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Chromoendoscopy with targeted biopsies is superior to white-light endoscopy for the long-term follow-up detection of dysplasia in ulcerative colitis patients: a multicenter randomized–controlled trial

BACKGROUND: Data from single-center experience or small sample-sized studies have shown that chromoendoscopy (CE) might be superior to white-light endoscopy (WLE) for dysplasia surveillance in ulcerative colitis (UC) patients. We performed a prospective randomized trial with a long-term follow-up to...

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Autores principales: Wan, Jian, Zhang, Qin, Liang, Shu-Hui, Zhong, Jie, Li, Jing-Nan, Ran, Zhi-Hua, Zhi, Fa-Chao, Wang, Xiao-Di, Zhang, Xiao-Lan, Wen, Zhong-Hui, Sheng, Jian-Qiu, Shi, Hua-Xiu, Mei, Qiao, Wu, Kai-Chun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7962735/
https://www.ncbi.nlm.nih.gov/pubmed/33747522
http://dx.doi.org/10.1093/gastro/goaa028
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author Wan, Jian
Zhang, Qin
Liang, Shu-Hui
Zhong, Jie
Li, Jing-Nan
Ran, Zhi-Hua
Zhi, Fa-Chao
Wang, Xiao-Di
Zhang, Xiao-Lan
Wen, Zhong-Hui
Sheng, Jian-Qiu
Shi, Hua-Xiu
Mei, Qiao
Wu, Kai-Chun
author_facet Wan, Jian
Zhang, Qin
Liang, Shu-Hui
Zhong, Jie
Li, Jing-Nan
Ran, Zhi-Hua
Zhi, Fa-Chao
Wang, Xiao-Di
Zhang, Xiao-Lan
Wen, Zhong-Hui
Sheng, Jian-Qiu
Shi, Hua-Xiu
Mei, Qiao
Wu, Kai-Chun
author_sort Wan, Jian
collection PubMed
description BACKGROUND: Data from single-center experience or small sample-sized studies have shown that chromoendoscopy (CE) might be superior to white-light endoscopy (WLE) for dysplasia surveillance in ulcerative colitis (UC) patients. We performed a prospective randomized trial with a long-term follow-up to compare the detection rate of dysplasia among WLE with targeted biopsies (WLT), WLE with random biopsies (WLR), and dye-based CE with targeted biopsies (CET) in UC patients. METHODS: Patients with long-standing UC were enrolled from 11 medical centers from March 2012 to December 2013 and randomized into three arms (WLT, WLR, and CET). Only high-definition endoscopy was used in all three groups. The patients were followed up by annual endoscopy with biopsies through December 2017. RESULTS: With a median follow-up time of 55 months, a total of 122 patients with 447 colonoscopies were finally analysed in the per-protocol set: WLT (n = 43), WLR (n = 40), and CET (n = 39). A total of 34 dysplastic lesions were found in 29 colonoscopies of 21 patients. WLR and CET could identify more colonoscopies that diagnosed dysplasia than WLT (8.1% and 9.7% vs 1.9%; P = 0.014 and 0.004, respectively). WLR obtained more biopsied samples than WLT and CET (16.4 ± 5.1 vs 4.3 ± 1.4 and 4.3 ± 1.4; both P < 0.001). During the second half of the follow-up (37 − 69 months), CET could identify more colonoscopies that diagnosed dysplasia than WLT (13.3% vs 1.6%, P = 0.015) and showed a trend for increasing the detection rate compared with WLR (13.3% vs 4.9%, P = 0.107). CONCLUSIONS: For a better outcome of cancer/dysplasia surveillance in patients with long-standing UC, CET appeared to be more effective than WLT and less tedious than WLR. CET was found to be particularly useful when a long-term (>3 years) follow-up was conducted for dysplasia surveillance. The trial was registered on www.chictr.org.cn (ChiCTR1900023689).
