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低剂量东京172菌株与常规剂量康诺特菌株作为非肌层浸润性膀胱癌膀胱内卡介苗预防用药的疗效相当,且发病率最低:一项随机前瞻性比较的结果

Comparable effect with minimal morbidity of low-dose Tokyo 172 strain compared with regular dose Connaught strain as an intravesical bacillus Calmette-Guérin prophylaxis in nonmuscle invasive bladder cancer: Results of a randomized prospective comparison.

作者信息

Inamoto Teruo, Ubai Takanobu, Nishida Takeshi, Fujisue Yutaka, Katsuoka Yoji, Azuma Haruhito

机构信息

Department of Urology, Osaka Medical College, Osaka, Japan.

出版信息

Urol Ann. 2013 Jan;5(1):7-12. doi: 10.4103/0974-7796.106873.

Abstract

AIM

The aim was to compare patients' morbidity and response of bacillus Calmette-Guérin (BCG) prophylaxis after the intravesical instillation of low-dose Tokyo 172 strain and regular dose Connaught strain in patients with nonmuscle invasive bladder cancer (NMIBC).

PATIENTS AND METHODS

This was a randomized, active-controlled, open-label, monocenter study. Thirty-eight, NMIBC patients were treated sequentially, in a random order, with low-dose Tokyo 172 strain and regular dose Connaught strain, receiving each therapy for 6 weeks. A total of 18 and 20 patients were randomly assigned to a Tokyo 172 strain arm and a Connaught strain arm, respectively. Complication, morbidity, and recurrence-free survival (RFS) after each treatment were compared.

RESULTS

There was no significant difference in the 1-year RFS rate in patients treated with Tokyo 172 strain and Connaught strain (72.2% vs. 83.5%, respectively; P = 0.698). There were no significant differences in adverse events between the arms. Severe adverse events (>Grade 3) were seen in 15% of the Connaught strain group while no severe adverse events were observed as a result of Tokyo 172 strain.

CONCLUSION

Our results indicated that low-dose Tokyo 172 strain decreased adverse events although it was not significant, and the RFS difference was not statistically significant between the two arms. Further investigation is warranted.

摘要

目的

旨在比较非肌层浸润性膀胱癌(NMIBC)患者膀胱内灌注低剂量东京172株和常规剂量康诺特株卡介苗(BCG)后的发病率及反应。

患者与方法

这是一项随机、活性对照、开放标签的单中心研究。38例NMIBC患者按随机顺序依次接受低剂量东京172株和常规剂量康诺特株治疗,每种治疗持续6周。分别有18例和20例患者被随机分配至东京172株组和康诺特株组。比较每次治疗后的并发症、发病率及无复发生存期(RFS)。

结果

接受东京172株和康诺特株治疗的患者1年RFS率无显著差异(分别为72.2%和83.5%;P = 0.698)。两组间不良事件无显著差异。康诺特株组15%的患者出现严重不良事件(>3级),而东京172株治疗未观察到严重不良事件。

结论

我们的结果表明,低剂量东京172株虽未显著降低不良事件,但两组间RFS差异无统计学意义。有必要进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc02/3643329/c01fe3b7f49f/UA-5-7-g002.jpg

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