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http://hdl.handle.net/10553/128785
Título: | Comparative study of <i>BCR-ABL1</i> quantification: Xpert assay, a feasible solution to standardization concerns | Autores/as: | López-Jorge, CE Gómez-Casares, MT Jiménez-Velasco, A García-Bello, MA Barrios, M Lopez, J De La Iglesia Íñigo, Silvia Narcisa Ramírez, T Sánchez, G Heiniger, AI Molero Labarta, María Teresa |
Clasificación UNESCO: | 32 Ciencias médicas 320708 Hematología |
Palabras clave: | BCR-ABL QRT-PCR CML MDR |
Fecha de publicación: | 2012 | Publicación seriada: | Annals of Hematology | Resumen: | The level of BCR-ABL1 reached after treatment with tyrosine kinase inhibitors is an effective marker of the therapeutic response and a good survival predictor in chronic myeloid leukemia (CML) patients. However, no agreement has yet been achieved about either the standardization of the technique to determine BCR-ABL1 or the interpretation of the results. The aim of this study was to compare the method currently recommended by the European LeukemiaNet,which includes the application of a conversion factor to express the results in international scale, with an automated method (Xpert BCR-ABL™, Cepheid). BCR-ABL1 transcript quantification was performed in 117 samples from CML patients in two different laboratories by both methods, and the results were compared by statistical procedures. A high linear correlation was obtained in the results between the two methods. The concordance at logarithmic intervals reached 62 %. When the major molecular response (MMR) was analyzed, 85 % agreement was achieved. The automated method provides reproducible results and does not show significant differences compared with the traditional method. As a clinical tool, Xpert correctly classified the patients inMMR and can be considered a useful alternative for the molecular follow-up of CML patients. | URI: | http://hdl.handle.net/10553/128785 | ISSN: | 0939-5555 | DOI: | 10.1007/s00277-012-1468-4 | Fuente: | Annals of Hematology [0939-5555], v. 91, pág. 1245-1250 (abril 2012) |
Colección: | Artículos |
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