GU, CNS and Sarcoma Program, Department of Medical Oncology, Vall d'Hebron University Hospital, Universitat Autònoma Barcelona, Passeig Vall d'Hebron 119-129, 08035, Barcelona, Catalonia, Spain.
Clin Transl Oncol. 2014 Jan;16(1):102-6. doi: 10.1007/s12094-013-1045-x. Epub 2013 Apr 20.
To evaluate the efficacy and toxicity of docetaxel regimen as second-line after failure of a platinum-based chemotherapy.
Between May 2005 and June 2008, we retrospectively analyzed the data of 22 patients who had evidence of disease progression after one prior platinum-based regimen for metastatic urothelial carcinoma. Patients were treated with two different docetaxel dose schedules: (1) docetaxel 60 mg/m(2) every 21 days for unfit patients or (2) docetaxel 75 mg/m(2) every 21 days for fit patients.
Median number of docetaxel cycles was three. Overall disease control rate was 18 %. Of the 22 patients, no patient achieved complete or partial response and four patients had stable disease. Median progression-free survival was 1.67 months and median overall survival was 3.12 months. Neutropenia was the most common adverse event.
This study identifies that docetaxel as second-line chemotherapy has low activity and was associated with significant toxicity.
评估多西紫杉醇方案作为铂类化疗失败后的二线治疗的疗效和毒性。
2005 年 5 月至 2008 年 6 月,我们回顾性分析了 22 例先前接受过铂类化疗的转移性尿路上皮癌患者,这些患者在疾病进展后接受了两种不同的多西紫杉醇剂量方案治疗。(1)不适合的患者使用多西紫杉醇 60mg/m2,每 21 天一次;(2)适合的患者使用多西紫杉醇 75mg/m2,每 21 天一次。
中位多西紫杉醇治疗周期数为 3 个。总体疾病控制率为 18%。22 例患者中,无患者完全或部分缓解,4 例患者疾病稳定。中位无进展生存期为 1.67 个月,中位总生存期为 3.12 个月。中性粒细胞减少是最常见的不良反应。
本研究表明,多西紫杉醇作为二线化疗药物活性较低,且与严重毒性相关。