Laying the Foundation for Clinically Actionable Genomic Subtyping in Diffuse Large B-cell Lymphoma

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Authors: Margaret A. Shipp, Louis M. Staudt, Daniel J. Hodson, David W. Scott, Wei-Li Zhao, Riccardo Dalla‐Favera, Ash A. Alizadeh, Ryan D. Morin
Cited by: 1
References: 52

Abstract

Diffuse large B-cell lymphoma (DLBCL) is clinically and genetically heterogeneous. The existence of genetically defined subtypes with therapeutic implications is clear. Additional considerations that are yet to be fully resolved include defining boundaries between discrete classes, relevant molecular data types, and handling of unclassifiable/composite cases. In this review, we juxtapose points of view on the topic from experts in the field, outline practical workflow considerations, and distill lessons from clinical trials. These synthesize experimental design and analytic considerations that inform the development and evaluation of clinically relevant DLBCL subtyping approaches. SIGNIFICANCE: The most meaningful way to stratify DLBCL remains unresolved, and this represents a significant barrier to adopting a precision medicine paradigm.

Fields of Study & Subjects

Lymphoma Diagnosis and Treatment Cutaneous lymphoproliferative disorders research CNS Lymphoma Diagnosis and Treatment

Publication details

Journal / source
Blood Cancer Discovery
Publisher
American Association for Cancer Research (AACR)
Volume
7
Issue
4
Pages
520–531
Publication date
12 May 2026
Language
EN