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Immunoblastic morphology but not the immunohistochemical GCB/nonGCB classifier predicts outcome in diffuse large B-cell lymphoma in the RICOVER-60 trial of the DSHNHL
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 1193184
Author(s) Rosenwald, Andreas
Author(s) at UniBasel Cogliatti, Sergio Bruno
Year 2010
Title Immunoblastic morphology but not the immunohistochemical GCB/nonGCB classifier predicts outcome in diffuse large B-cell lymphoma in the RICOVER-60 trial of the DSHNHL
Journal Blood
Volume 116
Number 23
Pages / Article-Number 4916-25
Abstract The survival of diffuse large B-cell lymphoma patients varies considerably, reflecting the molecular diversity of tumors. In view of the controversy whether cytologic features, immunohistochemical markers or gene expression signatures may capture this molecular diversity, we investigated which features provide prognostic information in a prospective trial in the R-CHOP treatment era. Within the cohort of DLBCLs patients treated in the RICOVER-60 trial of the German High-Grade Lymphoma Study Group (DSHNHL), we tested the prognostic impact of IB morphology in 949 patients. The expression of immunohistochemical markers CD5, CD10, BCL2, BCL6, human leukocyte antigen (HLA)-DR, interferon regulatory factor-4/multiple myeloma-1 (IRF4/MUM1), and Ki-67 was assessed in 506 patients. Expression of the immunohistochemical markers tested was of modest, if any, prognostic relevance. Moreover, the Hans algorithm using the expression patterns of CD10, BCL6, and interferon regulatory factor-4/multiple myeloma-1 failed to show prognostic significance in the entire cohort as well as in patient subgroups. IB morphology, however, emerged as a robust, significantly adverse prognostic factor in multivariate analysis, and its diagnosis showed a good reproducibility among expert hematopathologists. We conclude, therefore, that IB morphology in DLBCL is likely to capture some of the adverse molecular alterations that are currently not detectable in a routine diagnostic setting, and that its recognition has significant prognostic power.
Publisher American Society of Hematology
ISSN/ISBN 1528-0020
edoc-URL http://edoc.unibas.ch/dok/A6003432
Full Text on edoc No
Digital Object Identifier DOI 10.1182/blood-2010-03-276766
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/20736456
ISI-Number WOS:000284880200029
Document type (ISI) Journal Article, Multicenter Study, Randomized Controlled Trial
 
   

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