| Literature DB >> 20513126 |
Stephen D Smith, Eric Hsi, Brian Bolwell, Brad Pohlman, Robert Dean, Meagan Effinger, Amanda Maggiotto, John Sweetenham.
Abstract
Mantle cell lymphoma (MCL) is a unique, recently recognized entity with a variable clinical course [1]. Its historical grouping as an indolent lymphoma belies its common behavior, which is generally aggressive and incurable, with a median survival of about 5 years with modern therapy [2]. In an effort to improve outcomes in MCL, intensified therapies, including the rituximab plus HyperCVAD regimen [3] and incorporation of hematopoetic progenitor cell transplantation (HPCT) [4-6], have been used. However, although capable of inducing remissions in most patients, there is little proof that intensive first-line therapy prolongs overall survival (OS), and a continual relapse pattern is commonly observed [4,7-10].Entities:
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Year: 2010 PMID: 20513126 DOI: 10.1002/ajh.21705
Source DB: PubMed Journal: Am J Hematol ISSN: 0361-8609 Impact factor: 10.047