PMID- 25441686 OWN - NLM STAT- MEDLINE DCOM- 20150129 LR - 20141202 IS - 2210-7762 (Print) VI - 207 IP - 7-8 DP - 2014 Jul-Aug TI - Population-based characterization of the genetic landscape of chronic lymphocytic leukemia patients referred for cytogenetic testing in British Columbia, Canada: the role of provincial laboratory standardization. PG - 316-25 LID - S2210-7762(14)00173-2 [pii] LID - 10.1016/j.cancergen.2014.08.006 [doi] AB - Detection of recurrent chromosome abnormalities by fluorescence in situ hybridization (FISH) is an essential component of care in chronic lymphocytic leukemia (CLL) patients. In the province of British Columbia (BC), Canada, population 4.6 million, CLL patients receive uniform evaluation and therapy with FISH testing performed in three jurisdictions. The aims of this study were to (i) validate CLL-FISH testing among the BC cytogenetic laboratories to ensure standardization of results and (ii) characterize population-level CLL-FISH abnormalities by pooling provincial data. From 2004 to 2011, 585 consecutive patients underwent pretreatment CLL-FISH testing at laboratory A (50.1%), laboratory B (32.3%), or laboratory C (17.6%). For validation purposes, 26 CLL-FISH abnormalities were tested by each laboratory's protocol, with 91% result concordance. Discordant results involved percent abnormalities at or near cutoff values; therefore, a 10% universal cutoff was established when pooling results. Applying the universal cutoff to the provincial cohort, CLL-FISH abnormalities were detected in 74.9%: 54.9% 13q-, 18.8% +12, 8.5% 11q-, and 7.7% 17p-. In this large population-based cohort of patients referred for CLL-FISH testing, frequencies of abnormalities detected by FISH analysis were highly consistent with those reported in single-institution and clinical trial populations. Provinces or districts that work together to care for CLL patients can effectively pool data with appropriate laboratory validation to ensure standardization of results. CI - Copyright (c) 2014 Elsevier Inc. All rights reserved. FAU - Gerrie, Alina S AU - Gerrie AS AD - Leukemia/BMT Program of BC, Vancouver General Hospital and British Columbia Cancer Agency, University of British Columbia, Vancouver, Canada. FAU - Huang, Steven J T AU - Huang SJ AD - Leukemia/BMT Program of BC, Vancouver General Hospital and British Columbia Cancer Agency, University of British Columbia, Vancouver, Canada; Pathology and Laboratory Medicine, Vancouver General Hospital, University of British Columbia, Vancouver, Canada. FAU - Bruyere, Helene AU - Bruyere H AD - Pathology and Laboratory Medicine, Vancouver General Hospital, University of British Columbia, Vancouver, Canada. FAU - Dalal, Chinmay AU - Dalal C AD - Leukemia/BMT Program of BC, Vancouver General Hospital and British Columbia Cancer Agency, University of British Columbia, Vancouver, Canada. FAU - Hrynchak, Monica AU - Hrynchak M AD - Cytogenetics Laboratory, Royal Columbian Hospital, New Westminster, Canada. FAU - Karsan, Aly AU - Karsan A AD - Cancer Genetics Laboratory, Pathology and Laboratory Medicine, British Columbia Cancer Agency, University of British Columbia, Vancouver, Canada. FAU - Ramadan, Khaled M AU - Ramadan KM AD - Division of Hematology, St. Paul's Hospital, University of British Columbia, Vancouver, Canada. FAU - Smith, Adam C AU - Smith AC AD - Cancer Genetics Laboratory, Pathology and Laboratory Medicine, British Columbia Cancer Agency, University of British Columbia, Vancouver, Canada; Instituto de Pesquisa Pele Pequeno Principe, Curitiba, Brazil. FAU - Tyson, Christine AU - Tyson C AD - Cytogenetics Laboratory, Royal Columbian Hospital, New Westminster, Canada. FAU - Toze, Cynthia L AU - Toze CL AD - Leukemia/BMT Program of BC, Vancouver General Hospital and British Columbia Cancer Agency, University of British Columbia, Vancouver, Canada. FAU - Gillan, Tanya L AU - Gillan TL AD - Pathology and Laboratory Medicine, Vancouver General Hospital, University of British Columbia, Vancouver, Canada. Electronic address: Tanya.Gillan@vch.ca. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20140829 PL - United States TA - Cancer Genet JT - Cancer genetics JID - 101539150 SB - IM MH - Adult MH - Aged MH - Aged, 80 and over MH - British Columbia/epidemiology MH - *Chromosome Aberrations MH - Chromosome Disorders/diagnosis/epidemiology/*genetics MH - Chromosomes, Human/*genetics MH - Cohort Studies MH - Cytogenetic Analysis/*standards MH - Female MH - Follow-Up Studies MH - Humans MH - In Situ Hybridization, Fluorescence/*standards MH - Laboratories, Hospital/*standards MH - Leukemia, Lymphocytic, Chronic, B-Cell/diagnosis/epidemiology/*genetics MH - Male MH - Middle Aged MH - Prognosis OTO - NOTNLM OT - Chronic lymphocytic leukemia OT - cytogenetic OT - fluorescence in situ hybridization OT - population-based OT - validation EDAT- 2014/12/03 06:00 MHDA- 2015/01/30 06:00 CRDT- 2014/12/03 06:00 PHST- 2014/02/15 00:00 [received] PHST- 2014/08/14 00:00 [revised] PHST- 2014/08/21 00:00 [accepted] PHST- 2014/12/03 06:00 [entrez] PHST- 2014/12/03 06:00 [pubmed] PHST- 2015/01/30 06:00 [medline] AID - S2210-7762(14)00173-2 [pii] AID - 10.1016/j.cancergen.2014.08.006 [doi] PST - ppublish SO - Cancer Genet. 2014 Jul-Aug;207(7-8):316-25. doi: 10.1016/j.cancergen.2014.08.006. Epub 2014 Aug 29.