A pilot study of everolimus and gefitinib in the treatment of recurrent glioblastoma (GBM)

被引:137
|
作者
Kreisl, Teri N. [2 ]
Lassman, Andrew B. [1 ]
Mischel, Paul S. [3 ]
Rosen, Neal [4 ]
Scher, Howard I. [4 ]
Teruya-Feldstein, Julie [5 ]
Shaffer, David [4 ]
Lis, Eric [6 ]
Abrey, Lauren E. [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Neurol, New York, NY 10065 USA
[2] NCI, Neurooncol Branch, Bethesda, MD 20892 USA
[3] Univ Calif Los Angeles, David Geffen Sch Med, Los Angeles, CA 90095 USA
[4] Mem Sloan Kettering Canc Ctr, Dept Med, New York, NY 10065 USA
[5] Mem Sloan Kettering Canc Ctr, Dept Pathol, New York, NY 10065 USA
[6] Mem Sloan Kettering Canc Ctr, Dept Radiol, New York, NY 10065 USA
关键词
Glioblastoma; mTOR; EGFR; PTEN; GROWTH-FACTOR RECEPTOR; PHASE-II TRIAL; MALIGNANT GLIOMA; MAMMALIAN TARGET; MULTIFORME; RAPAMYCIN; INHIBITION; PATHWAY; TEMOZOLOMIDE; COMBINATION;
D O I
10.1007/s11060-008-9741-z
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Twenty-two patients with recurrent glioblastoma (GBM) were prospectively treated with everolimus and gefitinib, designed to test the combined inhibition of mammalian target of rapamycin (mTOR) and epidermal growth factor receptor (EGFR) as part of a larger clinical trial. The primary endpoint was radiographic response rate. Secondary endpoints included progression-free survival and correlation of molecular profiles with treatment response. 36% of patients had stable disease and 14% a partial response; however, responses were not durable and only one patient was progression-free at six months. Radiographic changes were not well characterized by conventional response criteria, and implied differential effects of therapy within the tumor and/or antiangiogenic effects. EGFR and PTEN status did not clearly predict response to treatment.
引用
收藏
页码:99 / 105
页数:7
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