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临床试验/NCT01873469
NCT01873469已完成不适用

Observational Study of Impact of [11C]-Methionine PET/MRI as a Tool for Individual Tailoring Postoperative Radiochemotherapy for Patients With Glioblastoma Multiforme

Technische Universität Dresden1 个研究点 分布在 1 个国家目标入组 102 人开始时间: 2013年7月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
102
试验地点
1
主要终点
Time to recurrence as function of [11C]MET uptake before postoperative radiochemotherapy

研究概览

简要总结

Local recurrence is a major problem of clinical treatment of glioblastoma multiforme (GBM). Today a very sensitive imaging method to detect glioblastoma is [11C]MET Positron emission tomography (PET), where in some patients also tumour manifestations can be detected that are not visible in MRI investigations.

The aim of the study is to investigate the association of high [11C]MET tracer uptake before postoperative radiochemotherapy and concurrent temozolomide (TMZ) with time to recurrence in patients with glioblastoma multiforme. Also site of recurrence will be correlated with the [11C]MET imaging before and early during radiochemotherapy. All imaging information will be included in treatment planning or treatment decisions.

The study provides a basis for later radiation dose escalation trials on the base of [11C]MET imaging.

详细描述

The current study aims to investigate the association of high [11C]MET tracer uptake before postoperative radiochemotherapy and concurrent temozolomide (TMZ) with time to recurrence in patients with glioblastoma multiforme (GBM).

[11C]MET-PET is expected to provide diagnostic (quantitative and spatial information) as well as prognostic information, to monitor treatment, to help stratification of patients for radiotherapeutic interventions such as dose-painting in order to optimize clinical applications and potentially improve the treatment outcome.

This study aims to provide the basis (e.g. optimal threshold value, sensitivity, specificity of MET uptake) for later intervention trials for treatment intensification, e.g. proton boost irradiation based on specific biomarkers.

The trial is a one-arm single-center, non-randomized observational (biomarker) study. After resection or biopsy, patients with newly diagnosed glioblastoma multiforme will receive a [11C]MET-PET/MRI scan before start of concurrent radiochemotherapy (~1-4 weeks after surgery). A fusion with the planning CT for irradiation treatment planning will be performed. Postoperative radiotherapy will be applied in daily fractions of 2 Gy given 5 days per week for 6 weeks, for a total dose of 60 Gy (50 Gy and a boost of 10 Gy), with concomitant administration of daily Temozolomide (75 mg/m2 p.o.) from the 1st day to the last day of radiotherapy. Follow up with [11C]MET-PET/MRI will be performed every 3 months until recurrence or until death of the patient.

The uptake of [11C]MET-PET (as standard uptake value - SUV) in tumour and in normal contralateral grey matter before start of concurrent radiochemotherapy will be determined. For each tumour, the ratio between tracer uptake in the tumor and contralateral gray matter will be calculated (lesion-to-gray matter ratio [l/g]).

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • histologically confirmed newly diagnosed glioblastoma multiforme
  • macroscopic total tumour resection or biopsy
  • indication for combined radiochemotherapy with temozolomide
  • patients are allowed to take part in other clinical trials at the same time
  • beginning of radiochemotherapy no later than 7 weeks after surgery
  • Karnofsky Performance Score ≥ 60, ECOG ≤2
  • women with childbearing potential, (and men) adequate contraception
  • ability of subject to understand character and individual consequences of the clinical trial
  • written informed consent

排除标准

  • previous radiotherapy of the brain or chemotherapy with TMZ other than during the radiochemotherapy
  • time interval of > 7 weeks after surgery and beginning of radiochemotherapy
  • patients who are not suitable for radiochemotherapy
  • known other malignant disease that impacts prognosis of the patient and/or is likely to require treatment interfering with study therapy
  • pregnant or lactating women
  • patients with non-MRI compatible metal implants, pacemaker or non-MRI compatible external automatic defibrillators, insulin pumps, neurostimulators, cochlear implants
  • Claustrophobic patients
  • refusal of the patients to take part in the study

结局指标

主要结局

Time to recurrence as function of [11C]MET uptake before postoperative radiochemotherapy

时间窗: participants will be followed until tumour recurrence, an expected average of 7 months

次要结局

  • overall survival(expected average 15 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Mechthild Krause

PD Dr. med.

Technische Universität Dresden

研究点 (1)

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