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一项前瞻性、多中心 II 期临床试验表明,2 周膀胱内灌注卡介苗是安全、可耐受且有效的非肌层浸润性膀胱癌维持治疗方案。

A 2-week maintenance regimen of intravesical instillation of bacillus Calmette-Guerin is safe, adherent and effective in patients with non-muscle-invasive bladder cancer: a prospective, multicenter phase II clinical trial.

出版信息

Jpn J Clin Oncol. 2012 Sep;42(9):813-9. doi: 10.1093/jjco/hys097. Epub 2012 Jul 3.

Abstract

OBJECTIVE

To investigate the safety and efficacy of a maintenance regimen of bacillus Calmette-Guérin therapy including 6-week induction and 2-week maintenance instillation for patients with recurrent or multiple Ta, T1 tumors or carcinoma in situ of the urinary bladder.

METHODS

This study was performed as single-arm multi-institutional study. The enrolled patients had been diagnosed with urothelial carcinoma of the bladder, including the presence of at least two bladder tumors, single tumors recurring within 12 months of follow-up, any Grade 3 Stage Ta or T1 tumor, and primary or recurrent biopsy proven carcinoma in situ. Patients received 81 mg intravesical bacillus Calmette-Guérin (Connaught strain). The instillation was repeated once a week for another 5 weeks, followed by once a week for 2 weeks at months 3, 6, 12, 18, 24, 30 and 36, for a total of 20 instillations in 3 years.

RESULTS

From 28 hospitals, 202 patients were registered. A total of 186 patients matched the inclusion criteria: 139 patients in the Ta/T1group and 47 patients in the carcinoma in situ group. At the 4-year median point of follow-up, recurrence-free survival rates in the Ta/T1 group and the carcinoma in situ group were 76.7 and 77.7%, respectively. Completion rates for maintenance therapy in both groups at months 3, 6, 12, 24 and 36 were 81.7, 68.9, 58.1, 42.5 and 35.0%, respectively. Common toxicities were pain on urination, urinary frequency and gross hematuria. There was no treatment-related death.

CONCLUSIONS

This regimen may be feasible in patients with Ta/T1 tumor or carcinoma in situ; however, future Phase III randomized study is needed to determine whether this regimen would be truly safe and effective compared with 3-week maintenance regimen.

摘要

目的

研究卡介苗治疗的维持方案的安全性和疗效,该方案包括 6 周诱导期和 2 周维持灌注期,适用于复发性或多发性 Ta、T1 肿瘤或膀胱原位癌患者。

方法

本研究为单臂多中心研究。纳入的患者被诊断为膀胱尿路上皮癌,包括至少两个膀胱肿瘤、随访 12 个月内复发的单个肿瘤、任何分级 3 期 Ta 或 T1 肿瘤、以及原发性或复发性经活检证实的原位癌。患者接受 81mg 卡介苗膀胱内灌注(康诺特株)。灌注每周重复一次,持续 5 周,随后在第 3、6、12、18、24、30 和 36 个月每周一次,共 3 年 20 次灌注。

结果

来自 28 家医院的 202 名患者被注册。共有 186 名患者符合纳入标准:Ta/T1 组 139 例,原位癌组 47 例。在 4 年的中位随访点,Ta/T1 组和原位癌组的无复发生存率分别为 76.7%和 77.7%。两组在第 3、6、12、24 和 36 个月时维持治疗的完成率分别为 81.7%、68.9%、58.1%、42.5%和 35.0%。常见的毒性反应为尿痛、尿频和肉眼血尿。无治疗相关死亡。

结论

该方案在 Ta/T1 肿瘤或原位癌患者中可能是可行的;然而,需要未来的 III 期随机研究来确定与 3 周维持方案相比,该方案是否真的安全有效。

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