Study of Low Dose Whole Brain Irradiation in the Treatment of Alzheimer's Disease

William Beaumont Hospitals

Status: Terminated

Conditions: Alzheimer's Disease

Treatments: Radiation: 5 daily fractions of 2 Gy; Radiation: 10 daily fractions of 2 Gy

Study type: Interventional

Funder types: Other

Identifiers

NCT02359864

2016-088 2017-471;

Details and patient eligibility

About

This study is designed to assess the safety and toxicity/adverse events associated with the use of low dose fractionated whole brain irradiation in those patients who have been diagnosed with probable Alzheimer's disease according to the National Institute of Neurological and Communicative Disorders and Stroke and the Alzheimer's Disease and Related Disorders Association (NINCDS-ADRDA) criteria. As a secondary goal it will establish whether or not the intervention with low dose whole brain irradiation might change the recognized progression of Alzheimer's Disease. The investigators will also collect information from the florbetaben F 18 Injection (AMYVID®) positron emission tomography (PET) Scans to determine if there is any correlation between neurocognitive/quality of life scores and changes in amyloid plaque size, number and location.

Full description

An initial 15 patients will be enrolled in the first treatment scheme (5 daily fractions of 2 Gy) and will be followed for 12 months after completion of treatment to assess safety and any toxicity/adverse events associated with treatment. In Arm 1 the 15 study participants will be enrolled in total at Botsford Radiation Oncology Center and William Beaumont Hospital (Royal Oak Campus). Once a total combined 15 patients are entered this Arm will be closed.

The second treatment arm will not be used until the last patient in the first dose arm has completed all follow up. At that point patients #16-30 will be enrolled in the second dose arm (10 daily fractions of 2 Gy). In Arm 2 the 15 study participants will be enrolled in total at both Botsford Hospital Radiation Oncology Center and William Beaumont Hospital (Royal Oak Campus). Once a total combined 15 patients are entered this Arm will be closed.

A total of 30 patients will be enrolled and each will be followed for 12 months to assess safety and toxicity/adverse events.

Enrollment: 2 patients

Sex: All

Ages: 55+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

Criteria for Eligibility (All responses must be YES)

Inclusion Criteria:

Patients must meet all eligibility criteria to be included in the study:

1. Must be 55 years of age or older
2. Patient must meet NINCDS-ADRDA criteria for Alzheimer's Disease
3. Patient must be able to complete Mini-Mental Examination (MMSE) and Alzheimer's Disease Assessment Scale - Cognitive (ADAS-Cog) questionnaire Score Sheets
4. Patient has a Rosen Modified Hachinski Ischemic Score of less than or equal to 4
5. Patient has a MMSE score of between 10-20
6. Patient has estimated survival of greater than 12 months
7. Patient or legally authorized representative must be able to give consent

Exclusion criteria

Patients will be excluded from the study if they meet any of the following criteria:

1. The patient has a history of cancer except non-melanoma skin cancer
2. Patient is taking anti-epileptic medication.
3. Dermatological skin disease of the scalp
4. Patient taking Alzheimer medication within the last 3 months, i.e. Exelon, Aricept, Namenda, Reminyl or Ebixa.
5. Current presence of a clinically significant major psychiatric disorder (e.g. major depressive disorder, bipolar disorder, schizophrenia, etc., according to the Diagnostic and Statistical Manual of Mental Disorders, 4th Edition (DSM-IV))
6. Patient currently participating in another Clinical Trial.
7. Patient and legally authorized representative unable to give informed consent
8. Patient with history of focal neurological deficits (with the exception of vibratory peripheral neuropathy)
9. Non-Alzheimer dementia
10. Patient has previous history of central nervous system radiation
11. Patient has evidence of substance abuse (alcohol / or other drugs of dependence) during previous 12 months
12. History of subdural hygroma / subdural hematoma
13. History of cerebral infection / hemorrhage.
14. History that the patient is immunocompromised
15. History of seizure activity
16. History of hydrocephalus

Trial design

Primary purpose: Treatment

Allocation: Non-Randomized

Interventional model: Single Group Assignment

Masking: None (Open label)

---

2 participants in 2 patient groups

Cohort One

Experimental group

Description:

An initial 15 patients will be enrolled in the first treatment scheme (5 daily fractions of 2 Gy) and will be followed for 12 months after completion of treatment to assess safety and any toxicity/adverse events associated with treatment. 15 patients will be enrolled and each will be followed for 12 months to assess safety and toxicity/adverse events.

Treatment:

Radiation: 5 daily fractions of 2 Gy

Cohort Two

Experimental group

Description:

The second treatment arm will not be used until the last patient in the first dose arm has completed all follow up. At that point patients #16-30 will be enrolled in the second dose arm (10 daily fractions of 2 Gy). 15 patients will be enrolled and each will be followed for 12 months to assess safety and toxicity/adverse events.

Treatment:

Radiation: 10 daily fractions of 2 Gy