Abstract
Circulating tumour cells (CTCs) can provide information on patient prognosis and treatment efficacy. However, there is no universal method to detect CTC currently available. Here, we compared the performance of two CTC detection systems based on the expression of the EpCAM antigen (CellSearch assay) or on cell size (ISET assay). Circulating tumour cells were enumerated in 60 patients with metastatic carcinomas of breast, prostate and lung origins using CellSearch according to the manufacturer's protocol and ISET by studying cytomorphology and immunolabelling with anti-cytokeratin or lineage-specific antibodies. Concordant results were obtained in 55% (11 out of 20) of the patients with breast cancer, in 60% (12 out of 20) of the patients with prostate cancer and in only 20% (4 out of 20) of lung cancer patients. Our results highlight important discrepancies between the numbers of CTC enumerated by both techniques. These differences depend mostly on the tumour type. These results suggest that technologies limiting CTC capture to EpCAM-positive cells, may present important limitations, especially in patients with metastatic lung carcinoma.
MeSH Terms
Adult
Aged
Aged, 80 and over
Antigens, Neoplasm/metabolism
Cell Adhesion Molecules/metabolism
Cell Count/methods
Cell Size
Epithelial Cell Adhesion Molecule
Female
Humans
Image Interpretation, Computer-Assisted/methods
Male
Middle Aged
Neoplasm Metastasis
Neoplasms/blood
Neoplastic Cells, Circulating
Chemicals
Antigens, Neoplasm
Cell Adhesion Molecules
Epithelial Cell Adhesion Molecule
Authors & Affiliations
15 authors, click to expand affiliations / ORCID
Farace F
Translational Research Laboratory, Institut de Cancérologie Gustave Roussy, 94805 Villejuif, France. farace@gr.fr
Massard C
Vimond N
Drusch F
Jacques N
Billiot F
Laplanche A
Chauchereau A
Lacroix L
Planchard D
Le Moulec S
André F
Fizazi K
Soria J C
Vielh P
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