Patel Prashant, Young J Graham, Mautner Vivien, Ashdown Daniel, Bonney Sarah, Pineda Robert G, Collins Stuart I, Searle Peter F, Hull Diana, Peers Elizabeth, Chester John, Wallace D Michael, Doherty Alan, Leung Hing, Young Lawrence S, James Nicholas D
CR UK Institute for Cancer Studies, University of Birmingham, UK.
Mol Ther. 2009 Jul;17(7):1292-9. doi: 10.1038/mt.2009.80. Epub 2009 Apr 14.
We report a phase I/II clinical trial in prostate cancer (PCa) using direct intraprostatic injection of a replication defective adenovirus vector (CTL102) encoding bacterial nitroreductase (NTR) in conjunction with systemic prodrug CB1954. One group of patients with localized PCa scheduled for radical prostatectomy received virus alone, prior to surgery, in a dose escalation to establish safety, tolerability, and NTR expression. A second group with local failure following primary treatment received virus plus prodrug to establish safety and tolerability. Based on acceptable safety data and indications of prostate-specific antigen (PSA) responses, an extended cohort received virus at a single dose level plus prodrug. The vector was well tolerated with minimal side effects, had a short half-life in the circulation, and stimulated a robust antibody response. Immunohistochemistry of resected prostate demonstrated NTR staining in tumor and glandular epithelium at all dose levels [5 x 10(10)-1 x 10(12) virus particles (vp)]. A total of 19 patients received virus plus prodrug and 14 of these had a repeat treatment; minimal toxicity was observed and there was preliminary evidence of change in PSA kinetics, with an increase in the time to 10% PSA progression in 6 out of 18 patients at 6 months.
我们报告了一项针对前列腺癌(PCa)的I/II期临床试验,该试验采用直接前列腺内注射编码细菌硝基还原酶(NTR)的复制缺陷型腺病毒载体(CTL102)并联合全身使用前药CB1954。一组计划进行根治性前列腺切除术的局限性PCa患者在手术前单独接受病毒注射,剂量逐步递增以确定安全性、耐受性和NTR表达情况。第二组在初次治疗后出现局部失败的患者接受病毒加前药治疗,以确定安全性和耐受性。基于可接受的安全性数据和前列腺特异性抗原(PSA)反应的迹象,一个扩大队列接受了单剂量水平的病毒加前药治疗。该载体耐受性良好,副作用极小,在循环中的半衰期较短,并刺激了强烈的抗体反应。切除前列腺的免疫组织化学显示,在所有剂量水平[5×10(10)-1×10(12)病毒颗粒(vp)]下,肿瘤和腺上皮中均有NTR染色。共有19名患者接受了病毒加前药治疗,其中14名患者接受了重复治疗;观察到的毒性极小,并且有初步证据表明PSA动力学发生了变化,在6个月时,18名患者中有6名患者的PSA进展至10%的时间有所延长。