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| Status |
Public on Dec 21, 2011 |
| Title |
Routine use of microarray-based gene expression profiling to identify patients with low cytogenetic risk acute myeloid leukemia: accurate results can be obtained even with suboptimal samples (training samples) |
| Organism |
Homo sapiens |
| Experiment type |
Expression profiling by array
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| Summary |
Background: Gene expression profiling has shown its ability to identify with high accuracy low cytogenetic risk acute myeloid leukemia such as acute promyelocytic leukemia and leukemias with t(8;21) or inv(16). The aim of this gene expression profiling study was to evaluate to what extent suboptimal samples with low leukemic blast load (range, 2-59%) and/or poor quality control criteria could also be correctly identified. Methods: Specific signatures were first defined so that all 71 acute promyelocytic leukemia, leukemia with t(8;21) or inv(16)-AML as well as cytogenetically normal acute myeloid leukemia samples with at least 60% blasts and good quality control criteria were correctly classified (training set). The classifiers were then evaluated for their ability to assign to the expected class 111 samples considered as suboptimal because of a low leukemic blast load (n=101) and/or poor quality control criteria (n=10) (test set). Results: With 10-marker classifiers, all training set samples as well as 97 of the 101 test samples with a low blast load, and all 10 samples with poor quality control criteria were correctly classified. Regarding test set samples, the overall error rate of the class prediction was below 4 percent, even though the leukemic blast load was as low as 2%. Sensitivity, specificity, negative and positive predictive values of the class assignments ranged from 91% to 100%. Of note, for acute promyelocytic leukemia and leukemias with t(8;21) or inv(16), the confidence level of the class assignment was influenced by the leukemic blast load. Conclusion: Gene expression profiling and a supervised method requiring 10-marker classifiers enable the identification of favorable cytogenetic risk acute myeloid leukemia even when samples contain low leukemic blast loads or display poor quality control criterion.
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| Overall design |
Training set.
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| Contributor(s) |
Raingeard de la Blétière D, Blanchet O, Cornillet-Lefèbvre P, Coutolleau A, Baranger L, Geneviève F, Luquet I, Hunault-Berger M, Beucher A, Schmidt-Tanguy A, Zandecki M, Delneste Y, Ifrah N, Guardiola P |
| Citation(s) |
22289410 |
| Submission date |
Dec 20, 2011 |
| Last update date |
Aug 16, 2018 |
| Contact name |
Philippe Guardiola |
| E-mail(s) |
Phguardiol@aol.com
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| Phone |
+33 2 41 35 44 82
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| Fax |
+33 2 41 35 45 82
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| Organization name |
Angers University Hospital
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| Lab |
Plateforme SNP, Transcriptome & Epigenomique
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| Street address |
4 rue Larrey
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| City |
Angers |
| State/province |
Maine et Loire |
| ZIP/Postal code |
49000 |
| Country |
France |
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| Platforms (1) |
| GPL6947 |
Illumina HumanHT-12 V3.0 expression beadchip |
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| Samples (89)
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| This SubSeries is part of SuperSeries: |
| GSE34823 |
Routine use of microarray-based gene expression profiling to identify patients with low cytogenetic risk acute myeloid leukemia: accurate results can be obtained even with suboptimal samples |
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| Relations |
| BioProject |
PRJNA156199 |
| Supplementary file |
Size |
Download |
File type/resource |
| GSE34577_RAW.tar |
6.2 Mb |
(http)(custom) |
TAR |
| GSE34577_non-normalized.txt.gz |
15.6 Mb |
(ftp)(http) |
TXT |
| Processed data included within Sample table |
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