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UNIty-Based MR-Linac Guided AdapTive RadiothErapy for High GraDe Glioma: A Phase 2 Trial (UNITED)

Primary Purpose

Glioblastoma Multiforme

Status
Active
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Reduced margin adaptive radiotherapy
Sponsored by
Sunnybrook Health Sciences Centre
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Glioblastoma Multiforme

Eligibility Criteria

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

Inclusion Criteria:

  • Patients aged 18 years and older
  • Histopathologically confirmed malignant glioma of the brain, Grade 4 (GBM)
  • Eligible for RT in 15 or 30 fractions with or without chemotherapy (temozolamide)
  • Expected survival greater than 12 weeks
  • WHO performance status less than or equal to 2
  • Able to converse and answer questionnaires in English language
  • Has a maximum final planning volume less than 150 cm3

Exclusion Criteria:

  • Contraindications to MRI examination as per standard MRI screening policy
  • Contraindication to Gadolinium-based contrast media
  • Unable to lie flat in a supine position for 30 minutes
  • Poor baseline kidney function with an eGFR < 60 mL/min
  • Unable to tolerate immobilization in a head thermoplastic mask
  • Patients >140 kg and/or a circumference >60cm
  • Previous cranial irradiation
  • Infratentorial tumour extent, multifocal of leptomeningeal disease
  • Unable to give informed consent

Sites / Locations

  • Sunnybrook Health Sciences Centre

Outcomes

Primary Outcome Measures

Imaging-detected tumor recurrence at the edge of the radiation volume ("marginal" failure)
The presence of tumor on contrast-enhanced MRI between 1-2 cm from the edge of the treated radiation volume (commonly known as a marginal failure) within 1 year from radiation.

Secondary Outcome Measures

Tumor volume changes during RT
Change in gross tumor volume (%) from start to end of RT
Acute radiation toxicity based on RTOG/EORTC Common Toxicity Criteria
Grades 1-4 toxicity during RT in the following categories: skin, CNS, eye, ear, and hematological
Quality of life changes based on EORTC QLQ-C30
Changes in quality of life during and after RT based on accepted EORTC cancer quality of life instruments administered each week on RT, 1 month post RT, and every 3 months subsequently
Dexamethasone usage
Amount of dexamethasone required during RT
Quality of life based on EORTC QLQ-BN20
Changes in quality of life during and after RT based on accepted EORTC brain tumor quality of life instruments administered each week on RT, 1 month post RT, and every 3 months subsequently

Full Information

First Posted
January 19, 2021
Last Updated
April 26, 2023
Sponsor
Sunnybrook Health Sciences Centre
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1. Study Identification

Unique Protocol Identification Number
NCT04726397
Brief Title
UNIty-Based MR-Linac Guided AdapTive RadiothErapy for High GraDe Glioma: A Phase 2 Trial
Acronym
UNITED
Official Title
UNIty-Based MR-Linac Guided AdapTive RadiothErapy for High GraDe Glioma: A Phase 2 Trial (UNITED Trial)
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
March 29, 2021 (Actual)
Primary Completion Date
May 2024 (Anticipated)
Study Completion Date
May 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Sunnybrook Health Sciences Centre

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Glioblastoma (GBM) is a high grade glioma (brain tumor) that is treated with surgery or biopsy followed by radiotherapy (RT) given daily over 3 or 6 weeks with or without an oral chemotherapy. Radiation is targeted to the visible residual tumor on magnetic resonance imaging (MRI) images plus a large margin of 15 to 30 mm to account for possible cancer cells outside the visible tumor and for potential growth or shifts in tumor position throughout the prolonged RT course. Standard RT uses MRI to create a reference plan (with large margins) and treats that same volume every day. This exposes a large amount of healthy brain tissue to radiation leading to toxicity and reduced quality of life. A new technology, the MR-Linac, combines an MRI scanner and a Linac (radiation delivery machine) into one unit. This allows for "adaptive" RT by obtaining an updated MRI scan each day just prior to treatment, adapting the RT plan to take into account any changes in the tumor or the patient's anatomy on that given day. This allows for a smaller (5 mm) margin on the visible tumor as its position can be tracked daily. The goal of this study is to use adaptive RT with small margins to demonstrate that the local control of the visible tumor is not compromised compared to the large volumes used with standard non-adaptive RT, while determining whether smaller margins lead to decreased radiation toxicity and therefore improved quality of life by minimizing radiation exposure.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Glioblastoma Multiforme

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
108 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Radiation
Intervention Name(s)
Reduced margin adaptive radiotherapy
Intervention Description
Reduced (5 mm) clinical target volume margin with weekly contrast-enhanced adaptive radiation on the MR-Linac treatment machine
Primary Outcome Measure Information:
Title
Imaging-detected tumor recurrence at the edge of the radiation volume ("marginal" failure)
Description
The presence of tumor on contrast-enhanced MRI between 1-2 cm from the edge of the treated radiation volume (commonly known as a marginal failure) within 1 year from radiation.
Time Frame
Within 1 year from end of radiation
Secondary Outcome Measure Information:
Title
Tumor volume changes during RT
Description
Change in gross tumor volume (%) from start to end of RT
Time Frame
6 weeks
Title
Acute radiation toxicity based on RTOG/EORTC Common Toxicity Criteria
Description
Grades 1-4 toxicity during RT in the following categories: skin, CNS, eye, ear, and hematological
Time Frame
6 weeks
Title
Quality of life changes based on EORTC QLQ-C30
Description
Changes in quality of life during and after RT based on accepted EORTC cancer quality of life instruments administered each week on RT, 1 month post RT, and every 3 months subsequently
Time Frame
1 year
Title
Dexamethasone usage
Description
Amount of dexamethasone required during RT
Time Frame
10 weeks
Title
Quality of life based on EORTC QLQ-BN20
Description
Changes in quality of life during and after RT based on accepted EORTC brain tumor quality of life instruments administered each week on RT, 1 month post RT, and every 3 months subsequently
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients aged 18 years and older Histopathologically confirmed malignant glioma of the brain, Grade 4 (GBM) Eligible for RT in 15 or 30 fractions with or without chemotherapy (temozolamide) Expected survival greater than 12 weeks WHO performance status less than or equal to 2 Able to converse and answer questionnaires in English language Has a maximum final planning volume less than 150 cm3 Exclusion Criteria: Contraindications to MRI examination as per standard MRI screening policy Contraindication to Gadolinium-based contrast media Unable to lie flat in a supine position for 30 minutes Poor baseline kidney function with an eGFR < 60 mL/min Unable to tolerate immobilization in a head thermoplastic mask Patients >140 kg and/or a circumference >60cm Previous cranial irradiation Infratentorial tumour extent, multifocal of leptomeningeal disease Unable to give informed consent
Facility Information:
Facility Name
Sunnybrook Health Sciences Centre
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M4N3M5
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

UNIty-Based MR-Linac Guided AdapTive RadiothErapy for High GraDe Glioma: A Phase 2 Trial

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