EC-145,叶酸靶向长春花生物碱偶联物,用于叶酸受体表达癌症的潜在治疗。

Franco Dosio, Paola Milla, Luigi Cattel
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摘要

Endocyte公司正在开发的EC-145是一种由去乙酰vinblastine单肼组成的偶联物,通过肽间隔剂连接到靶向部分叶酸,用于叶酸受体过表达的肿瘤,特别是卵巢癌和肺癌的潜在静脉治疗。体外研究表明EC-145选择性结合过表达叶酸受体的细胞,引起剂量依赖性细胞毒性。此外,KB人鼻咽癌细胞系与EC-145和阿霉素共孵育可产生协同抗肿瘤活性。小鼠肿瘤异种移植模型的实验证实了EC-145的效力,并在侵袭性淋巴瘤异种移植模型中证实了药物偶联物的疗效。在一项针对晚期或转移性实体瘤患者的I期临床试验中,不良事件通常为中等严重程度,最常见的是疲劳、便秘和周围感觉神经病变。一项针对晚期卵巢癌患者的II期临床试验的初步数据表明,EC-145三线或四线治疗比二线或三线阿霉素脂质体治疗的疾病控制效果更好。在铂耐药卵巢癌患者中,EC-145和阿霉素脂质体联合使用比标准治疗可显著提高无进展生存期。III期临床试验有望证实这些有希望的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
EC-145, a folate-targeted Vinca alkaloid conjugate for the potential treatment of folate receptor-expressing cancers.

EC-145, under development by Endocyte, is a conjugate composed of desacetylvinblastine monohydrazide linked through a peptide spacer to the targeting moiety folic acid, for the potential intravenous treatment of folate receptor-overexpressing tumors, in particular ovarian and lung cancers. In vitro studies demonstrated that EC-145 selectively binds to cells that overexpress the folate receptor, causing dose-dependent cytotoxicity. Furthermore, coincubation of the KB human nasopharyngeal carcinoma cell line with EC-145 and doxorubicin resulted in synergistic antitumor activity. Experiments in mouse tumor xenograft models have confirmed the potency of EC-145 and the curative effects of the drug conjugate were demonstrated in an aggressive lymphoma xenograft model. In a phase I clinical trial in patients with advanced or metastatic solid tumors, adverse events were generally of moderate severity with the most frequent being fatigue, constipation and peripheral sensory neuropathy. Preliminary data from a phase II clinical trial in patients with advanced ovarian cancer demonstrated that third- or fourth-line treatment with EC-145 yielded better disease control than second- or third-line liposomal doxorubicin. Coadministration of EC-145 and liposomal doxorubicin produced a statistically significant increase in progression-free survival over standard therapy in patients with platinum-resistant ovarian cancer. Phase III clinical trials are expected to confirm these promising results.

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