Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104-4318, USA.
Pediatr Blood Cancer. 2010 Jul 15;55(1):26-34. doi: 10.1002/pbc.22430.
MLN8237 is a small molecule inhibitor of Aurora Kinase A (AURKA) that is currently in early phase clinical testing. AURKA plays a pivotal role in centrosome maturation and spindle formation during mitosis.
MLN8237 was tested against the Pediatric Preclinical Testing Program (PPTP) in vitro panel at concentrations ranging from 1.0 nM to 10 microM and was tested against the PPTP in vivo panels at a dose of 20 mg/kg administered orally twice daily x 5 days. Treatment duration was 6 weeks for solid tumor xenografts and 3 weeks for ALL xenografts.
MLN8237 had a median IC(50) of 61 nM against the PPTP in vitro panel. The ALL cell lines were more sensitive and the rhabdomyosarcoma cell lines less sensitive than the remaining PPTP cell lines. In vivo, MLN8237 induced significant differences in event-free survival (EFS) distributions compared to controls in 32/40 (80%) solid tumor models and all (6/6) ALL models. Maintained complete responses (CRs) were observed in 3 of 7 neuroblastoma xenografts, and all 6 evaluable ALL xenografts achieved CR (n = 4) or maintained CR (n = 2) status. Maintained CRs were observed among single xenografts in other panels, including the Wilms tumor, rhabdoid tumor, rhabdomyosarcoma, Ewing sarcoma, osteosarcoma, and medulloblastoma.
The in vivo activity observed against the neuroblastoma panel far exceeds that observed for standard agents evaluated against the panel by the PPTP. High levels of in vivo activity were also observed against the ALL xenograft panel. These data support expedited clinical development of MLN8237 in childhood cancer.
MLN8237 是一种小分子 Aurora 激酶 A(AURKA)抑制剂,目前处于临床早期阶段。AURKA 在有丝分裂过程中对中心体成熟和纺锤体形成起着关键作用。
MLN8237 在浓度为 1.0 nM 至 10 μM 的范围内,在儿科临床前测试计划(PPTP)的体外面板中进行了测试,并在 20 mg/kg 的剂量下在 PPTP 的体内面板中进行了测试,每天口服两次,连续 5 天。治疗时间为实体瘤异种移植 6 周,ALL 异种移植 3 周。
MLN8237 在 PPTP 体外面板中的中位 IC(50)为 61 nM。ALL 细胞系比剩余的 PPTP 细胞系更敏感,横纹肌肉瘤细胞系比剩余的 PPTP 细胞系更不敏感。在体内,与对照组相比,MLN8237 诱导的无事件生存(EFS)分布差异在 32/40(80%)实体瘤模型和所有(6/6)ALL 模型中均有显著意义。在 7 个神经母细胞瘤异种移植瘤中,有 3 个观察到完全缓解(CR),所有 6 个可评估的 ALL 异种移植瘤均达到 CR(n=4)或维持 CR(n=2)状态。在其他面板中的单个异种移植瘤中也观察到维持 CR,包括肾母细胞瘤、横纹肌瘤、横纹肌肉瘤、尤文肉瘤、骨肉瘤和髓母细胞瘤。
在神经母细胞瘤面板中观察到的体内活性远远超过了 PPTP 评估该面板的标准药物的观察结果。在 ALL 异种移植面板中也观察到高水平的体内活性。这些数据支持加快 MLN8237 在儿童癌症中的临床开发。