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Treatment for gastric ‘indefinite for neoplasm/dysplasia’ lesions based on predictive factors

BACKGROUND: Gastric ‘indefinite for neoplasm/dysplasia’ (IFND) is a borderline lesion that is difficult to diagnose as either regenerative or neoplastic. There is a need for guidance in the identification of a subset of patients, who have an IFND lesion with a higher risk of malignant potential, to...

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Autores principales: Kwon, Mi Jung, Kang, Ho Suk, Kim, Hyeon Tae, Choo, Jin Woo, Lee, Bo Hyun, Hong, Sung Eun, Park, Kun Ha, Jung, Dong Min, Lim, Hyun, Soh, Jae Seung, Moon, Sung Hoon, Kim, Jong Hyeok, Park, Hye-Rim, Min, Soo Kee, Seo, Jin won, Choe, Ji-Young
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6350171/
https://www.ncbi.nlm.nih.gov/pubmed/30700943
http://dx.doi.org/10.3748/wjg.v25.i4.469
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author Kwon, Mi Jung
Kang, Ho Suk
Kim, Hyeon Tae
Choo, Jin Woo
Lee, Bo Hyun
Hong, Sung Eun
Park, Kun Ha
Jung, Dong Min
Lim, Hyun
Soh, Jae Seung
Moon, Sung Hoon
Kim, Jong Hyeok
Park, Hye-Rim
Min, Soo Kee
Seo, Jin won
Choe, Ji-Young
author_facet Kwon, Mi Jung
Kang, Ho Suk
Kim, Hyeon Tae
Choo, Jin Woo
Lee, Bo Hyun
Hong, Sung Eun
Park, Kun Ha
Jung, Dong Min
Lim, Hyun
Soh, Jae Seung
Moon, Sung Hoon
Kim, Jong Hyeok
Park, Hye-Rim
Min, Soo Kee
Seo, Jin won
Choe, Ji-Young
author_sort Kwon, Mi Jung
collection PubMed
description BACKGROUND: Gastric ‘indefinite for neoplasm/dysplasia’ (IFND) is a borderline lesion that is difficult to diagnose as either regenerative or neoplastic. There is a need for guidance in the identification of a subset of patients, who have an IFND lesion with a higher risk of malignant potential, to enable risk stratification and optimal management. AIM: To determine the clinical and pathologic factors for the accurate diagnosis of gastric IFND lesions. METHODS: In total, 461 gastric lesions diagnosed via biopsy as IFND lesions were retrospectively evaluated. Endoscopic resection (n = 134), surgery (n = 22), and follow-up endoscopic biopsy (n = 305) were performed to confirm the diagnosis. The time interval from initial biopsy to cancer diagnosis was measured, and diagnostic delays were categorized as > 2 wk, > 2 mo, > 6 mo, and > 1 year. The IFND lesions presenting as regenerating atypia (60%) or atypical epithelia (40%) at initial biopsy were adenocarcinomas in 22.6%, adenomas in 8.9%, and gastritis in 68.5% of the cases. RESULTS: Four clinical factors [age ≥ 60 years (2.445, 95%CI: 1.305-4.580, P = 0.005), endoscopic size ≥ 10 mm (3.519, 95%CI: 1.891-6.548, P < 0.001), single lesion (5.702, 95%CI: 2.212-14.696, P < 0.001), and spontaneous bleeding (4.056, 95%CI: 1.792-9.180, P = 0.001)], and two pathologic factors [atypical epithelium (25.575, 95%CI: 11.537-56.695, P < 0.001], and repeated IFND diagnosis [6.022, 95%CI: 1.822-19.909, P = 0.003)] were independent risk factors for gastric cancer. With two or more clinical factors, the sensitivity and specificity for carcinoma were 91.3% and 54.9%, respectively. Ten undifferentiated carcinomas were initially diagnosed as IFND. In the subgroup analysis, fold change (5.594, 95%CI: 1.458-21.462, P = 0.012) predicted undifferentiated or invasive carcinoma in the submucosal layers or deeper. Diagnostic delays shorter than 1 year were not associated with worse prognoses. Extremely well-differentiated adenocarcinomas accounted for half of the repeated IFND cases and resulted in low diagnostic accuracy even on retrospective blinded review. CONCLUSION: More than two clinical and pathologic factors each had significant cut-off values for gastric carcinoma diagnosis; in such cases, endoscopic resection should be considered.
