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Neurocognitive Functioning With Genu-Sparing Whole Brain Radiation Therapy for Brain Metastases

Primary Purpose

Brain Metastases

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
whole brain radiation therapy
Sponsored by
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Brain Metastases focused on measuring whole brain radiation therapy, genu of corpus callosum, cognitive function

Eligibility Criteria

18 Years - 100 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Histologic proof or unequivocal cytologic proof solid tumor malignancy. This may be obtained from either the primary or any metastatic site
  • Mini Mental State Examination (MMSE) ≥24
  • Age≥ 18 years
  • Karnofsky Performance Status (KPS) ≥70
  • Patient does not have metastases to the genu
  • Patient must be scheduled to undergo treatment with whole brain radiation therapy (WBRT) to manage the brain metastases
  • Patients of childbearing potential (male or female) must practice adequate contraception due to possible harmful effects of radiation therapy on an unborn child
  • Patient must have the ability to understand and the willingness to sign a written informed consent document
  • All patients must be informed of the investigational nature of this study and must be given written informed consent in accordance with institutional and federal guidelines
  • Patient must have a minimal life expectancy of at least 6 months
  • Patients receiving prior stereostatic radiosurgery (SRS) for brain metastases are eligible

Exclusion Criteria:

  • Prior WBRT
  • MMSE<24
  • Patient has brain metastases in the genu
  • Patients must not have a serious medical or psychiatric illness that would, in the opinion of the treating physician prevent informed consent or completion of protocol treatment, and/or follow-up visits.
  • KPS<70
  • Non-native English speakers will be excluded since patients often lose their faculty with the language they acquired second before their native language is affected in the context of cognitive decline. This could adversely affect performance on verbal cognitive tasks.
  • Patients with absolute contraindication to MRI imaging are not eligible for the study

Sites / Locations

  • Sibley Memorial HospitalRecruiting
  • The SKCCC at Johns HopkinsRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Corpus Callosum Genu-Sparing Whole Brain Radiation Therapy

Arm Description

Genu-sparing whole brain radiation therapy (GS-WBRT) 30 Gy in 3 Gy per fraction

Outcomes

Primary Outcome Measures

Rate of change of cognitive function
Evaluate changes in cognition from baseline to 4 months following genu-sparing whole brain radiation therapy (GS-WBRT)

Secondary Outcome Measures

Rate of change of white matter microstructure
Evaluate change in white matter microstructure following GS-WBRT utilizing diffusion tensor imaging
Rate of change of cognition
Evaluate changes in cognition from baseline to 4, 6 and 12 months following GS-WBRT
Time to brain metastasis
Document development of brain metastases in the spared genu of the corpus callosum
Rate of change in QoL
Document changes in QOL, neuropsychiatric symptoms, and functioning in patients receiving GS-WBRT from pre-treatment to 4, 6 and 12 months following GS-WBRT
Rate of change in other frontally-mediated functions
Document the stability of other frontally-mediated cognitive functions in those receiving GS-WBRT from pre-treatment to 4, 6 and 12 months following GS-WBRT.

Full Information

First Posted
July 12, 2017
Last Updated
May 30, 2023
Sponsor
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
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1. Study Identification

Unique Protocol Identification Number
NCT03223922
Brief Title
Neurocognitive Functioning With Genu-Sparing Whole Brain Radiation Therapy for Brain Metastases
Official Title
Preservation of Cognition and Neuropsychiatric Functioning With Corpus Callosum Genu-Sparing Whole Brain Radiation Therapy for Brain Metastases: A Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
July 19, 2017 (Actual)
Primary Completion Date
December 2025 (Anticipated)
Study Completion Date
December 2030 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins

4. Oversight

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

5. Study Description

Brief Summary
This is a trial that evaluates the preservation of cognition and neuropsychiatric function following genu-sparing whole brain radiation in patients with brain metastases.
Detailed Description
Efforts at treating radiation-induced cognitive and neuropsychiatric declines with medications have shown only minimal preliminary cognitive benefit and do not affect quality of life (QOL). Given the structural and functional brain alterations associated with WBRT, preventing rather than treating these radiation-induced changes may produce more favorable outcomes. Innovative radiotherapy techniques can limit the dose of radiation applied to specific brain structures without compromising tumor coverage. In this light, Radiation Therapy Oncology Group (RTOG) recently published a study evaluating the hippocampal avoidance whole brain radiation therapy (WBRT) in patients with brain metastases. They suggest potential preservation of cognitive function with this approach with no perceived detriment in survival. This concept is currently undergoing investigation in a definitive randomized controlled study (NRG-CC003) in patients receiving prophylactic cranial irradiation for small cell lung cancer. However, no other studies to date have prospectively evaluated avoidance of other particularly sensitive brain regions. One brain region that has received little attention in the radiotherapy literature is the corpus callosum. The genu of the corpus callosum contains thin, densely packed neural fibers that primarily connect the prefrontal association areas and the anterior inferior parietal regions of the brain. Damage or thinning of the genu is associated with reduced functioning on tests of executive functioning, attention, working memory, processing speed, verbal fluency and memory in a variety of healthy and patient groups including aging, cerebral small vessel disease, traumatic brain injury, multiple sclerosis , human immunodeficiency virus, mild cognitive impairment secondary to Parkinson's disease, and euthymic bipolar disorder. The limited existing data in adults receiving WBRT for brain metastases suggest that they also perceive progressive declines in motivation following treatment. Given its apparent involvement in a wide range of cognitive processes, the genu of the corpus callosum is an excellent candidate for sparing in WBRT. This relatively small area has the potential to preserve cognitive functioning across several domains if guarded from the damaging effects of radiation. In this study patients will receive the standard whole brain radiation dose of 3000 centigray (cGy) in 10 fractions, but intensity modulated radiation therapy will be utilized to limit radiation dose to the genu of the corpus callosum. Patients will undergo cognitive testing at baseline and at 4-, 6- and 12-months following completion of brain radiation to evaluate the study hypothesis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Brain Metastases
Keywords
whole brain radiation therapy, genu of corpus callosum, cognitive function

