Natural History Analysis of 101 Severe Dysplasia and Esophageal Carcinoma Cases by Endoscopy

Objectives. Our research is to realize the natural history from dysplasia to carcinoma and to provide evidence for exploring proper screening intervals. Methods. After the onset endoscopy screening, 2093 of the patients participated in the endoscopic follow-up voluntarily. Totally, 101 severe dyspla...

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Main Authors: Jin-Wu Wang, Chen-Tao Guan, Li-Li Wang, Ling-Yun Chang, Chang-Qing Hao, Bian-Yun Li, Ning Lu, Wen-Qiang Wei
Format: Article
Language:English
Published: Wiley 2017-01-01
Series:Gastroenterology Research and Practice
Online Access:http://dx.doi.org/10.1155/2017/9612854
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author Jin-Wu Wang
Chen-Tao Guan
Li-Li Wang
Ling-Yun Chang
Chang-Qing Hao
Bian-Yun Li
Ning Lu
Wen-Qiang Wei
author_facet Jin-Wu Wang
Chen-Tao Guan
Li-Li Wang
Ling-Yun Chang
Chang-Qing Hao
Bian-Yun Li
Ning Lu
Wen-Qiang Wei
author_sort Jin-Wu Wang
collection DOAJ
description Objectives. Our research is to realize the natural history from dysplasia to carcinoma and to provide evidence for exploring proper screening intervals. Methods. After the onset endoscopy screening, 2093 of the patients participated in the endoscopic follow-up voluntarily. Totally, 101 severe dysplasia and carcinoma cases, either diagnosed in the first endoscopy without treatment or diagnosed in the second endoscopy, were included in our study. We compared the pathologic results of their two endoscopies and calculate the mean and median progression time. Results. Of the 39 severe dysplasia cases diagnosed by the onset endoscopy, only 8 progressed to carcinoma. For severe dysplasia cases diagnosed by the follow-up endoscopy, mean progression times are 55.0, 49.8, and 38.0 months and median progression times are 43, 56, and 31 months for esophagitis, mild dysplasia, and moderate dysplasia, respectively. For superficial carcinoma cases diagnosed by the second endoscopy, mean progression times are 76.0, 57.4, and 47.0 months and median progression times are 77, 63, and 35 months for mild dysplasia, moderate dysplasia, and severe dysplasia, respectively. Conclusions. Population-based severe dysplasia cases may have much lower carcinoma progression rate than specific-selected ones. The progression time for most enrolled cases seems longer than that of the recent screening protocol recommended.
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publishDate 2017-01-01
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series Gastroenterology Research and Practice
spelling doaj-art-e179c2a2862f4210a7923c4d66437c6d2025-02-03T05:46:35ZengWileyGastroenterology Research and Practice1687-61211687-630X2017-01-01201710.1155/2017/96128549612854Natural History Analysis of 101 Severe Dysplasia and Esophageal Carcinoma Cases by EndoscopyJin-Wu Wang0Chen-Tao Guan1Li-Li Wang2Ling-Yun Chang3Chang-Qing Hao4Bian-Yun Li5Ning Lu6Wen-Qiang Wei7Department of Pathology, Cancer Hospital of Linzhou, Henan, ChinaDepartment of Cancer Epidemiology, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing, ChinaDepartment of Epidemiology, Cancer Hospital of Linzhou, Henan, ChinaDepartment of Pathology, Cancer Hospital of Linzhou, Henan, ChinaDepartment of Endoscopy, Cancer Hospital of Linzhou, Henan, ChinaDepartment of Epidemiology, Cancer Hospital of Linzhou, Henan, ChinaDepartment of Pathology, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing, ChinaDepartment of Cancer Epidemiology, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing, ChinaObjectives. Our research is to realize the natural history from dysplasia to carcinoma and to provide evidence for exploring proper screening intervals. Methods. After the onset endoscopy screening, 2093 of the patients participated in the endoscopic follow-up voluntarily. Totally, 101 severe dysplasia and carcinoma cases, either diagnosed in the first endoscopy without treatment or diagnosed in the second endoscopy, were included in our study. We compared the pathologic results of their two endoscopies and calculate the mean and median progression time. Results. Of the 39 severe dysplasia cases diagnosed by the onset endoscopy, only 8 progressed to carcinoma. For severe dysplasia cases diagnosed by the follow-up endoscopy, mean progression times are 55.0, 49.8, and 38.0 months and median progression times are 43, 56, and 31 months for esophagitis, mild dysplasia, and moderate dysplasia, respectively. For superficial carcinoma cases diagnosed by the second endoscopy, mean progression times are 76.0, 57.4, and 47.0 months and median progression times are 77, 63, and 35 months for mild dysplasia, moderate dysplasia, and severe dysplasia, respectively. Conclusions. Population-based severe dysplasia cases may have much lower carcinoma progression rate than specific-selected ones. The progression time for most enrolled cases seems longer than that of the recent screening protocol recommended.http://dx.doi.org/10.1155/2017/9612854
spellingShingle Jin-Wu Wang
Chen-Tao Guan
Li-Li Wang
Ling-Yun Chang
Chang-Qing Hao
Bian-Yun Li
Ning Lu
Wen-Qiang Wei
Natural History Analysis of 101 Severe Dysplasia and Esophageal Carcinoma Cases by Endoscopy
Gastroenterology Research and Practice
title Natural History Analysis of 101 Severe Dysplasia and Esophageal Carcinoma Cases by Endoscopy
title_full Natural History Analysis of 101 Severe Dysplasia and Esophageal Carcinoma Cases by Endoscopy
title_fullStr Natural History Analysis of 101 Severe Dysplasia and Esophageal Carcinoma Cases by Endoscopy
title_full_unstemmed Natural History Analysis of 101 Severe Dysplasia and Esophageal Carcinoma Cases by Endoscopy
title_short Natural History Analysis of 101 Severe Dysplasia and Esophageal Carcinoma Cases by Endoscopy
title_sort natural history analysis of 101 severe dysplasia and esophageal carcinoma cases by endoscopy
url http://dx.doi.org/10.1155/2017/9612854
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