject>Carcinoma, Non-Small-Cell Lung - drug therapy</subject><subject>Carcinoma, Non-Small-Cell Lung - mortality</subject><subject>Carcinoma, Non-Small-Cell Lung - pathology</subject><subject>Carcinoma, Squamous Cell - drug therapy</subject><subject>Carcinoma, Squamous Cell - mortality</subject><subject>Carcinoma, Squamous Cell - pathology</subject><subject>Chemotherapy</subject><subject>Cisplatin - administration &amp; 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We therefore investigated the clinical significance of changes in CECs count after three cycles of platinum-based chemotherapy in patients with advanced non-small cell lung cancer (NSCLC). Methods Peripheral blood samples were collected from 89 naive NSCLC patients at diagnosis and after chemotherapy. The CECs were quantified by an immuno-magnetic technique and fluorescent microscopy. After chemotherapy, patients were assessed according to the response evaluation criteria in solid tumors as partial response (PR), stable disease (SD) or progression disease (PD). Results Baseline CECs levels were significantly higher in PR patients ( n  = 62) than those in patients with SD/PD ( n  = 27) ( p  = 0.0007). Although there was no significant correlation between baseline CECs levels and progression-free survival (PFS) ( p  = 0.287), patients with high percentage change in CECs count after chemotherapy had significantly longer PFS than those with low percentage change ( p  = 0.048). Regarding treatment efficacy, CECs count significantly decreased after chemotherapy in comparison with CECs count at baseline in patients with PR ( p  &lt; 0.0001). By contrast, CECs levels after chemotherapy were significantly higher than those at diagnosis in patients with PD ( p  = 0.002). Moreover, there was no significant change between pre- and post-treatment CECs amount in patients with SD ( p  = 0.681). Conclusions Baseline CECs levels might be an early predictive biomarker for treatment efficacy in advanced NSCLC patients. Our results suggest the change in CECs count after chemotherapy as a prognostic factor for tumor response and PFS in NSCLC.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>25037116</pmid><doi>10.1007/s00432-014-1778-0</doi><tpages>7</tpages></addata></record>
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subjects Adenocarcinoma - drug therapy
Adenocarcinoma - mortality
Adenocarcinoma - pathology
Adult
Aged
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Biomarkers
Biomarkers, Tumor - analysis
Cancer Research
Carboplatin - administration & dosage
Carcinoma, Non-Small-Cell Lung - drug therapy
Carcinoma, Non-Small-Cell Lung - mortality
Carcinoma, Non-Small-Cell Lung - pathology
Carcinoma, Squamous Cell - drug therapy
Carcinoma, Squamous Cell - mortality
Carcinoma, Squamous Cell - pathology
Chemotherapy
Cisplatin - administration & dosage
Clinical outcomes
Deoxycytidine - administration & dosage
Deoxycytidine - analogs & derivatives
Endothelium
Endothelium, Vascular - pathology
Female
Follow-Up Studies
Hematology
Humans
Internal Medicine
Lung cancer
Lung Neoplasms - drug therapy
Lung Neoplasms - mortality
Lung Neoplasms - pathology
Male
Medicine
Medicine & Public Health
Middle Aged
Neoplasm Staging
Neoplastic Cells, Circulating - pathology
Oncology
Original Article – Clinical Oncology
Prognosis
Prospective Studies
ROC Curve
Survival Rate
Taxoids - administration & dosage
Vinblastine - administration & dosage
Vinblastine - analogs & derivatives
title Predictive and prognostic value of circulating endothelial cells in non-small cell lung cancer patients treated with standard chemotherapy
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