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临床试验/NCT06108206
NCT06108206进行中(未招募)不适用

Adaptive Radiotherapy Based on Multi-Parametric Diffusion- and Perfusion-weighted Magnetic Resonance Imaging in Patients With Newly Diagnosed High-Grade Glioma

Columbia University2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2024年1月30日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
20
试验地点
2
主要终点
Prediction of progression of disease in patients with high-grade glioma.

研究概览

简要总结

The purpose of this study is to find out if performing additional Magnetic Resonance Image (MRI) scans of the subjects' brain during each week of the radiation treatment of their high-grade glioma will help improve the radiation treatment.

详细描述

Diffusion weighted imaging (DWI) and Perfusion-weighted imaging (PWI) are validated MRI techniques that aid in diagnosis, prognosis, and assessment of treatment efficacy and, while they are utilized in select clinical settings, they have yet to make their way into routine clinical practice at most centers. DWI is a non-invasive MRI modality that has demonstrated an ability to predict for a response to radiation therapy in the primary treatment of patients with glioblastoma (GBM). PWI is one collection of measures that includes dynamic susceptibility contrast (DSC) enhancement and dynamic contrast-enhanced (DCE) imaging. The latter methods of MRI-adapted radiotherapy allow the opportunity to direct high-dose radiation to areas most likely to harbor resistant tumor while avoiding regions having a low likelihood of future recurrence. Multiple MRI sequences have been developed and validated that may identify high-risk areas in patients with High-grade glioma (HGG) and the ability to acquire multiple sequential time points creates an opportunity for dynamic radiotherapy that has not previously been explored. The current standard of care in radiotherapy does not incorporate any additional neuroimaging data.

This study hypothesizes that pre- and mid-treatment advanced imaging with (DWI) and (PWI) in patients with HGG can be used to generate an adaptive radiotherapy boost volume that correlates with areas of future recurrence and that this volume has a higher spatial correlation relative to the current standard of care.

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

  • Histopathologically proven diagnosis of glioblastoma, anaplastic astrocytoma, or anaplastic oligodendroglioma
  • History and physical examination within 28 days prior to enrollment
  • Karnofsky performance status 70 or greater
  • Age 18 years or greater
  • Negative pregnancy test for females of childbearing potential before 1st research MRI, performed in accordance to institutional guidelines.
  • Plan to receive standard of care 59.4-60 Gy in 30-33 fractions of radiotherapy. Glioblastoma patients over 65 year-old can receive standard of care hypofractionated radiotherapy including 40 Gy in 15 fractions.

排除标准

  • Prior therapy for tumor except for biopsy or resection, including prior radiotherapy to the brain.
  • Clinical or radiological evidence of metastatic disease outside the brain
  • Prior malignancy (except non-melanomatous skin cancer) unless disease free for a minimum of 2 years

研究组 & 干预措施

Patients with primary high-grade glioma

Patients will receive standard of care radiotherapy over 30-33 once-daily fractions. Subjects receiving hypofractionated radiotherapy will receive radiotherapy per standard of care over 15 once-daily fractions.

结局指标

主要结局

Prediction of progression of disease in patients with high-grade glioma.

时间窗: 3 years

To compare the volume of the current standard of care conedown volume definition with an MRI-based adaptive plan in predicting the location of disease progression in patients with high-grade glioma.

次要结局

  • Estimate the progression-free and overall survival in patient with high-grade glioma.(3 years)

研究者

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

Tony Jau Cheng Wang

Professor of Radiation Oncology (in Neurological Surgery)

Columbia University

研究点 (2)

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