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丝裂霉素C膀胱内电动药物输注治疗非肌层浸润性膀胱癌

[Intravesical Electromotive Drug Administration®(EMDA)with Mitomycin-C for non-muscle invasive bladder cancer].

作者信息

Di Stasi S M, Dutto L, Verri C

出版信息

Urologia. 2008 Oct-Dec;75(4):214-20.

Abstract

Electromotive Drug Administration® (EMDA) offers a means of controlling and enhancing the tissue transport of certain drugs, when applied to a surface epithelium, where they have a local therapeutic effect, in order to increase their efficacy. One application option is the treatment of non-muscle invasive bladder cancer with intravesical mitomycin-C (MMC). Laboratory studies demonstrated that EMDA/MMC can reduce the variability and enhance the drug administration rate into all layers of the bladder wall, and that the applied electric current causes no histological damage to tissue and no chemical modification of MMC. A prospective randomized study, performed in patients with in situ carcinoma, validated the prediction that electromotive enhancement of MMC delivery would provide results superior to those achieved using passive MMC transport. A further randomized study in patients with pT1 bladder cancer demonstrated that a regimen combining intravesical BCG and EMDA/MMC increased the disease-free interval and reduced the recurrence rate, as well as the disease progression and mortality rate if compared with BCG alone. The possibility that BCG may enhance the efficacy of MMC against high-grade pT1 transitional cell carcinoma and in situ carcinoma represents an important new therapeutic perspective in the high-risk non-muscle invasive bladder cancer.

摘要

电动药物导入疗法(Electromotive Drug Administration®,EMDA)提供了一种控制和增强某些药物经体表上皮组织转运的方法,这些药物在体表上皮组织发挥局部治疗作用,以此提高其疗效。一种应用方式是膀胱内灌注丝裂霉素C(MMC)治疗非肌层浸润性膀胱癌。实验室研究表明,EMDA/MMC可降低变异性并提高药物进入膀胱壁各层的给药速率,且施加的电流不会对组织造成组织学损伤,也不会对MMC产生化学修饰。一项针对原位癌患者的前瞻性随机研究证实了以下预测:电动增强MMC递送的效果优于被动MMC转运。另一项针对pT1期膀胱癌患者的随机研究表明,与单独使用卡介苗(BCG)相比,膀胱内灌注BCG与EMDA/MMC联合方案可延长无病间期,降低复发率、疾病进展率和死亡率。BCG可能增强MMC对高级别pT1期移行细胞癌和原位癌疗效的可能性,代表了高危非肌层浸润性膀胱癌重要的新治疗前景。

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