Memantine to preserve memory and neurocognition following craniospinal irradiation (MEMENTO)- A randomised control trial
Trial Snapshot
- Phase
- Phase 2/3
- Status
- Recruiting
- Sponsor
- Tata Memorial Hospital
- Enrollment
- 101
- Locations
- 1
- Primary Endpoint
- Cognitive-deterioration-free survival
Study Overview
Brief Summary
Craniospinal irradiation involving radiation of brain and spine, along with tumor-bed boost with or without chemotherapy, is the current standard treatment for medulloblastoma and other primitive embryonal tumors of the central nervous system. The delayed side effects following CSI include memory loss, hearing and balance difficulties, hormonal imbalance, and secondary cancers. Decline in memory severely affects the quality of life in long term survivors of these diseases. Hence, various strategies are being tried to prevent it. Memantine has been proven to effectively prevent the memory decline induced by RT. It is FDA-approved for Alzheimer’s disease and is widely used in the children for several developmental disorders. With this study, we are trying to investigate the role of memantine in patients receiving CSI to prevent memory decline.
After screening for the study, eligible patients will be randomly allocated by computerised system to one of the two arms that are described as follows. Patients in the experimental arm memantine will be started on memantine, starting dose of the same will be 5mg once daily at bedtime for 1 week, followed by 5mg twice daily for 1 week, and finally increased to the full dose of 10 mg twice daily for 6 months. Patients will continue radiation and chemotherapy when indicated as per schedule. All patients in the study will undergo neurocognitive evaluation, the time points for which will be pre-radiation baseline, 6 months post-RT, 1-year post-RT, and annually after that for 5 years from radiation. Following completion of RT or treatment, standard follow-up protocols will include a clinical examination 3 monthly for the first 2 years, followed by 6 monthly visits till 5 years post-RT. No additional risk is expected from the current study other than the common side effects of the standard treatment. Based on the results from the study, if primary endpoints are achieved, it will establish the role of memantine in preventing memory decline from CSI, which can be used as a standard treatment measure to help patients in the future.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Masking
- None
Eligibility Criteria
- Ages
- 5.00 Year(s) to 39.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •Planned for CSI, with or without boost dose with or without systemic chemotherapy Informed consent or assent taken Karnofsky Performance Status, Lanksy Performance Status≥60.
Exclusion Criteria
- •Re-irradiation Prior exposure to memantine Inability to undergo Wechsler test.
Outcomes
Primary Outcomes
Cognitive-deterioration-free survival
Time Frame: 2yrs after accrual
Secondary Outcomes
- Overall survival (OS)(at the completion of the study)
- Progression free survival (PFS)(until progression at any time point during the study)
Investigators
Dr Tejpal Gupta
Tata Memorial Hospital
