Dana-Farber Cancer Institute and Harvard Medical School, Boston, MA 02215, United States.
Eur J Cancer. 2013 Jan;49(1):121-31. doi: 10.1016/j.ejca.2012.07.020. Epub 2012 Aug 21.
The purpose was to assess the activity and side effect profile of ENMD-2076, an oral anti-angiogenic and anti-proliferative kinase inhibitor, in platinum-resistant recurrent epithelial ovarian cancer (EOC), fallopian tube or peritoneal cancer. Archival tumour tissue was obtained for correlative analyses.
This was an open-label single-arm Phase II study of single agent ENMD-2076 taken daily orally (PO). The primary objective was to determine the progression free survival (PFS) rate at 6 months of ENMD-2076 in platinum-resistant cancer based on RECIST v1.1. Secondary objectives included response rate (RR), duration of response, overall survival (OS) and safety. An exploratory analysis of archival tissue for mitotic index and angiogenesis was conducted in an attempt to identify a sensitive or resistant patient phenotype.
64 patients were enrolled, and the PFS rate at 6 months was 22% with a median time to progression of 3.6 months. The median number of prior regimens was 2. The most common adverse events were fatigue, hypertension and diarrhoea with the most common Grade 3/4 events being hypertension and fatigue. None of the markers of mitotic index or angiogenesis evaluated in the archival tissue samples were predictive of greater benefit or resistance to ENMD-2076 treatment.
ENMD-2076 has activity in platinum-resistant ovarian cancer, and observed toxicities were similar to other PO kinase inhibitors. Additional studies with ENMD-2076 are warranted, especially in combination with active chemotherapeutic agents in platinum-resistant patients. Further work to determine appropriate biomarkers for ENMD-2076 should be incorporated into new clinical studies.
评估口服抗血管生成和抗增殖激酶抑制剂 ENMD-2076 在铂耐药复发性卵巢上皮癌(EOC)、输卵管或腹膜癌中的活性和副作用谱。获得存档肿瘤组织进行相关分析。
这是一项开放标签、单臂 II 期研究,评估单药 ENMD-2076 每日口服(PO)的疗效。主要目的是根据 RECIST v1.1 确定 ENMD-2076 在铂耐药癌症中的 6 个月无进展生存期(PFS)率。次要目标包括反应率(RR)、缓解持续时间、总生存期(OS)和安全性。对存档组织进行有丝分裂指数和血管生成的探索性分析,试图确定敏感或耐药的患者表型。
共纳入 64 例患者,ENMD-2076 的 6 个月 PFS 率为 22%,中位无进展生存期为 3.6 个月。既往治疗方案中位数为 2 个。最常见的不良反应是疲劳、高血压和腹泻,最常见的 3/4 级事件是高血压和疲劳。在存档组织样本中评估的有丝分裂指数或血管生成标志物均未预测对 ENMD-2076 治疗的获益或耐药性更大。
ENMD-2076 在铂耐药卵巢癌中有活性,观察到的毒性与其他 PO 激酶抑制剂相似。需要进一步研究 ENMD-2076,尤其是在铂耐药患者中与活性化疗药物联合使用。应将确定 ENMD-2076 合适生物标志物的进一步工作纳入新的临床研究中。