2016
DOI: 10.3748/wjg.v22.i39.8831
|View full text |Cite
|
Sign up to set email alerts
|

Progression from low-grade dysplasia to malignancy in patients with Barrett's esophagus diagnosed by two or more pathologists

Abstract: AIMTo evaluate annual incidence of low grade dysplasia (LGD) progression to high grade dysplasia (HGD) and/or esophageal adenocarcinoma (EAC) when diagnosis was made by two or more expert pathologists.METHODSStudies evaluating the progression of LGD to HGD or EAC were included. The diagnosis of LGD must be made by consensus of two or more expert gastrointestinal pathologists. Articles were searched in Medline, Pubmed, and Embase. Pooled proportions were calculated using fixed and random effects model. Heteroge… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
6
0
1

Year Published

2018
2018
2023
2023

Publication Types

Select...
10

Relationship

0
10

Authors

Journals

citations
Cited by 20 publications
(7 citation statements)
references
References 58 publications
0
6
0
1
Order By: Relevance
“…It is also important to note that the diagnosis of BE-LGD requires expert pathology review [26]. There is significant intra-and interobserver variability among pathologists, especially in the differentiation between NDBE, indefinite for dysplasia and LGD.…”
Section: Discussionmentioning
confidence: 99%
“…It is also important to note that the diagnosis of BE-LGD requires expert pathology review [26]. There is significant intra-and interobserver variability among pathologists, especially in the differentiation between NDBE, indefinite for dysplasia and LGD.…”
Section: Discussionmentioning
confidence: 99%
“…32 but a recent pooled analysis estimated the annual progression rate from HGD to EAC to be 28.6%. 33 Based on above data, confirmed LGD and HGD (which is routinely confirmed by 2 pathologists) are important predictors of BE transforming to cancer.…”
Section: Risk Of Be Progression Based On the Degree Of Dysplasiamentioning
confidence: 60%
“…22,[47][48][49][50][51][52][53][54] A recent pooled analysis found the rate from LGD to HGD/EAC and the rate from HGD to EAC to be 10.5% per annum and 28.6% per annum, respectively. 52 Given the cumulative ongoing risk of EAC, developing strategies to predict progression of disease has clinical relevance and may assist in targeting therapy to ensure effective treatment of disease and minimize the morbidity associated with overtreatment. One example is a validated model developed by Sravanthi et al using male sex, smoking, BE length, and the presence of dysplasia to predict the annual risk of progression after initial diagnosis of NDBE from a low-risk category (0.21% per annum) to a high-risk category (2.1% per annum).…”
Section: Disease Progressionmentioning
confidence: 99%