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[Cancer Research 53, 1317-1321, March 15, 1993]
© 1993 American Association for Cancer Research

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Precancerous Gastric Lesions in a Population at High Risk of Stomach Cancer

Wei-cheng You1, William J. Blot2, Ji-you Li, Yun-sheng Chang, Mao-lin Jin, Robert Kneller, Lian Zhang, Zhong-xiang Han, Xiang-rui Zeng, Wei-dong Liu, Lei Zhao, Pelayo Correa, Joseph F. Fraumeni, Jr.3 and Guang-wei Xu

Beijing Institute for Cancer Research, Beijing, China 100034 [W-c. Y., J-y. L., Le. Z, G-w. X., M-l. J., Li. Z.]; National Cancer Institute, Bethesda, Maryland 20892 [W. J. B., R. K., J. F. F.]; Weifang Medical Institute, Weifang, Shandong, China 261041 [Y-s. C.]; Linqu Public Health Bureau, Linqu, Shandong, China 262600 [Z-x. H., X-r. Z., W-d. L.] and Louisiana State University Medical Center, New Orleans, Louisiana 70112 [P. C.]

A population-based screening for detection of early cancers evaluated the prevalence of precancerous gastric lesions in an area in Shandong province, China, with one of the world's highest rates of stomach cancer. A total of 3433 residents aged 35 to 64 yr received gastroscopical examinations with biopsies taken from standard locations. Chronic atrophic gastritis was nearly universal; less than 2% of the population had biopsies showing entirely normal mucosa or only superficial gastritis. Intestinal metaplasia was the most advanced lesion for 33% and gastric dysplasia for 20%, although the prevalence of each increased significantly with age. Intestinal metaplasia and gastric dysplasia were detected throughout the stomach, but the lesions were more pronounced along the lesser curvature, especially in the angulus and antrum. There was no sex difference in rates of chronic atrophic gastritis, but males had a slightly higher prevalence of intestinal metaplasia, a 1.6-fold increase in dysplasia, and a 3-fold excess of gastric cancer. The data quantify the extensiveness of gastric lesions likely to be involved in the natural history of stomach cancer in this high-risk population.

1 To whom requests from China for reprints should be addressed.

2 To whom requests from other countries for reprints should be addressed.

3 Recipient of support in part from National Cancer Institute Contracts N01-CP-15620, 05631, and 95660.

Received 2/ 3/92. Accepted 1/ 8/93.




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HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1993 by the American Association for Cancer Research.