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Stromal gene signatures in large-B-cell lymphomas

  • G. Lenz
  • , G. Wright
  • , S. S. Dave
  • , W. Xiao
  • , J. Powell
  • , H. Zhao
  • , W. Xu
  • , B. Tan
  • , N. Goldschmidt
  • , J. Iqbal
  • , J. Vose
  • , M. Bast
  • , K. Fu
  • , D. D. Weisenburger
  • , T. C. Greiner
  • , J. O. Armitage
  • , A. Kyle
  • , L. May
  • , R. D. Gascoyne
  • , J. M. Connors
  • G. Troen, H. Holte, S. Kvaloy, D. Dierickx, G. Verhoef, J. Delabie, E. B. Smeland, P. Jares, A. Martinez, A. Lopez-Guillermo, E. Montserrat, E. Campo, R. M. Braziel, T. P. Miller, L. M. Rimsza, J. R. Cook, B. Pohlman, J. Sweetenham, R. R. Tubbs, R. I. Fisher, E. Hartmann, A. Rosenwald, G. Ott, H. K. Muller-Hermelink, D. Wrench, T. A. Lister, E. S. Jaffe, W. H. Wilson, W. C. Chan, L. M. Staudt

Research output: Contribution to journalArticlepeer-review

Abstract

BACKGROUND: The addition of rituximab to combination chemotherapy with cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP), or R-CHOP, has significantly improved the survival of patients with diffuse large-B-cell lymphoma. Whether gene-expression signatures correlate with survival after treatment of diffuse large-B-cell lymphoma is unclear. METHODS: We profiled gene expression in pretreatment biopsy specimens from 181 patients with diffuse large-B-cell lymphoma who received CHOP and 233 patients with this disease who received R-CHOP. A multivariate gene-expression-based survival-predictor model derived from a training group was tested in a validation group. RESULTS: A multivariate model created from three gene-expression signatures - termed "germinal-center B-cell," "stromal-1," and "stromal-2" - predicted survival both in patients who received CHOP and patients who received R-CHOP. The prognostically favorable stromal-1 signature reflected extracellular-matrix deposition and histiocytic infiltration. By contrast, the prognostically unfavorable stromal-2 signature reflected tumor blood-vessel density. CONCLUSIONS: Survival after treatment of diffuse large-B-cell lymphoma is influenced by differences in immune cells, fibrosis, and angiogenesis in the tumor microenvironment.

Original languageEnglish (US)
Pages (from-to)2313-2323
Number of pages11
JournalNew England Journal of Medicine
Volume359
Issue number22
DOIs
StatePublished - Nov 27 2008

ASJC Scopus subject areas

  • General Medicine

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