首页> 外文期刊>The Journal of Urology >Phase II marker lesion study with intravesical instillation of apaziquone for superficial bladder cancer: toxicity and marker response.
【24h】

Phase II marker lesion study with intravesical instillation of apaziquone for superficial bladder cancer: toxicity and marker response.

机译:膀胱内滴注阿帕奇醌治疗浅表性膀胱癌的II期标志物病变研究:毒性和标志物反应。

获取原文
获取原文并翻译 | 示例
       

摘要

PURPOSE: We studied the ablative activity of intravesical apaziquone (EOquin) on a papillary marker tumor and determined the incidence of side effects. MATERIALS AND METHODS: A total of 46 patients with multiple pTa or pT1 bladder tumors underwent visible lesion resection except for 1 marker tumor. Patients were then treated with 6 instillations of apaziquone at weekly intervals. The response was determined 2 to 4 weeks after the last instillation. RESULTS: One patient withdrew informed consent and refused the last treatment due to side effects. A histologically proven complete response was seen in 30 patients. Progression to invasive stage was not observed. Local side effects in this study were comparable to those due to other chemotherapy instillations, such as mitomycin C and epirubicin, but less severe and less frequent compared to those of bacillus Calmette-Guerin instillations. CONCLUSIONS: The histological complete response rate after 6 consecutive instillations of apaziquone in patients with superficial bladder cancer was 67% (95% CI 51 to 80). Local side effects were comparable to side effects due to other chemotherapy instillations.
机译:目的:我们研究了膀胱内apaziquone(EOquin)对乳头状标志物肿瘤的消融活性,并确定了副作用的发生率。材料与方法:除1个标记肿瘤外,共有46例患有多个pTa或pT1膀胱肿瘤的患者接受了可见的病灶切除。然后,每隔一周对患者进行6次阿帕西醌滴注治疗。在最后滴注后2至4周确定反应。结果:一名患者因副作用退出知情同意并拒绝最后治疗。经组织学证实的完全缓解在30例患者中可见。未观察到进展为侵入性阶段。这项研究中的局部副作用与其他化学疗法滴注(如丝裂霉素C和表柔比星)所产生的副作用相当,但与卡介苗-卡林芽孢杆菌滴注相比,其严重程度较低且频率较低。结论:连续6次滴注阿帕奇醌治疗浅表性膀胱癌患者的组织学完全缓解率为67%(95%CI 51至80)。局部副作用与其他化学疗法滴注的副作用相当。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号