Dawson N A, Wilding G, Weiss R B, McLeod D G, Linehan W M, Frank J A, Jacob J L, Gelmann E P
Department of Medicine, Walter Reed Army Medical Center, Washington, DC 20307-5001.
Cancer. 1992 Jan 1;69(1):213-8. doi: 10.1002/1097-0142(19920101)69:1<213::aid-cncr2820690135>3.0.co;2-v.
Fifteen patients with previously untreated metastatic prostate cancer were treated on a pilot trial with a combination of maximal androgen blockade plus intermittent cytotoxic therapy after androgen priming to stimulate cell division. Androgen blockage was carried out using a gonadotropin-releasing hormone analog (leuprolide) plus a nonsteroidal antiandrogen (flutamide). Carboplatin (CBDCA) (800 mg/m2) was given intravenously every 28 days, preceded for 3 days and followed for 3 days by androgen treatment with fluoxymesterone (5 mg orally twice a day), during which time flutamide was discontinued. Three patients (20%) achieved a complete response (CR), and eight patients (53.3%) achieved a partial response (PR). Four patients (26.7%) had stable disease (SD). The median progression-free survival (PFS) time was 31 months. Nine of 15 patients (60%) remain alive with a median follow-up time of 42+ months (range, 22 to 54 months). Grade 4 thrombocytopenia and Grades 3 or 4 leukopenia were experienced in 87% and 80% of patients, respectively, requiring dose reductions of CBDCA in 85% of the cycles. Six of 15 patients experienced a flare in bone pain with androgen priming. There were no associated spinal cord compressions; however, exclusion of impending spinal cord compression was required before entrance on study.
15例既往未接受过治疗的转移性前列腺癌患者参加了一项试验性研究,采用最大雄激素阻断联合间歇性细胞毒性疗法,并在雄激素启动以刺激细胞分裂后进行。雄激素阻断采用促性腺激素释放激素类似物(亮丙瑞林)加非甾体类抗雄激素药物(氟他胺)。每28天静脉注射卡铂(CBDCA)(800mg/m²),在注射前3天及注射后3天给予氟甲睾酮雄激素治疗(口服5mg,每日2次),在此期间停用氟他胺。3例患者(20%)达到完全缓解(CR),8例患者(53.3%)达到部分缓解(PR)。4例患者(26.7%)疾病稳定(SD)。无进展生存期(PFS)的中位数为31个月。15例患者中有9例(60%)仍然存活,中位随访时间为42+个月(范围22至54个月)。分别有87%和80%的患者出现4级血小板减少和3级或4级白细胞减少,85%的周期需要减少CBDCA剂量。15例患者中有6例在雄激素启动时出现骨痛加剧。无相关脊髓压迫情况;然而,在入组研究前需要排除即将发生的脊髓压迫。