A BSTRACT Background: Diffuse large B cell lymphoma (DLBCL) within non-Hodgkin lymphoma has several morphologic and clinicopathologic variants. DLBCL has two prognostically important subtypes, germinal center B cell (GCB) and nongerminal center (Non-GCB) with the non-GCB having an inferior outcome. Immunohistochemical co-expression of cellular myelocytomatosis (CMYC) and BCL2 in DLBCL has poor prognosis and is considered as double-expressor lymphoma (DEL). Aims and Objectives: This study was done to identify DEL using immunohistochemistry among GCB and non-GCB DLBCL and to assess their treatment response. Methods and Material: A retrospective analysis of 97 DLBCL cases received in our department was done. Formalin-fixed paraffin blocks were used to prepare Hematoxylin and eosin–stained sections, immunohistochemical subtyping (into GCB and non-GCB using CD10, BCL6, and MUM1) and further to identify DEL (using CMYC and BCL2). Statistical Analysis: Analysis was done using Chi-square test (Statistical Package for Social Sciences version 18), and P <.05 was considered significant. Kaplan-Meier test was used to estimate overall survival. Results: Of the total 97 DLBCL cases analyzed, 33 (34%) were DEL and 64 (66%) were non-DEL. Of the DEL, 13 (13.40%) were GCB subtype and 20 (20.6%) were non-GCB. However, there was no statistically significant difference in the overall survival and treatment response between DEL and non-DEL. Conclusions: In this study, we found that DEL constituted about one-third of the total DLBCL and within the DEL non-GCB subtype was more common. Further studies should be performed in large population to study the difference in clinical outcome.
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Rani et al. (2024) studied this question.
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