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Multicenter Study
. 2005 Oct;14(4):895-9.

Detection of circulating tumor cells from renal carcinoma patients: experiences of a two-center study

Karen Blümke  1 , Udo Bilkenroth, Uta Schmidt, Andres Melchior, Susanne Füssel, Frank Bartel, Hans Heynemann, Paolo Fornara, Helge Taubert, Manfred P Wirth, Axel Meye
Affiliations
  • PMID: 16142348
Multicenter Study

Detection of circulating tumor cells from renal carcinoma patients: experiences of a two-center study

Karen Blümke et al. Oncol Rep. 2005 Oct.

Abstract

Approximately 30-40% of primary and localized renal cell carcinoma (RCC) will eventually become metastatic disease. Therefore, the detection and molecular characterization of circulating tumor cells (CTC) in RCC may have important prognostic and therapeutic implications. Venous blood samples were obtained from a total of 214 RCC patients before and after nephrectomy or during adjuvant immune chemotherapy in two urological centers. After density gradient centrifugation, the CD45-negative cell population was isolated from peripheral blood samples (BS) by a semi-automated immunomagnetic depletion procedure using the MACS technology. Enriched cell populations potentially containing CTC were stained for cytokeratin and evaluated by a trained pathologist. CTC were found in 105 out of 363 BS (29%) originating from 80 out of 214 patients (37%). The median tumor cell number was five (range 1-51) per BS, i.e. approximately one CTC was detectable per 2-3 ml peripheral blood after tumor cell enrichment. For a subpopulation, follow-up data indicate that 62% of the patients with CTC detection in the blood developed progressive disease with single or multiple distant metastases or died because of RCC within two years. Here we show that the standardized immunomagnetic depletion protocol is a powerful tool for detecting and isolating intact RCC-derived CTC. The occurrence and the quantity of CTC in RCC patients is an early disease event. Furthermore, the occurrence of CTC is correlated with an advanced tumor stage and seems to be associated with a more aggressive tumor phenotype.

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