PMID- 28265829 OWN - NLM STAT- MEDLINE DCOM- 20170503 LR - 20191210 IS - 1573-2568 (Electronic) IS - 0163-2116 (Print) IS - 0163-2116 (Linking) VI - 62 IP - 5 DP - 2017 May TI - A Multicenter Study of a Fluorescence In Situ Hybridization Probe Set for Diagnosing High-Grade Dysplasia and Adenocarcinoma in Barrett's Esophagus. PG - 1216-1222 LID - 10.1007/s10620-017-4517-y [doi] AB - BACKGROUND AND AIMS: Preliminary single-institution data suggest that fluorescence in situ hybridization (FISH) may be useful for detecting high-grade dysplasia (HGD) and esophageal adenocarcinoma (EA) in patients with Barrett's esophagus (BE). This multicenter study aims to validate the measurement of polysomy (gain of at least two loci) by FISH as a way to discriminate degrees of dysplasia in BE specimens. METHODS: Tissue specimens were collected from four different hospitals and read by both the local pathology department ("Site diagnosis") and a single central pathologist ("Review diagnosis") at a separate institution. The specimens then underwent FISH analysis using probes 8q24 (MYC), 9p21 (CDKN2A), 17q12 (ERBB2), and 20q13 (ZNF217) for comparison. A total of 46 non-BE, 42 non-dysplastic specialized intestinal metaplasia (SIM), 23 indefinite-grade dysplasia (IGD), 10 low-grade dysplasia (LGD), 29 HGD, and 42 EA specimens were analyzed. RESULTS: We found that polysomy, as detected by FISH, was the predominant chromosomal abnormality present as dysplasia increased. Polysomy was also the best predictor for the presence of dysplasia or EA when comparing its area under the curve to that of other FISH abnormalities. We observed that if at least 10% of cells had polysomy within a specimen, the FISH probe was able to differentiate between EA/HGD and the remaining pathologies with a sensitivity of 80% and a specificity of 88%. CONCLUSIONS: This study demonstrates that using FISH to determine the percentage of cells with polysomy can accurately and objectively aid in the diagnosis of HGD/EA in BE specimens. FAU - Poneros, John M AU - Poneros JM AD - Department of Gastroenterology, Columbia University Medical Center, 161 Fort Washington Avenue, Suite 862, New York, NY, 10032, USA. jmp14@cumc.columbia.edu. FAU - Faye, Adam S AU - Faye AS AD - Department of Internal Medicine, Columbia University Medical Center, 177 Fort Washington Avenue, Milstein 6C-12, New York, NY, 10032, USA. FAU - Barr Fritcher, Emily G AU - Barr Fritcher EG AD - Department of Laboratory Medicine and Pathology, Mayo Clinic, 200 First SW, Rochester, MN, 55905, USA. FAU - Sen, Ananda AU - Sen A AD - Department of Biostatistics, University of Michigan Medical Center, Ann Arbor, MI, USA. AD - Department of Family Medicine, University of Michigan Medical School, 1018 Fuller St., Ann Arbor, MI, 48104, USA. FAU - Anandasabapathy, Sharmila AU - Anandasabapathy S AD - Department of Gastroenterology, Baylor College of Medicine, Baylor St. Luke's Medical Center Clinic, 7200 Cambridge Street Suite 10C, Houston, TX, 77030, USA. FAU - Bresalier, Robert S AU - Bresalier RS AD - Department of Gastroenterology, University of Texas M.D. Anderson Cancer Center, 1515 Holcombe Blvd, Unit 1466, Houston, TX, 77030, USA. FAU - Marcon, Norman AU - Marcon N AD - Department of Gastroenterology, University of Toronto, Toronto, ON, Canada. AD - St. Michael's Hospital, University of Toronto, 30 Bond Street, 16-062 Cardinal Carter South Wing, Toronto, ON, M5B 1W8, Canada. FAU - Turgeon, D Kim AU - Turgeon DK AD - Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor, MI, USA. AD - Department of Gastroenterology, University of Michigan Health System, Taubman Center Floor 3, Reception D, 1500 E Medical Center Dr, Ann Arbor, MI, 48109, USA. FAU - Appelman, Henry AU - Appelman H AD - Department of Pathology, University of Michigan Medical Center, 1301 Catherine St., Ann Arbor, MI, 48109, USA. FAU - Normolle, Daniel AU - Normolle D AD - Department of Biostatistics, University of Pittsburgh Cancer Institute, 201 North Craig Street, Sterling Plaza Suite 325, Pittsburgh, PA, 15213, USA. FAU - Morrison, Larry E AU - Morrison LE AD - Abbott Molecular, Inc., Des Plaines, IL, USA. AD - Ventana Medical Systems Inc., 1910 E. Innovation Park Dr., Tucson, AZ, 85755, USA. FAU - Brenner, Dean E AU - Brenner DE AD - Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor, MI, USA. AD - Department of Pharmacology, University of Michigan Medical Center, 1500 E Medical Center Dr #2150, Ann Arbor, MI, 48109, USA. FAU - Halling, Kevin C AU - Halling KC AD - Department of Laboratory Medicine and Pathology, Mayo Clinic, 200 First SW, Rochester, MN, 55905, USA. LA - eng GR - P30 CA047904/CA/NCI NIH HHS/United States GR - U01 CA086400/CA/NCI NIH HHS/United States PT - Journal Article PT - Multicenter Study PT - Validation Study DEP - 20170306 PL - United States TA - Dig Dis Sci JT - Digestive diseases and sciences JID - 7902782 SB - IM MH - Adenocarcinoma/*diagnosis/pathology MH - Barrett Esophagus/*complications/*pathology MH - Esophageal Neoplasms/*diagnosis/pathology MH - Humans MH - In Situ Hybridization, Fluorescence MH - ROC Curve MH - Sensitivity and Specificity PMC - PMC6052443 MID - NIHMS981417 OTO - NOTNLM OT - Barrett's esophagus OT - Dysplasia OT - Endoscopy OT - FISH OT - Histopathology OT - Polysomy EDAT- 2017/03/08 06:00 MHDA- 2017/05/04 06:00 PMCR- 2018/07/19 CRDT- 2017/03/08 06:00 PHST- 2016/12/10 00:00 [received] PHST- 2017/02/26 00:00 [accepted] PHST- 2017/03/08 06:00 [pubmed] PHST- 2017/05/04 06:00 [medline] PHST- 2017/03/08 06:00 [entrez] PHST- 2018/07/19 00:00 [pmc-release] AID - 10.1007/s10620-017-4517-y [pii] AID - 10.1007/s10620-017-4517-y [doi] PST - ppublish SO - Dig Dis Sci. 2017 May;62(5):1216-1222. doi: 10.1007/s10620-017-4517-y. Epub 2017 Mar 6.