Treatment of High-grade Gliomas Using Hypofractionated Radiation Therapy -a Phase I Clinical Trial
2017年3月17日 更新者:Xue Xiaoying
Treatment of High-grade Gliomas Using Escalating Doses of Hypofractionated Simultaneous Integrated Boost-intensity Modulated Radiation Therapy in Combination With Temozolomide - a Modified Phase I Clinical Trial
Postoperative conventional radiation at 60 Gy/30f is currently still considered the standard radiotherapy mode for high-grade gliomas; however, the efficacy is still unsatisfactory.
Studies in recent years have shown that hypofractionated simultaneous integrated boost-intensity modulated radiation therapy (SIB-IMRT) has certain survival benefits over other fractionation methods; but, the best hypofractionation mode and its efficacy have not been confirmed.
The purpose of this study is to investigate the maximum tolerated dose (MTD) of hypofractionated SIB-IMRT with stepwise escalating of doses combined with temozolomide (TMZ) for the treatment of malignant gliomas.
研究概览
详细说明
Background: Postoperative conventional radiation at 60 Gy/30f is currently still considered the standard radiotherapy mode for high-grade gliomas; however, the efficacy is still unsatisfactory.
Studies in recent years have shown that hypofractionated simultaneous integrated boost-intensity modulated radiation therapy (SIB-IMRT) has certain survival benefits over other fractionation methods; but, the best hypofractionation mode and its efficacy have not been confirmed.
The purpose of this study is to investigate the maximum tolerated dose (MTD) of hypofractionated SIB-IMRT with stepwise escalating of doses combined with temozolomide (TMZ) for the treatment of malignant gliomas.
Methods: Malignant gliomas patients receive concurrent postoperative radiotherapy and chemotherapy.
The simultaneous integrated boost-intensity modulated technology is adopted to increase both the dose in the surgical cavity and residual tumor (PTV1).
The dose at each fraction is gradually increased from 2.8 Gy/f (total of 20 times) with an escalating dose interval of 0.4 Gy.
The planning target volume (PTV2) including the 2cm region around surgical cavity and residual tumor remain unchanged, with 2.5 Gy each time and a total of 50 Gy/20f.
The subsequent group of patients is advanced to the next dose level until dose-limiting toxicity (DLT) is present.
The dose, one level lower than the DLT, is the MTD.
The highest target single dose is 4 Gy/f.
TMZ is administered orally every day at 75 mg/m2 during radiotherapy and at 150-200 mg/m2 for 12 cycles following completion of chemoradiotherapy.
研究类型
介入性
注册 (实际的)
16
阶段
- 不适用
参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
18年 至 70年 (成人、年长者)
接受健康志愿者
不
有资格学习的性别
全部
描述
Inclusion Criteria:
- Postoperative grades III and IV glioma patients confirmed by pathology.
- The ages are between 18-70 years.
- Karnofsky performance score(KSP)≧60.
- Expected survival period ≧3 months.
- Blood routine and liver and kidney functions are normal.
- Receive cranial MRI examination after 48 h of surgery.
- Radiotherapy is performed after 2-4 weeks of surgery.
- Patients with restricted lesions and non-diffuse growth.
- Maximum diameter of the residual tumor, surgical cavity, and primary tumor bed are ≦6 cm.
Exclusion Criteria:
- Lesions are in the brain stem and thalamus.
- Pregnant and lactating women.
- Secondary primary malignant tumor.
- Severe pulmonary infection.
- Combination with mental illness or another disease that require hospitalization.
- Patients had received chemotherapy or brain radiotherapy previously.
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:不适用
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:hypofractionated group
hypofractionated group using hypofractionated radiation with temozolomide chemotherapy: Malignant gliomas patients received concurrent postoperative radiotherapy and chemotherapy.Intensity-modulated radiotherapy is adopted, the dose at each fraction is gradually increased from 2.8 Gy/f (total of 20 times) with an escalating dose interval of 0.4 Gy in PTV1.
The planning target volume (PTV2) remain unchanged with 2.5 Gy each time and a total of 50 Gy/20 f.
Temozolomide is administered orally every day at 75 mg/m2 during radiotherapy and at 150-200 mg/m2 for 12 cycles following completion of chemoradiotherapy.
|
The simultaneous integrated boost-intensity modulated technology is adopted to increase both the dose in the surgical cavity and residual tumor (PTV1).The dose at each fraction is gradually increased from 2.8 Gy/f (total of 20 times) with an escalating dose interval of 0.4 Gy in PTV1, until dose-limiting toxicity is present,the highest target single dose is 4 Gy/f.
The planning target volume (PTV2) including the 2 cm region around surgical cavity and residual tumor remain unchanged, with 2.5 Gy each time and a total of 50 Gy/20f.
Temozolomide(TMZ) is administered orally every day at 75 mg/m2 during radiotherapy and at 150-200 mg/m2 for 12 cycles following completion of chemoradiotherapy.
其他名称:
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
the maximum tolerated dose(MTD)
大体时间:1year
|
Safety and tolerability of hypofractionated simultaneous integrated boost intensity modulated radiation therapy (SIB-IMRT) combined with standard temozolomide chemotherapy. The maximum tolerated dose of hypofractionated radiation combined with concurrent temozolomide in newly diagnosed highgrade glioma is being explored. |
1year
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Progression free survival
大体时间:1 year
|
From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 1 year.
|
1 year
|
合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
赞助
调查人员
- 研究主任:xiaoying xue, doctor、Department of Radiotherapy
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (实际的)
2014年1月1日
初级完成 (实际的)
2016年11月7日
研究完成 (实际的)
2016年12月3日
研究注册日期
首次提交
2017年2月22日
首先提交符合 QC 标准的
2017年3月12日
首次发布 (实际的)
2017年3月17日
研究记录更新
最后更新发布 (实际的)
2017年3月21日
上次提交的符合 QC 标准的更新
2017年3月17日
最后验证
2017年3月1日
更多信息
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