Longitudinal Prospective Study of Neurocognition & Neuroimaging in Primary BT Patients

Sponsor
Jona Hattangadi-Gluth (Other)
Overall Status
Recruiting
CT.gov ID
NCT05576103
Collaborator
(none)
100
1
143
0.7

Study Details

Study Description

Brief Summary

In this proposal, the investigators introduce a novel, translational study to prospectively examine primary brain tumor patients undergoing fractionated radiation therapy to the brain. Quantitative neuroimaging, radiation dose information, and directed neurocognitive testing will be acquired through this study to improve understanding of cognitive changes associated with radiation dosage to non-targeted tissue, and will provide the basis for evidence-based cognitive- sparing brain radiotherapy.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Background: Fractionated radiation therapy (RT) is a mainstay in the treatment of primary and metastatic brain tumors. However, RT to the brain is associated with an inevitable decline in neurocognitive function in up to 90% of patients who survive more than 6 months after irradiation. Radiation to the brain results in an inevitable decline in neurocognitive function, mediated by tissue injury to white matter, cortex and subcortical areas. With quantitative magnetic resonance imaging (MRI) techniques, investigators can directly and non-invasively measure such changes.

    Objective/Hypothesis:

    The purpose of this study is to examine radiation-induced imaging changes in normal brain tissue over time in primary brain tumor patients, and correlate these with neurocognitive outcomes. The overarching goal is to better identify sensitive brain regions so that future radiation techniques can be optimally designed to mitigate collateral damage.

    Specific Aims:
    1. To identify microstructural changes in subcortical white matter, hippocampus, and cortex associated with quantified regional exposure to fractionated brain radiotherapy using advanced quantitative neuroimaging imaging

    2. To identify changes in neurocognitive functioning in primary brain tumor patients after brain radiotherapy

    Study Design:

    The investigators will prospectively enroll primary brain tumor patients undergoing fractionated partial brain radiation therapy. Patients will undergo volumetric and diffusion brain MRI (per clinical standard-of-care) and a neurocognitive battery of tests at baseline (pre-treatment), 3 months, 6 months, and 12 months post-treatment. Clinical data including age, gender, educational status, tumor size and histology, steroid use, antiepileptic drug use and chemotherapy will be recorded.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    100 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Longitudinal Prospective Study of Neurocognitive Outcomes and Multimodal Quantitative Neuroimaging Outcomes in Primary Brain Tumor Patients Receiving Brain Radiotherapy
    Actual Study Start Date :
    Jan 1, 2015
    Anticipated Primary Completion Date :
    Dec 1, 2026
    Anticipated Study Completion Date :
    Dec 1, 2026

    Arms and Interventions

    Arm Intervention/Treatment
    Primary brain tumour patients receiving RT

    Primary brain tumor patients are screened at time of consultation for this observational study, and the study population is diverse across sex/gender, and racial/ethnic groups.

    Outcome Measures

    Primary Outcome Measures

    1. Longitudinal changes in imaging biomarker volume (cc) from volumetric MR imaging [baseline (pre-treatment), 3 months, 6 months, 12 months post-treatment]

      To measure longitudinal changes in volume (cc) from volumetric MR imaging

    2. Longitudinal changes in imaging biomarker mean diffusivity (MD) in white matter from DTI imaging [baseline (pre-treatment), 3 months, 6 months, 12 months post-treatment]

      To measure longitudinal changes in MD (mm squared/second) from DTI imaging

    3. Longitudinal changes in imaging biomarker fractional anisotropy (FA) in white matter from DTI imaging [baseline (pre-treatment), 3 months, 6 months, 12 months post-treatment]

      To measure longitudinal changes in FA (unitless index between 0 and 1) from DTI imaging

