AZD2171, a pan-VEGF receptor tyrosine kinase inhibitor, normalizes tumor vasculature and alleviates edema in glioblastoma patients

被引:1355
作者
Batchelor, Tracy T. [1 ]
Sorensen, A. Gregory
di Tomaso, Emmanuelle
Zhang, Wei-Ting
Duda, Dan G.
Cohen, Kenneth S.
Kozak, Kevin R.
Cahill, Daniel P.
Chen, Poe-Jou
Zhu, Mingwang
Ancukiewicz, Marek
Mrugala, Maciej M.
Plotkin, Scott
Drappatz, Jan
Louis, David N.
Ivy, Percy
Scadden, David T.
Benner, Thomas
Loeffler, Jay S.
Wen, Patrick Y.
Jain, Rakesh K.
机构
[1] Massachusetts Gen Hosp, Dept Neurol, Boston, MA 02114 USA
[2] Massachusetts Gen Hosp, Dept Radiat Oncol, Boston, MA 02114 USA
[3] Massachusetts Gen Hosp, Dept Radiol, Boston, MA 02114 USA
[4] Massachusetts Gen Hosp, Ctr Regenerat Med, Boston, MA 02114 USA
[5] Massachusetts Gen Hosp, Dept Pathol, Boston, MA 02114 USA
[6] Harvard Univ, Sch Med, Boston, MA 02114 USA
[7] Massachusetts Gen Hosp, HST AA Martinos Ctr Biomed Imaging, Boston, MA 02114 USA
[8] Harvard Univ, Sch Med, Div Hlth Sci & Technol, Boston, MA 02114 USA
[9] MIT, Dept Nucl Sci & Engn, Cambridge, MA 02139 USA
[10] Childrens Hosp, Dana Farber Canc Inst, Dept Adult Oncol, Boston, MA 02115 USA
[11] NCI, Canc Therapy Evaluat Program, Bethesda, MD 20892 USA
关键词
D O I
10.1016/j.ccr.2006.11.021
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Using MRI techniques, we show here that normalization of tumor vessels in recurrent glioblastoma patients by daily administration of AZD2171-an oral tyrosine kinase inhibitor of VEGF receptors-has rapid onset, is prolonged but reversible, and has the significant clinical benefit of alleviating edema. Reversal of normalization began by 28 days, though some features persisted for as long as four months. Basic FGF, SDF1 alpha, and viable circulating endothelial cells (CECs) increased when tumors escaped treatment, and circulating progenitor cells (CPCs) increased when tumors progressed after drug interruption. Our study provides insight into different mechanisms of action of this class of drugs in recurrent glioblastoma patients and suggests that the timing of combination therapy may be critical for optimizing activity against this tumor.
引用
收藏
页码:83 / 95
页数:13
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