Raghavan D, Coorey G, Rosen M, Page J, Farebrother T
Urological Cancer Research Unit, Royal Prince Alfred Hospital, Sydney, Australia.
Semin Oncol. 1996 Dec;23(6 Suppl 14):20-3.
The management of metastatic prostate cancer that has relapsed after initial hormonal manipulation remains a major problem, with the majority of patients dying within 12 months. Their clinical course is frequently characterized by progressive debilitation, pain, and other tumor-related symptoms. A phase II, non-randomized multicenter clinical trial was carried out in Australia in 1985-1986 to assess the efficacy and toxicity of mitoxantrone. Substantial anticancer activity was shown against hormone-refractory prostate cancer, indicated by reduction in tumor-related symptoms, improvement in quality of life indices, and a median survival of 10 months in patients with a heavy tumor burden. Although it is not possible to equate this nonrandomized series more fully with current experience since routine prostate-specific antigen measurement was not performed, the median survival of 10 months was equivalent to or better than the survival times reported from most other institutional reports of the time. Even more importantly, however, major improvements were noted in such subjective indices as reduction in pain, weight gain, and performance status. Toxicity was also acceptable, with the major side effect being asymptomatic myelosuppression.
初始激素治疗后复发的转移性前列腺癌的管理仍然是一个主要问题,大多数患者在12个月内死亡。他们的临床病程通常以进行性衰弱、疼痛和其他肿瘤相关症状为特征。1985 - 1986年在澳大利亚进行了一项II期非随机多中心临床试验,以评估米托蒽醌的疗效和毒性。对激素难治性前列腺癌显示出显著的抗癌活性,表现为肿瘤相关症状减轻、生活质量指数改善,以及肿瘤负荷重的患者中位生存期为10个月。尽管由于未进行常规前列腺特异性抗原测量,无法将这个非随机系列与当前经验更全面地等同起来,但10个月的中位生存期与当时大多数其他机构报告的生存时间相当或更好。然而,更重要的是,在疼痛减轻、体重增加和身体状况等主观指标上有了显著改善。毒性也是可以接受的,主要副作用是无症状骨髓抑制。