Blombäck M, Hedlund P O, Säwe U
Dept of Clinical Chemistry and Blood Coagulation, Karolinska Hospital, Stockholm, Sweden.
Thromb Res. 1988 Jan 1;49(1):111-21. doi: 10.1016/0049-3848(88)90364-7.
An analysis of haemostatic variables was done in 31 prostate cancer patients treated with oestrogens (13 pts), estramustine phosphate (7 pts) or orchidectomy (11 pts) before, at about 7 weeks and 6 months of treatment. Six patients treated with either of the drugs developed venous thromboembolism or ischemic vascular disease. Already before treatment there were changes indicating some activation of blood coagulation, fibrinolysis and kallikrein systems. The drug treated group showed significant changes in several variables: i.e. increase in factor VII, plasminogen and prekallikrein but also a decrease in antithrombin and in inhibitors to the fibrinolytic and kallikrein system. Significant difference between the drug treated groups was found in circulating platelet aggregates and in kallikrein inhibiting activity. Tissue plasminogen activator capacity was significantly lower in the drug treated patients with complications than in those without. The study also showed that in addition to the assay of the tissue plasminogen activator capacity during the first weeks of therapy it might be helpful in predicting cardiovascular complications to investigate platelet aggregates, prothrombin complex, factor X, von Willebrand factor antigen, fibrinogen, antithrombin, fibrino-peptide A, and the inhibitors of fibrinolysis as well as C1-esterase inhibitor.
对31例接受雌激素治疗(13例)、磷酸雌莫司汀治疗(7例)或睾丸切除术治疗(11例)的前列腺癌患者在治疗前、治疗约7周和6个月时的止血变量进行了分析。接受这两种药物之一治疗的6例患者发生了静脉血栓栓塞或缺血性血管疾病。在治疗前就已经有一些变化,表明凝血、纤维蛋白溶解和激肽释放酶系统有一定程度的激活。药物治疗组在几个变量上有显著变化:即因子VII、纤溶酶原和前激肽释放酶增加,但抗凝血酶以及纤维蛋白溶解和激肽释放酶系统的抑制剂减少。在循环血小板聚集体和激肽释放酶抑制活性方面,发现药物治疗组之间存在显著差异。有并发症的药物治疗患者的组织纤溶酶原激活剂能力显著低于无并发症的患者。该研究还表明,除了在治疗的第一周测定组织纤溶酶原激活剂能力外,研究血小板聚集体、凝血酶原复合物、因子X、血管性血友病因子抗原、纤维蛋白原、抗凝血酶、纤维肽A以及纤维蛋白溶解抑制剂和C1酯酶抑制剂可能有助于预测心血管并发症。