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Myelosuppression in patients benefiting from imatinib with hydroxyurea for recurrent malignant gliomas.接受伊马替尼联合羟基脲治疗复发性恶性胶质瘤患者的骨髓抑制情况。
J Neurooncol. 2007 Nov;85(2):217-22. doi: 10.1007/s11060-007-9408-1. Epub 2007 Jun 27.
2
Phase II study of imatinib mesylate and hydroxyurea for recurrent grade III malignant gliomas.甲磺酸伊马替尼与羟基脲用于复发性III级恶性胶质瘤的II期研究。
J Neurooncol. 2007 May;83(1):53-60. doi: 10.1007/s11060-006-9302-2. Epub 2007 Jan 24.
3
Temozolomide 3 weeks on and 1 week off as first-line therapy for recurrent glioblastoma: phase II study from gruppo italiano cooperativo di neuro-oncologia (GICNO).替莫唑胺采用3周用药、1周停药方案作为复发性胶质母细胞瘤的一线治疗:意大利神经肿瘤协作组(GICNO)的II期研究
Br J Cancer. 2006 Nov 6;95(9):1155-60. doi: 10.1038/sj.bjc.6603376. Epub 2006 Oct 3.
4
Phase I/II study of imatinib mesylate for recurrent malignant gliomas: North American Brain Tumor Consortium Study 99-08.甲磺酸伊马替尼用于复发性恶性胶质瘤的I/II期研究:北美脑肿瘤联盟99-08研究
Clin Cancer Res. 2006 Aug 15;12(16):4899-907. doi: 10.1158/1078-0432.CCR-06-0773.
5
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Cancer Res. 2006 Aug 15;66(16):8042-8. doi: 10.1158/0008-5472.CAN-06-0900.
6
Radiotherapy and temozolomide for newly diagnosed glioblastoma: recursive partitioning analysis of the EORTC 26981/22981-NCIC CE3 phase III randomized trial.新诊断胶质母细胞瘤的放疗与替莫唑胺治疗:EORTC 26981/22981-NCIC CE3 三期随机试验的递归划分分析
J Clin Oncol. 2006 Jun 1;24(16):2563-9. doi: 10.1200/JCO.2005.04.5963.
7
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J Clin Oncol. 2005 Dec 20;23(36):9359-68. doi: 10.1200/JCO.2005.03.2185.
8
Phase I trial of irinotecan plus temozolomide in adults with recurrent malignant glioma.伊立替康联合替莫唑胺治疗复发性恶性胶质瘤成人患者的I期试验
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Ann Oncol. 2005 Oct;16(10):1702-8. doi: 10.1093/annonc/mdi317. Epub 2005 Jul 20.
10
Autocrine platelet-derived growth factor-dependent gene expression in glioblastoma cells is mediated largely by activation of the transcription factor sterol regulatory element binding protein and is associated with altered genotype and patient survival in human brain tumors.胶质母细胞瘤细胞中自分泌血小板衍生生长因子依赖性基因表达主要由转录因子固醇调节元件结合蛋白的激活介导,并与人脑肿瘤的基因型改变和患者生存相关。
Cancer Res. 2005 Jul 1;65(13):5523-34. doi: 10.1158/0008-5472.CAN-04-2582.

高剂量甲磺酸伊马替尼联合替莫唑胺的安全性和药代动力学:成人恶性胶质瘤的1期试验

Safety and pharmacokinetics of dose-intensive imatinib mesylate plus temozolomide: phase 1 trial in adults with malignant glioma.

作者信息

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

机构信息

Department of Surgery, Duke University Medical Center, Box 3624, Durham, NC 27710, USA.

出版信息

Neuro Oncol. 2008 Jun;10(3):330-40. doi: 10.1215/15228517-2008-003. Epub 2008 Mar 21.

DOI:10.1215/15228517-2008-003
PMID:18359865
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2563055/
Abstract

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.

摘要

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。