首页> 外文期刊>British Journal of Clinical Pharmacology >Effect of local hyperthermia of the bladder on mitomycin C pharmacokinetics during intravesical chemotherapy for the treatment of superficial transitional cell carcinoma.
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Effect of local hyperthermia of the bladder on mitomycin C pharmacokinetics during intravesical chemotherapy for the treatment of superficial transitional cell carcinoma.

机译:膀胱局部热疗对膀胱浅表移行细胞癌化疗期间丝裂霉素C药代动力学的影响。

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AIMS: To assess the effect of local hyperthermia on the systemic absorption of mitomycin C (MMC) during intravesical chemotherapy for the treatment of superficial transitional cell carcinoma of the bladder, and to establish the likely safety of this procedure. METHODS: Group 1 (n = 12) received 20 mg intravesical MMC plus local hyperthermia, group 2 (n = 13) 20 mg MMC alone, group 3 (n = 16) 40 mg MMC plus local hyperthermia and group 4 (n = 10) 40 mg MMC alone. Patients in groups 1, 2, and 4 underwent post-tumour resection adjuvant treatment, whereas those in group 3 still had tumour present and were treated to eradicate it. Intravesical instillation lasted 60 min, with the solution (50 ml) being replaced after the first 30 min. Blood samples were taken before, and every 15 min during instillation. MMC concentrations in plasma and in urine were determined by h.p.l.c. RESULTS: The highest MMC plasma concentration (67.9 ng ml(-1)) occurred in a patient in group 3. This value was well below the threshold concentration (400 ng ml-1) for myelosuppression. Local hyperthermia associated with the intravesical chemotherapy enhanced plasma MMC concentrations at 30, 45 and 60 min compared with chemotherapy alone (Group 1 vs 2, P < or = 0.008). Systemic exposure to MMC was not significantly increased by doubling the intravesical dose when intravesical chemotherapy alone was administered. Patients in group 3 displayed the highest degree of MMC absorption and the greatest variability in pharmacokinetics between patients. CONCLUSIONS: Local hyperthermia enhances the systemic absorption of MMC during intravesical chemotherapy for bladder cancer. In the doses used, plasma MMC concentrations were always more than six times lower than those shown to cause toxicity.
机译:目的:评估局部热疗对膀胱浅表移行细胞癌的膀胱内化疗期间丝裂霉素C(MMC)全身吸收的影响,并确定该程序的可能安全性。方法:第1组(n = 12)接受20 mg膀胱内MMC加局部热疗,第2组(n = 13)单独接受20 mg MMC,第3组(n = 16)接受40 mg MMC加局部热疗,第4组(n = 10) )单独40毫克MMC。第1、2和4组的患者接受了肿瘤切除后的辅助治疗,而第3组的患者仍然存在肿瘤,并接受了根除治疗。膀胱内滴注持续60分钟,在前30分钟后更换溶液(50 ml)。在滴注之前和滴注期间每15分钟采集一次血样。通过h.p.l.c.测定血浆和尿液中MMC的浓度。结果:3组患者的最高MMC血浆浓度(67.9 ng ml(-1))发生在该水平,远低于骨髓抑制的阈值浓度(400 ng ml-1)。与单独化疗相比,与膀胱内化疗相关的局部热疗在30、45和60分钟时提高了血浆MMC浓度(第1组与第2组,P <或= 0.008)。当单独进行膀胱内化疗时,通过将膀胱内剂量加倍不会显着增加对MMC的全身暴露。第3组患者之间的MMC吸收程度最高,药代动力学差异最大。结论:局部热疗可增强膀胱癌膀胱内化疗期间MMC的全身吸收。在使用的剂量中,血浆MMC的浓度总是比显示出毒性的浓度低六倍以上。

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