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Laboratory quality assessment of candidate gene panel testing for acute myeloid leukaemia: a joint ALLG / RCPAQAP initiative.
Corboy, Greg; Othman, Jad; Lee, Linda; Wei, Andrew; Ivey, Adam; Blombery, Piers; Agarwal, Rishu; Fong, Chun; Brown, Anna; Scott, Hamish; Grove, Carolyn; Louw, Alison; Enjeti, Anoop; Iland, Harry; Paul, Cheryl; Bohlander, Stefan; Kakadia, Purvi; Horan, Martin; Stevenson, William.
Affiliation
  • Corboy G; LabPlus, Auckland City Hospital, Grafton, New Zealand; Department of Molecular Medicine and Pathology, The University of Auckland, Grafton, New Zealand; Australasian Leukaemia and Lymphoma Group (ALLG), Richmond, Vic, Australia. Electronic address: gregc@adhb.govt.nz.
  • Othman J; Department of Haematology, Royal North Shore Hospital, St Leonards, NSW, Australia.
  • Lee L; Molecular Haematology, NSW Health Pathology, Royal North Shore Hospital, St Leonards, NSW, Australia.
  • Wei A; Australasian Leukaemia and Lymphoma Group (ALLG), Richmond, Vic, Australia; Department of Haematology, Alfred Health, Prahran, Vic, Australia.
  • Ivey A; Department of Pathology, Alfred Health, Prahran, Vic, Australia.
  • Blombery P; Australasian Leukaemia and Lymphoma Group (ALLG), Richmond, Vic, Australia; Peter MacCallum Cancer Centre, Parkville, Vic, Australia; Sir Peter MacCallum Department of Oncology, University of Melbourne, Melbourne, Vic, Australia.
  • Agarwal R; Australasian Leukaemia and Lymphoma Group (ALLG), Richmond, Vic, Australia; Department of Haematology, Austin Health, Heidelberg, Vic, Australia.
  • Fong C; Australasian Leukaemia and Lymphoma Group (ALLG), Richmond, Vic, Australia; Department of Haematology, Austin Health, Heidelberg, Vic, Australia.
  • Brown A; Department of Genetics and Molecular Pathology, SA Pathology, Adelaide, SA, Australia; Centre for Cancer Biology, SA Pathology and University of South Australia, Adelaide, SA, Australia; School of Medicine, University of Adelaide, Adelaide, SA, Australia; ACRF Cancer Genomics Facility, Centre for Ca
  • Scott H; Department of Genetics and Molecular Pathology, SA Pathology, Adelaide, SA, Australia; Centre for Cancer Biology, SA Pathology and University of South Australia, Adelaide, SA, Australia; School of Medicine, University of Adelaide, Adelaide, SA, Australia; ACRF Cancer Genomics Facility, Centre for Ca
  • Grove C; Australasian Leukaemia and Lymphoma Group (ALLG), Richmond, Vic, Australia; PathWest Laboratory Medicine, Perth, WA, Australia; Sir Charles Gairdner Hospital, Perth, WA, Australia.
  • Louw A; Australasian Leukaemia and Lymphoma Group (ALLG), Richmond, Vic, Australia; PathWest Laboratory Medicine, Perth, WA, Australia.
  • Enjeti A; Australasian Leukaemia and Lymphoma Group (ALLG), Richmond, Vic, Australia; Department of Haematology and Molecular Medicine, NSW Health Pathology - Hunter, John Hunter Hospital, Newcastle, NSW, Australia.
  • Iland H; Australasian Leukaemia and Lymphoma Group (ALLG), Richmond, Vic, Australia; Department of Haematology, Royal Prince Alfred Hospital, Camperdown, NSW, Australia.
  • Paul C; Department of Haematology, Royal Prince Alfred Hospital, Camperdown, NSW, Australia.
  • Bohlander S; Australasian Leukaemia and Lymphoma Group (ALLG), Richmond, Vic, Australia; Leukaemia and Blood Cancer Research Unit, Department of Molecular Medicine and Pathology, The University of Auckland, Grafton, New Zealand.
  • Kakadia P; Leukaemia and Blood Cancer Research Unit, Department of Molecular Medicine and Pathology, The University of Auckland, Grafton, New Zealand.
  • Horan M; Royal College of Pathologists of Australasia Quality Assurance Programs (RCPAQAP), St Leonards, NSW, Australia.
  • Stevenson W; Australasian Leukaemia and Lymphoma Group (ALLG), Richmond, Vic, Australia; Department of Haematology, Royal North Shore Hospital, St Leonards, NSW, Australia; Molecular Haematology, NSW Health Pathology, Royal North Shore Hospital, St Leonards, NSW, Australia.
Pathology ; 53(4): 487-492, 2021 Jun.
Article in En | MEDLINE | ID: mdl-33272691
ABSTRACT
Accurate classification of acute myeloid leukaemia (AML) has become increasingly reliant on molecular characterisation of this blood cancer. Throughout Australia and New Zealand massively parallel sequencing (MPS) is being adopted by diagnostic laboratories for the routine evaluation of patients with AML. This technology enables the surveying of many genes simultaneously, with many technical advantages over single gene testing approaches. However, there are many variations in wet and dry lab MPS procedures, which raises the prospect of discordant results between laboratories. This study compared the results obtained from MPS testing of ten diagnostic AML bone marrow aspirate samples sent to eight participating laboratories across Australasia. A reassuringly high concordance of 94% was observed with regard to variant detection and characterisation of pathogenicity. The level of discordance observed, although low, demonstrates the need for ongoing assessment of concordance between diagnostic testing laboratories through quality assurance programs.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Quality Assurance, Health Care / Leukemia, Myeloid, Acute / Laboratories Type of study: Diagnostic_studies / Prognostic_studies Limits: Humans Country/Region as subject: Oceania Language: En Journal: Pathology Year: 2021 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Quality Assurance, Health Care / Leukemia, Myeloid, Acute / Laboratories Type of study: Diagnostic_studies / Prognostic_studies Limits: Humans Country/Region as subject: Oceania Language: En Journal: Pathology Year: 2021 Document type: Article