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Paclitaxel and carboplatin in patients with metastatic transitional cell cancer of the urinary tract.

机译:紫杉醇和卡铂在尿路转移性移行细胞癌患者中的应用。

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OBJECTIVES: The combination of methotrexate, vinblastine, doxorubicin, and cisplatin (MVAC) is currently considered the most effective chemotherapy for metastatic transitional cell cancer (TCC) of the urinary tract, but because of its considerable toxicity, alternative regimens appear very interesting. We evaluated the efficacy and toxicity of a combination of paclitaxel and carboplatin as first-line therapy for metastatic TCC. METHODS: Thirty-two patients (8 women, 24 men; mean age 67.03 years, range 50 to 79) with metastatic TCC of the bladder or upper urinary tract were included in the study. Paclitaxel (175 mg/m2) was given as a 3-hour intravenous infusion, carboplatin was dosed to an area under the plasma concentration curve of 5 mg/m/min calculated according to the Calvert formula [(creatinine clearance + 25) x 5] as a 30-minute intravenous infusion immediately after paclitaxel. Response evaluation was performed after every 2 cycles and additional therapy depended on response. The maximum number of cycles was 6. RESULTS: With a mean follow-up of 13.1 months (range 2 to 28), 23 of 32 patients responded to treatment (response rate 71.9%), with 31.3% complete remission (CR) (10 of 32) and 40.6% partial remission (PR) (13 of 32). Four patients (12.5%) had stable disease, and 5 patients (15.6%) showed progression. These results compare well with the outcome after MVAC. Toxicity was mainly characterized by neurotoxicity grade 3 and 4 in 9.4%, grade 3 and 4 leukopenia in 37.5%, and grade 3 thrombocytopenia in 3.1% of the patients. No nephrotoxicity was observed, but all patients developed alopecia. Time to progression after CR was a mean of 7.0 months (range 4 to 13) and after PR a mean of 5.9 months (range 2 to 9). CONCLUSIONS: Paclitaxel/carboplatin is an effective therapy for metastatic TCC, with low toxicity.
机译:目的:甲氨蝶呤,长春碱,阿霉素和顺铂(MVAC)的组合目前被认为是治疗泌尿系转移性移行细胞癌(TCC)的最有效的化学疗法,但由于其毒性大,替代疗法显得非常有趣。我们评估了紫杉醇和卡铂联合作为转移性TCC一线治疗的疗效和毒性。方法:本研究纳入了32例膀胱或上尿路转移性TCC患者(8名女性,24名男性;平均年龄67.03岁,范围50至79)。紫杉醇(175 mg / m2)静脉输注3小时,根据Calvert公式[(肌酐清除率+ 25)x 5,将卡铂给药至血浆浓度曲线下5 mg / m / min的区域。紫杉醇治疗后立即静脉输注30分钟。每2个周期后进行反应评估,其他治疗取决于反应。最大周期数为6。结果:平均随访13.1个月(范围2至28),32例患者中有23例对治疗有反应(缓解率71.9%),完全缓解(CR)占31.3%(10占32)和40.6%的部分缓解(PR)(32之13)。 4名患者(12.5%)病情稳定,而5名患者(15.6%)表现为进展。这些结果与MVAC后的结果相当。毒性的主要特征是神经毒性的3级和4级分别为9.4%,3级和4级白细胞减少症为37.5%,3级血小板减少症为3.1%。没有观察到肾毒性,但所有患者均出现脱发。 CR后平均进展时间为7.0个月(范围4至13),PR后平均进展时间为5.9个月(范围2至9)。结论:紫杉醇/卡铂是治疗转移性TCC的有效方法,毒性低。

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