Pilot Study on the Determination of Therapy Resistant Areas Within the Tumor in Patients With High-grade Glioma by Repeated 18F-FDG-PET-CT Scans
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 发起方
- 入组人数
- 10
- 试验地点
- 1
- 主要终点
- To determine the localisation within the primary tumour of the therapy resistant cells, before and during radiotherapy to determine the accurate boost volume. To determine changes during treatment intra- and extratumoral within the irradiated area.
研究概览
简要总结
The objectives of the trial are:
- To determine the localisation within the primary tumor of the therapy resistant cells, before and during radiotherapy to determine a possible accurate boost volume.
- To determine changes during treatment intra- and extratumoral within the irradiated area.(Intratumoral: change of up-take - decrease, increase, change of localization/ Extratumoral: effects of temporal changes in up-take - e.g. due to oedema).
详细描述
Patients harboring a primary intracerebral high grade tumor (WHO III- IV) have a median survival of six to 12 months. Combined chemoradiotherapy with temozolomide is now the standard of care since results of the joint EORTC-NCIC phase III study randomizing between radiotherapy alone and combined radiochemotherapy with temozolomide showed a significant improvement in 2-years survival from 8% to 24% for the combined treatment arm (Stupp 2005).
A differentiation between possible responders and non-responders before the start of irradiation may eventual be possible by the use of 18F-FDG PET-CT. Preliminary own results have shown that a higher metabolic activity in glioblastoma as measured on a simulation 18F-FDG PET-CT scan can be a prognosticator for shortened survival (Baumert, 2006).
Our preliminary data show that a high uptake of 18F-FDG on a PET-CT scan before radiotherapy in glioblastoma could be a marker for reduced survival.
Popperl et al showed that dual phase FDG PET imaging is superior in differentiating low-grade from high-grade recurrent astrocytomas (Popperl, 2006). Visual analysis of delineation of glioma showed that the delayed images (imaged first 0-90 min and once or twice later at 180-480 min after injection) better distinguished the high uptake in tumors relative to uptake in gray matter. SUV comparisons also showed greater uptake in the tumors than in gray matter, brain, or white matter at the delayed times (Spence et al).
These findings support the view that by using FDG-PET scans we could image active areas within the tumor. Indeed, in vivo, a cancer is made up by different types of cells, including hypoxic cells, cells that proliferate more fast, as well as by non-malignant tissues, including inflammatory cells and vasculature.
研究设计
- 研究类型
- Observational
- 观察模型
- Case Only
- 时间视角
- Prospective
入排标准
- 年龄范围
- 19 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Histologically confirmed gliomas III - IV (glioblastoma, anaplastic astrocytoma, gliosarcoma) at primary diagnosis;
- •WhO PFS <= 2
- •Tumours which do enhance on pre-operative imaging.
- •Post-operative enough visible residual tumour on PET or status after biopsy only
- •Age >18 years
- •Availability of deep fresh frozen tissue for molecular biologic evaluation - if possible
- •Patient able to tolerate full course of conventional RT and follow serial scanning
- •No previous radiotherapy to the head and neck and brain area.
- •Prior neurosurgery within 6 weeks of treatment
- •No previous chemotherapy before treatment of the glioma. Standard radiochemotherapy with temozolomide is not excluded
- •No prior or concurrent medical condition which would make treatment difficult to complete. Medication with steroids is allowed.
- •No incapacitated patients.
排除标准
- •Not histologically confirmed gliomas III - IV (glioblastoma, anaplastic astrocytoma, gliosarcoma) at primary diagnosis;
- •WhO PFS > 2
- •No tumours which do enhance on pre-operative imaging.
- •Post-operative not enough visible residual tumor on PET or status after biopsy only
- •Age <18 years
- •No availability of deep fresh frozen tissue for molecular biologic evaluation
- •Patient not able to tolerate full course of conventional RT and follow serial scanning
- •Previous radiotherapy to the head and neck and brain area.
- •Prior neurosurgery not within 6 weeks of treatment
- •Previous chemotherapy before treatment of the glioma.
- •Prior or concurrent medical condition which would make treatment difficult to complete.
- •Incapacitated patients.
结局指标
主要结局
To determine the localisation within the primary tumour of the therapy resistant cells, before and during radiotherapy to determine the accurate boost volume. To determine changes during treatment intra- and extratumoral within the irradiated area.
时间窗: after acquisition of all planned PET CTs
次要结局
未报告次要终点