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 in | The New England journal of medicine Vol. 350; no. 16; pp. 1605 - 1616 |
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| Main Authors | , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
Boston, MA
Massachusetts Medical Society
15.04.2004
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| Subjects | |
| Online Access | Get full text |
| ISSN | 0028-4793 1533-4406 1533-4406 |
| DOI | 10.1056/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.
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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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| Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-General Information-1 content type line 14 ObjectType-Feature-3 ObjectType-Article-1 ObjectType-Feature-2 content type line 23 ObjectType-Feature-1 |
| ISSN: | 0028-4793 1533-4406 1533-4406 |
| DOI: | 10.1056/NEJMoa031046 |