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首页> 外文期刊>Urologic oncology >Phase II study of intravesical therapy with AD32 in patients with papillary urothelial carcinoma or carcinoma in situ (CIS) refractory to prior therapy with bacillus Calmette-Guerin (E3897): a trial of the Eastern Cooperative Oncology Group.
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Phase II study of intravesical therapy with AD32 in patients with papillary urothelial carcinoma or carcinoma in situ (CIS) refractory to prior therapy with bacillus Calmette-Guerin (E3897): a trial of the Eastern Cooperative Oncology Group.

机译:乳头尿路上皮癌或原位癌(CIS)难以治疗的乳头尿路上皮癌或原位癌(CIS)患者进行AD32膀胱内治疗的II期研究:东方合作肿瘤小组的一项试验。

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摘要

OBJECTIVE: To assess the safety and effectiveness of AD32, a doxorubicin analogue with little systemic exposure when administered intravesically, in patients with recurrent or refractory superficial urothelial carcinoma (formerly called transitional cell carcinoma [TCC]), or carcinoma in situ (CIS), who have failed prior BCG-based immunotherapy. METHODS: Eligible patients received six weekly doses (800 mg) of intravesical AD32 and were evaluated at 12-week intervals for 24 months or until date of worsening disease. Primary analysis was the proportion of all patients recurrence-free at 12 months. Treatment-related and GU-specific toxicities were also examined. All participating institutions submitted the protocol for Institutional Review Board (IRB) approval. RESULTS: The study was halted due to unavailability of study drug after accrual of 48 of a planned 64 patients; 42 were included in the analysis. Of these, 28 (67%) were still alive after median follow-up of 61.1 months. Of 21 TCC patients, 18 (85.7%) experienced disease recurrence (median time to recurrence, 5.3 months). Of the 5 CIS patients with complete response (CR), 3 (60%) experienced disease recurrence; (median time to recurrence, 37.3 months). Recurrence-free rates at 12 and 24 months were 20% (90% CI, 7.8%, 36.1%) and 15% (90 CI, 4.9%, 30.2%), respectively, for patients with TCC and 80% (90% CI, 31.4%, 95.8%) at both intervals for CIS patients with CR. Infection was the most common treatment-related toxicity; no grade 4 or higher toxicity was observed. The most common GU-specific toxicity was increased frequency/urgency. CONCLUSIONS: AD32 is safe and active for treatment of recurrent or refractory superficial bladder carcinoma. The agent awaits more complete characterization when drug production problems can be solved.
机译:目的:评估患有复发性或难治性浅表尿路上皮癌(以前称为移行细胞癌[TCC])或原位癌(CIS)的患者,经静脉内注射后几乎没有全身暴露的阿霉素类似物AD32的安全性和有效性,先前基于BCG的免疫治疗失败的人。方法:符合条件的患者每周接受六次剂量(800毫克)的膀胱内AD32治疗,并每隔12周评估一次,持续24个月或直至疾病恶化之日。初步分析是所有患者在12个月无复发的比例。还检查了与治疗有关的毒性和GU特异性毒性。所有参与机构均已将协议提交机构审查委员会(IRB)批准。结果:由于计划中的64位患者中有48位获得了研究药物而停止了研究。分析中包括42个。在中位随访61.1个月后,其中28例(67%)仍然存活。在21例TCC患者中,有18例(85.7%)经历了疾病复发(中位复发时间为5.3个月)。在5例完全缓解(CR)的CIS患者中,3例(60%)经历了疾病复发。 (中位复发时间为37.3个月)。对于TCC和80%(90%CI)患者,在12和24个月时的无复发率分别为20%(90%CI,7.8%,36.1%)和15%(90 CI,4.9%,30.2%)。 ,分别为31.4%,95.8%)。感染是最常见的治疗相关毒性。没有观察到4级或更高的毒性。 GU特异的最常见毒性是频率/紧急性增加。结论:AD32治疗复发性或难治性浅表性膀胱癌是安全有效的。当药物生产问题可以解决时,试剂等待更完整的表征。

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