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Quality assurance in RT-PCR-based BCR/ABL diagnostics - results of an interlaboratory test and a standardization approach

Here we describe the results of an interlaboratory test for RT-PCR-based BCR/ABL analysis. The test was organized in two parts. The number of participating laboratories in the first and second part was 27 and 20, respectively. In the first part samples containing various concentrations of plasmids w...

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Detalles Bibliográficos
Autores principales: Burmeister, Thomas (Autor) , Maurer, J. (Autor) , Aivado, M. (Autor) , Elmaagacli, A. H. (Autor) , Grünebach, F. (Autor) , Held, K. R. (Autor) , Heß, G. (Autor) , Hochhaus, Andreas (Autor) , Höppner, W. (Autor) , Lentes, K. U. (Autor) , Lübbert, M. (Autor) , Schäfer, K. L. (Autor) , Schafhausen, P. (Autor) , Schmidt, C. A. (Autor) , Schüler, F. (Autor) , Seeger, K. (Autor) , Seelig, R. (Autor) , Thiede, C. (Autor) , Viehmann, S. (Autor) , Weber, C. (Autor) , Wilhelm, S. (Autor) , Christmann, A. (Autor) , Clement, J. H. (Autor) , Ebener, U. (Autor) , Enczmann, J. (Autor) , Leo, R. (Autor) , Schleuning, M. (Autor) , Schoch, R. (Autor) , Thiel, E. (Autor)
Formato: Article (Journal)
Lenguaje:inglés
Publicado: 10 October 2000
In: Leukemia
Year: 2000, Volumen: 14, Número: 10, Pages: 1850-1856
ISSN:1476-5551
DOI:10.1038/sj.leu.2401899
Acceso en línea:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1038/sj.leu.2401899
Verlag, lizenzpflichtig, Volltext: https://www.nature.com/articles/2401899
Enlace del recurso
Notas de Autor:T. Burmeister, J. Maurer, M. Aivado, A.H. Elmaagacli, F. Grünebach, K.R. Held, G. Heß, A. Hochhaus, W. Höppner, K.U. Lentes, M. Lübbert, K.L. Schäfer, P. Schafhausen, C.A. Schmidt, F.Schüler, K. Seeger, R. Seelig, C. Thiede, S. Viehmann, C. Weber, S. Wilhelm, A. Christmann, J.H. Clement, U. Ebener, J. Enczmann, R. Leo, M. Schleuning, R. Schoch, E. Thiel
Descripción
Sumario:Here we describe the results of an interlaboratory test for RT-PCR-based BCR/ABL analysis. The test was organized in two parts. The number of participating laboratories in the first and second part was 27 and 20, respectively. In the first part samples containing various concentrations of plasmids with the ela2, b2a2 or b3a2 BCR/ABL transcripts were analyzed by PCR. In the second part of the test, cell samples containing various concentrations of BCR/ABL-positive cells were analyzed by RT-PCR. Overall PCR sensitivity was sufficient in approximately 90% of the tests, but a significant number of false positive results were obtained. There were significant differences in sensitivity in the cell-based analysis between the various participants. The results are discussed, and proposals are made regarding the choice of primers, controls, conditions for RNA extraction and reverse transcription.
Notas:Gesehen am 13.04.2022
Descripción Física:Online Resource
ISSN:1476-5551
DOI:10.1038/sj.leu.2401899

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