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Bladder preservation by neoadjuvant chemotherapy followed by gemcitabine as radiosensitizer for muscle-invasive transitional cell carcinoma of the urinary bladder after maximal TURBT

机译:新辅助化疗后膀胱保存,继而吉西他滨作为放射增敏剂治疗最大TURBT后膀胱肌肉浸润性移行细胞癌

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Objectives: To evaluate prospective phase II study of neoadjuvant chemotherapy and gemcitabine as radiosensetizer in conservative management of muscle-invasive transitional cell carcinoma of the urinary bladder . Patients and methods: Forty eight patients with transitional cell carcinoma, stage T2b-T4aN0M0, bladder cancer underwent maximal TURBT followed by neoadjuvant chemotherapy carboplatin AUC5 D1 and gemcitabine 1000 mg/m2 D1and D8 repeated every 21 days for 2 cycles followed by concurrent radiation 65Gy with Gemcitabine given intravenously at 100 mg/m2 on days 1, 8, 15, 22, 29, 36. The end points were tumor response, toxicity and survival. Results: The neoadjuvant as well as concurrent chemoradiotherapy were tolerated with low toxicity rates as the following, Urinary Bladder irritative symptoms developed in 2 patients (4.1%) and successfully managed with antimuscarinic. Neutropenia occurred in 4 patients (8.3%) while febrile neutropenis in 1 patient (2%). Nausea and vomiting occurred in 6 patients (12.5%) while nephrotoxicity occurred in 2 patients (4.1%). Complete response was noted in 28 patients (58.3%). Partial response was observed in 15 patients (31.25%). At time of analysis, there were fourteen deaths (29.1%) due to bladder cancer. Three-year cancer specific survival (CSS) and overall survival (OS) were 69.9% and 66.6%. Twenty one patients (43.7%) were tumor free and kept their bladder at time of analysis . Conclusion: Neoadjuvant chemotherapy followed by gemcitabine as radiosensitizer for muscle-invasive transitional cell carcinoma of the urinary bladder was tolerable with good bladder preservation and overall survival .
机译:目的:评价新辅助化疗和吉西他滨作为放射增敏剂在保守治疗膀胱肌浸润性移行细胞癌中的Ⅱ期研究。患者和方法:对48例T2b-T4aN0M0期移行细胞癌,膀胱癌患者进行最大的TURBT治疗,然后每21天重复进行新辅助化疗卡铂AUC5 D1和吉西他滨1000 mg / m 2 D1和D8在第1、8、15、22、29、36天第2个周期后,同时以100 mg / m 2 静脉给予吉西他滨65Gy放射。终点为肿瘤反应,毒性和生存期。结果:新辅助疗法和同期放化疗均具有较低的毒性,耐受性如下:2例患者(4.1%)出现膀胱膀胱刺激性症状,并成功使用抗毒蕈碱治疗。中性粒细胞减少症发生在4例患者中(8.3%),而发热性中性粒细胞减少症在1例患者中发生(2%)。恶心和呕吐发生在6例患者中(12.5%),而肾毒性发生在2例患者中(4.1%)。 28名患者(58.3%)观察到完全缓解。在15例患者中观察到部分缓解(31.25%)。在分析时,有14例(29.1%)因膀胱癌死亡。三年癌症特异性生存率(CSS)和总体生存率(OS)分别为69.9%和66.6%。在分析时有21名患者(43.7%)没有肿瘤并且保留了膀胱。结论:新辅助化疗后联合吉西他滨作为放射增敏剂治疗膀胱肌浸润性移行细胞癌具有良好的膀胱保存能力和总体生存率。

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