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Evaluation of Circulating Tumor Cells and Related Events as Prognostic Factors and Surrogate Biomarkers in Advanced NSCLC Patients Receiving First-Line Systemic Treatment

Anido Herranz, Urbano; Vieito Villar, María; Abalo Piñeiro, Alicia; Muinelo Romay , Laura; Alonso Nocelo, Marta; Abal Posada, Miguel; López López, Rafael; Vázquez Rivera, Francisca; Barón Duarte, Francisco Javier; Brozos Vázquez, Elena María; Aguin Losada, Santiago
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URI: http://hdl.handle.net/20.500.11940/5543
PMID: 24452143
DOI: 10.3390/cancers6010153
ISSN: 2072-6694
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Cancers (Basel) . 2014 Jan 21;6(1):153-65 (501.2Kb)
Date issued
2014
Journal title
Cancers (Basel)
Type of content
Artigo
DeCS
Carcinoma de Pulmón de Células no Pequeñas | Células Neoplásicas Circulantes
MeSH
Carcinoma, Non-Small-Cell Lung | Neoplastic Cells, Circulating
Abstract
In the present study we investigated the prognostic value of Circulating Tumour Cells (CTC) and their utility for therapy monitoring in non-small cell lung cancer (NSCLC). A total of 43 patients newly diagnosed with NSCLC were prospectively enrolled. Blood samples were obtained before the 1st, 2nd and 5th cycles of chemotherapy and analyzed using CellSearch technology. Both CTC and CTC-related objects (not morphological standard or broken epithelial cells) were counted. At baseline 18 (41.9%) patients were positive for intact CTC count and 10 (23.2%) of them had ≥5 CTC, while CK positive events were found in 79.1% of patients. The group of patients with CTC ³5 at baseline presented worse PFS and OS than those with <5 CTC (p = 0.034 and p = 0.008, respectively). Additionally, high levels of total CK positive events were associated with poor prognosis in the group of patients with <5 CTC. Regarding therapy monitoring, patients presenting increased levels of CTC during the treatment demonstrated lower OS and PFS rates. All these data supported the value of CTC as a prognostic biomarker and as a surrogate indicator of chemotherapy effectiveness in advanced NSCLC patients, with the additional value of analyzing other "objects" such as apoptotic CTC or CK fragments to guide the clinical management of these patients.

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