Jean-Claude Cutz1, Kenneth J Craddock, Emina Torlakovic, Guilherme Brandao, Ronald F Carter, Gilbert Bigras, Jean Deschenes, Iyare Izevbaye, Zhaolin Xu, Wenda Greer, Yasushi Yatabe, Diana Ionescu, Aly Karsan, Sungmi Jung, Richard S Fraser, Miriam Blumenkrantz, Josee Lavoie, Flechere Fortin, Anna Bojarski, Gilbert B Côté, Janette A van den Berghe, Fariborz Rashid-Kolvear, Martin Trotter, Harmanjatinder S Sekhon, Roula Albadine, Danh Tran-Thanh, Isabelle Gorska, Joan H M Knoll, Jie Xu, Ben Blencowe, A John Iafrate, David M Hwang, Melania Pintilie, Rania Gaspo, Christian Couture, Ming-Sound Tsao. 1. *Department of Pathology and Molecular Medicine, McMaster University Health Sciences Centre and McMaster University, Hamilton, Ontario; †Department of Pathology, University Health Network, Princess Margaret Cancer Centre and University of Toronto, Toronto, Ontario; ‡Department of Pathology, Jewish General Hospital and Lady David Institute, McGill University, Montreal, Québec; §Cross Cancer Institute and Department of Laboratory Medicine & Pathology, University of Alberta, Edmonton, Alberta; ‖Department of Molecular Pathology, University of Alberta Hospital, Edmonton, Alberta; ¶Department of Pathology, Queen Elizabeth II Health Sciences Centre and Dalhousie University, Halifax, Nova Scotia; #Department of Pathology, Aichi Cancer Center Hospital, Nagoya, Japan; **Department of Pathology, British Columbia Cancer Agency and University of British Columbia, Vancouver, British Columbia; ††Department of Pathology, McGill University Health Centre, Montreal, Québec; ‡‡Department of Human Genetics, McGill University, Montreal, Québec; §§Department of Pathology, Health Sciences North, Sudbury, Ontario; ‖‖Department of Pathology and Laboratory Medicine, University of Calgary, Calgary, Alberta; ¶¶Department of Pathology, The Ottawa Hospital and University of Ottawa, Ottawa, Ontario; ##Centre hospitalier de l'Universite de Montreal, Montreal, Québec; ***Department of Pathology, London Health Sciences Centre, London, Ontario; †††Department of Molecular Genetics, University of Toronto, Toronto, Ontario; ‡‡‡Department of Pathology, Harvard Medical School, Massachusetts General Hospital, Boston, MA; §§§Pfizer Oncology Canada, Kirkland, Québec; and ‖‖‖Institut Universitaire de Cardiologie et de Pneumologie de Québec (Hôpital Laval), Université Laval, Québec, Québec.
Abstract
INTRODUCTION: Fluorescence in situ hybridization (FISH) is currently the standard for diagnosing anaplastic lymphoma kinase (ALK)-rearranged (ALK+) lung cancers for ALK inhibitor therapies. ALK immunohistochemistry (IHC) may serve as a screening and alternative diagnostic method. The Canadian ALK (CALK) study was initiated to implement a multicenter optimization and standardization of laboratory developed ALK IHC and FISH tests across 14 hospitals. METHODS:Twenty-eight lung adenocarcinomas with known ALK status were used as blinded study samples. Thirteen laboratories performed IHC using locally developed staining protocols for 5A4, ALK1, or D5F3 antibodies; results were assessed by H-score. Twelve centers conducted FISH using protocols based on Vysis' ALK break-apart FISH kit. Initial IHC results were used to optimize local IHC protocols, followed by a repeat IHC study to assess the results of standardization. Three laboratories conducted a prospective parallel IHC and FISH analysis on 411 consecutive clinical samples using post-validation optimized assays. RESULTS: Among study samples, FISH demonstrated 22 consensus ALK+ and six ALK wild type tumors. Preoptimization IHC scores from 12 centers with 5A4 and the percent abnormal cells by FISH from 12 centers showed intraclass correlation coefficients of 0.83 and 0.68, respectively. IHC optimization improved the intraclass correlation coefficients to 0.94. Factors affecting FISH scoring and outliers were identified. Post-optimization concurrent IHC/FISH testing in 373 informative cases revealed 100% sensitivity and specificity for IHC versus FISH. CONCLUSIONS: Multicenter standardization study may accelerate the implementation of ALK testing protocols across a country/region. Our data support the use of an appropriately validated IHC assay to screen for ALK+ lung cancers.
RCT Entities:
INTRODUCTION: Fluorescence in situ hybridization (FISH) is currently the standard for diagnosing anaplastic lymphoma kinase (ALK)-rearranged (ALK+) lung cancers for ALK inhibitor therapies. ALK immunohistochemistry (IHC) may serve as a screening and alternative diagnostic method. The Canadian ALK (CALK) study was initiated to implement a multicenter optimization and standardization of laboratory developed ALK IHC and FISH tests across 14 hospitals. METHODS: Twenty-eight lung adenocarcinomas with known ALK status were used as blinded study samples. Thirteen laboratories performed IHC using locally developed staining protocols for 5A4, ALK1, or D5F3 antibodies; results were assessed by H-score. Twelve centers conducted FISH using protocols based on Vysis' ALK break-apart FISH kit. Initial IHC results were used to optimize local IHC protocols, followed by a repeat IHC study to assess the results of standardization. Three laboratories conducted a prospective parallel IHC and FISH analysis on 411 consecutive clinical samples using post-validation optimized assays. RESULTS: Among study samples, FISH demonstrated 22 consensus ALK+ and six ALK wild type tumors. Preoptimization IHC scores from 12 centers with 5A4 and the percent abnormal cells by FISH from 12 centers showed intraclass correlation coefficients of 0.83 and 0.68, respectively. IHC optimization improved the intraclass correlation coefficients to 0.94. Factors affecting FISH scoring and outliers were identified. Post-optimization concurrent IHC/FISH testing in 373 informative cases revealed 100% sensitivity and specificity for IHC versus FISH. CONCLUSIONS: Multicenter standardization study may accelerate the implementation of ALK testing protocols across a country/region. Our data support the use of an appropriately validated IHC assay to screen for ALK+ lung cancers.
Authors: C Lim; H S Sekhon; J C Cutz; D M Hwang; S Kamel-Reid; R F Carter; G da Cunha Santos; T Waddell; M Binnie; M Patel; N Paul; T Chung; A Brade; R El-Maraghi; C Sit; M S Tsao; N B Leighl Journal: Curr Oncol Date: 2017-04-27 Impact factor: 3.677
Authors: M von Laffert; P Schirmacher; A Warth; W Weichert; R Büttner; R M Huber; J Wolf; F Griesinger; M Dietel; C Grohé Journal: Pathologe Date: 2016-03 Impact factor: 1.011
Authors: B Melosky; P Cheema; J Agulnik; R Albadine; D G Bebb; N Blais; R Burkes; C Butts; P B Card; A M Y Chan; V Hirsh; D N Ionescu; R Juergens; W Morzycki; Z Poonja; R Sangha; M Tehfe; M S Tsao; M Vincent; Z Xu; G Liu Journal: Curr Oncol Date: 2018-10-31 Impact factor: 3.677