Molecular Diagnosis of Burkitt's Lymphoma

Sandeep S. Davé(National Institutes of Health), Kai Fu(University of Nebraska Medical Center), George W. Wright(National Institutes of Health), Lloyd T. Lam(National Institutes of Health), Philip M. Kluin(University Medical Center Groningen), Evert-Jan Boerma(University Medical Center Groningen), Timothy C. Greiner(University of Nebraska Medical Center), Dennis D. Weisenburger(University of Nebraska Medical Center), Andreas Rosenwald(University of Würzburg), German Ott(University of Würzburg), Hans-Konrad Müller-Hermelink, Randy D. Gascoyne(BC Cancer Agency), Jan Delabie, Lisa M. Rimsza(University of Arizona), Rita M. Braziel(Oregon Health & Science University), Thomas M. Grogan(University of Arizona), Elı́as Campo(Universitat de Barcelona), Elaine S. Jaffe(National Institutes of Health), Bhavana J. Davé(University of Nebraska Medical Center), Warren G. Sanger(University of Nebraska Medical Center), Martin Bast(National Institutes of Health), Julie M. Vose(University of Nebraska Medical Center), Jamés O. Armitage(University of Nebraska Medical Center), Joseph M. Connors(BC Cancer Agency), Erlend B. Smeland(University of Oslo), Stein Kvaløy, Harald Holte, Richard I. Fisher(University of Rochester Medical Center), Thomas P. Miller(University of Arizona), Emilio Montserrat(Universitat de Barcelona), Wyndham H. Wilson(National Institutes of Health), Manisha Bahl(National Institutes of Health), Hong Zhao(National Institutes of Health), Liming Yang(Center for Information Technology), John Powell(Center for Information Technology), Richard Simon(National Institutes of Health), Wing C. Chan(University of Nebraska Medical Center), Louis M. Staudt(National Institutes of Health)
New England Journal of Medicine
June 7, 2006
Cited by 903Open Access
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Abstract

BACKGROUND: The distinction between Burkitt's lymphoma and diffuse large-B-cell lymphoma is crucial because these two types of lymphoma require different treatments. We examined whether gene-expression profiling could reliably distinguish Burkitt's lymphoma from diffuse large-B-cell lymphoma. METHODS: Tumor-biopsy specimens from 303 patients with aggressive lymphomas were profiled for gene expression and were also classified according to morphology, immunohistochemistry, and detection of the t(8;14) c-myc translocation. RESULTS: A classifier based on gene expression correctly identified all 25 pathologically verified cases of classic Burkitt's lymphoma. Burkitt's lymphoma was readily distinguished from diffuse large-B-cell lymphoma by the high level of expression of c-myc target genes, the expression of a subgroup of germinal-center B-cell genes, and the low level of expression of major-histocompatibility-complex class I genes and nuclear factor-kappaB target genes. Eight specimens with a pathological diagnosis of diffuse large-B-cell lymphoma had the typical gene-expression profile of Burkitt's lymphoma, suggesting they represent cases of Burkitt's lymphoma that are difficult to diagnose by current methods. Among 28 of the patients with a molecular diagnosis of Burkitt's lymphoma, the overall survival was superior among those who had received intensive chemotherapy regimens instead of lower-dose regimens. CONCLUSIONS: Gene-expression profiling is an accurate, quantitative method for distinguishing Burkitt's lymphoma from diffuse large-B-cell lymphoma.


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