Long term experience in high grade glial tumors with temozolomide

被引:0
|
作者
Demirci, U. [1 ]
Buyukberber, S. [2 ]
Coskun, U. [2 ]
Akmansu, M. [3 ]
Yaman, E. [4 ]
Baykara, M. [2 ]
Yamac, D. [2 ]
Uner, A. [2 ]
Benekli, M. [2 ]
机构
[1] Ataturk Educ & Res Hosp, Dept Med Oncol, TR-0906800 Ankara, Turkey
[2] Gazi Univ, Dept Med Oncol, Fac Med, Ankara, Turkey
[3] Gazi Univ, Dept Radiat Oncol, Fac Med, Ankara, Turkey
[4] Mersin State Hosp, Dept Med Oncol, Mersin, Turkey
来源
JOURNAL OF BUON | 2012年 / 17卷 / 02期
关键词
elderly; malignant glioma; radiation; temozolomide; RADIOTHERAPY PLUS CONCOMITANT; MALIGNANT GLIOMA; ADJUVANT TEMOZOLOMIDE; PHASE-II; GLIOBLASTOMA-MULTIFORME; PROGNOSTIC-FACTORS; MANAGEMENT; SURVIVAL; COHORT; DRUG;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Temozolomide is used concurrently with radiotherapy (RT) and as consolidation therapy in high grade gliomas (HGGs). In the present study we present our experience of long-term efficacy and toxicity of temozolomide in HGGs. Methods: After surgery, temozolomide was administered at 75 mg/m(2) daily concurrently with RT, followed by 6 courses of consolidation therapy (150-200 mg/m(2) for 5 days every 28 days). Results: A total of 172 patients with either glioblastoma multiforme (GBM) (n= 142; 82.6%) or anaplastic astrocytoma (AA) (n= 30; 17.4%) were studied. The objective response rate (ORR) was 42.5%, including 12 (7%) complete responses (CRs) and 61 (35.5%) partial responses (PRs). In the GBM group, median progression free survival (PFS) and overall survival (OS) were 9 and 16 months, respectively. In the AA group, median PFS and OS were 16 and 24 months, respectively. Three-year OS was 18.2% for GBM, and 39.4% for AA. In elderly patients (14.5%), median PFS and OS were 8 and 11 months respectively for both HGGs. Serious toxicities were mainly hematologic. Conclusion: Temozolomide is an effective agent in HGGs with favorable outcome and low toxicity profile even in advanced age.
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页码:357 / 362
页数:6
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