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一项比较卡介苗(Tokyo 株或 Connaught 株)膀胱内灌注治疗非肌层浸润性膀胱癌的前瞻性研究。

A prospective comparative study of intravesical bacillus Calmette-Guérin therapy with the Tokyo or Connaught strain for nonmuscle invasive bladder cancer.

机构信息

Department of Urology, Japanese Red Cross Otsu Hospital, Otsu, Shiga, Japan.

出版信息

J Urol. 2013 Jul;190(1):50-4. doi: 10.1016/j.juro.2013.01.084. Epub 2013 Jan 30.

Abstract

PURPOSE

We prospectively compared the efficacy and adverse events of the bacillus Calmette-Guérin Tokyo 172 and Connaught strains for nonmuscle invasive bladder cancer.

MATERIALS AND METHODS

Between January 2004 and May 2012 patients with pTa/T1 and pTis, multiple tumors and a recurrence-free period of 3 months or less who required intravesical bacillus Calmette-Guérin therapy were prospectively allocated randomly to receive the Tokyo or Connaught strain. The primary study end points were the complete response rate in patients with pTis and concomitant carcinoma in situ (pTa or pT1), recurrence-free survival in patients with pTa, pT1 and carcinoma in situ who achieved a complete response after therapy and the frequency of adverse events.

RESULTS

Administration of the Connaught strain ceased because its production was suspended in June 2012. Therefore, analysis was performed using data gathered to date. Overall, 66 and 63 patients who received the Tokyo and Connaught strains, respectively, were included in efficacy analysis. Patient and tumor characteristics were well balanced between the 2 groups. Median followup was 855 days. Adverse events were similar in the groups. The complete response rate was 90.3% and 85.0% in patients given the Tokyo and Connaught strains, respectively, which did not significantly differ (p = 0.896). The 2-year recurrence-free survival rate was 73.2% and 68.8%, respectively.

CONCLUSIONS

Results suggest no significant differences between the Tokyo and Connaught strains in the complete response, recurrence-free survival or adverse event rate.

摘要

目的

我们前瞻性地比较了卡介苗东京 172 株和康诺特株在非肌肉浸润性膀胱癌中的疗效和不良反应。

材料与方法

2004 年 1 月至 2012 年 5 月,我们前瞻性地将需要膀胱内卡介苗治疗的 pTa/T1 和 pTis、多发性肿瘤和无复发生存期小于 3 个月的患者随机分配接受东京株或康诺特株。主要研究终点是 pTis 合并原位癌(pTa 或 pT1)患者的完全缓解率、治疗后完全缓解的 pTa、pT1 和原位癌患者的无复发生存率以及不良反应的频率。

结果

由于康诺特株于 2012 年 6 月停产,故分析使用了截至目前的数据。总体而言,分别接受东京株和康诺特株治疗的 66 例和 63 例患者纳入疗效分析。两组患者和肿瘤特征均均衡。中位随访时间为 855 天。两组不良反应相似。分别给予东京株和康诺特株的患者完全缓解率分别为 90.3%和 85.0%,差异无统计学意义(p=0.896)。2 年无复发生存率分别为 73.2%和 68.8%。

结论

结果表明,东京株和康诺特株在完全缓解率、无复发生存率或不良反应率方面无显著差异。

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