Radiotherapy and temozolomide for anaplastic astrocytic gliomas

被引:4
作者
Nayak, Lakshmi [1 ]
Panageas, Katherine S. [2 ]
Reiner, Anne S. [2 ]
Huse, Jason T. [3 ]
Pentsova, Elena [1 ]
Braunthal, Stephanie G. [1 ]
Abrey, Lauren E. [1 ]
DeAngelis, Lisa M. [1 ]
Lassman, Andrew B. [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Neurol, New York, NY 10021 USA
[2] Mem Sloan Kettering Canc Ctr, Dept Epidemiol & Biostat, New York, NY 10021 USA
[3] Mem Sloan Kettering Canc Ctr, Dept Pathol, New York, NY 10021 USA
关键词
Anaplastic astrocytoma; Temozolomide; Radiotherapy; Chemotherapy; Clinical trial; NEWLY-DIAGNOSED GLIOBLASTOMA; HIGH-GRADE GLIOMA; PHASE-III; CELL-PROLIFERATION; MALIGNANT GLIOMA; MGMT METHYLATION; IDH1; MUTATION; DOSE-DENSE; SURVIVAL; TRIAL;
D O I
10.1007/s11060-015-1771-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:129 / 134
页数:6
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