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Cerebral Morbidity After Radiation Therapy for Brain Tumors

Cerebral Morbidity After Radiation Therapy for Brain Tumors

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04292353
Acronym
WP-12
Enrollment
67
Registered
2020-03-03
Start date
2016-07-01
Completion date
2024-09-30
Last updated
2021-05-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Brain Tumor, Cognitive Impairment, Radiation Toxicity

Keywords

Brain tumor, Cognitive function, Radiation Therapy, Hippocampus

Brief summary

This study will assess cognitive function in patients with a primary brain tumour treated with radiation therapy (RT) to generate radio-sensitivity and volume effect parameters for the development of cognitive dysfunction. All types of brain tumours apart from glioblastoma will be included.

Detailed description

RT to brain tumours causes cognitive dysfunction. The extent of RT induced changes in cognitive function and radio-sensitivity of the brain is unknown. RT with protons instead of photons spares the healthy brain tissue more and is believed to reduce the risk of cognitive dysfunction. There is modest knowledge on which parts of the brain we need to spare, to prevent cognitive dysfunction. The study is a prospective nationwide study including approximately 60 brain tumour patients from the four neuro oncology centres in Denmark. The patients will do patient reported outcome (PRO) and undergo neuropsychological assessment with standardized tests: They will do this prior to RT treatment and ½, 1, 3 and 5 years afterwards. The PRO's included measures on quality of life, fatigue, sleep, depression, anxiety, and socio demografica. The standardized tests are: Trail making Test (TMT); Hopkins Verbal Learning Test (HVLT); Controlled Oral Word Association Test (COWAT) - Animals and S; Coding and Digit Span from WAIS-IV; Paced Auditory Serial Addition Test (PASAT). The correlation between cognitive scores and RT dose-volume parameters to specific areas in the brain will be tested. This study will elucidate the dose-response relationship in radiation-induced damage to substructures of the brain such as hippocampus, thalamus, temporal and frontal lobes that will allow the clinician to prioritize these structures in planning of proton radiotherapy.

Interventions

OTHERCognitive tests and Patient Reported Outcome

Sponsors

University of Aarhus
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
Yes

Inclusion criteria

* 18 years or older and Danish speaking. * Performance status WHO 0-2 * Capable of cooperating on testing * Tumor histology (WHO 2016 classification) of the following types: anaplastic astrocytoma (IDH mutant), diffuse astrocytoma (IDH-mutant), gemistocytic astrocytoma (IDH mutant), diffuse astrocytoma (NOS), oligidendroglioma, meningioma, medulloblastoma (NOS), pituitary adenoma, other brain tumours including skull base sarcomas

Exclusion criteria

* Glioblastoma * Performance status 3-4

Design outcomes

Primary

MeasureTime frameDescription
Impairment of memory as assessed by the HVLT-r test5 YearsExamined by the Hopkins Verbal Learning Test. It will be correlated to the mean radiation dose to the hippocampus. Outcome is number of correct words (0-24)

Secondary

MeasureTime frameDescription
Attention and working memory5 YearsExamined by WAIS\_IV\_digit\_span and PASAT (Pased Auditory Seriel Addition Test). Outcome on WAIS digit span is number of correct (0-36) and outcome for PASAT is number of incorrects (0-60)
Verbal learning and memory5 YearsExamine by the Hopkins Verbal Learning Test (HVLT) - total and delayed. Outcome is number of correct words (0-24)
Verbal fluency5 YearsExamined by the Controlled Oral Word Association Test (COWAT) - Animals and letter\_S. Outcome is number of words produced in 1 minute (0-100)
Executive function5 YearsExamined by Trail making Test part B (TMT-B) and the STROOP colour and word test (STROOP). Outcome for TMT\_B is time in seconds (0-300). Outcome for STROOP is number of corrects (0-120)
Processing speed5 YearsExamined by the Trail making Test part A (TMT\_A) and the Coding from WAIS-IV. Outcome for TMT\_A is time in seconds (0-120 seconds). Outcome for Coding is number of correct (within 2 minutes) (0-100)
Fatigue5 yearsAssessed by questionnaire: FACIT-Fatigue scale (version 4) in order to explore the level of fatigue in brain tumour patients who has received radiation therapy.
Qulity of Sleep5 yearsAssessed by questionnaire:Pittsburg Sleep Quality INDEX, PSQI in order to explore the level of quality of sleep in brain tumour patients who has received radiation therapy
Depression/Anxiety5 yearsAssessed by questionnaire: Hospital anxiety and depression Scale (HADS) in order to explore level of depression and anxiety in patients treated with radiation therapy for their brain tumour
Patient's Assessment of Own Functioning Inventory5 yearsAssessed by questionnaire; Patient's Assessment of Own Functioning Inventory (PAOFI), in order to assess patients own perception of cognitive function
Global Health - Quality of life5 YearsAssessed by questionnaire; EORTC QlQ-C30 in order to examine the level of quality of life in brain tumour patients who has received radiation therapy. Quality of life will be assessed by EORTC QIQ-C-30

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026