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How I treat primary mediastinal B-cell lymphoma.

Authors :
Giulino-Roth L
Source :
Blood [Blood] 2018 Aug 23; Vol. 132 (8), pp. 782-790. Date of Electronic Publication: 2018 Jul 05.
Publication Year :
2018

Abstract

The World Health Organization now recognizes primary mediastinal B-cell lymphoma (PMBCL) as a unique clinical and biologic entity. PMBCL is distinct from other B-cell non-Hodgkin lymphoma subtypes and has features that overlap with classical Hodgkin lymphoma, including a peak incidence in the adolescent and young adult population, mediastinal presentation of disease, and molecular alterations in JAK2 and programmed death ligands. Because PMBCL is rare, there are few prospective clinical trials to guide therapy, resulting in no single standard of care. Given the long life expectancy of survivors of PMBCL, treatment approaches must balance maximizing cure while minimizing long-term toxicity. In this article, I review my approach to the treatment of PMBCL, incorporating data from adult and pediatric studies, as well as recent advances in our understanding of the molecular basis of PMBCL.<br /> (© 2018 by The American Society of Hematology.)

Details

Language :
English
ISSN :
1528-0020
Volume :
132
Issue :
8
Database :
MEDLINE
Journal :
Blood
Publication Type :
Academic Journal
Accession number :
29976557
Full Text :
https://doi.org/10.1182/blood-2018-04-791566