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Cancer Epidemiology Biomarkers & Prevention Vol. 10, 75-78, January 2001
© 2001 American Association for Cancer Research


Short Communication

Histological Classification of Gastric Adenocarcinoma for Epidemiological Research: Concordance between Pathologists1

Atsuko Shibata2, Teri A. Longacre, Balaram Puligandla, Julie Parsonnet and Laurel A. Habel

Departments of Health Research and Policy [A. S., J. P.], Pathology [T. A. L.], and Medicine [J. P.], Stanford University School of Medicine, Stanford, California 94305, and Department of Pathology [B. P.] and Division of Research [L. A. H.], Kaiser Foundation Research Institute, Oakland, California 94611

Epidemiology of gastric adenocarcinoma suggests that intestinal-type and diffuse-type cancers develop through distinct causal pathways. To examine the differences in risk factors and molecular changes between the histological types, reliable data on histological typing are essential. We evaluated the concordance between two pathologists in assessment of 95 gastric adenocarcinomas for Laurén classification and tumor grade. Two pathologists, each blinded to the other’s assessment, reviewed H&E-stained slides of gastric tumor. The responses of the two pathologists for histological type were considered as concordant if they fell on one of the three categories (intestinal type, diffuse type, or other). Tumor grade was classified into three categories (well, moderately, or poorly differentiated). The pathologists agreed on the classification of histological type for 71 of 92 (77%) tumors. {kappa} coefficient was 0.59 (95% confidence interval, 0.44–0.73). Concordance for tumor grade was 87%, with a {kappa} coefficient of 0.72 (95% confidence interval, 0.57–0.87). Both observed concordance and {kappa} coefficient for histological type and tumor grade were similar across three calendar periods of study. Interobserver agreement was virtually identical between tumors with biopsy specimens only and those with surgical specimens. Although the level of disagreement for histological type observed in this study is comparable with that in other studies, the resulting misclassification would lead to the reduction in observed differences in prevalence and odds ratio estimates between two histological types.




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A. Shibata, J. Parsonnet, T. A. Longacre, M. I. Garcia, B. Puligandla, R.E. Davis, J. H. Vogelman, N. Orentreich, and L. A. Habel
CagA status of Helicobacter pylori infection and p53 gene mutations in gastric adenocarcinoma
Carcinogenesis, March 1, 2002; 23(3): 419 - 424.
[Abstract] [Full Text] [PDF]




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Copyright © 2001 by the American Association for Cancer Research.