Chi Kim N, Eisenhauer Elizabeth, Fazli Ladan, Jones Edward C, Goldenberg S Larry, Powers Jean, Tu Dongsheng, Gleave Martin E
Vancouver Cancer Centre, BC Cancer Agency, Vancouver, British Columbia, V5Z 4E6, Canada.
J Natl Cancer Inst. 2005 Sep 7;97(17):1287-96. doi: 10.1093/jnci/dji252.
Clusterin is a cytoprotective chaperone protein that promotes cell survival and confers broad-spectrum treatment resistance. OGX-011 is a 2'-methoxyethyl modified phosphorothioate antisense oligonucleotide that is complementary to clusterin mRNA and has been reported to inhibit clusterin expression and enhance drug efficacy in xenograft models. The primary objective of this clinical study was to determine a biologically effective dose of OGX-011 that would inhibit clusterin expression in human cancer.
Subjects (n = 25) with localized prostate cancer with high-risk features who were candidates for prostatectomy were treated with OGX-011 by 2-hour intravenous infusion on days 1, 3, and 5 and then weekly from days 8-29 combined with androgen blockade starting on day 1; prostatectomy was performed on days 30-36. Six different doses were tested, from 40 to 640 mg. OGX-011 plasma and prostate tissue concentrations were measured by an enzyme-linked immunosorbent assay method, and the pharmacokinetics of OGX-011 were determined from these data. Prostate cancer tissue, lymph nodes, and serial samples of peripheral blood mononuclear cells were assessed for clusterin expression using quantitative real-time polymerase chain reaction and immunohistochemistry. All statistical tests were two-sided.
Only grade 1 and 2 toxicities were observed. The plasma half-life of OGX-011 was approximately 2-3 hours, and the area under the concentration versus time curve and CMAX (peak plasma concentration) increased proportionally with dose (Ptrend < .001). OGX-011 in prostate tissue increased with dose (Ptrend < .001). Dose-dependent decreases in prostate cancer and lymph node clusterin expression were observed by polymerase chain reaction of greater than 90% (Ptrend = .008 and Ptrend < .001, respectively) and by immunohistochemistry (Ptrend < .001 and Ptrend = .01, respectively).
OGX-011 is well tolerated and reduces clusterin expression in primary prostate tumors. The optimal biologic dose for OGX-011 at the schedule used is 640 mg.
聚集素是一种细胞保护伴侣蛋白,可促进细胞存活并赋予广谱治疗抗性。OGX-011是一种2'-甲氧基乙基修饰的硫代磷酸酯反义寡核苷酸,与聚集素mRNA互补,据报道在异种移植模型中可抑制聚集素表达并增强药物疗效。这项临床研究的主要目的是确定能抑制人类癌症中聚集素表达的OGX-011的生物学有效剂量。
25名具有高危特征的局限性前列腺癌患者,这些患者均为前列腺切除术的候选对象,于第1、3和5天通过2小时静脉输注接受OGX-011治疗,然后从第8 - 29天每周一次,并于第1天开始联合雄激素阻断治疗;在第30 - 36天进行前列腺切除术。测试了六种不同剂量,从40至640毫克。通过酶联免疫吸附测定法测量OGX-011的血浆和前列腺组织浓度,并根据这些数据确定OGX-011的药代动力学。使用定量实时聚合酶链反应和免疫组织化学评估前列腺癌组织、淋巴结和外周血单核细胞系列样本中的聚集素表达。所有统计检验均为双侧检验。
仅观察到1级和2级毒性。OGX-011的血浆半衰期约为2 - 3小时,浓度-时间曲线下面积和CMAX(血浆峰浓度)随剂量成比例增加(Ptrend <.001)。前列腺组织中的OGX-011随剂量增加(Ptrend <.001)。通过聚合酶链反应观察到前列腺癌和淋巴结聚集素表达呈剂量依赖性下降,下降幅度大于90%(分别为Ptrend =.008和Ptrend <.001),通过免疫组织化学观察到的下降幅度分别为(Ptrend <.001和Ptrend =.01)。
OGX-011耐受性良好,并可降低原发性前列腺肿瘤中聚集素的表达。按照所使用的方案,OGX-011的最佳生物学剂量为640毫克。