Biological heterogeneity in diffuse large B-cell lymphoma

被引:11
作者
Hilton, Laura K. [1 ,2 ]
Scott, David W. [1 ,3 ]
Morin, Ryan D. [1 ,2 ,4 ]
机构
[1] BC Canc Ctr Lymphoid Canc, 675 W 10th Ave, Vancouver, BC V5Z 1L3, Canada
[2] Simon Fraser Univ, Dept Mol Biol & Biochem, Burnaby, BC, Canada
[3] Univ British Columbia, Dept Med, Div Med Oncol, Vancouver, BC, Canada
[4] BC Canc Res Ctr, Canadas Michael Smith Genome Sci Ctr, Vancouver, BC, Canada
关键词
Genomics; Molecular subgroups; LymphGen; Biomarkers; Precision medicine; OF-ORIGIN SUBTYPES; GENE-EXPRESSION; MOLECULAR SUBTYPES; DIFFERENTIAL EFFICACY; PHASE-III; R-CHOP; CLASSIFICATION; MUTATIONS; CHEMOTHERAPY; RITUXIMAB;
D O I
10.1053/j.seminhematol.2023.11.006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Diffuse large B -cell lymphoma (DLBCL) is heterogeneous both in clinical outcomes and the underlying disease biology. Over the last 2 decades, several different approaches for dissecting biological heterogeneity have emerged. Gene expression profiling (GEP) stratifies DLBCL into 3 broad groups (ABC, GCB, and DZsig/MHG), each with parallels to different normal mature B cell developmental states and prognostic implications. More recently, several different genomic approaches have been developed to categorize DLBCL based on the co -occurrence of tumor somatic mutations, identifying more granular biologically unified subgroups that complement GEP-based approaches. We review the molecular approaches and clinical evidence supporting the stratification of DLBCL patients based on tumor biology. By offering a platform for subtype -guided therapy, these divisions remain a promising avenue for improving patient outcomes, especially in subgroups with inferior outcomes with current standard -of -care therapy. (c) 2023 The Author(s). Published by Elsevier Inc. This is an open access article under the CC BY -NC -ND license ( http://creativecommons.org/licenses/by-nc-nd/4.0/ )
引用
收藏
页码:267 / 276
页数:10
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