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Tumour-derived extracellular vesicles in blood of metastatic cancer patients associate with overall survival.
Nanou, Afroditi; Miller, M Craig; Zeune, Leonie L; de Wit, Sanne; Punt, Cornelis J A; Groen, Harry J M; Hayes, Daniel F; de Bono, Johann S; Terstappen, Leon W M M.
  • Nanou A; Department of Medical Cell BioPhysics, Faculty of Science and Technology, University of Twente, Enschede, The Netherlands. a.nanou@utwente.nl.
  • Miller MC; ClarifyDx Consulting, Quakertown, PA, USA.
  • Zeune LL; Department of Medical Cell BioPhysics, Faculty of Science and Technology, University of Twente, Enschede, The Netherlands.
  • de Wit S; Department of Medical Cell BioPhysics, Faculty of Science and Technology, University of Twente, Enschede, The Netherlands.
  • Punt CJA; Department of Medical Oncology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
  • Groen HJM; Department of Pulmonary Diseases, University of Groningen and University Medical Centre of Groningen, Groningen, The Netherlands.
  • Hayes DF; Department of Internal Medicine, University of Michigan Rogel Cancer Center, Ann Arbor, MI, USA.
  • de Bono JS; Prostate Cancer Targeted Therapy Group, The Royal Marsden NHS Foundation Trust, London, UK.
  • Terstappen LWMM; Division of Clinical Studies, The Institute of Cancer Research, Royal Marsden Hospital, London, UK.
Br J Cancer ; 122(6): 801-811, 2020 03.
Article en En | MEDLINE | ID: mdl-31937922
BACKGROUND: Circulating tumour cells (CTCs) in blood associate with overall survival (OS) of cancer patients, but they are detected in extremely low numbers. Large tumour-derived extracellular vesicles (tdEVs) in castration-resistant prostate cancer (CRPC) patients are present at around 20 times higher frequencies than CTCs and have equivalent prognostic power. In this study, we explored the presence of tdEVs in other cancers and their association with OS. METHODS: The open-source ACCEPT software was used to automatically enumerate tdEVs in digitally stored CellSearch® images obtained from previously reported CTC studies evaluating OS in 190 CRPC, 450 metastatic colorectal cancer (mCRC), 179 metastatic breast cancer (MBC) and 137 non-small cell lung cancer (NSCLC) patients before the initiation of a new treatment. RESULTS: Presence of unfavourable CTCs and tdEVs is predictive of OS, with respective hazard ratios (HRs) of 2.4 and 2.2 in CRPC, 2.7 and 2.2 in MBC, 2.3 and 1.9 in mCRC and 2.0 and 2.4 in NSCLC, respectively. CONCLUSIONS: tdEVs have equivalent prognostic value as CTCs in the investigated metastatic cancers. CRPC, mCRC, and MBC (but not NSCLC) patients with favourable CTC counts can be further prognostically stratified using tdEVs. Our data suggest that tdEVs could be used in clinical decision-making.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Vesículas Extracelulares / Células Neoplásicas Circulantes / Metástasis de la Neoplasia / Neoplasias Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Año: 2020 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Vesículas Extracelulares / Células Neoplásicas Circulantes / Metástasis de la Neoplasia / Neoplasias Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Año: 2020 Tipo del documento: Article