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spelling pubmed-79627352021-03-19 Chromoendoscopy with targeted biopsies is superior to white-light endoscopy for the long-term follow-up detection of dysplasia in ulcerative colitis patients: a multicenter randomized–controlled trial Wan, Jian Zhang, Qin Liang, Shu-Hui Zhong, Jie Li, Jing-Nan Ran, Zhi-Hua Zhi, Fa-Chao Wang, Xiao-Di Zhang, Xiao-Lan Wen, Zhong-Hui Sheng, Jian-Qiu Shi, Hua-Xiu Mei, Qiao Wu, Kai-Chun Gastroenterol Rep (Oxf) Original Articles BACKGROUND: Data from single-center experience or small sample-sized studies have shown that chromoendoscopy (CE) might be superior to white-light endoscopy (WLE) for dysplasia surveillance in ulcerative colitis (UC) patients. We performed a prospective randomized trial with a long-term follow-up to compare the detection rate of dysplasia among WLE with targeted biopsies (WLT), WLE with random biopsies (WLR), and dye-based CE with targeted biopsies (CET) in UC patients. METHODS: Patients with long-standing UC were enrolled from 11 medical centers from March 2012 to December 2013 and randomized into three arms (WLT, WLR, and CET). Only high-definition endoscopy was used in all three groups. The patients were followed up by annual endoscopy with biopsies through December 2017. RESULTS: With a median follow-up time of 55 months, a total of 122 patients with 447 colonoscopies were finally analysed in the per-protocol set: WLT (n = 43), WLR (n = 40), and CET (n = 39). A total of 34 dysplastic lesions were found in 29 colonoscopies of 21 patients. WLR and CET could identify more colonoscopies that diagnosed dysplasia than WLT (8.1% and 9.7% vs 1.9%; P = 0.014 and 0.004, respectively). WLR obtained more biopsied samples than WLT and CET (16.4 ± 5.1 vs 4.3 ± 1.4 and 4.3 ± 1.4; both P < 0.001). During the second half of the follow-up (37 − 69 months), CET could identify more colonoscopies that diagnosed dysplasia than WLT (13.3% vs 1.6%, P = 0.015) and showed a trend for increasing the detection rate compared with WLR (13.3% vs 4.9%, P = 0.107). CONCLUSIONS: For a better outcome of cancer/dysplasia surveillance in patients with long-standing UC, CET appeared to be more effective than WLT and less tedious than WLR. CET was found to be particularly useful when a long-term (>3 years) follow-up was conducted for dysplasia surveillance. The trial was registered on www.chictr.org.cn (ChiCTR1900023689). Oxford University Press 2020-09-20 /pmc/articles/PMC7962735/ /pubmed/33747522 http://dx.doi.org/10.1093/gastro/goaa028 Text en © The Author(s) 2020. Published by Oxford University Press and Sixth Affiliated Hospital of Sun Yat-sen University http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Articles
Wan, Jian
Zhang, Qin
Liang, Shu-Hui
Zhong, Jie
Li, Jing-Nan
Ran, Zhi-Hua
Zhi, Fa-Chao
Wang, Xiao-Di
Zhang, Xiao-Lan
Wen, Zhong-Hui
Sheng, Jian-Qiu
Shi, Hua-Xiu
Mei, Qiao
Wu, Kai-Chun
Chromoendoscopy with targeted biopsies is superior to white-light endoscopy for the long-term follow-up detection of dysplasia in ulcerative colitis patients: a multicenter randomized–controlled trial
title Chromoendoscopy with targeted biopsies is superior to white-light endoscopy for the long-term follow-up detection of dysplasia in ulcerative colitis patients: a multicenter randomized–controlled trial
title_full Chromoendoscopy with targeted biopsies is superior to white-light endoscopy for the long-term follow-up detection of dysplasia in ulcerative colitis patients: a multicenter randomized–controlled trial
title_fullStr Chromoendoscopy with targeted biopsies is superior to white-light endoscopy for the long-term follow-up detection of dysplasia in ulcerative colitis patients: a multicenter randomized–controlled trial
title_full_unstemmed Chromoendoscopy with targeted biopsies is superior to white-light endoscopy for the long-term follow-up detection of dysplasia in ulcerative colitis patients: a multicenter randomized–controlled trial
title_short Chromoendoscopy with targeted biopsies is superior to white-light endoscopy for the long-term follow-up detection of dysplasia in ulcerative colitis patients: a multicenter randomized–controlled trial
title_sort chromoendoscopy with targeted biopsies is superior to white-light endoscopy for the long-term follow-up detection of dysplasia in ulcerative colitis patients: a multicenter randomized–controlled trial
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7962735/
https://www.ncbi.nlm.nih.gov/pubmed/33747522
http://dx.doi.org/10.1093/gastro/goaa028
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