Barroso-Sousa Romualdo, da Fonseca Leonardo Gomes, Souza Karla Teixeira, Chaves Ana Carolina Ribeiro, Kann Ariel Galapo, de Castro Gilberto, Dzik Carlos
Division of Medical Oncology, Instituto do Câncer do Estado de São Paulo (ICESP), Hospital das Clínicas da Faculdade de Medicina, Universidade de São Paulo, Av. Dr. Arnaldo 251, 5o andar, São Paulo, 01246-000, São Paulo, Brazil,
Med Oncol. 2015 Jan;32(1):443. doi: 10.1007/s12032-014-0443-4. Epub 2014 Dec 18.
We evaluated the efficacy and safety of metronomic oral cyclophosphamide (CTX) and prednisone in metastatic castration-resistant prostate cancer (mCRPC) patients. We analyzed retrospectively patients with mCRPC previously treated with docetaxel, and who received metronomic CTX (from 50 mg PO daily to 150 mg PO, 14 days/7 days off) and prednisone 10 mg PO daily between September 2009 and April 2014 were analyzed. The primary endpoint was prostate-specific antigen (PSA) decrease ≥50 %. Secondary analysis included PSA decrease ≥30 %, time-to-treatment failure (TTF) and toxicity. Demographics and baseline characteristics were summarized using descriptive statistics. PSA response and adverse events were reported as relative rates. Kaplan-Meier estimates were calculated and plotted for time-to-event endpoints. Forty patients were evaluated. The median age was 69 years old (52-86), 12 (30.0 %) patients presented a Karnofsky performance status (KPS) of <80 %, and 34 (85 %) presented with bone with or without nodal metastases. Median pre-treatment PSA was 192 ng/dL (7-2696 ng/dL). All patients were previously exposed to docetaxel, including 33 (82.5 %) with docetaxel-refractory disease. PSA response rate was achieved in eight (20.0 %) out of 40 patients. Additionally, PSA declines of ≥30 % occurred in 14 (35.0 %) patients. The median TTF was 3 months (95 % confidence interval 2.5-3.5). The treatment was well tolerated. Grade 3/4 lymphopenia was reported in 11 (27.5 %) patients and was the only grade 3-4 toxicity reported. Metronomic oral CTX showed activity and safety in docetaxel-pretreated mCRPC patients. This regimen deserves further investigation in this setting.
我们评估了节拍口服环磷酰胺(CTX)和泼尼松在转移性去势抵抗性前列腺癌(mCRPC)患者中的疗效和安全性。我们回顾性分析了先前接受多西他赛治疗的mCRPC患者,这些患者在2009年9月至2014年4月期间接受了节拍CTX(从每日口服50毫克至150毫克,服用14天,停药7天)和每日口服10毫克泼尼松治疗。主要终点是前列腺特异性抗原(PSA)下降≥50%。次要分析包括PSA下降≥30%、治疗失败时间(TTF)和毒性。使用描述性统计总结人口统计学和基线特征。PSA反应和不良事件以相对率报告。计算Kaplan-Meier估计值并绘制事件发生时间终点图。对40名患者进行了评估。中位年龄为69岁(52 - 86岁),12名(30.0%)患者的卡诺夫斯基体能状态(KPS)<80%,34名(85%)患者有骨转移,伴或不伴有淋巴结转移。治疗前PSA中位数为192 ng/dL(7 - 2696 ng/dL)。所有患者均曾接受多西他赛治疗,其中33名(82.5%)患有多西他赛难治性疾病。40名患者中有8名(20.0%)达到PSA反应率。此外,14名(35.0%)患者的PSA下降≥30%。中位TTF为3个月(95%置信区间2.5 - 3.5)。该治疗耐受性良好。11名(27.5%)患者报告有3/4级淋巴细胞减少,这是唯一报告的3 - 4级毒性。节拍口服CTX在接受多西他赛预处理的mCRPC患者中显示出活性和安全性。该方案在这种情况下值得进一步研究。