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Prognostic significance of CEACAM5mRNA-positive circulating tumor cells in patients with metastatic colorectal cancer.

Authors :
Messaritakis, Ippokratis
Sfakianaki, Maria
Papadaki, Chara
Koulouridi, Asimina
Vardakis, Nikolaos
Koinis, Filippos
Hatzidaki, Dora
Georgoulia, Nefeli
Kladi, Athina
Kotsakis, Athanasios
Souglakos, John
Georgoulias, Vassilis
Source :
Cancer Chemotherapy & Pharmacology. Nov2018, Vol. 82 Issue 5, p767-775. 9p.
Publication Year :
2018

Abstract

<bold>Purpose: </bold>Τo evaluate the clinical relevance of CEACAM5mRNA-positive circulating tumor cells (CTCs) in patients with metastatic colorectal cancer (mCRC).<bold>Methods: </bold>Peripheral blood was obtained from 436 patients with mCRC before the initiation of systemic therapy. A second sample was obtained on treatment assessment from 296 (67.9%) patients. The detection of CEACAM5mRNA-positive CTCs was performed using a real-time PCR assay.<bold>Results: </bold>The patients' median age was 67 years and PS (EGOG 0-1) 92%; KRAS exon 2 and BRAFV600E mutated primary tumors were identified in 31.9% and 6.4% of the tested patients, respectively, whereas metastasectomy was performed in 17.7% of the patients. Circulating CEACAM5mRNA-positive CTCs were detected in 125 (28.7%) and 85 (28.7%) patients at baseline and on treatment assessment, respectively. The detection of CEACAM5mRNA-positive cells was revealed, in multivariate analysis, as an independent prognostic factor associated with decreased PFS (HR 1.6; 95% CI 1.1-2.5; p = 0.026) and OS (HR 2.2; 95% CI 1.3-3.2; p < 0.001). The detection of CEACAM5mRNA-positive CTCs in patients with KRAS and BRAFV600E mutations was correlated with shorter PFS (p = 0.041 and p = 0.022, respectively). Moreover, OS was significantly shorter in patients with CEACAM5+/KRAS mutations compared to those with CEACAM5+/KRAS wt tumors (p = 0.023).<bold>Conclusions: </bold>Detection of peripheral blood CEACAM5mRNA-positive CTCs is an adverse prognostic factor correlated with poor clinical outcome in patients with mCRC, especially in patients with KRAS and BRAF mutated tumors. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03445704
Volume :
82
Issue :
5
Database :
Academic Search Index
Journal :
Cancer Chemotherapy & Pharmacology
Publication Type :
Academic Journal
Accession number :
132223018
Full Text :
https://doi.org/10.1007/s00280-018-3666-9