TY - JOUR
T1 - A systematic literature review on clonal evolution events preceding relapse in multiple myeloma
AU - Jakobsen, Maja Zimmer
AU - Brøndum, Rasmus Froberg
AU - Gregersen, Henrik
AU - Due, Hanne
AU - Dybkær, Karen
N1 - Copyright © 2024. Published by Elsevier B.V.
PY - 2025/1
Y1 - 2025/1
N2 - Despite considerable treatment advances, multiple myeloma (MM) remains an incurable hematological cancer due to treatment resistance. A systematic literature search was conducted to identify determinants for clonal evolution driving relapse and drug resistance in MM. A total of 631 non-duplicate publications were screened of which 28 articles were included for data extraction. Genetic alterations, mutational signatures, evolutionary trajectories, and non-genetic determinants were identified as key topics to characterize clonal evolution in relapsed MM. A variety of factors led to clonal diversification and increased tumor mutation burden, such as MAPK-Ras mutations and incremental changes related to chromosomal bands 1 and 17, while mutational signature analyses revealed that APOBEC activity and melphalan treatment leave a distinct impact on the clonal composition in MM genomes. To capture and dissect tumor heterogeneity, our review suggests combining methods or using technical approaches with high resolution to assess the impact of clonal evolution.
AB - Despite considerable treatment advances, multiple myeloma (MM) remains an incurable hematological cancer due to treatment resistance. A systematic literature search was conducted to identify determinants for clonal evolution driving relapse and drug resistance in MM. A total of 631 non-duplicate publications were screened of which 28 articles were included for data extraction. Genetic alterations, mutational signatures, evolutionary trajectories, and non-genetic determinants were identified as key topics to characterize clonal evolution in relapsed MM. A variety of factors led to clonal diversification and increased tumor mutation burden, such as MAPK-Ras mutations and incremental changes related to chromosomal bands 1 and 17, while mutational signature analyses revealed that APOBEC activity and melphalan treatment leave a distinct impact on the clonal composition in MM genomes. To capture and dissect tumor heterogeneity, our review suggests combining methods or using technical approaches with high resolution to assess the impact of clonal evolution.
KW - Clonal evolution
KW - Drug resistance
KW - Genetic alterations
KW - Multiple myeloma
KW - Mutational Signatures
UR - http://www.scopus.com/inward/record.url?scp=85209996335&partnerID=8YFLogxK
U2 - 10.1016/j.critrevonc.2024.104560
DO - 10.1016/j.critrevonc.2024.104560
M3 - Review article
C2 - 39549892
SN - 1040-8428
VL - 205
JO - Critical Reviews in Oncology/Hematology
JF - Critical Reviews in Oncology/Hematology
M1 - 104560
ER -