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Patients will be treated to a total dose of 30 Gy with a once daily fractionation schedule of 3 Gy per fraction, administered five days per week.
Masking
None (Open Label)
Allocation
N/A
Enrollment
24 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Corpus Callosum Genu-Sparing Whole Brain Radiation Therapy
Arm Type
Experimental
Arm Description
Genu-sparing whole brain radiation therapy (GS-WBRT) 30 Gy in 3 Gy per fraction
Intervention Type
Radiation
Intervention Name(s)
whole brain radiation therapy
Other Intervention Name(s)
WBRT
Intervention Description
Corpus Callosum Genu-Sparing Whole Brain Radiation Therapy Genu-sparing whole brain radiation therapy (GS-WBRT) 30 Gy in 3 Gy per fraction
Primary Outcome Measure Information:
Title
Rate of change of cognitive function
Description
Evaluate changes in cognition from baseline to 4 months following genu-sparing whole brain radiation therapy (GS-WBRT)
Time Frame
4 months
Secondary Outcome Measure Information:
Title
Rate of change of white matter microstructure
Description
Evaluate change in white matter microstructure following GS-WBRT utilizing diffusion tensor imaging
Time Frame
4, 6 and 12 months
Title
Rate of change of cognition
Description
Evaluate changes in cognition from baseline to 4, 6 and 12 months following GS-WBRT
Time Frame
4, 6 and 12 months
Title
Time to brain metastasis
Description
Document development of brain metastases in the spared genu of the corpus callosum
Time Frame
4, 6 and 12 months
Title
Rate of change in QoL
Description
Document changes in QOL, neuropsychiatric symptoms, and functioning in patients receiving GS-WBRT from pre-treatment to 4, 6 and 12 months following GS-WBRT
Time Frame
4, 6 and 12 months
Title
Rate of change in other frontally-mediated functions
Description
Document the stability of other frontally-mediated cognitive functions in those receiving GS-WBRT from pre-treatment to 4, 6 and 12 months following GS-WBRT.
Time Frame
4, 6 and 12 months

10. Eligibility

Sex
All
Gender Based
Yes
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
100 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Histologic proof or unequivocal cytologic proof solid tumor malignancy. This may be obtained from either the primary or any metastatic site Mini Mental State Examination (MMSE) ≥24 Age≥ 18 years Karnofsky Performance Status (KPS) ≥70 Patient does not have metastases to the genu Patient must be scheduled to undergo treatment with whole brain radiation therapy (WBRT) to manage the brain metastases Patients of childbearing potential (male or female) must practice adequate contraception due to possible harmful effects of radiation therapy on an unborn child Patient must have the ability to understand and the willingness to sign a written informed consent document All patients must be informed of the investigational nature of this study and must be given written informed consent in accordance with institutional and federal guidelines Patient must have a minimal life expectancy of at least 6 months Patients receiving prior stereostatic radiosurgery (SRS) for brain metastases are eligible Exclusion Criteria: Prior WBRT MMSE<24 Patient has brain metastases in the genu Patients must not have a serious medical or psychiatric illness that would, in the opinion of the treating physician prevent informed consent or completion of protocol treatment, and/or follow-up visits. KPS<70 Non-native English speakers will be excluded since patients often lose their faculty with the language they acquired second before their native language is affected in the context of cognitive decline. This could adversely affect performance on verbal cognitive tasks. Patients with absolute contraindication to MRI imaging are not eligible for the study
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kristin Redmond, MD
Phone
410-614-1642
Email
kjanson3@jhmi.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kristin Janson
Organizational Affiliation
The SKCCC at Johns Hopkins
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sibley Memorial Hospital
City
Washington
State/Province
District of Columbia
ZIP/Postal Code
20016
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Victoria Croog, MD
Phone
202-537-4787
Email
vcroog@jhmi.edu
Facility Name
The SKCCC at Johns Hopkins
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21287
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kristin Redmond, MD
Phone
410-614-1642
Email
kjanson3@jhmi.edu
First Name & Middle Initial & Last Name & Degree
Tracy Vannorsdall, PhD
First Name & Middle Initial & Last Name & Degree
Haris Sair, MD
First Name & Middle Initial & Last Name & Degree
Russell Hales, MD
First Name & Middle Initial & Last Name & Degree
Lawrence Kleinberg, MD
First Name & Middle Initial & Last Name & Degree
Brandi Page, MD
First Name & Middle Initial & Last Name & Degree
Deborah Frassica, MD
First Name & Middle Initial & Last Name & Degree
Fariba Asrari, MD

12. IPD Sharing Statement

Plan to Share IPD
No

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Neurocognitive Functioning With Genu-Sparing Whole Brain Radiation Therapy for Brain Metastases

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