Rearrangement of the BCL6 locus at 3q27 is an independent poor prognostic factor in nodal diffuse large B-cell lymphoma.

Br J Haematol

Academic Unit of Haematology and Oncology, HMDS, Algernon Firth Building, Leeds General Infirmary, Leeds LS1 3EX, UK.

Published: May 2002

AI Article Synopsis

  • Diffuse large B-cell lymphomas (DLBCL) are complex tumors with varying characteristics, and this study focused on the impact of BCL6 gene rearrangement on patient prognosis in those with primary nodal disease.
  • A new FISH technique was used to analyze tissue samples from 111 DLBCL cases, revealing that 25% had 3q27 rearrangements, and a significant portion expressed BCL2 protein and exhibited a germinal center phenotype.
  • The analysis indicated that the presence of 3q27 rearrangements, alongside BCL2 expression and absence of a germinal center phenotype, correlates with poorer patient outcomes, helping to refine risk assessment when combined with the International Prognostic Index (IPI).

Article Abstract

Diffuse large B-cell lymphomas (DLBCL) are a heterogeneous group of tumours, varying in clinical features, immunophenotype and cytogenetics. The aim of this study was to investigate the prognostic significance of BCL6 gene rearrangement at the 3q27 locus in patients with primary nodal disease, and to examine interrelationships with immunophenotype and International Prognostic Index (IPI). We have developed a fluorescent in situ hybridization (FISH)-based technique for the retrospective analysis of the effect of BCL6 gene rearrangements on survival, using nuclei extracted from paraffin-embedded tissue. FISH results were obtained in 111 presentation cases of nodal DLBCL. The IPI was calculated and each case was stained immunocytochemically for BCL6, BCL2 and CD10. 3q27 rearrangements were detected in 25% of cases. BCL2 protein and a germinal centre (GC) phenotype (defined as CD10+, BCL6+) were expressed in 56% and 41% of cases respectively. In multivariate analysis, rearrangement of 3q27 and BCL2 expression and the absence of a GC phenotype were associated with a poor prognosis. These factors can be used in conjunction with the IPI to improve risk stratification in nodal DLBCL.

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http://dx.doi.org/10.1046/j.1365-2141.2002.03435.xDOI Listing

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