Experience With Carbon Ion Radiotherapy for WHO Grade 2 Diffuse Astrocytomas

被引:18
作者
Hasegawa, Azusa [1 ]
Mizoe, Jun-Etsu [1 ]
Tsujii, Hirohiko [1 ]
Kamada, Tadashi [1 ]
Jingu, Keiichi [1 ]
Iwadate, Yasuo [2 ]
Nakazato, Youichi [3 ]
Matsutani, Masao [4 ]
Takakura, Kintomo [5 ]
机构
[1] Natl Inst Radiol Sci, Res Ctr Charged Particle Therapy Hosp, Chiba 260, Japan
[2] Chiba Univ, Grad Sch Med, Dept Neurol Surg, Chiba, Japan
[3] Gunma Univ, Grad Sch Med, Dept Human Pathol, Gunma, Japan
[4] Saitama Med Univ, Dept Neurol Surg, Saitama, Japan
[5] Tokyo Womens Med Univ, Dept Neurol Surg, Tokyo, Japan
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2012年 / 83卷 / 01期
关键词
Carbon ion radiotherapy; Diffuse astrocytomas; Dose escalation study; High-LET radiotherapy; Phase I/II clinical trial; RADIATION-THERAPY; PROGNOSTIC-FACTORS; RANDOMIZED-TRIAL; STEREOTACTIC RADIOTHERAPY; GLIOMA; ADULTS; SURVIVAL; EFFICACY; SURGERY;
D O I
10.1016/j.ijrobp.2011.06.1952
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To assess outcomes of carbon ion radiotherapy for diffuse astrocytomas in adults. Methods and Materials: Between October 1994 and February 2002, 14 patients with diffuse astrocytoma, identified as eligible for carbon ion radiotherapy, were enrolled in a phase I/II clinical trial. Carbon ion radiotherapy was administered in 24 fractions over 6 weeks. The normal tissue morbidity was monitored carefully, and the carbon ion dose was escalated from 50.4 Gy equivalent (GyE) to 55.2 GyE. Patients were divided into two groups according to their carbon ion doses: a low-dose group in which 2 patients were irradiated with 46.2 GyE and 7 patients were irradiated with 50.4 GyE, and a high-dose group in which 5 patients were irradiated with 55.2 GyE. Results: Toxicities were within acceptable limits, and none of the patients developed Grade 3 or higher acute or late reactions. The median progression-free survival (PFS) time was 18 months for the low-dose group and 91 months for the high-dose group (p = 0.0030). The median overall survival (OS) time was 28 months for the low-dose group and not reached for the high-dose group (p = 0.0208). Conclusion: High-dose group patients showed significant improvement in PFS and OS rates compared to those in the low-dose group, and both dose groups showed acceptable toxicity. (C) 2012 Elsevier Inc.
引用
收藏
页码:100 / 106
页数:7
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