RecruitingRecruiting
Neurocognitive Outcomes After Whole Brain Radiation Therapy for Hematologic Malignancies
NCT05011045 · M.D. Anderson Cancer Center
In plain English
Click the button to translate this study into plain language — what it is, who qualifies, and what participation looks like.
About this study
PRIMARY OBJECTIVE:
I. Record patients' cognitive outcomes after whole-brain radiation therapy (WBRT) for hematologic malignancies using standard-of-care neurocognitive function testing.
SECONDARY OBJECTIVES:
I. Assess patients' quality-of-life after WBRT for hematologic malignancies, based on a validated questionnaire.
II. Explore magnetic resonance imaging (MRI) changes in the brain after WBRT for hematologic malignancies, based on standard-of-care imaging studies.
III. Study the role of Memantine in patients' cognitive outcomes during and after WBRT for hematologic malignancies, based on standard-of-care use, utilizing standard-of-care neurocognitive function testing.
OUTLINE:
Patients undergo neurocognitive function assessments, complete questionnaires over 8-10 minutes and undergo standard of care MRI at baseline (within 4 weeks before the first day of WBRT), 2, 6, 12 months after RT completion, then annually for 5 years.
Eligibility criteria
Inclusion Criteria:
* Age 18 years or older
* Treatment with radiation therapy to the brain for a hematologic malignancy (ex. primary central nervous system lymphoma \[PCNSL\], secondary central nervous system lymphoma \[SCNSL\], leukemia, myeloma)
* Proficient and capable of completing tests in English
* Patients with claustrophobia are eligible if the claustrophobia is managed with medication
* Patients with cognitively-impairment are eligible if the impairment is managed with medication
* Patients who are pregnant
Study design
Enrollment target: 100 participants
Age groups: adult, older_adult
Timeline
Starts: 2020-01-09
Estimated completion: 2026-10-31
Last updated: 2026-05-20
Interventions
Procedure: Magnetic Resonance ImagingOther: Neurocognitive AssessmentOther: Quality-of-Life AssessmentOther: Questionnaire Administration
Primary outcomes
- • Cognitive outcomes (Up to 5 years)
Sponsor
M.D. Anderson Cancer Center · other
Contacts & investigators
ContactDustin M Silk · contact · dmdmsilk@mdanderson.orgsilk@mdanderson.org · 713-563-3090
InvestigatorBouthaina S Dabaja · principal_investigator, M.D. Anderson Cancer Center
All locations (1)
M D Anderson Cancer CenterRecruiting
Houston, Texas, United States