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Updates in intravesical electromotive drug administration® of mitomycin-C for non-muscle invasive bladder cancer

机译:丝裂霉素C膀胱电动药物管理®在非肌肉浸润性膀胱癌中的最新进展

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Electromotive drug administration® (EMDA) increases the local drug efficacy by controlling and enhancing transmembranous transport into tissue. EMDA of intravesical mitomycin-C (MMC) has been used for treatment of non-muscle invasive bladder cancer (NMIBC) for about a decade on the basis of laboratory studies that demonstrated an enhanced administration rate of MMC into all bladder wall layers after EMDA compared to standard instillation/passive diffusion (PD). Higher MMC concentrations might have a clinical impact since EMDA was associated with lower recurrence rates than PD in randomized studies. Further data suggest that EMDA/MMC is at least equivalent to BCG in treatment of high-risk bladder tumours. In addition, BCG combined with EMDA/MMC as well as preoperative EMDA/MMC are new therapeutic strategies with promising preliminary results in terms of higher remission rates and longer remission times. In summary, these findings suggest that EMDA for MMC delivery in the bladder could be a major therapeutic breakthrough in the treatment of NMIBC.
机译:电动药物施用(sup>®(EMDA)通过控制和增强跨膜向组织的运输来提高局部药物效力。在实验室研究的基础上,膀胱内丝裂霉素-C(MMC)的EMDA被用于治疗非肌肉浸润性膀胱癌(NMIBC)大约十年了,研究表明,与EMDA相比,MMC对所有膀胱壁层的给药率都有所提高达到标准滴注/被动扩散(PD)。由于随机研究中EMDA的复发率低于PD,因此较高的MMC浓度可能会产生临床影响。进一步的数据表明,EMDA / MMC在治疗高危膀胱肿瘤方面至少等同于BCG。此外,卡介苗联合EMDA / MMC以及术前EMDA / MMC是新的治疗策略,就更高的缓解率和更长的缓解时间而言,它们具有令人鼓舞的初步结果。总而言之,这些发现表明,EMDA用于膀胱内MMC的递送可能是NMIBC治疗的主要治疗突破。

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