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阿帕喹酮膀胱内灌注治疗浅表性膀胱癌的II期标记病变研究:毒性和标记反应。

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

作者信息

van der Heijden Antoine G, Moonen Paula M J, Cornel Erik B, Vergunst Henk, de Reijke Theo M, van Boven Erika, Barten Evert J, Puri Rajiv, van Kalken Coenraad K, Witjes J Alfred

机构信息

University Medical Centre Nijmegen, Nijmegen, The Netherlands.

出版信息

J Urol. 2006 Oct;176(4 Pt 1):1349-53; discussion 1353. doi: 10.1016/j.juro.2006.06.007.

Abstract

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.

摘要

目的

我们研究了膀胱内注射阿帕喹酮(EOquin)对乳头状标记肿瘤的消融活性,并确定了副作用的发生率。

材料与方法

共有46例患有多发性pTa或pT1膀胱肿瘤的患者接受了可见病变切除术,但有1个标记肿瘤除外。然后患者每周接受6次阿帕喹酮灌注治疗。在最后一次灌注后2至4周确定反应情况。

结果

1例患者因副作用撤回知情同意并拒绝最后一次治疗。30例患者出现组织学证实的完全缓解。未观察到进展至浸润期的情况。本研究中的局部副作用与其他化疗灌注(如丝裂霉素C和表柔比星)引起的副作用相当,但与卡介苗灌注相比,严重程度更低且发生率更低。

结论

浅表性膀胱癌患者连续6次灌注阿帕喹酮后的组织学完全缓解率为67%(95%可信区间51至80)。局部副作用与其他化疗灌注引起的副作用相当。

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