Literature DB >> 10640140

A multicenter investigation with D-FISH BCR/ABL1 probes.

G Dewald1, R Stallard, A Alsaadi, S Arnold, R Blough, T M Ceperich, B Rafael Elejalde, J Fink, J V Higgins, R R Higgins, G A Hoeltge, W T Hsu, E B Johnson, D Kronberger, D J McCorquodale, L F Meisner, M A Micale, L Oseth, J S Payne, S Schwartz, S Sheldon, A Sophian, P Storto, P Van Tuinen, G D Wenger, A Wiktor, L A Willis, J F Yung, J Zenger-Hain.   

Abstract

Twenty-eight laboratories evaluated a new fluorescence in situ hybridization (FISH) strategy for chronic myeloid leukemia. In a three-part study, bcr/abl1 D-FISH probes were used to study bone marrow specimens. First, laboratories familiarized themselves with the strategy by applying it to known normal and abnormal specimens. Then, collectively the laboratories studied 20 normal and 20 abnormal specimens blindly and measured workload. Finally, each laboratory and two experts studied six serial dilutions with 98-0% abnormal nuclei. Using the reported normal cutoff of < 1% abnormal nuclei, participants reported no false-negative cases and 15 false-positive cases (1-6.6% abnormal nuclei). Results provided by participants for serial dilutions approximated the expected percentages of abnormal nuclei, but those from the experts exhibited greater precision. The clinical sensitivity, precision, nomenclature, workload, recommendations for training, and quality assurance in methods using D-FISH in clinical practice are discussed.

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Year:  2000        PMID: 10640140     DOI: 10.1016/s0165-4608(99)00120-x

Source DB:  PubMed          Journal:  Cancer Genet Cytogenet        ISSN: 0165-4608


  6 in total

1.  Guidance for fluorescence in situ hybridization testing in hematologic disorders.

Authors:  Daynna J Wolff; Adam Bagg; Linda D Cooley; Gordon W Dewald; Betsy A Hirsch; Peter B Jacky; Kathleen W Rao; P Nagesh Rao
Journal:  J Mol Diagn       Date:  2007-04       Impact factor: 5.568

2.  Statistical treatment of fluorescence in situ hybridization validation data to generate normal reference ranges using Excel functions.

Authors:  Allison L Ciolino; Mary E Tang; Ron Bryant
Journal:  J Mol Diagn       Date:  2009-06-12       Impact factor: 5.568

3.  Canadian College of Medical Geneticists guidelines for the indications, analysis, and reporting of cancer specimens.

Authors:  A J Dawson; J McGowan-Jordan; J Chernos; J Xu; J Lavoie; J C Wang; M Steinraths; S Shetty
Journal:  Curr Oncol       Date:  2011-10       Impact factor: 3.677

Review 4.  FISH analysis for the detection of lymphoma-associated chromosomal abnormalities in routine paraffin-embedded tissue.

Authors:  Roland A Ventura; Jose I Martin-Subero; Margaret Jones; Joanna McParland; Stefan Gesk; David Y Mason; Reiner Siebert
Journal:  J Mol Diagn       Date:  2006-05       Impact factor: 5.568

5.  Standardization of fluorescence in situ hybridization studies on chronic lymphocytic leukemia (CLL) blood and marrow cells by the CLL Research Consortium.

Authors:  Stephanie A Smoley; Daniel L Van Dyke; Neil E Kay; Nyla A Heerema; Marie L Dell' Aquila; Paola Dal Cin; Prasad Koduru; Ayala Aviram; Laura Rassenti; John C Byrd; Kanti R Rai; Jennifer R Brown; Andrew W Greaves; Jeanette Eckel-Passow; Donna Neuberg; Thomas J Kipps; Gordon W Dewald
Journal:  Cancer Genet Cytogenet       Date:  2010-12

6.  Derivative chromosome 9 deletions in chronic myeloid leukaemia: interpretation of atypical D-FISH pattern.

Authors:  T S K Wan; S K Ma; W Y Au; L C Chan
Journal:  J Clin Pathol       Date:  2003-06       Impact factor: 3.411

  6 in total

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