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Paclitaxel, ifosfamide, nedaplatin (TIN) for patients with metastatic urothelial cancer

机译:紫杉醇,Ifosfamide,Nedaplatin(锡)用于转移性尿路上皮癌症

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TIN (ifosfamide 1.5 g/m2 daily for 3 days, paclitaxel 175 mg/m2, and nedaplatin 70 mg/m2 on day 1) was administered to patients with metastatic urothelial cancer previously treated by platinum-based chemotherapy and repeated every 4 weeks. Four patients received maintenance therapy, which consisted of 5'-DFUR 800 mg/day orally for 12 weeks and 1 subsequent course of TIN. This therapy regimen was repeated for 2 years from initiation of TIN. Eleven of 12 patients (91.6%) demonstrated a major response (3 complete responses, 8 partial responses), with durations of response ranging from 3 to 20 months. Progression-free survival time was from 0 to 20 months (median 8 months). One-year progression-free survival rate was 45.8%. Overall survival time was from 2 to 20 months (median 10.5 months). One-year overall survival rate was 53.5%. Grade 3/4 hematologic toxicity involved neutropenia in 100% and thrombocytopenia in 33.3%. Febrile neutropenia was observed in 5 patients (41.6%). Grade 3 nonhematologic toxicity involved malaise in 15.3%. No patient discontinued this therapy because of complications. TIN is a potent, well-tolerated regimen for previously treated patients with urothelial cancer.
机译:锡(Ifosfamide 1.5g / m 2每天3天,紫杉醇175mg / m 2和第1天的Nedaplatin 70mg / m 2)给先前通过铂类化疗先前治疗的转移性尿道癌患者施用,并每4周重复一次。四名患者接受维持治疗,其由5'-DFUR 800 mg /天口服组成12周和1个后续锡。将该治疗方案重复2年,从锡开始。 11名患者(91.6%)展示了一个重大反应(3个完全反应,8个部分反应),持续时间持续3至20个月。无进展的生存时间为0至20个月(中位数8个月)。一年的无进展生存率为45.8%。总生存时间为2至20个月(中位数10.5个月)。一年的总生存率为53.5%。 3/4级血液学毒性涉及100%和血小板减少的中性粒细胞减少症33.3%。在5名患者(41.6%)中观察到发热的中性粒细胞贫乏。 3级非活性学毒性涉及15.3%的萎靡。由于并发症,没有患者停止这种治疗。锡是一种有效的,可耐受耐受的方案,用于先前治疗的尿路上癌症患者。

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