Türkeri Levent, Tanıdır Yılören, Çal Çağ, Özen Haluk, Şahin Hayrettin
Department of Urology, Marmara University School of Medicine, Istanbul, Turkey.
Urol Int. 2010;85(3):261-5. doi: 10.1159/000300571. Epub 2010 Mar 20.
To investigate the efficacy of single or double epirubicin instillation during the early postoperative period (EPP) in intermediate-risk non-muscle-invasive urothelial cancer.
Patients with primary and solitary or multiple (3 or less) Ta (grade 2-3) or T1 (grade 1-2) tumors were enrolled. Patients were randomized to receive either a single dose of 100 mg epirubicin instillation within 6 h or a second 100 mg epirubicin instillation during the 12th-18th hours after a complete TUR-BT. At the end of the 60-month follow-up period, the available data were statistically analyzed. The end-points of the study were determined as disease-free survival, progression and recurrence rates, time to recurrence, and time to progression.
A total of 299 patients from 24 institutions were randomized between January 2002 and June 2004. There were 143 patients from 18 institutions who met the eligibility criteria. The follow-up and disease-free survival periods were 16.9 months and 16 months, respectively. There was no statistical difference in the demographic properties and the end-points between the groups.
A single dose of intravesical 100 mg epirubicin chemotherapy during the early postoperative period for primary intermediate-risk non-muscle-invasive urothelial cancer achieved 16 months of mean disease-free survival. A second intravesical epirubicin instillation did not provide any significant benefit.
探讨早期术后(EPP)单剂量或双剂量表柔比星灌注治疗中危非肌层浸润性尿路上皮癌的疗效。
纳入原发性单发或多发(3个及以下)Ta(2-3级)或T1(1-2级)肿瘤患者。患者被随机分为两组,一组在6小时内接受单剂量100mg表柔比星灌注,另一组在完全经尿道膀胱肿瘤电切术(TUR-BT)后的第12至18小时接受第二次100mg表柔比星灌注。在60个月随访期结束时,对可得数据进行统计学分析。研究的终点指标确定为无病生存期、进展和复发率、复发时间及进展时间。
2002年1月至2004年6月,来自24家机构的299例患者被随机分组。来自18家机构的143例患者符合纳入标准。随访期和无病生存期分别为16.9个月和16个月。两组间人口统计学特征和终点指标无统计学差异。
对于原发性中危非肌层浸润性尿路上皮癌,术后早期单剂量膀胱内灌注100mg表柔比星化疗的平均无病生存期达16个月。第二次膀胱内灌注表柔比星未带来任何显著益处。