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Gene expression predicts overall survival in paraffin-embedded tissues of diffuse large B-cell lymphoma treated with R-CHOP

  • Lisa M. Rimsza
  • , Michael L. LeBlanc
  • , Joseph M. Unger
  • , Thomas P. Miller
  • , Thomas M. Grogan
  • , Daniel O. Persky
  • , Ralph R. Mattel
  • , Constantine M. Sabalos
  • , Bruce Seligmann
  • , Rita M. Braziel
  • , Elias Campo
  • , Andreas Rosenwald
  • , Joseph M. Connors
  • , Laurie H. Sehn
  • , Nathalie Johnson
  • , Randy D. Gascoyne

Research output: Contribution to journalArticlepeer-review

Abstract

Gene expression profiling (GEP) on frozen tissues has identified genes predicting outcome in patients with diffuse large B-cell lymphoma (DLBCL). Confirmation of results in current patients is limited by availability of frozen samples and addition of monoclonal antibodies to treatment regimens. We used a quantitative nuclease protection assay (qNPA) to analyze formalin-fixed, paraffin-embedded tissue blocks for 36 previously identified genes (N=209, 93 chemotherapy; 116rituximab + chemotherapy). By qNPA, 208 cases were successfully analyzed (99.5%). In addition, 15 of 36 and 11 of 36 genes, representing each functional group previously identified by GEP, were associated with survival (P < .05) in the 2 treatment groups, respectively. In addition, 30 of 36 hazard ratios of death trended in the same direction versus the original studies. Multivariate and variable cut-off point analysis identified low levels of HLA-DRB (< 20%) and high levels of MYC (> 80%) as independent indicators of survival, together distinguishing cases with the worst prognosis. Our results solve a clinical research problem by demonstrating that prognostic genes can be meaningfully quantified using qNPA technology on formalin-fixed, paraffinembedded tissues; previous GEP findings in DLBCL are relevant with current treatments; and 2 genes, representing immune escape and proliferation, are the common features of the most aggressive DLBCL.

Original languageEnglish (US)
Pages (from-to)3425-3433
Number of pages9
JournalBlood
Volume112
Issue number8
DOIs
StatePublished - Oct 15 2008

ASJC Scopus subject areas

  • Biochemistry
  • Immunology
  • Hematology
  • Cell Biology

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