Seal U S, Doe R P, Byar D P, Corle D K
Cancer. 1976 Sep;38(3):1108-17. doi: 10.1002/1097-0142(197609)38:3<1108::aid-cncr2820380310>3.0.co;2-l.
Fibrinogen and plasminogen were measured in plasma samples from prostatic cancer patients before and after 3 months of treatment with either Premarin, Provera, Provera and diethylstilbestrol, one of three doses of diethylstilbestrol, or placebo. Plasminogen levels generally were increased significantly with the estrogens but were unchanged following placebo or Provera treatment. Pretreatment plasminogen levels in Study 3 were significantly lower (p less than .001) than in Study 2. Plasminogen pretreatment levels were significantly correlated with age, hemoglobin, body weight, and blood pressure. Fibrinogen pretreatment levels were significantly elevated above normal. They were not significantly with age, hemoglobin, body weight, or blood pressure. Fibrinogen levels generally were significantly decreased by the estrogens. Comparisons of means of pretreatment fibrinogen and plasminogen levels from patients dying during the first year of the study with the mean pretreatment levels of the patient group alive after 1 year on study yielded no significant differences. Death rates were calculated by pretreatment plasminogen or fibrinogen for all treatments of all Stage III and Stage IV patients combined for Study 2 and Study 3 separately. Such rates were calculated for all causes combined and for deaths from prostatic cancer or cardiovascular disease separately. The levels of plasminogen were significnatly negatively correlated with death rate from all causes combined and with cardiovascular disease considered separately, but not with death from prostatic cancer. The levels of fibrinogen were signigicantly positively correlated with death rates from all cuses and nearly significantly with prostatic cancer, but not cardiovascular disease. Elvated pretreatment fibrinogen levels were associated with an increased proportion of deaths at 1 year from all causes and from cancer of the prostate.
在前列腺癌患者接受以下治疗3个月前后,检测其血浆样本中的纤维蛋白原和纤溶酶原水平:结合雌激素、醋酸甲羟孕酮、醋酸甲羟孕酮与己烯雌酚、三种剂量己烯雌酚中的一种,或安慰剂。纤溶酶原水平通常在使用雌激素后显著升高,但在使用安慰剂或醋酸甲羟孕酮治疗后无变化。研究3中的治疗前纤溶酶原水平显著低于研究2(p<0.001)。纤溶酶原治疗前水平与年龄、血红蛋白、体重和血压显著相关。纤维蛋白原治疗前水平显著高于正常。它们与年龄、血红蛋白、体重或血压无显著相关性。纤维蛋白原水平通常在使用雌激素后显著降低。将研究第一年死亡患者的治疗前纤维蛋白原和纤溶酶原水平均值与研究1年后存活患者组的治疗前平均水平进行比较,未发现显著差异。分别计算研究2和研究3中所有III期和IV期患者接受所有治疗的治疗前纤溶酶原或纤维蛋白原的死亡率。计算所有原因合并的死亡率以及分别因前列腺癌或心血管疾病死亡的死亡率。纤溶酶原水平与所有原因合并的死亡率以及单独考虑的心血管疾病死亡率显著负相关,但与前列腺癌死亡率无关。纤维蛋白原水平与所有原因的死亡率显著正相关,与前列腺癌死亡率几乎显著正相关,但与心血管疾病死亡率无关。治疗前纤维蛋白原水平升高与1年时所有原因和前列腺癌死亡比例增加相关。