Reardon David A, Desjardins Annick, Vredenburgh James J, Sathornsumetee Sith, Rich Jeremy N, Quinn Jennifer A, Lagattuta Theodore F, Egorin Merrill J, Gururangan Sridharan, McLendon Roger, Herndon James E, Friedman Allan H, Salvado August J, Friedman Henry S
Department of Surgery, Duke University Medical Center, Box 3624, Durham, NC 27710, USA.
Neuro Oncol. 2008 Jun;10(3):330-40. doi: 10.1215/15228517-2008-003. Epub 2008 Mar 21.
We determined the maximum tolerated dose (MTD) and dose-limiting toxicity (DLT) of imatinib mesylate, an inhibitor of the receptor tyrosine kinases platelet-derived growth factor receptor (PDGFR), the proto-oncogene product c-kit, and the fusion protein Bcr-Abl, when administered for 8 days in combination with temozolomide (TMZ) to malignant glioma (MG) patients. MG patients who had not failed prior TMZ were eligible to receive TMZ at a dose of 150-200 mg/m(2) per day on days 4-8 plus imatinib mesylate administered orally on days 1-8 of each 4-week cycle. Patients were stratified based on concurrent administration of CYP3A4-inducing antiepileptic drugs (EIAEDs). The imatinib dose was escalated in successive cohorts of patients independently for each stratum. Imatinib, at doses ranging from 400 mg to 1,200 mg, was administered with TMZ to 65 patients: 52 (80%) with glioblastoma multiforme (GBM) and 13 (20%) with grade III MG. At enrollment, 34 patients (52%) had stable disease, and 33 (48%) had progressive disease; 30 patients (46%) were on EIAEDs. The MTD of imatinib for patients concurrently receiving or not receiving EIAEDs was 1,000 mg. DLTs were hematologic, gastrointestinal, renal, and hepatic. Pharmacokinetic analyses revealed lowered exposures and enhanced clearance among patients on EIAEDs. Among GBM patients with stable disease at enrollment (n=28), the median progression-free and overall survival times were 41.7 and 56.1 weeks, respectively. Imatinib doses up to 1,000 mg/day for 8 consecutive days are well tolerated when combined with standard TMZ dosing for MG patients. A subsequent phase 2 study is required to further evaluate the efficacy of this regimen for this patient population.
我们确定了甲磺酸伊马替尼(一种受体酪氨酸激酶抑制剂,可抑制血小板衍生生长因子受体(PDGFR)、原癌基因产物c-kit和融合蛋白Bcr-Abl)与替莫唑胺(TMZ)联合应用8天时对恶性胶质瘤(MG)患者的最大耐受剂量(MTD)和剂量限制毒性(DLT)。未接受过TMZ治疗且未出现治疗失败的MG患者,在每4周一个周期的第4至8天,每天接受剂量为150 - 200 mg/m²的TMZ治疗,同时在第1至8天口服甲磺酸伊马替尼。根据是否同时服用诱导CYP3A4的抗癫痫药物(EIAEDs)对患者进行分层。每个分层中,伊马替尼剂量在连续的患者队列中独立递增。65例患者接受了剂量范围为400 mg至1200 mg的伊马替尼与TMZ联合治疗:52例(80%)为多形性胶质母细胞瘤(GBM),13例(20%)为III级MG。入组时,34例患者(52%)病情稳定,33例(48%)病情进展;30例患者(46%)正在服用EIAEDs。同时接受或未接受EIAEDs的患者,伊马替尼的MTD均为1000 mg。DLT包括血液学、胃肠道、肾脏和肝脏方面的毒性。药代动力学分析显示,服用EIAEDs的患者药物暴露量降低,清除率提高。在入组时病情稳定的GBM患者(n = 28)中,无进展生存期和总生存期的中位数分别为41.7周和56.1周。对于MG患者,当伊马替尼与标准TMZ剂量联合应用时,连续8天每天剂量高达1000 mg耐受性良好。需要进行后续的2期研究,以进一步评估该方案对该患者群体的疗效。