Volumetric Modulated Arc Therapy (VMAT) for Brain Metastases
Primary Purpose
Brain Metastases
Status
Active
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
whole brain radiotherapy (WBRT) and a simultaneous integrated boost (SIB) using volumetric modulated arc therapy
Sponsored by
About this trial
This is an interventional treatment trial for Brain Metastases
Eligibility Criteria
Inclusion Criteria:
- Age ≥ 18
- pathologically confirmed solid malignancy diagnosed within the past 5 years (if the original pathological cancer diagnosis is more than 5 years earlier, a biopsy to confirm metastatic relapse within the past 5 years is required)
- 1-10 brain metastases
- Maximum diameter of largest metastasis ≤ 3 cm
- KPS ≥ 70
- Patient is neurologically stable with or without corticosteroids
- Extracranial disease well-controlled (6-month estimated median life expectancy).
- Available for regular clinical and imaging follow up
- Prior craniotomy permitted
Exclusion Criteria:
- Require craniotomy to relieve mass effect
- Previous cranial radiotherapy
- Metastatic germinoma, small cell carcinoma, multiple myeloma, lymphoma or leukaemia.
- Chemotherapy administered within one week before radiotherapy or planned within one week after radiotherapy.
- Metastases within 0.7 cm of the optic chiasm, brainstem or optic nerves
- Brainstem metastases
- Systemic lupus erythematosis, scleroderma, or other connective tissue disorders not in remission
- Multiple sclerosis
- Glomerular Filtration Rate < 60 ml/minute
- Non-small cell lung cancer with liver metastases
- Bilirubin > upper normal limit
- AST or ALT > 2X upper normal limit
- Pregnancy
- Summed volume of all metastasis PTVs > 50 cm3
Sites / Locations
- BC Cancer Agency - Vancouver Centre
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Whole brain radiotherapy
Arm Description
whole brain radiotherapy (WBRT) and a simultaneous integrated boost (SIB) using volumetric modulated arc therapy
Outcomes
Primary Outcome Measures
3 month treatment response of metastases evaluated using contrast-enhanced MRI scan of brain
Secondary Outcome Measures
1-year local control of treated metastases evaluated with contrast-enhanced MRI scan of brain
1-year brain control of metastases evaluated with contrast-enhanced MRI scan of brain
Median survival
Both acute neurological toxicity (within 3 months of treatment) and late neurological toxicity (beyond 3 months of treatment
Time to decline in activities of daily living evaluated using the Modified Barthel index
Time to decline in cognition evaluated with the Mini-mental state examination
Full Information
NCT ID
NCT01046123
First Posted
January 7, 2010
Last Updated
August 8, 2023
Sponsor
British Columbia Cancer Agency
1. Study Identification
Unique Protocol Identification Number
NCT01046123
Brief Title
Volumetric Modulated Arc Therapy (VMAT) for Brain Metastases
Official Title
A Phase II Study of Whole Brain Radiotherapy With Simultaneous Integrated Boost Using Volumetric Modulated Arc Therapy for One to Ten Brain Metastases
Study Type
Interventional
2. Study Status
Record Verification Date
August 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
January 2010 (undefined)
Primary Completion Date
June 2013 (Actual)
Study Completion Date
December 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
British Columbia Cancer Agency
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Radiotherapy to the whole brain is standard treatment for cancer that has spread to the brain (brain metastases) as it treats both the metastases that can be seen on scans and the brain metastases that are too small to be seen on scans.
This study will use a novel radiotherapy technique, called volumetric modulated arc therapy (VMAT), to treat patients with brain metastases. This technique allows delivery of both a standard radiation dose to the whole brain as well as a higher radiation dose to the brain metastases at the same time.
The study will assess the effectiveness of using VMAT in treating brain metastases, and examine its potential side-effects.
Detailed Description
This is a Phase II prospective clinical trial. Following registration, patients will be required to undertake a baseline questionnaire assessment of daily living activities using the Modified Barthel's index, as well as cognitive assessment using MMSE.
Patients will undergo MRI scan of the brain for radiotherapy planning purposes. During radiotherapy planning and for each of the five radiotherapy fractions, patients will be immobilised in a custom fitted stereotactic mask system, to minimise head movement. During treatment, patients will have daily online setup corrections to ensure treatment accuracy.
Patients will be treated with WBRT/SIB using VMAT, delivering a total of 20 Gy in 5 fractions to the whole brain and 50Gy in 5 fractions to the brain metastases, delivered once daily on working days. Anti-nausea and anti-inflammatory medication will be prescribed to minimise acute toxicity.
