Leukemic Variant of Mantle Cell Lymphoma: Clinical Presentation and Management.


Journal

Current oncology reports
ISSN: 1534-6269
Titre abrégé: Curr Oncol Rep
Pays: United States
ID NLM: 100888967

Informations de publication

Date de publication:
16 07 2021
Historique:
accepted: 20 05 2021
entrez: 16 7 2021
pubmed: 17 7 2021
medline: 24 2 2022
Statut: epublish

Résumé

This review summarizes the unique presentation and management of the leukemic variant of mantle cell lymphoma (LV-MCL, also referred to as non-nodal MCL) and highlights the biologic and clinical differentiation from classical mantle cell lymphoma (cMCL) in biomarker expression, clinical features, prognosis, disease course, and treatment. Several studies have evaluated the gene expression profile of mantle cell lymphoma, differentiating LV-MCL from cMCL. The typical immunophenotypic profile is CD5-positive, SOX 11-negative, CD23-low, CD200-low, and cyclin D1 overexpressed. LV-MCL commonly has mutated immunoglobulin heavy chain variable region genes. Data on treatment of LV-MCL is limited to retrospective analyses; the ideal treatment for these patients is unknown although many have a clinically indolent, asymptomatic presentation and often may be observed for an extended period without active treatment. LV-MCL is a clinically and biologically distinct entity. Clinically, it must be distinguished from chronic lymphocytic leukemia and cMCL. Future prospective, randomized clinical trials are required to optimize management, define the initial treatment, and appropriately sequence treatment modalities.

Identifiants

pubmed: 34269910
doi: 10.1007/s11912-021-01094-y
pii: 10.1007/s11912-021-01094-y
doi:

Substances chimiques

Biomarkers, Tumor 0
Immunoglobulin Heavy Chains 0
Immunoglobulin Variable Region 0
SOXC Transcription Factors 0
Cyclin D1 136601-57-5

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

102

Informations de copyright

© 2021. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

Auteurs

Krista M Isaac (KM)

Division of Hematology/Oncology, Department of Medicine, University of Virginia Cancer Center, Jefferson Park Avenue, PO 800716, Charlottesville, VA, 22908, USA.

Craig A Portell (CA)

Division of Hematology/Oncology, Department of Medicine, University of Virginia Cancer Center, Jefferson Park Avenue, PO 800716, Charlottesville, VA, 22908, USA.

Michael E Williams (ME)

Division of Hematology/Oncology, Department of Medicine, University of Virginia Cancer Center, Jefferson Park Avenue, PO 800716, Charlottesville, VA, 22908, USA. mew4p@virginia.edu.

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Classifications MeSH