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Circulating Tumour Cell Numbers Correlate with Platelet Count and Circulating Lymphocyte Subsets in Men with Advanced Prostate Cancer: Data from the ExPeCT Clinical Trial (CTRIAL-IE 15-21).
- Source :
-
Cancers [Cancers (Basel)] 2021 Sep 18; Vol. 13 (18). Date of Electronic Publication: 2021 Sep 18. - Publication Year :
- 2021
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Abstract
- Interactions between circulating tumour cells (CTCs) and platelets are thought to inhibit natural killer(NK)-cell-induced lysis. We attempted to correlate CTC numbers in men with advanced prostate cancer with platelet counts and circulating lymphocyte numbers. Sixty-one ExPeCT trial participants, divided into overweight/obese and normal weight groups on the basis of a BMI ≥ 25 or <25, were randomized to participate or not in a six-month exercise programme. Blood samples at randomization, and at three and six months, were subjected to ScreenCell filtration, circulating platelet counts were obtained, and flow cytometry was performed on a subset of samples ( n = 29). CTC count positively correlated with absolute total lymphocyte count (r <superscript>2</superscript> = 0.1709, p = 0.0258) and NK-cell count (r <superscript>2</superscript> = 0.49, p < 0.0001). There was also a positive correlation between platelet count and CTC count (r <superscript>2</superscript> = 0.094, p = 0.0001). Correlation was also demonstrated within the overweight/obese group ( n = 123, p < 0.0001), the non-exercise group ( n = 79, p = 0.001) and blood draw samples lacking platelet cloaking ( n = 128, p < 0.0001). By flow cytometry, blood samples from the exercise group ( n = 15) had a higher proportion of CD3+ T-lymphocytes ( p = 0.0003) and lower proportions of B-lymphocytes ( p = 0.0264) and NK-cells ( p = 0.015) than the non-exercise group ( n = 14). These findings suggest that CTCs engage in complex interactions with the coagulation cascade and innate immune system during intravascular transit, and they present an attractive target for directed therapy at a vulnerable stage in metastasis.
Details
- Language :
- English
- ISSN :
- 2072-6694
- Volume :
- 13
- Issue :
- 18
- Database :
- MEDLINE
- Journal :
- Cancers
- Publication Type :
- Academic Journal
- Accession number :
- 34572916
- Full Text :
- https://doi.org/10.3390/cancers13184690