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首页> 外文期刊>Urologic oncology >Phase II trial of cisplatin, 5-fluorouracil, and interferon-alpha-2B as first line treatment of advanced urothelial cancer.
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Phase II trial of cisplatin, 5-fluorouracil, and interferon-alpha-2B as first line treatment of advanced urothelial cancer.

机译:顺铂,5-氟尿嘧啶和干扰素-α-2B作为晚期尿路上皮癌的一线治疗的II期试验。

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摘要

Cisplatin based combination chemotherapy remains the mainstay for treatment of advanced urothelial cancer. The combination of 5-fluorouracil and interferon has been found to be effective second line treatment of advanced urothelial cancer. Hence, we tested the combination of cisplatin, 5-fluorouracil and interferon as first line therapy in advanced urothelial cancer. Eligible patients had to have no prior chemotherapy or interferon. Treatment consisted of cisplatin 80 mg/m(2) on day one, followed by 5-fluorouracil 750 mg/m(2) as a daily infusion for 5 days and interferon alpha 2 B 5 MU/m(2) subcutaneously daily on day 1-5 of 5-fluorouracil infusion. Cycles repeated every 21 days. Eighteen patients, of which sixteen were males were enrolled. Median age was 60 years. All patients had transitional-cell carcinoma. The median number of cycles given was 4. Thirteen patients were evaluable for response. Two patients achieved CR and 3 PR for an overall response rate of 28% (95% confidence interval 7% to 49%). Median response duration was 8.3 months. Median survival was 5.5 months. Four patients died secondary to chemotherapy toxicities. Those were GI perforation in one, bronchopneumonia in one, acute renal failure in one and one patient died at home 3 weeks following the third cycle. The above regimen demonstrates excessive toxicity and moderate activity. It cannot be recommended in its present format. Novel anti-cancer agents need to explored.
机译:基于顺铂的联合化疗仍然是治疗晚期尿路上皮癌的主要手段。已经发现5-氟尿嘧啶和干扰素的组合是晚期尿路上皮癌的有效二线治疗。因此,我们测试了顺铂,5-氟尿嘧啶和干扰素的组合作为晚期尿路上皮癌的一线治疗方法。符合条件的患者必须事先没有化疗或干扰素。治疗包括在第一天的顺铂80 mg / m(2),然后每天输注5-氟尿嘧啶750 mg / m(2),持续5天,每天第二天皮下注射干扰素α2 B 5 MU / m(2)。 1-5的5-氟尿嘧啶输注。周期每21天重复一次。入选了18位患者,其中16位是男性。中位年龄为60岁。所有患者均患有移行细胞癌。给出的周期中位数为4。13位患者的反应可评估。两名患者获得CR和3 PR,总缓解率为28%(95%置信区间为7%至49%)。中位反应持续时间为8.3个月。中位生存期为5.5个月。 4例患者因化疗毒性而死亡。那些是胃肠穿孔,一是支气管肺炎,一是急性肾衰竭,一是三例,在第三周期3周后在家中死亡。上述方案显示出过度的毒性和中等活性。不能推荐采用当前格式。需要探索新型抗癌药。

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