Following therapy completion, patients will be seen every 3 months for the 1st year, then every 6 months thereafter. At each clinic visit, clinicians or study investigators will monitor for toxicity from therapy, document neurologic symptoms and signs and performance status as well as Modified Barthel's index and cognitive assessment.
Patients will have contrast-enhanced MRI brain at 3 months and 1 year, and contrast-enhanced CT brain at 6 months and 9 months in the first year and every 6 months after the first year. Serum creatinine levels will be done prior to each scan to ensure safety of intravenous contrast administration.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Brain Metastases
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
60 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Whole brain radiotherapy
Arm Type
Experimental
Arm Description
whole brain radiotherapy (WBRT) and a simultaneous integrated boost (SIB) using volumetric modulated arc therapy
Intervention Type
Radiation
Intervention Name(s)
whole brain radiotherapy (WBRT) and a simultaneous integrated boost (SIB) using volumetric modulated arc therapy
Intervention Description
Patients will be treated with WBRT/SIB using VMAT, delivering a total of 20 Gy in 5 fractions to the whole brain and 50Gy in 5 fractions to the brain metastases, delivered once daily on working days.
Primary Outcome Measure Information:
Title
3 month treatment response of metastases evaluated using contrast-enhanced MRI scan of brain
Time Frame
3 months post treatment
Secondary Outcome Measure Information:
Title
1-year local control of treated metastases evaluated with contrast-enhanced MRI scan of brain
Time Frame
1 year post-treatment
Title
1-year brain control of metastases evaluated with contrast-enhanced MRI scan of brain
Time Frame
1 year post-treatment
Title
Median survival
Time Frame
No time frame
Title
Both acute neurological toxicity (within 3 months of treatment) and late neurological toxicity (beyond 3 months of treatment
Time Frame
3 months and beyond
Title
Time to decline in activities of daily living evaluated using the Modified Barthel index
Time Frame
No time frame
Title
Time to decline in cognition evaluated with the Mini-mental state examination
Time Frame
No time frame
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
100 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age ≥ 18
pathologically confirmed solid malignancy diagnosed within the past 5 years (if the original pathological cancer diagnosis is more than 5 years earlier, a biopsy to confirm metastatic relapse within the past 5 years is required)
1-10 brain metastases
Maximum diameter of largest metastasis ≤ 3 cm
KPS ≥ 70
Patient is neurologically stable with or without corticosteroids
Extracranial disease well-controlled (6-month estimated median life expectancy).
Available for regular clinical and imaging follow up
Prior craniotomy permitted
Exclusion Criteria:
Require craniotomy to relieve mass effect
Previous cranial radiotherapy
Metastatic germinoma, small cell carcinoma, multiple myeloma, lymphoma or leukaemia.
Chemotherapy administered within one week before radiotherapy or planned within one week after radiotherapy.
Metastases within 0.7 cm of the optic chiasm, brainstem or optic nerves
Brainstem metastases
Systemic lupus erythematosis, scleroderma, or other connective tissue disorders not in remission
Multiple sclerosis
Glomerular Filtration Rate < 60 ml/minute
Non-small cell lung cancer with liver metastases
Bilirubin > upper normal limit
AST or ALT > 2X upper normal limit
Pregnancy
Summed volume of all metastasis PTVs > 50 cm3
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alan M Nichol, MD
Organizational Affiliation
British Columbia Cancer Agency
Official's Role
Principal Investigator
Facility Information:
Facility Name
BC Cancer Agency - Vancouver Centre
City
Vancouver
State/Province
British Columbia
ZIP/Postal Code
V5Z 4E6
Country
Canada
12. IPD Sharing Statement
Citations:
PubMed Identifier
33239056
Citation
Chan M, Ferguson D, Ni Mhurchu E, Yuan R, Gondara L, McKenzie M, Olson R, Thiessen B, Lalani N, Ma R, Nichol A. Patients with pretreatment leukoencephalopathy and older patients have more cognitive decline after whole brain radiotherapy. Radiat Oncol. 2020 Nov 25;15(1):271. doi: 10.1186/s13014-020-01717-x.
Results Reference
derived
PubMed Identifier
26678660
Citation
Nichol A, Ma R, Hsu F, Gondara L, Carolan H, Olson R, Schellenberg D, Germain F, Cheung A, Peacock M, Bergman A, Vollans E, Vellani R, McKenzie M. Volumetric Radiosurgery for 1 to 10 Brain Metastases: A Multicenter, Single-Arm, Phase 2 Study. Int J Radiat Oncol Biol Phys. 2016 Feb 1;94(2):312-21. doi: 10.1016/j.ijrobp.2015.10.017. Epub 2015 Oct 22.
Results Reference
derived
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Volumetric Modulated Arc Therapy (VMAT) for Brain Metastases
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