Confirmation of the molecular classification of diffuse large B-cell lymphoma by immunohistochemistry using a tissue microarray
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Résumé
Diffuse large B-cell lymphoma (DLBCL) can be divided into prognostically important subgroups with germinal center B-cell-like (GCB), activated B-cell-like (ABC), and type 3 gene expression profiles using a cDNA microarray. Tissue microarray (TMA) blocks were created from 152 cases of DLBCL, 142 of which had been successfully evaluated by cDNA microarray (75 GCB, 41 ABC, and 26 type 3). Sections were stained with antibodies to CD10, bcl-6, MUM1, FOXP1, cyclin D2, and bcl-2. Expression of bcl-6 (P <.001) or CD10 (P =.019) was associated with better overall survival (OS), whereas expression of MUM1 (P =.009) or cyclin D2 (P <.001) was associated with worse OS. Cases were subclassified using CD10, bcl-6, and MUM1 expression, and 64 cases (42%) were considered GCB and 88 cases (58%) non-GCB. The 5-year OS for the GCB group was 76% compared with only 34% for the non-GCB group (P <.001), which is similar to that reported using the cDNA microarray. Bcl-2 and cyclin D2 were adverse predictors in the non-GCB group. In multivariate analysis, a high International Prognostic Index score (3-5) and the non-GCB phenotype were independent adverse predictors (P <.0001). In summary, immunostains can be used to determine the GCB and non-GCB subtypes of DLBCL and predict survival similar to the cDNA microarray.
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La notice
- Revue
- Blood
- Thématique
- Lymphoma Diagnosis and Treatment
- Domaine
- Medicine
- Établissements canadiens
- BC Cancer Agency
- Organismes subventionnaires
- National Cancer InstituteAssociazione Italiana per la Ricerca sul CancroU.S. Department of Health and Human Services
- Mots-clés
- Tissue microarrayMicroarrayLymphomaGerminal centerImmunohistochemistryDiffuse large B-cell lymphomaPathologyBiologyInternational Prognostic IndexGene expression profilingMicroarray analysis techniquesComplementary DNAGene expressionMedicineB cellAntibodyGeneImmunologyGenetics
- Résumé présent dans OpenAlex
- oui