A new four-year research study, with an estimated budget of US$100 million, has been announced by the Alzheimer’s Association and the American College of Radiology (ACR). The Imaging dementia—Evidence for amyloid scanning (IDEAS) study will determine the clinical usefulness and value in diagnosing Alzheimer’s and other dementias in certain situations of a brain positron emission tomography (PET) scan that detects a core feature of Alzheimer’s disease.
The IDEAS study will assess the impact of brain amyloid PET imaging on a variety of patient outcomes. The study protocol received approval with requirements by the Centers for Medicare & Medicaid Services (CMS). Participating providers will be reimbursed for the PET scans under the CMS Coverage with Evidence Development (CED) policy that requires research study participation as a condition of Medicare payment.
IDEAS is led by the Alzheimer’s Association and managed by the ACR and American College of Radiology Imaging Network (ACRIN).
Why the IDEAS study is needed
Two abnormal structures called plaques and tangles are prime suspects in damaging and killing nerve cells in Alzheimer’s. The plaques are deposits of a protein fragment called amyloid-beta that build up in the spaces between nerve cells. Amyloid PET imaging represents a potential major advance in the clinical assessment of people with cognitive impairment. The technology makes amyloid plaques light up on a brain PET scan, enabling for the first time accurate detection of plaques in living people.
“The purpose of the IDEAS study is to examine how brain imaging, specifically an amyloid PET scan, helps guide doctors in diagnosing and treating Alzheimer’s and other dementias in cases where the cause of cognitive impairment is difficult to diagnose,” says Gil D Rabinovici, IDEAS study chair and Associate Professor of Neurology at the University of California, San Francisco, USA. “We believe the study will show that, in diagnostically uncertain cases, knowledge of amyloid status will lead to significant changes in patient management—such as earlier counselling and prescription of more appropriate drugs—that will translate into improved long-term outcomes.”
The IDEAS study was developed in response to the 2013 CMS National Coverage Decision (NCD) on amyloid PET imaging in dementia and neurodegenerative disease (CAG-00431N) not cover the scans because “the evidence is insufficient to conclude that the use of positron emission tomography (PET) amyloid-beta (A) imaging is reasonable and necessary for the diagnosis or treatment of illness or injury or to improve the functioning of…Medicare beneficiaries with dementia or neurodegenerative disease.”
CMS questioned the ability of PET amyloid imaging to lead to improved health outcomes, such as: avoidance of futile treatment or tests, improving or slowing the decline of quality of life, and survival. However, CMS did find sufficient evidence that the use of PET A imaging is promising: (1) to exclude Alzheimer’s in narrowly defined and clinically difficult diagnoses, and (2) to enrich clinical trials seeking better treatments or prevention strategies for Alzheimer’s. Under the NCD, Medicare will provide coverage for one amyloid PET scan per patient enrolled in an approved clinical study.
“I am confident that, at the end of this study, we will have amassed sufficient data to assess whether amyloid imaging has a positive impact on patient outcomes leading to expansion of beneficiary access to this important procedure beyond the IDEAS study,” says Maria Carrillo, a co-chair of the IDEAS study and chief science officer at the Alzheimer’s Association.
The IDEAS study in more detail
Amyloid PET imaging alone does not establish a diagnosis of Alzheimer’s disease, but must be considered in the context of the person’s medical history, physical examination, and cognitive testing. To guide clinicians on how best to apply amyloid PET in the clinical evaluation of people with cognitive decline, a working group convened by the Alzheimer’s Association and the Society of Nuclear Medicine and Molecular Imaging (SNMMI) developed appropriate use criteria (AUC) for brain amyloid PET scans.
The AUC indicate that amyloid PET should only be considered in patients with clear, measurable cognitive deficits when there is substantial diagnostic uncertainty after a comprehensive evaluation by a dementia specialist. According to AUC, amyloid PET may have greatest value in patients with either: (1) progressive, unexplained mild cognitive impairment (MCI); or (2) dementia of uncertain cause due to atypical or mixed symptoms, or unusually early age-of-onset.
A total of 18,488 Medicare beneficiaries age 65 and older meeting AUC will be enrolled over 24 months at roughly 200 sites throughout the United States. Study participants will be recruited into one of two sub-groups: (1) progressive, unexplained MCI, and (2) dementia of uncertain cause.
All referrals to the study and for amyloid PET will come from dementia specialists, defined by the Alzheimer’s Association and SNMMI as “physicians trained and board-certified in neurology, psychiatry, or geriatric medicine who devote a substantial proportion of patient contact time to the evaluation and care of adults with acquired cognitive impairment or dementia, including probable or suspected Alzheimer’s disease.” Dementia specialists will be recruited through societies such as the International Association of Gerontology and Geriatrics, American Academy of Neurology, American Society of Neuroradiology; plus clinician outreach through psychiatrists, members of the Alzheimer’s Association, and news media outreach.
