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J Neurooncol. 2014 Jun;118(2):377-383. doi: 10.1007/s11060-014-1443-0. Epub 2014 Apr 20.
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Dose-dense temozolomide for newly diagnosed glioblastoma: a randomized phase III clinical trial.替莫唑胺剂量密集疗法治疗新诊断的胶质母细胞瘤:一项随机 III 期临床试验。
J Clin Oncol. 2013 Nov 10;31(32):4085-91. doi: 10.1200/JCO.2013.49.6968. Epub 2013 Oct 7.
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A hypermethylated phenotype is a better predictor of survival than MGMT methylation in anaplastic oligodendroglial brain tumors: a report from EORTC study 26951.在间变性少突胶质细胞瘤的脑肿瘤中,超甲基化表型比 MGMT 甲基化更能预测生存:来自 EORTC 研究 26951 的报告。
Clin Cancer Res. 2011 Nov 15;17(22):7148-55. doi: 10.1158/1078-0432.CCR-11-1274. Epub 2011 Sep 13.
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Temozolomide and 13-cis retinoic acid in patients with anaplastic gliomas: a prospective single-arm monocentric phase-II study (RNOP-05).替莫唑胺和 13-顺式维甲酸治疗间变性神经胶质瘤患者的前瞻性单臂单中心 II 期研究(RNOP-05)。
J Neurooncol. 2011 Sep;104(3):801-9. doi: 10.1007/s11060-011-0548-y. Epub 2011 Mar 4.
5
Patients with IDH1 wild type anaplastic astrocytomas exhibit worse prognosis than IDH1-mutated glioblastomas, and IDH1 mutation status accounts for the unfavorable prognostic effect of higher age: implications for classification of gliomas.IDH1 野生型间变性星形细胞瘤患者的预后比 IDH1 突变型胶质母细胞瘤差,IDH1 突变状态解释了高龄的不良预后影响:对胶质瘤分类的影响。
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Temozolomide versus procarbazine, lomustine, and vincristine in recurrent high-grade glioma.替莫唑胺对比洛莫司汀、司莫司汀和长春新碱治疗复发性高级别胶质瘤。
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Integrated genomic analysis identifies clinically relevant subtypes of glioblastoma characterized by abnormalities in PDGFRA, IDH1, EGFR, and NF1.整合基因组分析确定了具有 PDGFRA、IDH1、EGFR 和 NF1 异常的胶质母细胞瘤的临床相关亚型。
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10
NOA-04 randomized phase III trial of sequential radiochemotherapy of anaplastic glioma with procarbazine, lomustine, and vincristine or temozolomide.NOA-04 间变性胶质瘤序贯放化疗(采用丙卡巴肼、洛莫司汀和长春新碱或替莫唑胺)的随机 III 期试验
J Clin Oncol. 2009 Dec 10;27(35):5874-80. doi: 10.1200/JCO.2009.23.6497. Epub 2009 Nov 9.

放疗与替莫唑胺治疗间变性星形细胞瘤

Radiotherapy and temozolomide for anaplastic astrocytic gliomas.

作者信息

Nayak Lakshmi, Panageas Katherine S, Reiner Anne S, Huse Jason T, Pentsova Elena, Braunthal Stephanie G, Abrey Lauren E, DeAngelis Lisa M, Lassman Andrew B

机构信息

Department of Neurology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

出版信息

J Neurooncol. 2015 May;123(1):129-34. doi: 10.1007/s11060-015-1771-8. Epub 2015 Apr 29.

DOI:10.1007/s11060-015-1771-8
PMID:25920709
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4606458/
Abstract

We previously reported results of a phase II non-comparative trial that randomized patients with glioblastoma following radiotherapy to one of two different temozolomide schedules, followed by 13-cis-retinoic acid (RA) maintenance. Here we report the results of an exploratory cohort of patients accrued with anaplastic astrocytic tumors. Patients with newly diagnosed anaplastic astrocytoma (AA) or anaplastic oligo-astrocytoma (AOA) were treated with concurrent radiotherapy (60 Gy over 6 weeks) and temozolomide (75 mg/m(2)), and six adjuvant 28-day cycles of either dose-dense (150 mg/m(2), days 1-7, 15-21) or metronomic (50 mg/m(2), days 1-28) temozolomide. Subsequently, maintenance RA (100 mg/m(2), days 1-21/28) was administered until disease progression. All outcome measures were descriptive without intention to compare between treatment arms. Survival was measured by the Kaplan-Meier method. There were 31 patients (21 men, 10 women) with median age 48 years (range 28-74), median KPS 90 (range 60-100). Extent of resection was gross-total in 35%, subtotal 23%, and biopsy 42%. Histology was AA in 90%, and AOA in 10%. MGMT promoter methylation was methylated in 20%, unmethylated in 50%, and uninformative in 30% of 30 tested. Median progression-free survival was 2.1 years (95% CI 0.95-Not Reached), and overall survival 2.9 years (95 % CI 2.0-Not Reached). We report outcomes among a homogeneously treated population with anaplastic astrocytic tumors. Survival was unexpectedly short compared to other reports. These data may be useful as a contemporary historic control for other ongoing or future randomized trials.

摘要

我们之前报告了一项II期非对照试验的结果,该试验将胶质母细胞瘤患者在放疗后随机分为两种不同替莫唑胺给药方案中的一种,随后进行13 - 顺式维甲酸(RA)维持治疗。在此,我们报告一组间变性星形细胞瘤患者的探索性队列结果。新诊断的间变性星形细胞瘤(AA)或间变性少突星形细胞瘤(AOA)患者接受同步放疗(6周内60 Gy)和替莫唑胺(75 mg/m²)治疗,以及六个辅助性28天周期的剂量密集型(150 mg/m²,第1 - 7天、15 - 21天)或节拍型(50 mg/m²,第1 - 28天)替莫唑胺治疗。随后,给予维持性RA(100 mg/m²,第1 - 21/28天)直至疾病进展。所有结局指标均为描述性,无意在各治疗组之间进行比较。生存情况采用Kaplan - Meier方法测量。共有31例患者(21例男性,10例女性),中位年龄48岁(范围28 - 74岁),中位KPS为90(范围60 - 100)。切除范围为全切的占35%,次全切除的占23%,活检的占42%。组织学类型为AA的占90%,AOA的占10%。在30例检测患者中,MGMT启动子甲基化的占20%,未甲基化的占50%,信息不明确的占30%。中位无进展生存期为2.1年(95%CI 0.95 - 未达到),总生存期为2.9年(95%CI 2.0 - 未达到)。我们报告了一组接受同质化治疗的间变性星形细胞瘤患者的结局。与其他报告相比,生存期意外地短。这些数据可能作为其他正在进行或未来随机试验的当代历史对照有用。