Noguchi Masanori, Noda Shinshi, Yoshida Masaki, Ueda Shoichi, Shiraishi Taizo, Itoh Kyogo
Department of Urology, Kurume University School of Medicine, Kurume, Japan.
Int J Urol. 2004 Feb;11(2):103-9. doi: 10.1111/j.1442-2042.2004.t01-1-00748.x.
The present study was undertaken mainly to investigate whether chemohormonal therapy with estramustine phosphate plus luteinizing hormone-releasing hormone (LHRH) agonist has a more beneficial effect than the hormonal therapy with flutamide plus LHRH agonist for newly diagnosed patients with metastatic prostate cancer.
A total of 57 patients with metastatic prostate cancer aged 59-80 years (median 74 years) were entered in the study and were randomized to the treatment of estramustine phosphate (560 mg/day) plus LHRH agonist (estramustine group) or flutamide (375 mg/day) plus LHRH agonist (flutamide group) with stratification for the degree of performance status, histological differentiation and bone metastasis.
Both of the treatment regimens were well tolerated with similar incidences of adverse drug reactions. The overall response rates (complete response plus partial response) at 12 weeks after treatment in the estramustine and flutamide groups were 76 and 55%, respectively. The median time to objective progression for the estramustine group (25.4 months) was longer than that of the flutamide group (14.6 months). The serum levels of follicle stimulating hormone and testosterone were significantly lower in the estramustine group.
Chemohormonal therapy with estramustine phosphate plus LHRH agonist showed longer clinical progression-free survival than the hormonal therapy with flutamide plus LHRH agonist (P = 0.03), although there was no significant difference in the overall survival. A larger-scaled trial with more statistical power is required to clarify that the former regimen is more beneficial than the latter for newly diagnosed patients with advanced prostate cancer.
本研究主要旨在调查对于新诊断的转移性前列腺癌患者,磷酸雌莫司汀联合促黄体生成激素释放激素(LHRH)激动剂的化学激素疗法是否比氟他胺联合LHRH激动剂的激素疗法具有更有益的效果。
共有57例年龄在59至80岁(中位年龄74岁)的转移性前列腺癌患者进入本研究,并根据体能状态、组织学分化程度和骨转移情况进行分层,随机分为接受磷酸雌莫司汀(560毫克/天)联合LHRH激动剂治疗组(雌莫司汀组)或氟他胺(375毫克/天)联合LHRH激动剂治疗组(氟他胺组)。
两种治疗方案耐受性良好,药物不良反应发生率相似。雌莫司汀组和氟他胺组治疗12周后的总缓解率(完全缓解加部分缓解)分别为76%和55%。雌莫司汀组至客观进展的中位时间(25.4个月)长于氟他胺组(14.6个月)。雌莫司汀组的促卵泡生成素和睾酮血清水平显著较低。
磷酸雌莫司汀联合LHRH激动剂的化学激素疗法比氟他胺联合LHRH激动剂的激素疗法显示出更长的临床无进展生存期(P = 0.03),尽管总生存期无显著差异。需要进行一项具有更大统计效力的更大规模试验,以阐明对于新诊断的晚期前列腺癌患者,前一种方案比后一种方案更有益。