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spelling pubmed-63501712019-01-30 Treatment for gastric ‘indefinite for neoplasm/dysplasia’ lesions based on predictive factors Kwon, Mi Jung Kang, Ho Suk Kim, Hyeon Tae Choo, Jin Woo Lee, Bo Hyun Hong, Sung Eun Park, Kun Ha Jung, Dong Min Lim, Hyun Soh, Jae Seung Moon, Sung Hoon Kim, Jong Hyeok Park, Hye-Rim Min, Soo Kee Seo, Jin won Choe, Ji-Young World J Gastroenterol Retrospective Study BACKGROUND: Gastric ‘indefinite for neoplasm/dysplasia’ (IFND) is a borderline lesion that is difficult to diagnose as either regenerative or neoplastic. There is a need for guidance in the identification of a subset of patients, who have an IFND lesion with a higher risk of malignant potential, to enable risk stratification and optimal management. AIM: To determine the clinical and pathologic factors for the accurate diagnosis of gastric IFND lesions. METHODS: In total, 461 gastric lesions diagnosed via biopsy as IFND lesions were retrospectively evaluated. Endoscopic resection (n = 134), surgery (n = 22), and follow-up endoscopic biopsy (n = 305) were performed to confirm the diagnosis. The time interval from initial biopsy to cancer diagnosis was measured, and diagnostic delays were categorized as > 2 wk, > 2 mo, > 6 mo, and > 1 year. The IFND lesions presenting as regenerating atypia (60%) or atypical epithelia (40%) at initial biopsy were adenocarcinomas in 22.6%, adenomas in 8.9%, and gastritis in 68.5% of the cases. RESULTS: Four clinical factors [age ≥ 60 years (2.445, 95%CI: 1.305-4.580, P = 0.005), endoscopic size ≥ 10 mm (3.519, 95%CI: 1.891-6.548, P < 0.001), single lesion (5.702, 95%CI: 2.212-14.696, P < 0.001), and spontaneous bleeding (4.056, 95%CI: 1.792-9.180, P = 0.001)], and two pathologic factors [atypical epithelium (25.575, 95%CI: 11.537-56.695, P < 0.001], and repeated IFND diagnosis [6.022, 95%CI: 1.822-19.909, P = 0.003)] were independent risk factors for gastric cancer. With two or more clinical factors, the sensitivity and specificity for carcinoma were 91.3% and 54.9%, respectively. Ten undifferentiated carcinomas were initially diagnosed as IFND. In the subgroup analysis, fold change (5.594, 95%CI: 1.458-21.462, P = 0.012) predicted undifferentiated or invasive carcinoma in the submucosal layers or deeper. Diagnostic delays shorter than 1 year were not associated with worse prognoses. Extremely well-differentiated adenocarcinomas accounted for half of the repeated IFND cases and resulted in low diagnostic accuracy even on retrospective blinded review. CONCLUSION: More than two clinical and pathologic factors each had significant cut-off values for gastric carcinoma diagnosis; in such cases, endoscopic resection should be considered. Baishideng Publishing Group Inc 2019-01-28 2019-01-28 /pmc/articles/PMC6350171/ /pubmed/30700943 http://dx.doi.org/10.3748/wjg.v25.i4.469 Text en ©The Author(s) 2019. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Retrospective Study
Kwon, Mi Jung
Kang, Ho Suk
Kim, Hyeon Tae
Choo, Jin Woo
Lee, Bo Hyun
Hong, Sung Eun
Park, Kun Ha
Jung, Dong Min
Lim, Hyun
Soh, Jae Seung
Moon, Sung Hoon
Kim, Jong Hyeok
Park, Hye-Rim
Min, Soo Kee
Seo, Jin won
Choe, Ji-Young
Treatment for gastric ‘indefinite for neoplasm/dysplasia’ lesions based on predictive factors
title Treatment for gastric ‘indefinite for neoplasm/dysplasia’ lesions based on predictive factors
title_full Treatment for gastric ‘indefinite for neoplasm/dysplasia’ lesions based on predictive factors
title_fullStr Treatment for gastric ‘indefinite for neoplasm/dysplasia’ lesions based on predictive factors
title_full_unstemmed Treatment for gastric ‘indefinite for neoplasm/dysplasia’ lesions based on predictive factors
title_short Treatment for gastric ‘indefinite for neoplasm/dysplasia’ lesions based on predictive factors
title_sort treatment for gastric ‘indefinite for neoplasm/dysplasia’ lesions based on predictive factors
topic Retrospective Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6350171/
https://www.ncbi.nlm.nih.gov/pubmed/30700943
http://dx.doi.org/10.3748/wjg.v25.i4.469
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