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临床试验/NCT04197297
NCT04197297招募中2 期

Imaging Trial of Biomarkers to Guide Individualized Therapy in Patients With Brain Metastasis Receiving Radiotherapy

University Health Network, Toronto1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2021年10月5日最近更新:
适应症
干预措施

试验速览

阶段
2 期
状态
招募中
入组人数
90
试验地点
1
主要终点
Response Assessment in Neuro-Oncology (RANO) to validate biomarkers

研究概览

简要总结

A biomarker is a measurable indicator of the severity or presence of some disease state. In this study, brain metastases patients who will be receiving radiation treatment, will undergo CT (Computed Tomography) and MRI (Magnetic Resonance Imaging) scans prior to and after radiation treatment to measure these biomarkers. This is a single-center phase II study to validate the predictive abilities of biomarkers, in terms of determining how patients will respond to radiation treatment.

详细描述

Advances in medical imaging can provide useful information to guide and look at the response to treatment. Previous studies suggest early changes in the tumor after radiation treatment may be detectable using special MRI (Magnetic Resonance Imaging), and CT (Computed Tomography) scans. A biomarker is a measureable indicator of the severity or presence of some disease state. Previous studies suggest that the change in several imaging biomarkers can predict who will respond to radiation treatment. In this study, patients will undergo CT and MRI scans prior to and after radiation treatment to measure these biomarkers. The purpose of this study is to validate the predictive abilities of biomarkers in terms of determining how patients will respond to radiation treatment. This is a single-center phase II study, which will be conducted at the Princess Margaret Cancer Center. The study will be enrolling up to a total of 90 patients who will be receiving radiation treatment for brain metastases. Patients will be asked to participate within this study for 2 years.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

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

  • Biopsy proven primary malignancy (original biopsy is adequate as long as the brain imaging is consistent with brain metastases)
  • At least one index lesion with diameter > 1cm and without imaging evidence of hemorrhage
  • Patients age > 18 years of age
  • Patients planned for RT to brain metastases
  • Ability to understand and the willingness to sign a written informed consent document.

排除标准

  • Previous Whole Brain Radiotherapy
  • Previous radiosurgery to the index lesion
  • Individuals unable to undergo contrasted MRI for whatever reason

研究组 & 干预措施

CT and MRI Scans

Other

Each patient will undergo a 3T MRI scan as well as a dynamic contrast-enhanced CT scan within one week prior to the start of treatment. Patients will also undergo a research 3T MRI scan and research dynamic contrast-enhanced CT scan at the one week post radiotherapy mark. An MRI scan during their 3 month post-treatment follow up visits will take place as per routine standard of care.

干预措施: CT and MRI Scans (Diagnostic Test)

结局指标

主要结局

Response Assessment in Neuro-Oncology (RANO) to validate biomarkers

时间窗: Up to 2 years.

Using RANO to validate imaging predictive biomarkers of response to radiotherapy

Progression Free Survival (PFS) to validate biomarkers

时间窗: Up to 2 years.

Using PFS to validate imaging predictive biomarkers of response to radiotherapy

Response Evaluation Criteria in Solid Tumors (RECIST) criteria to validate biomarkers

时间窗: Up to 2 years.

Using RECIST criteria to validate imaging predictive biomarkers of response to radiotherapy

次要结局

  • Objective (Radiological) Progression(Up to 2 years.)
  • Time to Intracranial Local Progression(Up to 2 years.)
  • Objective (Radiological) Response(Up to 2 years.)
  • Time to Intracranial Distant Progression(Up to 2 years.)
  • Brain Progression Free Survival(Up to 2 years.)
  • Unexpected and/or Serious Toxicities (AEs)(Up to 2 years.)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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