Stromal Gene Signatures in Large-B-Cell Lymphomas

Georg Lenz(National Cancer Institute), George W. Wright(National Institutes of Health), Sandeep S. Davé(National Institutes of Health), Wenming Xiao(National Institutes of Health), John Powell(National Institutes of Health), Hong Zhao(National Institutes of Health), Weihong Xu(National Institutes of Health), Bruce K. Tan(National Institutes of Health), Neta Goldschmidt(National Institutes of Health), Javeed Iqbal(University of Nebraska Medical Center), Julie Vose(University of Nebraska Medical Center), M. Bast(University of Nebraska Medical Center), Kai Fu(University of Nebraska Medical Center), DD Weisenburger(University of Nebraska Medical Center), Timothy C. Greiner(University of Nebraska Medical Center), Jamés O. Armitage(University of Nebraska Medical Center), Alastair H. Kyle(University of British Columbia), Lorraine F. May(University of British Columbia), Randy D. Gascoyne(University of British Columbia), Joseph M. Connors(University of British Columbia), Gunhild Trøen(University of Oslo), Harald Holte(University of Oslo), Stein Kvaløy(University of Oslo), Daan Dierickx(KU Leuven), G. Verhoef(KU Leuven), Jan Delabie(University of Oslo), Erlend B. Smeland(University of Oslo), Pedro Jares(Universitat de Barcelona), Antonio Martı́nez(Universitat de Barcelona), Armando López‐Guillermo(Universitat de Barcelona), Emili Montserrat(Universitat de Barcelona), Elı́as Campo(Universitat de Barcelona), Rita M. Braziel(Oregon Health & Science University), Thomas P. Miller(University of Arizona), Lisa M. Rimsza(University of Arizona), James R. Cook(Cleveland Clinic), Brad Pohlman(Cleveland Clinic), John Sweetenham(Cleveland Clinic), Raymond R. Tubbs(Cleveland Clinic), Richard I. Fisher(University of Rochester), Elena Hartmann(University of Würzburg), Andreas Rosenwald(University of Würzburg), German Ott(Robert Bosch (Germany)), Müller-Hermelink Hk(University of Würzburg), David Wrench(St Bartholomew's Hospital), T. Lister(St Bartholomew's Hospital), Elaine S. Jaffe(National Institutes of Health), Wyndham H. Wilson(National Institutes of Health), Wing C. Chan(University of Nebraska Medical Center), Louis M. Staudt(National Institutes of Health)
New England Journal of Medicine
November 26, 2008
Cited by 1,812Open Access
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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.


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