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Circulating tumor cells, tumor-derived extracellular vesicles and plasma cytokeratins in castration-resistant prostate cancer patients.
Nanou, Afroditi; Coumans, Frank A W; van Dalum, Guus; Zeune, Leonie L; Dolling, David; Onstenk, Wendy; Crespo, Mateus; Fontes, Mariane Sousa; Rescigno, Pasquale; Fowler, Gemma; Flohr, Penny; Brune, Christoph; Sleijfer, Stefan; de Bono, Johann S; Terstappen, Leon W M M.
Affiliation
  • Nanou A; Department of Medical Cell BioPhysics, MIRA Institute, University of Twente, Enschede, the Netherlands.
  • Coumans FAW; Department of Biomedical Engineering and Physics, Academic Medical Center, University of Amsterdam, the Netherlands.
  • van Dalum G; Department of General, Visceral and Pediatric Surgery, University Hospital and Medical Faculty of the Heinrich-Heine University, Düsseldorf, Germany.
  • Zeune LL; Department of Medical Cell BioPhysics, MIRA Institute, University of Twente, Enschede, the Netherlands.
  • Dolling D; Department of Applied Mathematics, MIRA Institute and Faculty of EEMCS, University of Twente, Enschede, the Netherlands.
  • Onstenk W; Division of Clinical Studies, The Institute of Cancer Research, London, United Kingdom.
  • Crespo M; Department of Medical Oncology, Erasmus MC - Cancer Institute, Rotterdam, The Netherlands.
  • Fontes MS; Division of Clinical Studies, The Institute of Cancer Research, London, United Kingdom.
  • Rescigno P; Division of Clinical Studies, The Institute of Cancer Research, London, United Kingdom.
  • Fowler G; Prostate Cancer Targeted Therapies Group, The Royal Marsden NHS Foundation Trust, London, United Kingdom.
  • Flohr P; Division of Clinical Studies, The Institute of Cancer Research, London, United Kingdom.
  • Brune C; Prostate Cancer Targeted Therapies Group, The Royal Marsden NHS Foundation Trust, London, United Kingdom.
  • Sleijfer S; Division of Clinical Studies, The Institute of Cancer Research, London, United Kingdom.
  • de Bono JS; Division of Clinical Studies, The Institute of Cancer Research, London, United Kingdom.
  • Terstappen LWMM; Department of Applied Mathematics, MIRA Institute and Faculty of EEMCS, University of Twente, Enschede, the Netherlands.
Oncotarget ; 9(27): 19283-19293, 2018 Apr 10.
Article in En | MEDLINE | ID: mdl-29721202
ABSTRACT

PURPOSE:

The presence of Circulating Tumor Cells (CTCs) in Castration-Resistant Prostate Cancer (CRPC) patients is associated with poor prognosis. In this study, we evaluated the association of clinical outcome in 129 CRPC patients with CTCs, tumor-derived Extracellular Vesicles (tdEVs) and plasma levels of total (CK18) and caspase-cleaved cytokeratin 18 (ccCK18). EXPERIMENTAL

DESIGN:

CTCs and tdEVs were isolated with the CellSearch system and automatically enumerated. Cut-off values dichotomizing patients into favorable and unfavorable groups of overall survival were set on a retrospective data set of 84 patients and validated on a prospective data set of 45 patients. Plasma levels of CK18 and ccCK18 were assessed by ELISAs.

RESULTS:

CTCs, tdEVs and both cytokeratin plasma levels were significantly increased in CRPC patients compared to healthy donors (HDs). All biomarkers except for ccCK18 were prognostic showing a decreased median overall survival for the unfavorable groups of 9.2 vs 21.1, 8.1 vs 23.0 and 10.0 vs 21.5 months respectively. In multivariable Cox regression analysis, tdEVs remained significant.

CONCLUSIONS:

Automated CTC and tdEV enumeration allows fast and reliable scoring eliminating inter- and intra- operator variability. tdEVs provide similar prognostic information to CTC counts.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Oncotarget Year: 2018 Document type: Article Affiliation country: Países Bajos

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Oncotarget Year: 2018 Document type: Article Affiliation country: Países Bajos