Literature DB >> 7849295

A clinical analysis of two indolent lymphoma entities: mantle cell lymphoma and marginal zone lymphoma (including the mucosa-associated lymphoid tissue and monocytoid B-cell subcategories): a Southwest Oncology Group study.

R I Fisher1, S Dahlberg, B N Nathwani, P M Banks, T P Miller, T M Grogan.   

Abstract

The objectives of this study were (1) to determine the clinical presentation and natural history associated with two newly recognized pathologic entities termed mantle cell lymphoma (MCL) and marginal zone lymphoma (MZL), including the mucosa-associated lymphoid tissue (MALT) and monocytoid B-cell subcategories, and (2) to determine whether these entities differ clinically from the other relatively indolent non-Hodgkin's lymphomas with which they have been previously classified. We reviewed the conventional pathology and clinical course of 376 patients who had no prior therapy; had stage III/IV disease; were classified as Working Formulation categories A, B, C, D, or E; and received cyclophosphamide, doxorubicin, vincristine, prednisone (CHOP) on Southwest Oncology Group (SWOG) studies no. 7204, 7426, or 7713. All slides were reviewed by the three pathologists who reached a consensus diagnosis. Age, sex, performance status, bone marrow and/or gastrointestinal involvement, failure-free survival, and overall survival were compared among all the categories. We found that (1) MCL and MZL each represent approximately 10% of stage III or IV patients previously classified as Working Formulation categories A through E and treated with CHOP on SWOG clinical trials; (2) the failure-free survival and overall survival of patients with MZL is the same as that of patients with Working Formulation categories A through E, but the failure-free survival and overall survival of the monocytoid B-cell patients were higher than that of the MALT lymphoma patients (P = .009 and .007, respectively); and (3) the failure-free survival and overall survival of patients with MCL is significantly worse than that of patients with Working Formulation categories A through E (P = .0002 and .0001, respectively). In conclusion, patients with advanced stage MALT lymphomas may have a more aggressive course than previously recognized. Patients with MCL do not have an indolent lymphoma and are candidates for innovative therapy.

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Year:  1995        PMID: 7849295

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  43 in total

Review 1.  Molecular diagnostic approach to non-Hodgkin's lymphoma.

Authors:  D A Arber
Journal:  J Mol Diagn       Date:  2000-11       Impact factor: 5.568

2.  Detection of translocation t(11;14)(q13;q32) in mantle cell lymphoma by fluorescence in situ hybridization.

Authors:  J Y Li; F Gaillard; A Moreau; J L Harousseau; C Laboisse; N Milpied; R Bataille; H Avet-Loiseau
Journal:  Am J Pathol       Date:  1999-05       Impact factor: 4.307

Review 3.  Current treatment strategy and new agents in mantle cell lymphoma.

Authors:  Michinori Ogura
Journal:  Int J Hematol       Date:  2010-06-08       Impact factor: 2.490

Review 4.  Mantle cell lymphoma.

Authors:  J J Densmore; M E Williams
Journal:  Curr Treat Options Oncol       Date:  2000-08

5.  Mantle cell lymphoma successfully treated in a patient with multiple endocrine neoplasia type 2: a rare combination of two malignancies.

Authors:  Maciej Machaczka
Journal:  Med Oncol       Date:  2012-09       Impact factor: 3.064

6.  How I treat mantle cell lymphoma.

Authors:  David J Straus
Journal:  J Oncol Pract       Date:  2007-09       Impact factor: 3.840

7.  Durable responses with the metronomic rituximab and thalidomide plus prednisone, etoposide, procarbazine, and cyclophosphamide regimen in elderly patients with recurrent mantle cell lymphoma.

Authors:  Jia Ruan; Peter Martin; Morton Coleman; Richard R Furman; Ken Cheung; Adam Faye; Rebecca Elstrom; Mark Lachs; Katherine A Hajjar; John P Leonard
Journal:  Cancer       Date:  2010-06-01       Impact factor: 6.860

8.  Mantle cell lymphoma cells express high levels of CXCR4, CXCR5, and VLA-4 (CD49d): importance for interactions with the stromal microenvironment and specific targeting.

Authors:  Antonina V Kurtova; Archito T Tamayo; Richard J Ford; Jan A Burger
Journal:  Blood       Date:  2009-02-19       Impact factor: 22.113

Review 9.  Low-grade lymphomas: new entities and treatment concepts.

Authors:  F B Hagemeister
Journal:  Med Oncol       Date:  1995-09       Impact factor: 3.064

10.  Synchronous adenocarcinoma and mantle cell lymphoma of the stomach.

Authors:  Yong Il Kim; Min Young Koo
Journal:  Yonsei Med J       Date:  2007-12-31       Impact factor: 2.759

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