Nagel R, Leistenschneider W
Urologe A. 1983 May;22(3):162-6.
In addition to surveying biochemistry, clinical findings and side effects of Estramustin Phosphate therapy, this paper gives an account of our own results with primary and secondary Estramustin Phosphate therapy. A total number of 118 patients have been examined in three different studies since 1970. Apart from conventional clinical control examinations, an additional accurate parameter applied to control therapy response was cytological analysis of therapy induced regression signs in primary tumor. Thus objective therapy response was established for 87% resp. 93% of the patients on primary Estramustin Phosphate therapy, and for 35% resp. 45% of those on secondary therapy. Patients with cytologically poor therapy response 3 months after beginning of therapy entered significantly earlier into clinical progression than patients with favorable therapy response, with clinical progression being additionally and essentially influenced by the pretherapeutical metastatic stage. Gastro-intestinal side-effects were prevalent in 79% of cases on intravenous administration of the drug, while on oral administration they were found to be three times less.
除了研究磷酸雌莫司汀疗法的生物化学、临床发现及副作用外,本文还介绍了我们在原发性和继发性磷酸雌莫司汀疗法方面取得的成果。自1970年以来,在三项不同研究中总共检查了118例患者。除了常规临床对照检查外,另一个用于控制治疗反应的精确参数是对原发性肿瘤中治疗引起的消退迹象进行细胞学分析。因此,接受原发性磷酸雌莫司汀治疗的患者中,分别有87%和93%出现了客观治疗反应,接受继发性治疗的患者中,这一比例分别为35%和45%。治疗开始3个月后细胞学治疗反应较差的患者比治疗反应良好的患者更早进入临床进展期,临床进展还受到治疗前转移阶段的额外且重要的影响。静脉给药时,79%的病例出现胃肠道副作用,而口服给药时副作用发生率则低三倍。