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Recent Advances in Aggressive Large B-cell Lymphomas: A Comprehensive Review
Penelope Korkolopoulou1, Theodoros Vassilakopoulos, Vassilios Milionis
1*First Department of Pathology †Department of Hematology, Athens University, School of Medicine, Laikon General Hospital, Athens ‡Department of Pathology, Faculty of Medicine, University of Thessaly, Larissa, Greece.
This review updates the clinical, pathologic, and molecular features of Diffuse Large B-cell Lymphoma (DLBCL), including new variants and diagnostic challenges. Genomic characterization advances offer insights into prognosis and targeted therapies for DLBCL patients.
Area of Science:
- Hematology
- Oncology
- Genetics
Background:
- Diffuse Large B-cell Lymphoma (DLBCL) exhibits significant heterogeneity, challenging its classification.
- Recent genome-wide studies reveal distinct molecular subsets in DLBCL linked to specific gene/pathway dysregulation.
Purpose of the Study:
- To provide an updated review of DLBCL, incorporating recent clinical, pathologic, and molecular findings.
- To highlight emerging DLBCL variants and challenging diagnostic entities.
- To discuss advances in genomic characterization for prognostication and targeted therapy.
Main Methods:
- Literature review of English-language publications in PubMed up to December 2015.
- Synthesis of information on DLBCL pathobiology, prognosis, and emerging variants.
- Focus on genomic characterization and its therapeutic implications.
Main Results:
- Identification of distinct molecular subsets within DLBCL.
- Emergence of new DLBCL variants (e.g., CD30 DLBCL, HIV-related, EBV DLBCL).
- Advances in understanding challenging entities like T-cell/histiocyte-rich large B-cell lymphoma.
Conclusions:
- DLBCL molecular complexity is increasingly understood through genetic and epigenetic studies.
- New variants and diagnostic challenges require updated clinical and pathologic insights.
- Genomic insights are crucial for improving DLBCL prognostication and developing tailored therapies.
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