Chu Quincy S C, Forouzesh Bahram, Syed Samira, Mita Monica, Schwartz Garry, Cooper Joshua, Curtright Janet, Rowinsky Eric K
Cross Cancer Institute, 11560 University Avenue, Edmonton, AB T6G 1Z2, Canada.
Invest New Drugs. 2007 Aug;25(4):359-67. doi: 10.1007/s10637-006-9031-6. Epub 2007 Jan 20.
This phase II study evaluated the antitumor activity of the tetracycline analog COL-3, a potent inhibitor of metalloproteinases (MMPs), particularly MMP-2 and MMP-9, on a continuous oral schedule at a dose of 50 mg/m2 daily in patients with advanced and/or metastatic soft tissue sarcoma (STS). The principal endpoints were the rate of objective tumor regression and the proportion of patients who did not experience disease progression during the first 8 weeks of treatment. Other study objectives included an assessment of pharmacology of COL-3, time to progression (TTP), and overall survival. A Simon two-stage design with multinomial stopping rule was employed, with 15 patients enrolled during the first stage of the study. Although COL-3 was generally well-tolerated, there were no objective responses and 5(33%) patients experienced disease progression during the first 8 weeks of treatment, which exceeded the criteria established a priori with regard to pursuing further evaluations of COL-3 in STS. The median values for TTP and survival were 109 and 279 days, respectively. Based on these results, further studies of COL-3 on this administration schedule in patients with STS are not warranted.
这项II期研究评估了四环素类似物COL-3(一种金属蛋白酶(MMPs),特别是MMP-2和MMP-9的强效抑制剂)对晚期和/或转移性软组织肉瘤(STS)患者每日口服50 mg/m²剂量的连续给药方案的抗肿瘤活性。主要终点是客观肿瘤消退率和在治疗的前8周内未经历疾病进展的患者比例。其他研究目标包括对COL-3的药理学评估、疾病进展时间(TTP)和总生存期。采用了带有多项停止规则的Simon两阶段设计,在研究的第一阶段招募了15名患者。尽管COL-3总体耐受性良好,但在治疗的前8周内没有客观反应,5名(33%)患者经历了疾病进展,这超过了预先设定的关于在STS中进一步评估COL-3的标准。TTP和生存期的中位数分别为109天和279天。基于这些结果,不建议对STS患者按此给药方案进一步研究COL-3。