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Tumour-derived extracellular vesicles in blood of metastatic cancer patients associate with overall survival

Nanou, A., Miller, M. C., Zeune, L. L., de Wit, S., Punt, C. J. A., Groen, H. J. M., Hayes, D. F., de Bono, J. S. & Terstappen, L. W. M. M., 15-Jan-2020, In : British Journal of Cancer. 11 p.

Research output: Contribution to journalArticleAcademicpeer-review

  • Afroditi Nanou
  • M Craig Miller
  • Leonie L Zeune
  • Sanne de Wit
  • Cornelis J A Punt
  • Harry J M Groen
  • Daniel F Hayes
  • Johann S de Bono
  • Leon W M M Terstappen

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 (R) 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.

Original languageEnglish
Number of pages11
JournalBritish Journal of Cancer
Publication statusPublished - 15-Jan-2020

    Keywords

  • RESISTANT PROSTATE-CANCER, BRANCHED EVOLUTION, PROGRESSION-FREE, CELLS, EXOSOMES, PREDICT, HETEROGENEITY, MICROVESICLES, EXPRESSION, BIOMARKERS

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