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Optimal number of endoscopic biopsies for diagnosis of early gastric cancer
Background and study aims No recommendations are available for optimal number of endoscopic biopsies for early gastric cancer (GC), and whether detection of early GC is improved by increasing the number of biopsy is unclear. We therefore evaluated the relationship between number of biopsies and dia...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
© Georg Thieme Verlag KG
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6887641/ https://www.ncbi.nlm.nih.gov/pubmed/31803818 http://dx.doi.org/10.1055/a-1007-1730 |
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author | Nishitani, Masaki Yoshida, Naohiro Tsuji, Shigetsugu Masunaga, Teppei Hirai, Hirokazu Miyajima, Saori Dejima, Akihiro Nakashima, Takashi Wakita, Shigenori Takemura, Kenichi Minato, Hiroshi Kaneko, Shuichi Doyama, Hisashi |
author_facet | Nishitani, Masaki Yoshida, Naohiro Tsuji, Shigetsugu Masunaga, Teppei Hirai, Hirokazu Miyajima, Saori Dejima, Akihiro Nakashima, Takashi Wakita, Shigenori Takemura, Kenichi Minato, Hiroshi Kaneko, Shuichi Doyama, Hisashi |
author_sort | Nishitani, Masaki |
collection | PubMed |
description | Background and study aims No recommendations are available for optimal number of endoscopic biopsies for early gastric cancer (GC), and whether detection of early GC is improved by increasing the number of biopsy is unclear. We therefore evaluated the relationship between number of biopsies and diagnostic accuracy. Materials and methods We retrospectively evaluated 858 early GCs (623 from endoscopic submucosal dissection and 235 surgical specimens), which we classified as obtained after one, two, or three or more biopsies. We assessed diagnostic accuracy by number of biopsies, and in subgroups by tumor diameter, gross type, and surface color. Results Almost half the lesions were obtained after one biopsy each, 30 % after two biopsies, and 20 % after three or more biopsies. Although diagnostic accuracy increased with biopsy number, it was significantly greater for the two-biopsy group than the one-biopsy group, (92.5 % vs. 83.9 %, P = 0.0009), but did not significantly differ between the two- and three or more-biopsy groups. This finding was seen when tumors were evaluated by size, but not by elevated type and surface color, for which more biopsies did not improve diagnostic accuracy. Multivariate analysis demonstrated that two or more biopsies was the independent significant factors for diagnostic accuracy. Conclusions Two biopsies are the optimal number required to diagnose early GC. |
format | Online Article Text |
id | pubmed-6887641 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | © Georg Thieme Verlag KG |
record_format | MEDLINE/PubMed |
spelling | pubmed-68876412019-12-04 Optimal number of endoscopic biopsies for diagnosis of early gastric cancer Nishitani, Masaki Yoshida, Naohiro Tsuji, Shigetsugu Masunaga, Teppei Hirai, Hirokazu Miyajima, Saori Dejima, Akihiro Nakashima, Takashi Wakita, Shigenori Takemura, Kenichi Minato, Hiroshi Kaneko, Shuichi Doyama, Hisashi Endosc Int Open Background and study aims No recommendations are available for optimal number of endoscopic biopsies for early gastric cancer (GC), and whether detection of early GC is improved by increasing the number of biopsy is unclear. We therefore evaluated the relationship between number of biopsies and diagnostic accuracy. Materials and methods We retrospectively evaluated 858 early GCs (623 from endoscopic submucosal dissection and 235 surgical specimens), which we classified as obtained after one, two, or three or more biopsies. We assessed diagnostic accuracy by number of biopsies, and in subgroups by tumor diameter, gross type, and surface color. Results Almost half the lesions were obtained after one biopsy each, 30 % after two biopsies, and 20 % after three or more biopsies. Although diagnostic accuracy increased with biopsy number, it was significantly greater for the two-biopsy group than the one-biopsy group, (92.5 % vs. 83.9 %, P = 0.0009), but did not significantly differ between the two- and three or more-biopsy groups. This finding was seen when tumors were evaluated by size, but not by elevated type and surface color, for which more biopsies did not improve diagnostic accuracy. Multivariate analysis demonstrated that two or more biopsies was the independent significant factors for diagnostic accuracy. Conclusions Two biopsies are the optimal number required to diagnose early GC. © Georg Thieme Verlag KG 2019-12 2019-12-02 /pmc/articles/PMC6887641/ /pubmed/31803818 http://dx.doi.org/10.1055/a-1007-1730 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License, which permits unrestricted reproduction and distribution, for non-commercial purposes only; and use and reproduction, but not distribution, of adapted material for non-commercial purposes only, provided the original work is properly cited. |
spellingShingle | Nishitani, Masaki Yoshida, Naohiro Tsuji, Shigetsugu Masunaga, Teppei Hirai, Hirokazu Miyajima, Saori Dejima, Akihiro Nakashima, Takashi Wakita, Shigenori Takemura, Kenichi Minato, Hiroshi Kaneko, Shuichi Doyama, Hisashi Optimal number of endoscopic biopsies for diagnosis of early gastric cancer |
title | Optimal number of endoscopic biopsies for diagnosis of early gastric cancer |
title_full | Optimal number of endoscopic biopsies for diagnosis of early gastric cancer |
title_fullStr | Optimal number of endoscopic biopsies for diagnosis of early gastric cancer |
title_full_unstemmed | Optimal number of endoscopic biopsies for diagnosis of early gastric cancer |
title_short | Optimal number of endoscopic biopsies for diagnosis of early gastric cancer |
title_sort | optimal number of endoscopic biopsies for diagnosis of early gastric cancer |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6887641/ https://www.ncbi.nlm.nih.gov/pubmed/31803818 http://dx.doi.org/10.1055/a-1007-1730 |
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