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Biology, Prognosis, and Therapy of Waldenström Macroglobulinemia | SpringerLink
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Waldenström Macroglobulinemia (WM) is a rare B-cell lymphoma characterized by the uncontrolled accumulation of malignant lymphoplasmacytic cells, mainly in the bone marrow, and monoclonal IgM production. Despite its rarity, our understanding of the biology of...
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ScholarlyArticle:
headline:Biology, Prognosis, and Therapy of Waldenström Macroglobulinemia
pageEnd:195
pageStart:177
image:https://media.springernature.com/w153/springer-static/cover/book/978-3-319-13150-4.jpg
genre:
Medicine
Medicine (R0)
isPartOf:
name:Non-Hodgkin Lymphoma
isbn:
978-3-319-13150-4
978-3-319-13149-8
type:Book
publisher:
name:Springer International Publishing
logo:
url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
type:ImageObject
type:Organization
author:
name:Jorge J. Castillo
affiliation:
name:Dana-Farber Cancer Institute, Harvard Medical School
address:
name:Division of Hematologic Malignancies, Dana-Farber Cancer Institute, Harvard Medical School, Boston, USA
type:PostalAddress
type:Organization
email:[email protected]
type:Person
name:Irene M. Ghobrial
affiliation:
name:Dana-Farber Cancer Institute, Harvard Medical School
address:
name:Division of Hematologic Malignancies, Dana-Farber Cancer Institute, Harvard Medical School, Boston, USA
type:PostalAddress
type:Organization
type:Person
name:Steven P. Treon
affiliation:
name:Dana-Farber Cancer Institute, Harvard Medical School
address:
name:Division of Hematologic Malignancies, Dana-Farber Cancer Institute, Harvard Medical School, Boston, USA
type:PostalAddress
type:Organization
type:Person
keywords:Waldenström Macroglobulinemia, MYD88, CXCR4, Biology, Therapy, Survival
description:Waldenström Macroglobulinemia (WM) is a rare B-cell lymphoma characterized by the uncontrolled accumulation of malignant lymphoplasmacytic cells, mainly in the bone marrow, and monoclonal IgM production. Despite its rarity, our understanding of the biology of this disease has improved significantly in recent years with the identification of recurrent mutations in the MYD88 and CXCR4 genes. Based on the diversity of clinical features observed in WM patients, therapy should be highly personalized having into account several factors such as age, co-morbidities, IgM levels, and presence of hyperviscosity, coagulopathy, cryoglobulinemia, or cold agglutinin disease. In this chapter, we review the recent advances in the biology of WM and the current therapeutic options for untreated and relapsed WM patients. Finally, we discuss the role of prognostic factors and current evidence supporting an improvement in the survival of WM patients in the last decade.
datePublished:2015
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