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膀胱内注射分枝杆菌细胞壁 - DNA 复合物用于治疗标准膀胱内治疗失败后的膀胱原位癌。

Intravesical mycobacterial cell wall-DNA complex in the treatment of carcinoma in situ of the bladder after standard intravesical therapy has failed.

作者信息

Morales Alvaro, Phadke Kiran, Steinhoff Gary

机构信息

Queen's University, Kingston, Ontario, Canada.

出版信息

J Urol. 2009 Mar;181(3):1040-5. doi: 10.1016/j.juro.2008.11.019. Epub 2009 Jan 16.

Abstract

PURPOSE

We assessed the clinical efficacy and safety of mycobacterial cell wall-DNA complex after intravesical administration in patients with carcinoma in situ in whom prior therapy with bacillus Calmette-Guerin failed or in those who were treatment naïve.

MATERIALS AND METHODS

Patients received 6 weekly instillations of 4 or 8 mg mycobacterial cell wall-DNA complex (formulated as an emulsion) followed by 3 weekly instillations at weeks 12 and 24. Efficacy and safety were evaluated throughout the treatment phase and at months 12 and 18.

RESULTS

A total of 55 patients (mean age 74 years, 74.6% male) received 4 mg (25) or 8 mg (30) mycobacterial cell wall-DNA complex emulsion. All patients were previously treated with bacillus Calmette-Guerin except for 8 who were treatment naïve and 2 who received chemotherapy. In the intent to treat population the complete response rate was 27.3% at weeks 12 and 26 in the 4 mg group while 46.4% of patients receiving 8 mg had a complete response at both points. Mycobacterial cell wall-DNA complex was well tolerated by both dose groups. Overall 90% of all adverse events were mild to moderate in severity.

CONCLUSIONS

Mycobacterial cell wall-DNA complex has shown antineoplastic activity in patients with bladder cancer with less toxicity than that associated with bacillus Calmette-Guerin administration. The tolerance and efficacy of mycobacterial cell wall-DNA complex might hold promise for the treatment of carcinoma in situ of the bladder.

摘要

目的

我们评估了膀胱内给药分枝杆菌细胞壁 - DNA复合物对卡介苗治疗失败或未接受过治疗的原位癌患者的临床疗效和安全性。

材料与方法

患者每周接受6次4毫克或8毫克分枝杆菌细胞壁 - DNA复合物(制成乳剂)的灌注,随后在第12周和第24周每周进行3次灌注。在整个治疗阶段以及第12个月和第18个月评估疗效和安全性。

结果

共有55例患者(平均年龄74岁,74.6%为男性)接受了4毫克(25例)或8毫克(30例)分枝杆菌细胞壁 - DNA复合物乳剂治疗。除8例未接受过治疗和2例接受过化疗的患者外,所有患者此前均接受过卡介苗治疗。在意向性治疗人群中,4毫克组在第12周和第26周的完全缓解率为27.3%,而接受8毫克治疗的患者在这两个时间点的完全缓解率为46.4%。两个剂量组对分枝杆菌细胞壁 - DNA复合物的耐受性均良好。总体而言,所有不良事件中有90%的严重程度为轻度至中度。

结论

分枝杆菌细胞壁 - DNA复合物在膀胱癌患者中显示出抗肿瘤活性,且毒性低于卡介苗给药。分枝杆菌细胞壁 - DNA复合物的耐受性和疗效可能为膀胱原位癌的治疗带来希望。

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