Perry C M, McTavish D
Adis International Limited, Auckland, New Zealand.
Drugs Aging. 1995 Jul;7(1):49-74. doi: 10.2165/00002512-199507010-00006.
Estramustine phosphate sodium (estramustine phosphate), a unique antitumour agent, is selectively taken up by prostate cells and exerts antineoplastic effects by interfering with microtubule of dynamics and by reducing plasma levels of testosterone. In noncomparative studies of estramustine phosphate in patients with hormone-refractory disease, objective response rates ranging from 19 to 69% have been reported. Preliminary clinical investigations indicate that combining estramustine phosphate with vinblastine, etoposide or paclitaxel improves objective response rates over single-agent treatment, although no survival benefit over single-agent treatment has been demonstrated to date. In comparative studies, estramustine phosphate produces similar objective response rates to conventional antineoplastic agents in patients with hormone-refractory prostate cancer. In previously untreated patients with advanced metastatic hormone-responsive prostate cancer, objective responses are achieved in approximately 80% of patients. Estramustine phosphate appears to be at least as effective as estrogen or flutamide therapy in these patients. Nausea and vomiting are the most frequently observed adverse effects of treatment with estramustine phosphate. While these symptoms are usually mild to moderate in nature, they may occasionally be more troublesome to the patient and necessitate withdrawal of treatment. Cardiovascular complications are a more serious, though less frequently encountered, adverse effect of the drug. However, these complications may be avoided by careful patient selection and prophylactic treatment measures. Unlike some other antineoplastic agents, estramustine phosphate is rarely associated with myelosuppression. In addition to producing similar objective response rates to other established agents, estramustine phosphate improves the subjective status of many patients and has been shown to reduce the intensity of pain and improve the performance status of patients.(ABSTRACT TRUNCATED AT 250 WORDS)
磷酸雌莫司汀钠(雌莫司汀磷酸盐)是一种独特的抗肿瘤药物,它能被前列腺细胞选择性摄取,并通过干扰微管动力学以及降低睾酮血浆水平发挥抗肿瘤作用。在对激素难治性疾病患者进行的磷酸雌莫司汀非对照研究中,报告的客观缓解率为19%至69%。初步临床研究表明,将磷酸雌莫司汀与长春碱、依托泊苷或紫杉醇联合使用,与单药治疗相比可提高客观缓解率,不过迄今为止尚未证明联合治疗比单药治疗有生存获益。在对照研究中,对于激素难治性前列腺癌患者,磷酸雌莫司汀产生的客观缓解率与传统抗肿瘤药物相似。在先前未经治疗的晚期转移性激素敏感性前列腺癌患者中,约80%的患者可实现客观缓解。在这些患者中,磷酸雌莫司汀似乎至少与雌激素或氟他胺治疗一样有效。恶心和呕吐是磷酸雌莫司汀治疗最常观察到的不良反应。虽然这些症状通常性质为轻至中度,但偶尔可能对患者来说更麻烦,需要停药。心血管并发症是该药物更严重但较少见的不良反应。然而,通过仔细选择患者和采取预防性治疗措施可避免这些并发症。与其他一些抗肿瘤药物不同,磷酸雌莫司汀很少引起骨髓抑制。除了产生与其他已确立药物相似的客观缓解率外,磷酸雌莫司汀还改善了许多患者的主观状态,并已证明可减轻疼痛强度和改善患者的体能状态。(摘要截选至250词)