Prediction of Adenocarcinoma in Esophagectomy Specimens Based Upon Analysis of Preresection Biopsies of Barrett Esophagus With At Least High-Grade Dysplasia: A Comparison of 2 Systems

被引:14
作者
Patil, Deepa T. [1 ]
Goldblum, John R. [1 ]
Rybicki, Lisa [6 ]
Plesec, Thomas P. [1 ]
Mendelin, Joel E. [2 ]
Bennett, Ana E. [1 ]
Castilla, Elias A. [3 ]
Henricks, Walter H. [1 ]
Schoenfield, Lynn [1 ]
Skacel, Marek [4 ]
Yerian, Lisa M. [1 ]
Rice, Thomas W. [7 ]
Bronner, Mary P. [5 ]
Downs-Kelly, Erinn [1 ]
机构
[1] Cleveland Clin, Dept Anat Pathol, Cleveland, OH 44195 USA
[2] St Marys Hosp, Dept Pathol, Madison, WI USA
[3] Bethesda N Hosp, Dept Pathol, Cincinnati, OH USA
[4] Dahl Chase Pathol Associates, Bangor, ME USA
[5] Univ Utah, Dept Anat Pathol, ARUP, Salt Lake City, UT USA
[6] Cleveland Clin, Dept Quantitat Hlth Sci, Cleveland, OH 44195 USA
[7] Cleveland Clin, Dept Thorac Surg, Cleveland, OH 44195 USA
关键词
Barrett esophagus; high-grade dysplasia; esophagectomy; adenocarcinoma; P53 GENE MUTATION; PROGRESSION; RISK; CANCER; ASSOCIATION; EPITHELIUM; EXPRESSION; DIAGNOSIS; THERAPY; MARKER;
D O I
10.1097/PAS.0b013e3182354e43
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Distinguishing Barrett esophagus with high-grade dysplasia (BE-HGD) from intramucosal and submucosal adenocarcinomas on biopsies is challenging, yet important, in the choice of therapy. The current study evaluates preresection biopsies from patients who underwent esophagectomy for at least BE-HGD, to compare the recently published histologic categories by the University of Michigan (UM) and Cleveland Clinic (CC), correlate prcresection and final resection diagnosis, and identify histologic features in biopsies that might be predictive of adenocarcinoma on esophagectomy. A total of 112 cases with a consensus biopsy diagnosis (agreement by >= 4 of 7 gastrointestinal pathologists) were statistically analyzed to identify histologic features that predicted adenocarcinoma on resection. Applying the UM criteria to the biopsy series showed excellent agreement with the CC system (kappa = 0.86) and significant correlation between preoperative and esophagectomy diagnoses (P < 0.001). The likelihood of finding carcinoma on resection was significantly higher with the category of HGD with marked glandular distortion cannot exclude intramucosal adenocarcinoma [CC; odd ratio (OR), 2.8; P = 0.046] or HGD suspicious for adenocarcinoma (UM; OR, 4.3; P = 0.008), compared to HGD alone. The presence of "never-ending" glands (OR, 3.7; P = 0.008), sheet-like growth (P < 0.001), angulated glands (OR, 8.5; P < 0.001), >= 3 dilated glands with intraluminal debris (OR, 2.6; P = 0.05), and > 1 focus of single-cell infiltration into the lamina propria (OR, 8.9; P < 0.001) increased the odds of finding carcinoma on resection. The latter 2 variables remained independent predictors of adenocarcinoma in multivariable analysis. In conclusion, the CC and UM systems show excellent agreement and define histologic categories that can improve prediction of adenocarcinoma on resection.
引用
收藏
页码:134 / 141
页数:8
相关论文
共 24 条
[1]   Paget cells in the esophagus: Assessment of their histopathologic features and near-universal association with underlying Esophageal adenocarcinoma [J].
Abraham, Susan C. ;
Wang, Huamin ;
Wang, Kenneth K. ;
Wu, Tsung-Teh .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2008, 32 (07) :1068-1074
[2]   p53 gene mutation and protein accumulation during neoplastic progression in Barrett's esophagus [J].
Bian, YS ;
Osterheld, MC ;
Bosman, FT ;
Benhattar, J ;
Fontolliet, C .
MODERN PATHOLOGY, 2001, 14 (05) :397-403
[3]  
BLOUNT PL, 1994, CANCER RES, V54, P2292
[4]   CLINICAL IMPLICATIONS OF P53 GENE MUTATION IN THE PROGRESSION OF BARRETTS EPITHELIUM TO INVASIVE ESOPHAGEAL CANCER [J].
CASSON, AG ;
MANOLOPOULOS, B ;
TROSTER, M ;
KERKVLIET, N ;
OMALLEY, F ;
INCULET, R ;
FINLEY, R ;
ROTH, JA .
AMERICAN JOURNAL OF SURGERY, 1994, 167 (01) :52-57
[5]   AMACR immunostaining is useful in detecting dysplastic epithelium in Barrett's esophagus, ulcerative colitis, and Crohn's disease [J].
Dorer, Russell ;
Odze, Robert D. .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2006, 30 (07) :871-877
[6]   Poor Interobserver Agreement in the Distinction of High-Grade Dysplasia and Adenocarcinoma in Pretreatment Barrett's Esophagus Biopsies [J].
Downs-Kelly, Erinn ;
Mendelin, Joel E. ;
Bennett, Ana E. ;
Castilla, Elias ;
Henricks, Walter H. ;
Schoenfield, Lynn ;
Skacel, Marek ;
Yerian, Lisa ;
Rice, Thomas W. ;
Rybicki, Lisa A. ;
Bronner, Mary P. ;
Goldblum, John R. .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2008, 103 (09) :2333-2340
[7]   DNA abnormalities as marker of risk for progression of Barrett's esophagus to adenocarcinoma: Image cytometric DNA analysis in formalin-fixed tissues [J].
Fang, M ;
Lew, E ;
Klein, M ;
Sebo, T ;
Su, YY ;
Goyal, R .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2004, 99 (10) :1887-1894
[8]   Clonal expansion and loss of heterozygosity at chromosomes 9p and 17p in premalignant esophageal (Barrett's) tissue [J].
Galipeau, PC ;
Prevo, LJ ;
Sanchez, CA ;
Longton, GM ;
Reid, BJ .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1999, 91 (24) :2087-2095
[9]   Quality control of endoscopic ultrasound in preoperative staging of esophageal cancer [J].
Kutup, A. ;
Link, B.-C. ;
Schurr, P. G. ;
Strate, T. ;
Kaifi, J. T. ;
Bubenheim, M. ;
Seewald, S. ;
Yekebas, E. F. ;
Soehendra, N. ;
Izbicki, J. R. .
ENDOSCOPY, 2007, 39 (08) :715-719
[10]   Expression of α-methylacyl-coenzyme A racemase in dysplastic Barrett's epithelium [J].
Lisovsky, Mikhail ;
Falkowski, Olga ;
Bhuiya, Tawfiqul .
HUMAN PATHOLOGY, 2006, 37 (12) :1601-1606