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PMID: 12424193 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

A significant diffuse component predicts for inferior survival in grade 3 follicular lymphoma, but cytologic subtypes do not predict survival.

Blood ·Vol. 101 ·No. 6 ·2003-03-15 ·Pages 2363-7

Hans CP, Weisenburger DD, Vose JM, Hock LM, Lynch JC, Aoun P, Greiner TC, Chan WC, Bociek RG, Bierman PJ, Armitage JO

Abstract

Grade 3 follicular lymphoma (FL3) is thought to have an aggressive clinical course. On the basis of possible biologic differences, the new World Health Organization (WHO) classification of lymphoma suggests further subdivision of FL3 into grades 3a and 3b and states that the percentage of involvement by diffuse large B-cell lymphoma (DLBCL) should also be reported. However, the clinical implications of these features are unclear. Therefore, we studied 190 newly diagnosed patients with lymph node-based FL3 who received anthracycline-containing combination chemotherapy. The follicular component was subclassified as grade 3a (FL3a) or grade 3b (FL3b) according to the WHO criteria, or as follicular large cleaved cell type (FLC). The percentage of a diffuse component, if present, was also recorded. Of the 190 cases, there were 107 FL3a (56%), 53 FL3b (28%), and 30 FLC (16%) cases. Diffuse areas were seen in 72 cases (31 FL3a, 28 FL3b, and 13 FLC). There were no significant differences in the clinical characteristics, overall survival, or event-free survival between patients with grades FL3a, FL3b, or FLC. However, those cases with a predominant diffuse component (> 50% diffuse) had a significantly worse overall survival (P =.0037) and event-free survival (P =.012). Therefore, we conclude that the subdivision of FL3 into cytologic subtypes does not appear to be important clinically. However, patients with FL3 having a diffuse component of more than 50% have an inferior survival that is similar to the survival of those with DLBCL.

MeSH Terms
Adolescent Adult Aged Aged, 80 and over Antineoplastic Combined Chemotherapy Protocols/therapeutic use Bleomycin/therapeutic use Cyclophosphamide/therapeutic use Doxorubicin/therapeutic use Female Humans Lymphoma, B-Cell/pathology Lymphoma, Follicular/drug therapy,mortality,pathology Lymphoma, Large B-Cell, Diffuse/pathology Male Middle Aged Mitoxantrone/therapeutic use Prednisolone/therapeutic use Prednisone/therapeutic use Procarbazine/therapeutic use Prognosis Survival Rate Vincristine/therapeutic use
Chemicals
Bleomycin Procarbazine Vincristine Doxorubicin Cyclophosphamide Prednisolone Mitoxantrone Prednisone
Authors & Affiliations
11 authors, click to expand affiliations / ORCID
Hans Christine P
Department of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, NE 68198-3135, USA.
Weisenburger Dennis D
Vose Julie M
Hock Lynette M
Lynch James C
Aoun Patricia
Greiner Timothy C
Chan Wing C
Bociek Robert G
Bierman Philip J
Armitage James O
Supplementary Concepts
CHOP protocol (Protocol) COP-BLAM protocol (Protocol) MCOP protocol (Protocol)
Article Info
Journal
Blood
Abbr.
Blood
ISSN
0006-4971
Published
2003-03-15
Epub
2002-00-07
Pages
2363-7
Language
English
Region
United States
NLM ID
7603509
Subset
IM
Grants
NCI NIH HHS · CA36727 · United States
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