Korean J Intern Med > Volume 41(2); 2026 > Article
ORIGINAL ARTICLE
Hemato-oncology
Korean J Intern Med. 2026;41(2):307-316.         doi: https://doi.org/10.3904/kjim.2025.224
High diffuse bone marrow uptake in 18F-FDG PET/CT may reflect the diverse mutational characteristics of multiple myeloma
Hee Jeong Cho1, Donghyeon Lee2,3, Tan Minh Le2,3, Hong Duc Thi Nguyen2,3, Juhyung Kim1, Jung Min Lee1, Dong Won Baek1, Ha-Jeong Kim5, Hyung Soo Han2,3, Sang Kyun Sohn1, Chae Moon Hong4, and Joon Ho Moon1
1Department of Hematology/Oncology, Kyungpook National University Hospital, School of Medicine, Kyungpook National University, Daegu, Korea
2Department of Biomedical Science, Kyungpook National University, Daegu, Korea
3BK21 Four Program, School of Medicine, Kyungpook National University, Daegu, Korea
4Department of Nuclear Medicine, Kyungpook National University Hospital, School of Medicine, Kyungpook National University, Daegu, Korea
5Department of Physiology, Kyungpook National University Hospital, School of Medicine, Kyungpook National University, Daegu, Korea
Corresponding Author: Joon Ho Moon  , Tel: +82-53-200-6314, Fax: +82-53-426-2046, Email: jhmoon@knu.ac.kr
Received: July 13, 2025;   Revised: October 15, 2025;   Accepted: November 14, 2025.
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Abstract
Background/Aims: To explore the biological implications of positron emission tomography/computed tomography (PET/CT) findings in multiple myeloma (MM), we investigated the mutational characteristics relevant to PET/CT findings using targeted DNA sequencing.
Methods: Fourteen newly diagnosed patients with MM who underwent 18F-fluorodeoxyglucose (FDG) PET/CT at diagnosis were retrospectively reviewed. Targeted sequencing was performed on their bone marrow samples using a customized panel covering 80 genes relevant to MM biology. In seven patients, serial PET/CT and sequencing were also conducted after firstline treatment.
Results: The most frequently identified mutant gene was ATM, followed by HUWE1, PABPC1, and TP53. Patients with high diffuse FDG uptake (high DU) in their bone marrow showed a higher tumor burden than those with low diffuse uptake (low DU), and they were likely to have an inferior overall survival. Mutations detected in high DU were associated with various oncogenic pathways relevant to the disease progression of MM. Notably, pathways involving epigenetic regulators were predominantly enriched in patients with high DU. In serial follow-ups, a patient with residual PET/CT findings showed the emergence of new mutations; however, those with complete resolution of PET/CT abnormalities demonstrated improved mutational characteristics.
Conclusions: Patients with high DU showed diverse mutational characteristics, which may reflect the heterogeneous nature of MM and contribute to inferior survival outcomes.
Keywords: Multiple myeloma ; PET/CT ; Diffuse uptake ; Mutations
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