A systematic literature review on clonal evolution events preceding relapse in multiple myeloma

IF 5.5 2区 医学 Q1 HEMATOLOGY Critical reviews in oncology/hematology Pub Date : 2024-11-15 DOI:10.1016/j.critrevonc.2024.104560
Maja Zimmer Jakobsen , Rasmus Froberg Brøndum , Henrik Gregersen , Hanne Due , Karen Dybkær
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Abstract

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.
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关于多发性骨髓瘤复发前克隆进化事件的系统性文献综述。
尽管多发性骨髓瘤(MM)的治疗取得了很大进展,但由于耐药性,它仍然是一种无法治愈的血液肿瘤。为了确定导致多发性骨髓瘤复发和耐药性的克隆进化的决定因素,我们进行了系统的文献检索。共筛选出 631 篇非重复文献,其中 28 篇被纳入数据提取范围。基因改变、突变特征、进化轨迹和非基因决定因素被确定为描述复发 MM 中克隆进化特征的关键主题。多种因素导致了克隆多样化和肿瘤突变负荷的增加,如MAPK-Ras突变以及与1号和17号染色体带相关的增量变化,而突变特征分析表明,APOBEC活性和美法仑治疗对MM基因组中的克隆组成有明显影响。为了捕捉和剖析肿瘤的异质性,我们的综述建议结合各种方法或使用高分辨率的技术方法来评估克隆演变的影响。
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来源期刊
CiteScore
11.00
自引率
3.20%
发文量
213
审稿时长
55 days
期刊介绍: Critical Reviews in Oncology/Hematology publishes scholarly, critical reviews in all fields of oncology and hematology written by experts from around the world. Critical Reviews in Oncology/Hematology is the Official Journal of the European School of Oncology (ESO) and the International Society of Liquid Biopsy.
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