AI Article Synopsis

  • * Recent advancements in DNA-based genomic subtyping provide a potential framework for developing personalized and targeted therapies for DLBCL patients.
  • * The review discusses the need for a unified genomic classification system to facilitate effective clinical trials and improve daily practice, along with suggestions for necessary laboratory techniques and infrastructure to support this effort.

Article Abstract

Diffuse large B-cell lymphoma (DLBCL) is a widely heterogeneous disease in presentation, treatment response and outcome that results from a broad biological heterogeneity. Various stratification approaches have been proposed over time but failed to sufficiently capture the heterogeneous biology and behavior of the disease in a clinically relevant manner. The most recent DNA-based genomic subtyping studies are a major step forward by offering a level of refinement that could serve as a basis for exploration of personalized and targeted treatment for the years to come. To enable consistent trial designs and allow meaningful comparisons between studies, harmonization of the currently available knowledge into a single genomic classification widely applicable in daily practice is pivotal. In this review, we investigate potential avenues for harmonization of the presently available genomic subtypes of DLBCL inspired by consensus molecular classifications achieved for other malignancies. Finally, suggestions for laboratory techniques and infrastructure required for successful clinical implementation are described.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9648119PMC
http://dx.doi.org/10.3389/fonc.2022.970063DOI Listing

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