The expression of 16 genes related to the cell of origin and immune response predicts survival in elderly patients with diffuse large B-cell lymphoma treated with CHOP and rituximab

Leukemia. 2008 Oct;22(10):1917-24. doi: 10.1038/leu.2008.188. Epub 2008 Jul 10.

Abstract

Gene expression profiles have been associated with clinical outcome in patients with diffuse large B-cell lymphoma (DLBCL) treated with anthracycline-containing chemotherapy. Using Affymetrix HU133A microarrays, we analyzed the lymphoma transcriptional profile of 30 patients treated with CHOP (cyclophosphamide, doxorubicin, vincristine, prednisone) and 23 patients treated with rituximab (R)-CHOP in the Groupe d'Etude des Lymphomes de l'Adulte clinical centers. We used this data set to select transcripts showing an association with progression-free survival in all patients or showing a differential effect in the two treatment groups. We performed real-time quantitative reverse transcription-PCR in the 23 R-CHOP samples of the screening set and an additional 44 R-CHOP samples set to evaluate the prognostic significance of these transcripts. In these 67 patients, the level of expression of 16 genes and the cell-of-origin classification were significantly associated with overall survival, independently of the International Prognostic Index. A multivariate model comprising four genes of the cell-of-origin signature (LMO2, MME, LPP and FOXP1) and two genes related to immune response, identified for their differential effects in R-CHOP patients (APOBEC3G and RAB33A), demonstrated a high predictive efficiency in this set of patients, suggesting that both features affect outcome in DLBCL patients receiving immunochemotherapy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • APOBEC-3G Deaminase
  • Adaptor Proteins, Signal Transducing
  • Aged
  • Aged, 80 and over
  • Antibodies, Monoclonal / administration & dosage*
  • Antibodies, Monoclonal, Murine-Derived
  • Antineoplastic Combined Chemotherapy Protocols / administration & dosage*
  • Cyclophosphamide / administration & dosage
  • Cytidine Deaminase / genetics
  • Cytoskeletal Proteins / genetics
  • DNA-Binding Proteins / genetics
  • Doxorubicin / administration & dosage
  • Female
  • Forkhead Transcription Factors / genetics
  • Gene Expression Profiling*
  • Humans
  • LIM Domain Proteins
  • Lymphoma, Large B-Cell, Diffuse / drug therapy*
  • Lymphoma, Large B-Cell, Diffuse / genetics
  • Lymphoma, Large B-Cell, Diffuse / immunology
  • Lymphoma, Large B-Cell, Diffuse / mortality
  • Male
  • Metalloproteins / genetics
  • Middle Aged
  • Multivariate Analysis
  • Prednisone / administration & dosage
  • Proto-Oncogene Proteins
  • Repressor Proteins / genetics
  • Reverse Transcriptase Polymerase Chain Reaction
  • Rituximab
  • Vincristine / administration & dosage
  • rab GTP-Binding Proteins / genetics

Substances

  • Adaptor Proteins, Signal Transducing
  • Antibodies, Monoclonal
  • Antibodies, Monoclonal, Murine-Derived
  • Cytoskeletal Proteins
  • DNA-Binding Proteins
  • FOXP1 protein, human
  • Forkhead Transcription Factors
  • LIM Domain Proteins
  • LMO2 protein, human
  • LPP protein, human
  • Metalloproteins
  • Proto-Oncogene Proteins
  • RAB33A protein, human
  • Repressor Proteins
  • Rituximab
  • Vincristine
  • Doxorubicin
  • Cyclophosphamide
  • APOBEC-3G Deaminase
  • APOBEC3G protein, human
  • Cytidine Deaminase
  • rab GTP-Binding Proteins
  • Prednisone

Supplementary concepts

  • CHOP protocol