    4. Change in Memory after RT [baseline (pre-treatment), 3 months, 6 months, 12 months post-treatment]

      To evaluate the change from baseline to post-RT verbal memory performance when performing fractionated partial brain RT. Verbal memory outcomes and measurements include: Hopkins Verbal Learning Test-Revised (HVLT-R)-Immediate, Delayed Recall. Brief Visuospatial Memory Test-Revised (BVMT-R)- Total, Delayed Recall Scale of scores is: Hopkins Verbal Learning Test-Revised (HVLT-R)-Immediate, Delayed Recall: 0-36 for Immediate, 0-12 for Delayed. For both tests, higher scores indicate better performance. Brief Visuospatial Memory Test-Revised (BVMT-R)- Total, Delayed Recall: l: 0-36 for Immediate, 0-12 for Delayed. For both tests, higher scores indicate better performance.

    5. Change in Executive Functioning after RT [baseline (pre-treatment), 3 months, 6 months, 12 months post-treatment]

      To evaluate the change from baseline to post-RT executive functioning performance when performing fractionated partial brain RT. Executive functioning outcomes and measurements include: Controlled Oral Word Association Test (COWA): letter fluency, Trail Making Test Part B (TMT-B). Scale of scores is: Controlled Oral Word Association Test (COWA): letter fluency: 0- no upper limit. Higher score indicates better performance Trail Making Test Part B (TMT-B): 0-240. Higher score indicates poorer performance

    6. Change in Attention/Processing Speed after RT [baseline (pre-treatment), 3 months, 6 months, 12 months post-treatment]

      To evaluate the change from baseline to post-RT Attention/Processing Speed performance when performing fractionated partial brain RT. Attention/Processing Speed outcomes and measurements include: Trail Making Test Part A (TMT-A) Scale of scores is: Trail Making Test Part A (TMT-A): 0-240. Higher score indicates poorer performance.

    7. Change in Language functioning after RT [baseline (pre-treatment), 3 months, 6 months, 12 months post-treatment]

      To evaluate the change from baseline to post-RT Language performance when performing fractionated partial brain RT in patients with primary brain tumor. Language outcomes and measurements include: Boston Naming Test (BNT), Controlled Oral Word Association Test (COWA): category fluency Scale of scores is: Boston Naming Test (BNT): 0-60 Controlled Oral Word Association Test (COWA): category fluency: 0-no upper limit. For both tests, higher score indicates better performance.

    8. Change in Fine Motor Skills after RT [baseline (pre-treatment), 3 months, 6 months, 12 months post-treatment]

      To evaluate the change from baseline to post-RT Fine Motor Skills performance when performing fractionated partial brain RT in patients with primary brain tumor. Fine Motor Skills outcomes and measurements include: Trail Making Test Motor Speed; Grooved Pegboard Test

    9. Change in health-related quality of life (hrQoL) from baseline to 5 years after RT [baseline (pre-treatment), 3 months, 6 months, 12 months post-treatment]

      To evaluate the change from baseline to post-RT health-related quality of life (hrQoL) when performing fractionated partial brain RT in patients with primary brain tumor. Quality of life outcomes and measurements include: Beck Depression inventory II (BDI II), Beck Anxiety Inventory (BAI) and FACT-BR (Functional Assessment of Cancer Therapy - Brain). FACT-BR (Functional Assessment of Cancer Therapy - Brain) higher scores on each subscale indicate greater hrQoL.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. Patients 18 years or older

    2. Karnofsky performance status (KPS) ≥70

    3. Life expectancy of ≥1 year

    4. Primary brain tumor patients who will receive fractionated partial brain RT

    5. Able to complete neurocognitive assessments

    Exclusion Criteria:
    1. Inability to undergo MRI with contrast

    2. Prior brain RT

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Moores Cancer Center San Diego California United States 92037

    Sponsors and Collaborators

    • Jona Hattangadi-Gluth

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Jona Hattangadi-Gluth, Professor, University of California, San Diego
    ClinicalTrials.gov Identifier:
    NCT05576103
    Other Study ID Numbers:
    • 131457
    First Posted:
    Oct 12, 2022
    Last Update Posted:
    Oct 12, 2022
    Last Verified:
    Oct 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 12, 2022