University of Maryland Greenebaum Cancer Center, Baltimore, MD, USA.
J Thorac Oncol. 2012 Oct;7(10):1618-21. doi: 10.1097/JTO.0b013e318267d051.
EC145 is a novel folate-receptor targeted agent consisting of a folate molecule linked to a vinca alkaloid. EC20 is a technetium-labeled folate that assesses the presence of folate receptors (FR) in vivo. The objective of this study was to determine the activity of EC145 in patients with chemotherapy refractory lung adenocarcinoma, whose tumors expressed the FR as determined by EC20 imaging.
Patients with advanced adenocarcinoma of the lung, Eastern Cooperative Oncology Group performance status 0 to 2, normal organ function, those who had progressed after at least two prior cytotoxic regimens, and with EC 20 uptake in at least one index lesion were eligible. The primary objective of the study was the ability to receive four or more cycles of therapy.
Sixty patients were screened and 43 patients were enrolled. Eleven patients (26%) received more than four cycles (95% confidence interval [CI] 14%, 41%), and one patient had partial response (response rate (RR) = 2.3%, 95% CI 0%, 12%). Patients in whom all target tumor lesions expressed FR by EC 20 scans had a trend toward superior results in terms of clinical benefit response (50% versus 14.3 %; p = 0.10) and survival (47.2 weeks versus 14.9 weeks [HR = 0.539, p = 0.101]) compared with those in whom at least one but not all target lesions were positive for FR (FR+).
EC145 demonstrated clinical activity with a good toxicity profile in this population. Uniform uptake of EC20 may predict activity of EC145 and be useful for prospective selection of patients in future trials.
EC145 是一种新型叶酸受体靶向药物,由叶酸分子与长春碱类药物连接而成。EC20 是一种锝标记的叶酸,用于评估体内叶酸受体(FR)的存在。本研究的目的是确定 EC145 在经 EC20 成像确定为 FR 阳性的化疗耐药肺腺癌患者中的活性。
符合条件的患者为晚期肺腺癌,东部肿瘤协作组体能状态 0 至 2 分,器官功能正常,至少接受过两种细胞毒性方案治疗后进展,且至少一个指数病变存在 EC20 摄取。研究的主要目的是能够接受至少四个周期的治疗。
对 60 名患者进行了筛选,其中 43 名患者入组。11 名患者(26%)接受了超过四个周期的治疗(95%置信区间[CI]为 14%,41%),1 名患者有部分缓解(缓解率[RR]为 2.3%,95%CI 为 0%,12%)。所有目标肿瘤病灶均通过 EC20 扫描表达 FR 的患者在临床获益反应(50%比 14.3%;p=0.10)和生存(47.2 周比 14.9 周[HR=0.539,p=0.101])方面有更好的趋势,与至少一个但不是所有目标病灶为 FR 阳性(FR+)的患者相比。
在该人群中,EC145 表现出良好的疗效和毒性特征。EC20 的均匀摄取可能预测 EC145 的活性,并有助于未来试验中患者的前瞻性选择。