AL Amyloidosis, Monoclonal Gammopathy, Monoclonal Gammopathy of Undetermined Significance (MGUS), Multiple Myeloma, Systemic Amyloidosis
Conditions
Keywords
MGUS, MGCS, Amyloid PET, PET/MRI, Florbetaben, Early detection, Systemic amyloidosis, Monoclonal gammopathy, AL amyloidosis
Brief summary
The goal of this clinical trial is to evaluate whether ¹⁸F-florbetaben PET/MR can detect systemic amyloid deposits early and noninvasively in patients with monoclonal gammopathy. The main question it aims to answer is: Can ¹⁸F-florbetaben PET/MR identify systemic amyloid deposits across clinically and histologically defined patient groups? Participants will: * Be screened for eligibility and asked to sign an informed consent form * Have their vital signs measured * Receive a single intravenous injection of approximately 300 MBq ¹⁸F-florbetaben (Neuraceq®), followed by whole-body PET/MR imaging from skull base to below the kidneys. If MRI is contraindicated (e.g., pacemaker, severe claustrophobia), PET/CT will be performed instead. The scan takes approximately one hour, during which participants lie still in the scanner * Be monitored during and after the scan for any side effects or adverse events * Complete study participation at the end of the imaging session (single visit, no follow-up required)
Detailed description
Aim of the Project: The overarching goal is to establish a non-invasive, sensitive method for early detection of systemic amyloid deposits, laying the foundation for earlier diagnosis and improved treatment of AL amyloidosis. * Primary Aim: Validate 18F-florbetaben PET for detection of systemic AL amyloidosis versus negative controls. * Secondary Aim: Compare the sensitivity of amyloid PET with established methods (echocardiography, MRI, serological biomarkers) for the detection of early organ involvement. * Tertiary Aim: Quantify and characterize systemic amyloid burden across early and manifest disease stages. Hypotheses: 1. Amyloid PET shows pathological tracer uptake in patients with AL amyloidosis and remains unremarkable in negative controls. 2. Amyloid PET detects amyloid deposits at a stage in which conventional methods do not yet show structural or functional changes. 3. Systemic amyloid burden follows a graded pattern, with intermediate values in early disease and the highest values in manifest AL amyloidosis. Study Design and Methods Prospective, observational cohort study at the University Hospital Zurich (USZ). 50 participants will be recruited from the established COSMO-AL cohort at the Department of Hematology, which systematically captures patients with clinically significant monoclonal gammopathy and provides standardized skin biopsy data. Participants: * Negative controls: monoclonal gammopathy without histologic amyloid (n = 10). * Early disease (study cohort): monoclonal gammopathy with local, histologically confirmed amyloid deposits (n = 20). * Positive controls: biopsy-confirmed systemic AL amyloidosis (n = 20). Patients with confirmed amyloid involvement will be additionally stratified by organ involvement to allow exploratory analysis of organ-specific tracer uptake.
Interventions
DRUG¹⁸F-florbetaben
Single intravenous dose of \~300 MBq ¹⁸F-florbetaben followed by PET/MR (or PET/CT, if MRI is contraindicated), from the skull base to below the kidneys
Sponsors
University of Zurich
Study design
Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE
Intervention model description
Single-center, prospective, observational cohort study, which will include three predefined patient groups: negative controls, study cohort, positive controls
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Participation in the COSMO-AL study * Available biopsy test result * Written informed consent
Exclusion criteria
* Pregnant or lactating women
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Systemic ¹⁸F-florbetaben PET positivity rate | At time of PET/MR imaging (Day 1) | Rate of positive ¹⁸F-florbetaben PET scans assessed by visual qualitative analysis across the three patient groups (monoclonal gammopathy without biopsy-proven amyloid, biopsy-positive monoclonal gammopathy, biopsy-proven systemic AL). PET positivity is defined as any tracer uptake in the myocardium or in any organ outside the liver. Imaging performed with PET/MR or PET/CT, if MRI is contraindicated. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Correlation of myocardial ¹⁸F-Florbetaben uptake with cardiac biomarker and MRI parameters | At time of PET/MR imaging (Day 1) | Correlation of myocardial percent injected dose (%ID) with NT-proBNP (pg/mL) and cardiac MR parameters (indexed LV mass (g/m²), left ventricular ejection fraction (LVEF, %), and extracellular volume fraction (ECV, %) |
| Association of Myocardial ¹⁸F-Florbetaben Uptake with Histological Amyloid Status | At time of PET/MR imaging (Day 1) | Association of myocardial %ID with histological amyloid status (positive vs. negative) as determined by biopsy data from the parallel COSMO-AL study cohort. |
Countries
Switzerland
Contacts
CONTACTDominik C Benz, PD Dr. med.
CONTACTMirjam Marty
PRINCIPAL_INVESTIGATORDominik C Benz, PD Dr. med.
University of Zurich
Outcome results
None listed