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基于DNA的白喉毒素A BC-819疗法:一项针对中度风险非肌肉浸润性膀胱癌患者的2b期标记病变试验。

DNA based therapy with diphtheria toxin-A BC-819: a phase 2b marker lesion trial in patients with intermediate risk nonmuscle invasive bladder cancer.

作者信息

Gofrit Ofer N, Benjamin Shalva, Halachmi Sarel, Leibovitch Ilan, Dotan Zohar, Lamm Donald L, Ehrlich Nahum, Yutkin Vladimir, Ben-Am Monique, Hochberg Abraham

机构信息

Hadassah Ein-Kerem Medical Center, Jerusalem, Israel.

Edith Wolfson Medical Center, Sackler Faculty of Medicine, Holon, Israel.

出版信息

J Urol. 2014 Jun;191(6):1697-702. doi: 10.1016/j.juro.2013.12.011. Epub 2013 Dec 14.

Abstract

PURPOSE

H19 is a paternally imprinted oncofetal gene expressed in various embryonic tissues and in 85% of bladder tumors but suppressed in the adult healthy bladder. BC-819 is a DNA plasmid that carries the gene for diphtheria toxin-A under regulation of the H19 promoter sequence. We assessed the efficacy and toxicity of intravesical BC-819 instillations to prevent tumor recurrence and ablate a marker lesion in a phase 2b trial.

MATERIALS AND METHODS

A total of 47 patients with recurrent, multiple nonmuscle invasive bladder tumors in whom prior intravesical therapy had failed underwent transurethral resection of all except 1 marker tumor. Patients expressing H19 received a 6-week induction course of intravesical BC-819. Patients who achieved a complete response (absent new tumors at 3 months) were given 3 maintenance courses of 3-weekly instillations every 3 months.

RESULTS

All patients were evaluable for adverse effects and 39 were evaluable for efficacy. Complete tumor ablation was achieved in 33% of patients and in 64% there were no new tumors at 3 months. Median time to recurrence was 11.3 months in all cases but significantly longer (22.1 months) when analyzed by response status at 3 months. Adverse events were mild. The study was limited by the small number of patients.

CONCLUSIONS

BC-819 prevented new tumor growth in two-thirds of the patients and ablated a third of the marker lesions. Prolonged time to recurrence was observed in responding patients. These results along with the good safety profile make BC-819 a potential medication for bladder cancer.

摘要

目的

H19是一种父系印记的癌胚基因,在各种胚胎组织以及85%的膀胱肿瘤中表达,但在成人健康膀胱中受到抑制。BC - 819是一种DNA质粒,其携带在H19启动子序列调控下的白喉毒素A基因。我们在一项2b期试验中评估了膀胱内灌注BC - 819预防肿瘤复发和消融标记性病变的疗效及毒性。

材料与方法

共有47例复发性、多发性非肌层浸润性膀胱肿瘤患者,他们之前的膀胱内治疗均失败,除1个标记性肿瘤外,其余均接受了经尿道切除术。表达H19的患者接受为期6周的膀胱内BC - 819诱导疗程。达到完全缓解(3个月时无新肿瘤)的患者每3个月接受3个疗程、每周1次共3周的维持灌注。

结果

所有患者均可评估不良反应,39例可评估疗效。33%的患者实现了肿瘤完全消融,64%的患者在3个月时无新肿瘤。所有病例的中位复发时间为11.3个月,但按3个月时的反应状态分析,复发时间显著延长(22.1个月)。不良事件较轻。该研究受患者数量较少的限制。

结论

BC - 819使三分之二的患者预防了新肿瘤生长,并消融了三分之一的标记性病变。反应性患者观察到复发时间延长。这些结果连同良好的安全性使BC - 819成为膀胱癌的一种潜在药物。

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