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Brain Imaging Biomarkers in Patients With Brain Metastasis

Primary Purpose

Brain Metastases, Adult

Status
Recruiting
Phase
Phase 2
Locations
Canada
Study Type
Interventional
Intervention
CT and MRI Scans
Sponsored by
University Health Network, Toronto
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Brain Metastases, Adult focused on measuring Radiation Therapy, Radiotherapy, Biomarkers, Magnetic Resonance Imaging, Computed Tomography, Radiosurgery

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 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.

Exclusion Criteria:

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

Sites / Locations

  • University Health NetworkRecruiting

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

CT and MRI Scans

Arm Description

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.

Outcomes

Primary Outcome Measures

Response Assessment in Neuro-Oncology (RANO) to validate biomarkers
Using RANO to validate imaging predictive biomarkers of response to radiotherapy
Response Evaluation Criteria in Solid Tumors (RECIST) criteria to validate biomarkers
Using RECIST criteria to validate imaging predictive biomarkers of response to radiotherapy
Progression Free Survival (PFS) to validate biomarkers
Using PFS to validate imaging predictive biomarkers of response to radiotherapy

Secondary Outcome Measures

Objective (Radiological) Progression
Defined as increase in volume of contrast uptake on MRI of > 25% as measured by two perpendicular tumor diameters compared to the smallest measurement ever for the same lesion by the same technique.
Objective (Radiological) Response
Defined as stable or reduced volume of contrast uptake on MRI (i.e., all non-progression).
Time to Intracranial Local Progression
Defined as the time interval between the date of first treatment and the date of objective radiological progression of any one of the treated lesions.
Time to Intracranial Distant Progression
Defined as the time interval between the date of first treatment and the date of new brain metastases, with or without progression of the treated lesions.
Brain Progression Free Survival
Defined as the time interval between the date of first treatment and the date of disease progression in the brain or death due to disease in the brain, whichever comes first.
Unexpected and/or Serious Toxicities (AEs)
AEs that are deemed by the PI to be possibly, probably or definitely attributable to the research MRI and/or CT will be reported according to CTCAE version 4.3.

Full Information

First Posted
November 25, 2019
Last Updated
April 5, 2023
Sponsor
University Health Network, Toronto
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1. Study Identification

Unique Protocol Identification Number
NCT04197297
Brief Title
Brain Imaging Biomarkers in Patients With Brain Metastasis
Official Title
Imaging Trial of Biomarkers to Guide Individualized Therapy in Patients With Brain Metastasis Receiving Radiotherapy
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 5, 2021 (Actual)
Primary Completion Date
January 2024 (Anticipated)
Study Completion Date
January 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Health Network, Toronto

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
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.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Brain Metastases, Adult
Keywords
Radiation Therapy, Radiotherapy, Biomarkers, Magnetic Resonance Imaging, Computed Tomography, Radiosurgery

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Model Description
Participants will undergo CT and MRIs before and after radiation therapy.
Masking
None (Open Label)
Allocation
N/A
Enrollment
90 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
CT and MRI Scans
Arm Type
Other
Arm Description
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.
Intervention Type
Diagnostic Test
Intervention Name(s)
CT and MRI Scans
Intervention Description
CT and MRI scans will occur before and after radiation therapy.
Primary Outcome Measure Information:
Title
Response Assessment in Neuro-Oncology (RANO) to validate biomarkers
Description
Using RANO to validate imaging predictive biomarkers of response to radiotherapy
Time Frame
Up to 2 years.
Title
Response Evaluation Criteria in Solid Tumors (RECIST) criteria to validate biomarkers
Description
Using RECIST criteria to validate imaging predictive biomarkers of response to radiotherapy
Time Frame
Up to 2 years.
Title
Progression Free Survival (PFS) to validate biomarkers
Description
Using PFS to validate imaging predictive biomarkers of response to radiotherapy
Time Frame
Up to 2 years.
Secondary Outcome Measure Information:
Title
Objective (Radiological) Progression
Description
Defined as increase in volume of contrast uptake on MRI of > 25% as measured by two perpendicular tumor diameters compared to the smallest measurement ever for the same lesion by the same technique.
Time Frame
Up to 2 years.
Title
Objective (Radiological) Response
Description
Defined as stable or reduced volume of contrast uptake on MRI (i.e., all non-progression).
Time Frame
Up to 2 years.
Title
Time to Intracranial Local Progression
Description
Defined as the time interval between the date of first treatment and the date of objective radiological progression of any one of the treated lesions.
Time Frame
Up to 2 years.
Title
Time to Intracranial Distant Progression
Description
Defined as the time interval between the date of first treatment and the date of new brain metastases, with or without progression of the treated lesions.
Time Frame
Up to 2 years.
Title
Brain Progression Free Survival
Description
Defined as the time interval between the date of first treatment and the date of disease progression in the brain or death due to disease in the brain, whichever comes first.
Time Frame
Up to 2 years.
Title
Unexpected and/or Serious Toxicities (AEs)
Description
AEs that are deemed by the PI to be possibly, probably or definitely attributable to the research MRI and/or CT will be reported according to CTCAE version 4.3.
Time Frame
Up to 2 years.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 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. Exclusion Criteria: Previous Whole Brain Radiotherapy Previous radiosurgery to the index lesion Individuals unable to undergo contrasted MRI for whatever reason
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
David Shultz, M.D., Ph. D
Phone
416-946-6899
Email
david.shultz@rmp.uhn.on.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Catherine Coolens, Ph. D
Phone
416-946-5011
Email
catherine.coolens@rmp.uhn.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Catherine Coolens, Ph. D
Organizational Affiliation
Princess Margaret Cancer Center - UHN
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Health Network
City
Toronto
State/Province
Ontario
ZIP/Postal Code
L4W4C2
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
David Shultz, MD
Phone
416 946 4501
Email
david.shultz@rmp.uhn.ca

12. IPD Sharing Statement

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Brain Imaging Biomarkers in Patients With Brain Metastasis

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