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11C-Methionine PET/CT in Assessment of Multiple Myeloma Patients: Comparison to 18F-FDG PET/CT and Prognostic Value
Maria I Morales-Lozano1, Paula Rodriguez-Otero2, Lidia Sancho1
1Department of Nuclear Medicine, Clinica Universidad de Navarra, CCUN Applied Medical Research, Instituto de Investigación Sanitaria de Navarra, 31008 Pamplona, Spain.
Abstract:
Multiple myeloma (MM) is the second most common haematological malignancy and remains incurable despite therapeutic advances. 18F-FDG (FDG) PET/CT is a relevant tool MM for staging and it is the reference imaging technique for treatment evaluation. However, it has limitations, and investigation of other PET tracers is required. Preliminary results with L-methyl-[11C]- methionine (MET), suggest higher sensitivity than 18F-FDG. This study aimed to compare the diagnostic accuracy and prognostic value of 1FDG and MET in MM patients. We prospectively compared FDG and MET PET/CT for assessment of bone disease and extramedullary disease (EMD) in a series of 52 consecutive patients (8 smoldering MM, 18 newly diagnosed MM and 26 relapsed MM patients). Bone marrow (BM) uptake patterns and the detection of focal lesions (FLs) and EMD were compared. Furthermore, FDG PET parameters with known MM prognostic value were explored for both tracers, as well as total lesion MET uptake (TLMU). Median patient age was 61 years (range, 37-83 years), 54% were male, 13% of them were in stage ISS (International Staging System) III, and 31% had high-risk cytogenetics. FDG PET/CT did not detect active disease in 6 patients, while they were shown to be positive by MET PET/CT. Additionally, MET PET/CT identified a higher number of FLs than FDG in more than half of the patients (63%). For prognostication we focussed on the relapsed cohort, due to the low number of progressions in the two other cohorts. Upon using FDG PET/CT in relapsed patients, the presence of more than 3 FLs (HR 4.61, p = 0.056), more than 10 FLs (HR 5.65, p = 0.013), total metabolic tumor volume (TMTV) p50 (HR 4.91, p = 0.049) or TMTV p75 (HR 5.32, p = 0.016) were associated with adverse prognosis. In MET PET/CT analysis, TMTV p50 (HR 4.71, p = 0.056), TMTV p75 (HR 6.27, p = 0.007), TLMU p50 (HR 8.8, p = 0.04) and TLMU p75 (HR 6.3, p = 0.007) adversely affected PFS. This study confirmed the diagnostic and prognostic value of FDG in MM. In addition, it highlights that MET has higher sensitivity than FDG PET/CT for detection of myeloma lesions, including FLs. Moreover, we show, for the first time, the prognostic value of TMTV and TLMU MET PET/CT in the imaging evaluation of MM patients.
Insights
New PET tracer L-methyl-[11C]-methionine (MET) shows higher sensitivity than 18F-FDG for detecting multiple myeloma (MM) lesions. MET PET/CT also offers valuable prognostic information, complementing FDG PET/CT in MM patient evaluation.
Area of Science:
- Nuclear Medicine
- Oncology
- Radiopharmaceuticals
Background:
- Multiple myeloma (MM) is a significant hematological malignancy with limited cure rates.
- 18F-FDG (FDG) PET/CT is standard for MM staging and treatment response, but has limitations.
- Investigating novel PET tracers like L-methyl-[11C]-methionine (MET) is crucial for improved MM assessment.
Purpose of the Study:
- To prospectively compare the diagnostic accuracy of FDG PET/CT and MET PET/CT in MM patients.
- To evaluate the prognostic value of FDG and MET PET/CT parameters in MM.
- To assess the detection capabilities of MET PET/CT for bone disease and extramedullary disease (EMD) compared to FDG PET/CT.
Main Methods:
- A prospective study involving 52 MM patients (smoldering, newly diagnosed, relapsed).
- Comparison of FDG PET/CT and MET PET/CT for bone marrow uptake, focal lesions (FLs), and EMD.
- Analysis of prognostic parameters including total lesion MET uptake (TLMU) and total metabolic tumor volume (TMTV) for both tracers.
Main Results:
- MET PET/CT detected active disease in 6 patients missed by FDG PET/CT.
- MET PET/CT identified more focal lesions than FDG PET/CT in 63% of patients.
- Both FDG and MET PET/CT parameters (TMTV, TLMU) showed prognostic value in relapsed MM patients, with MET demonstrating significant associations with progression-free survival (PFS).
Conclusions:
- MET PET/CT demonstrates higher sensitivity than FDG PET/CT for detecting myeloma lesions, including focal lesions.
- MET PET/CT provides significant prognostic information, particularly regarding PFS in relapsed MM.
- This study establishes the prognostic value of TMTV and TLMU using MET PET/CT in MM imaging evaluation.
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