Particle radiation therapy in the management of malignant glioma: Early experience at the Shanghai Proton and Heavy Ion Center

被引:24
|
作者
Kong, Lin [1 ,2 ]
Wu, Jinsong [3 ]
Gao, Jing [2 ,4 ]
Qiu, Xianxin [2 ,4 ]
Yang, Jing [2 ,4 ]
Hu, Jiyi [2 ,4 ]
Hu, Weixu [2 ,4 ]
Mao, Ying [3 ]
Lu, Jiade J. [2 ,4 ]
机构
[1] Fudan Univ, Shanghai Proton & Heavy Ion Ctr, Dept Radiat Oncol, Shanghai Canc Ctr, Shanghai, Peoples R China
[2] Shanghai Engn Res Ctr Proton & Heavy Ion Radiat, Shanghai, Peoples R China
[3] Fudan Univ, Dept Neurosurg, Shanghai Huashan Hosp, Shanghai, Peoples R China
[4] Shanghai Proton & Heavy Ion Ctr, Dept Radiat Oncol, Shanghai, Peoples R China
关键词
glioblastoma; high-grade glioma; particle radiotherapy; survival; temozolomide; GLIOBLASTOMA CELL-LINES; DOUBLE-STRAND BREAKS; CONCURRENT TEMOZOLOMIDE; RESPONSE ASSESSMENT; CARBON; RADIOTHERAPY; PHOTON; BEAMS; IRRADIATION; MULTIFORME;
D O I
10.1002/cncr.32828
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background The objective of this study was to evaluate the outcomes of patients with high-grade glioma who received treatment with particle radiotherapy. Methods Between June 2015 and October 2018, 50 consecutive and nonselected patients with glioblastoma multiforme (n = 34) or anaplastic glioma (n = 16) were treated at the Shanghai Proton and Heavy Ion Center. Twenty-four patients received proton radiotherapy (at a dose of 60 gray-equivalents in 30 daily fractions), and 26 patients received proton radiotherapy plus a carbon-ion radiotherapy (CIRT) boost in various dose-escalating schemes. All patients received temozolomide because of their age or their O-6-methylguanine-DNA methyltransferase (MGMT) promoter methylation status. Progression-free survival (PFS) and overall survival (OS) rates, as well as treatment-induced toxicities, were analyzed. Results At a median follow-up of 14.3 months (range, 4.8-39.6 months), the 12-month and 18-month OS rates were 87.8% (95% CI, 77.6%-98.0%) and 72.8% (95% CI, 56.7%-88.9%), respectively, and the 12-month and 18-month PFS rates were 74.2% (95% CI, 60.9%-87.5%) and 59.8% (95% CI, 43.1%-76.5%), respectively. Univariate analyses revealed that age (>50 vs <= 50 years), World Health Organization grade (3 vs 4), and Karnofsky performance status (>80 vs <= 80) were significant prognosticators for OS, and IDH mutation and World Health Organization grade were significant for predicting PFS. Furthermore, MGMT promoter methylation, performance status, and age showed a trend toward predicting PFS. No significant predictive factors for PFS or OS were identified in multivariate analyses. Twenty-nine patients experienced grade 1 treatment-related acute adverse effects, and 11 developed grade 1 (n = 6) or grade 2 (n = 5) late adverse effect of radiation-induced brain necrosis. No grade 3, 4, or 5 toxicities were observed. Conclusions Particle radiotherapy produced 18-month OS and PFS rates of 72.8% and 59.8%, respectively, with acceptable adverse effects in patients with high-grade glioma. Particle radiotherapy at a dose >= 60 gray-equivalents appears to be safe and potentially effective.
引用
收藏
页码:2802 / 2810
页数:9
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