Use of Gene-Expression Profiling to Identify Prognostic Subclasses in Adult Acute Myeloid Leukemia

This study demonstrates that the genes expressed by peripheral-blood monocytes of adults with acute myeloid leukemia provide prognostic information over and above that provided by established indicators such as cytogenetic status. The authors analyzed the gene-expression profiles of samples obtained...

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Published inThe New England journal of medicine Vol. 350; no. 16; pp. 1605 - 1616
Main Authors Bullinger, Lars, Döhner, Konstanze, Döhner, Hartmut, Bair, Eric, Fröhling, Stefan, Schlenk, Richard F, Tibshirani, Robert, Pollack, Jonathan R
Format Journal Article
LanguageEnglish
Published Boston, MA Massachusetts Medical Society 15.04.2004
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ISSN0028-4793
1533-4406
1533-4406
DOI10.1056/NEJMoa031046

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Summary:This study demonstrates that the genes expressed by peripheral-blood monocytes of adults with acute myeloid leukemia provide prognostic information over and above that provided by established indicators such as cytogenetic status. The authors analyzed the gene-expression profiles of samples obtained from 116 patients, who were subsequently assigned to receive various intensive treatments. They identified good- and poor-outcome classes of gene expression that were associated with differences in overall survival — even when the analysis was restricted to specimens with a normal karyotype. Genes expressed by monocytes identified good- and poor-outcome classes even with a normal karyotype. Acute myeloid leukemia (AML) is the most common acute leukemia in adults. Chemotherapy induces a complete remission in 70 to 80 percent of younger patients (age, 16 to 60 years), but many of them have a relapse and die of their disease. Myeloablative conditioning followed by allogeneic stem-cell transplantation can prevent relapse, but this approach is associated with a high treatment-related mortality. 1 Therefore, accurate predictors of the clinical outcome are needed to determine appropriate treatment for individual patients. (See Glossary.) Currently used prognostic indicators include age, cytogenetic findings, the white-cell count, and the presence or absence of an antecedent hematologic . . .
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ISSN:0028-4793
1533-4406
1533-4406
DOI:10.1056/NEJMoa031046