Prospective Comparison of 18F-Choline Positron Emission Tomography/Computed Tomography (PET/CT) and 18F-Fluorodeoxyglucose (FDG) PET/CT in the Initial Workup of Multiple Myeloma: Study Protocol of a Prospective Imaging Trial
Autor: | Charles Mesguich, Gerald Marit, Valerie Latrabe, Laurence Bordenave, Elif Hindié, Paul Perez, Julien Asselineau, Cyrille Hulin |
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Jazyk: | angličtina |
Rok vydání: | 2020 |
Předmět: |
PET/CT
Computer applications to medicine. Medical informatics medical imaging skeletal system R858-859.7 030218 nuclear medicine & medical imaging 18F-choline 03 medical and health sciences 0302 clinical medicine McNemar's test medicine Medical imaging Protocol cancer Pelvis Multiple myeloma Fluorodeoxyglucose PET-CT medicine.diagnostic_test business.industry Magnetic resonance imaging General Medicine medicine.disease multiple myeloma medicine.anatomical_structure 18-FDG Positron emission tomography 030220 oncology & carcinogenesis Medicine business Nuclear medicine medicine.drug MRI |
Zdroj: | JMIR Research Protocols, Vol 9, Iss 9, p e17850 (2020) JMIR Research Protocols |
ISSN: | 1929-0748 |
Popis: | Background The International Myeloma Working Group recommends the use of 18-fluorodeoxyglucose (FDG) positron emission tomography/computed tomography (PET/CT) for treatment response evaluation, as it is superior to magnetic resonance imaging (MRI). However, at initial staging, the sensitivity of FDG-PET remains inferior to that of MRI. Therefore, there is a need for an imaging technique that could have a sensitivity equal to that of MRI at diagnosis and could serve to evaluate therapy. 18F-choline has shown increased sensitivity when compared with 18-FDG, with about 75% more lesions detected in patients with relapsed or progressive multiple myeloma (MM). Objective Our primary objective is to prospectively compare the detection rate of bone lesions by 18F-choline PET/CT (FCH-PET) and FDG-PET in newly diagnosed MM. Our secondary objectives are to assess the accuracy of both PET modalities for the detection of bone lesions and the diagnosis of diffuse disease, to assess the detection rate of extramedullary lesions. Methods We will prospectively include 30 patients in a paired comparative accuracy study. Patients with de novo MM will undergo FCH-PET, FDG-PET, and whole-body MRI (WB-MRI) within a 3-week period. WB-MRI will be composed of conventional sequences on the spine and pelvis and of whole-body diffusion axial sequences. The following 6 skeletal areas will be defined: skull, sternum/costal grid, spine, pelvis, superior limbs, and inferior limbs. The number of focal lesions, their respective localization, and intensity of uptake will be retrieved for each skeletal area. Readings will be performed blinded from other imaging techniques. The reference standard will be WB-MRI. Focal lesions present on PET/CT but not on WB-MRI will require a decision made with a consensus of experts based on clinical and imaging data. The number of bone lesions and number of extramedullary lesions will be compared using the Wilcoxon test. The accuracy of FCH-PET and FDG-PET will be compared using the McNemar test. Results The study started in September 2019, and enrollment is ongoing. As of June 2020, 8 participants have been included. Data collection is expected to be completed in June 2021, and the results are expected to be available in December 2021. Conclusions This study will assess if FCH-PET is superior to FDG-PET for the evaluation of MM tumor burden. This will pave the way for future prospective evaluations of the prognostic value of 18-FCH for treatment response evaluation in MM patients. Additionally, this work may provide new perspectives for better assessment of the risk of smoldering MM progressing to MM. Trial Registration ClinicalTrials.gov NCT03891914; https://clinicaltrials.gov/ct2/show/NCT03891914 International Registered Report Identifier (IRRID) DERR1-10.2196/17850 |
Databáze: | OpenAIRE |
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