Medical Oncology & Hematology, Princess Margaret Hospital, 610 University Avenue, Toronto, Ontario, Canada.
Expert Opin Investig Drugs. 2012 May;21(5):717-32. doi: 10.1517/13543784.2012.668882. Epub 2012 Mar 8.
Aurora kinases are key regulators of mitosis and inhibition of Aurora kinase activity is a rational therapeutic strategy in the treatment of solid tumors and hematological malignancies.
This paper will provide an updated summary of preclinical and clinical experience with ENMD-2076 in hematological malignancies. The MEDLINE (OVID) (1980 through 31 January 2012) was searched with the term combinations including Aurora, multiple myeloma, leukemia, lymphoma, myelodysplastic syndrome and myeloproliferative neoplasms. In addition, the American Society of Clinical Oncology (ASCO) (1997 - 2011) and the American Society of Hematology (ASH) (1997 - 2011) conference proceedings were searched for reports of new or ongoing trials.
ENMD-2076 is a multi-kinase inhibitor, with activity against Aurora A kinase, FLT3, c-KIT, c-FMS and VEGFR-2 and -3. It appears to be tolerable, exhibits favorable pharmacokinetic profiles and has activity in patients with acute myeloid leukemia and multiple myeloma. Further evaluation with cytotoxic chemotherapy and targeted agents, which affect different pathways and have non-overlapping toxicities, in patients with hematological malignancies are warranted.
极光激酶是有丝分裂的关键调节因子,抑制极光激酶的活性是治疗实体瘤和血液恶性肿瘤的合理治疗策略。
本文将提供血液恶性肿瘤中 ENMD-2076 的临床前和临床经验的最新总结。检索 MEDLINE(OVID)(1980 年至 2012 年 1 月 31 日),使用的术语组合包括极光、多发性骨髓瘤、白血病、淋巴瘤、骨髓增生异常综合征和骨髓增生性肿瘤。此外,还检索了美国临床肿瘤学会(ASCO)(1997-2011 年)和美国血液学会(ASH)(1997-2011 年)会议记录,以寻找新的或正在进行的试验报告。
ENMD-2076 是一种多激酶抑制剂,对极光激酶 A、FLT3、c-KIT、c-FMS 和 VEGFR-2 和 -3 具有活性。它似乎耐受性良好,表现出有利的药代动力学特征,并且在急性髓性白血病和多发性骨髓瘤患者中具有活性。在血液恶性肿瘤患者中,有必要进一步评估细胞毒性化疗和靶向药物的疗效,这些药物影响不同的途径,且毒性不重叠。