Initial Testing of the Aurora Kinase A Inhibitor MLN8237 by the Pediatric Preclinical Testing Program (PPTP)

被引:182
作者
Maris, John M. [1 ,2 ]
Morton, Christopher L. [3 ]
Gorlick, Richard [4 ]
Kolb, E. Anders [5 ]
Lock, Richard [6 ]
Carol, Hernan [6 ]
Keir, Stephen T. [7 ]
Reynolds, C. Patrick [8 ]
Kang, Min H. [8 ]
Wu, Jianrong [3 ]
Smith, Malcolm A. [9 ]
Houghton, Peter J. [3 ]
机构
[1] Univ Penn, Childrens Hosp Philadelphia, Sch Med, Philadelphia, PA 19104 USA
[2] Abramson Family Canc Res Inst, Philadelphia, PA USA
[3] St Jude Childrens Hosp, Memphis, TN 38105 USA
[4] Childrens Hosp Montefiore, Bronx, NY USA
[5] Alfred I DuPont Hosp Children, Wilmington, DE USA
[6] Childrens Canc Inst Australia Med Res, Randwick, NSW, Australia
[7] Duke Univ, Med Ctr, Durham, NC USA
[8] Texas Tech Univ, Hlth Sci Ctr, Lubbock, TX 79430 USA
[9] NCI, Canc Therapy Evaluat Program, Bethesda, MD 20892 USA
关键词
preclinical testing; developmental therapeutics; MLN8237; XENOGRAFT MODELS; CANCER MODELS; DRUG TARGETS; IN-VIVO; N-MYC; CHECKPOINT; PROTEIN; AGENTS; CELLS; GENE;
D O I
10.1002/pbc.22430
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background. 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. Procedures. MLN8237 was tested against the Pediatric Preclinical Testing Program (PPTP) in vitro panel at concentrations ranging from 1.0 nM to 10 mu M 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. Results. 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. Conclusions. 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. Pediatr Blood Cancer 2010;55:26-34. (C) 2010 Wiley-Liss, Inc.
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收藏
页码:26 / 34
页数:9
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