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Analytical Validation of a Highly Sensitive, Multiplexed Chronic Myeloid Leukemia Monitoring System Targeting BCR-ABL1 RNA.
Brown, Justin T; Beldorth, Ion J; Laosinchai-Wolf, Walairat; Fahey, Marie E; Jefferson, Keri L; Ruskin, Adam K; Roth, Jacquelyn J; Cai, Li; Watt, Christopher D; Press, Richard D; Yang, Fei; Hedges, John B; Andruss, Bernard F.
Afiliación
  • Brown JT; Asuragen, Inc., Austin, Texas. Electronic address: jbrown@asuragen.com.
  • Beldorth IJ; Asuragen, Inc., Austin, Texas.
  • Laosinchai-Wolf W; Asuragen, Inc., Austin, Texas.
  • Fahey ME; Asuragen, Inc., Austin, Texas.
  • Jefferson KL; Asuragen, Inc., Austin, Texas.
  • Ruskin AK; Asuragen, Inc., Austin, Texas.
  • Roth JJ; Department of Pathology and Laboratory Medicine, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania.
  • Cai L; Center for Molecular Biology and Pathology, Laboratory Corporation of America Holdings, Research Triangle Park, North Carolina.
  • Watt CD; Department of Pathology and Laboratory Medicine, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania.
  • Press RD; Department of Pathology and Knight Cancer Institute, Oregon Health and Science University, Portland, Oregon.
  • Yang F; Department of Pathology and Knight Cancer Institute, Oregon Health and Science University, Portland, Oregon.
  • Hedges JB; Asuragen, Inc., Austin, Texas.
  • Andruss BF; Asuragen, Inc., Austin, Texas.
J Mol Diagn ; 21(4): 718-733, 2019 07.
Article en En | MEDLINE | ID: mdl-31026597
This study describes the analytical performance of the QuantideX qPCR BCR-ABL IS Kit, the first Food and Drug Administration-cleared assay designed to monitor breakpoint cluster region-Abelson tyrosine-protein kinase 1 (BCR-ABL1) fusion transcripts isolated from peripheral blood specimens from patients with chronic myeloid leukemia. This multiplex real-time quantitative RT-PCR assay amplifies both e13a2 and e14a2 Major BCR-ABL1 transcripts and the reference target ABL1. The test results are provided in international scale (IS) values by incorporating armored RNA-based calibrators that have defined IS values tied directly to the World Health Organization BCR-ABL1 Primary Reference Materials, without the necessity of determining and maintaining conversion factors. For each batch run, the integrated interpretive software evaluates run and specimen quality control metrics (including a sufficient amount of ABL1 control transcripts to ensure a minimal limit of detection) and calculates both molecular response (MR) and %IS values for each specimen. The test has a limit of detection of MR4.7 (0.002%IS) and a linear range from MR0.3 (50%IS) to MR4.7 (0.002%IS) for both Major transcripts. Single-site and multisite precision studies demonstrated a maximum SD of 0.13 MR (30% CV within the assay range between MR0.7 and MR3.7). The performance of this BCR-ABL1 monitoring test meets all of the clinical guideline recommendations for sensitivity and IS reporting for the management of chronic myeloid leukemia patients.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Leucemia Mielógena Crónica BCR-ABL Positiva / Proteínas de Fusión bcr-abl / Reacción en Cadena de la Polimerasa Multiplex / Reacción en Cadena en Tiempo Real de la Polimerasa Tipo de estudio: Diagnostic_studies / Guideline Límite: Humans Idioma: En Revista: J Mol Diagn Asunto de la revista: BIOLOGIA MOLECULAR Año: 2019 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Leucemia Mielógena Crónica BCR-ABL Positiva / Proteínas de Fusión bcr-abl / Reacción en Cadena de la Polimerasa Multiplex / Reacción en Cadena en Tiempo Real de la Polimerasa Tipo de estudio: Diagnostic_studies / Guideline Límite: Humans Idioma: En Revista: J Mol Diagn Asunto de la revista: BIOLOGIA MOLECULAR Año: 2019 Tipo del documento: Article