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Updated: Jul 2, 2026

A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
Tissue factor-related biomarkers during combined androgen blockade in patients with prostate cancer: A brief report
Athanasios Klampatsas1, Panagiota Tsiatsiou2, Paraskevoula Koutra2
1Urology Department, ‛Theagenio' Cancer Hospital of Thessaloniki, 43 Paraskevopoulou Str, Thessaloniki, 55133, Greece. aklampat@auth.gr.
Abstract:
Men undergoing combined androgen blockade therapy (CAB) for prostate cancer are at risk of thromboembolism. Tissue factor (TF) and microparticle-associated tissue factor activity (MP-TF) play a role in coagulation and may detect early coagulation changes during hormonal therapy. However, therapy-related hemostatic alterations remain poorly understood. We prospectively studied men with localized and locally advanced prostate cancer treated with CAB through two pathways: radiotherapy (RT) plus CAB (RT + CAB) for localized disease, and radical prostatectomy (RP) followed by adjuvant radiotherapy (ART) and CAB (RP + ART+CAB) for locally advanced disease. We assessed whether TF-related biomarkers were modified during diagnosis and whether this profile remained after 6 months of CAB. We evaluated longitudinal biomarker changes, pathway differences, and their relationship with routine coagulation tests. Circulating TF levels were elevated at baseline and increased after CAB. MP-TF activity remained elevated, with no significant longitudinal change. No significant differences were observed between the treatment pathways (p > 0.05). Routine coagulation parameters remained stable and did not reflect biomarker changes. CAB therapy was associated with increased circulating TF levels and a persistent procoagulant microparticle profile, not reflected by routine coagulation assays. Larger studies with clinical thrombotic endpoints are needed to confirm their clinical relevance.
