CC BY-NC-ND 4.0 · Endoscopy 2024; 56(05): 376-383
DOI: 10.1055/a-2239-8145
Original article

Linked-color imaging with or without artificial intelligence for adenoma detection: a randomized trial

Kazuya Miyaguchi
1   Department of Gastroenterology, Saitama Medical University, Saitama, Japan
,
Yoshikazu Tsuzuki
1   Department of Gastroenterology, Saitama Medical University, Saitama, Japan
,
Nobutaka Hirooka
2   Department of General Internal Medicine, Saitama Medical University, Saitama, Japan
,
Hisashi Matsumoto
2   Department of General Internal Medicine, Saitama Medical University, Saitama, Japan
,
Hideki Ohgo
3   Department of Gastroenterology, Saitama Medical University, Saitama, Japan
,
Hidetomo Nakamoto
2   Department of General Internal Medicine, Saitama Medical University, Saitama, Japan
,
1   Department of Gastroenterology, Saitama Medical University, Saitama, Japan
› Author Affiliations
Clinical Trial: Registration number (trial ID): UMIN000046361, Trial registry: UMIN Japan (http://www.umin.ac.jp/english/), Type of Study: Randomized control trial

Abstract

Background Adenoma detection rate (ADR) is an important indicator of colonoscopy quality and colorectal cancer incidence. Both linked-color imaging (LCI) with artificial intelligence (LCA) and LCI alone increase adenoma detection during colonoscopy, although it remains unclear whether one modality is superior. This study compared ADR between LCA and LCI alone, including according to endoscopists’ experience (experts and trainees) and polyp size.

Methods Patients undergoing colonoscopy for positive fecal immunochemical tests, follow-up of colon polyps, and abdominal symptoms at a single institution were randomly assigned to the LCA or LCI group. ADR, adenoma per colonoscopy (APC), cecal intubation time, withdrawal time, number of adenomas per location, and adenoma size were compared.

Results The LCA (n=400) and LCI (n=400) groups showed comparable cecal intubation and withdrawal times. The LCA group showed a significantly higher ADR (58.8% vs. 43.5%; P<0.001) and mean (95%CI) APC (1.31 [1.15 to 1.47] vs. 0.94 [0.80 to 1.07]; P<0.001), particularly in the ascending colon (0.30 [0.24 to 0.36] vs. 0.20 [0.15 to 0.25]; P=0.02). Total number of nonpolypoid-type adenomas was also significantly higher in the LCA group (0.15 [0.09 to 0.20] vs. 0.08 [0.05 to 0.10]; P=0.02). Small polyps (≤5, 6–9mm) were detected significantly more frequently in the LCA group (0.75 [0.64 to 0.86] vs. 0.48 [0.40 to 0.57], P<0.001 and 0.34 [0.26 to 0.41] vs. 0.24 [0.18 to 0.29], P=0.04, respectively). In both groups, ADR was not significantly different between experts and trainees.

Conclusions LCA was significantly superior to LCI alone in terms of ADR.

Supplementary Material



Publication History

Received: 18 May 2023

Accepted after revision: 03 January 2024

Accepted Manuscript online:
08 January 2024

Article published online:
01 February 2024

© 2024. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial-License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/).

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  • References

  • 1 Sung H, Ferlay J, Siegel RL. et al. Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin 2021; 71: 209-249
  • 2 Rex DK, Schoenfeld PS, Cohen J. et al. Quality indicators for colonoscopy. Gastrointest Endosc 2015; 81: 31-53
  • 3 Corley DA, Jensen CD, Marks AR. et al. Adenoma detection rate and risk of colorectal cancer and death. N Engl J Med 2014; 370: 1298-1306
  • 4 Kaminski MF, Regula J, Kraszewska E. et al. Quality indicators for colonoscopy and the risk of interval cancer. N Engl J Med 2010; 362: 1795-1803
  • 5 Samadder NJ, Curtin K, Tuohy TM. et al. Characteristics of missed or interval colorectal cancer and patient survival: a population-based study. Gastroenterology 2014; 146: 950-960
  • 6 Sakamoto T, Cho H, Saito Y. Clinical applications of linked color imaging and blue laser/light imaging in the screening, diagnosis, and treatment of superficial colorectal tumors. Clin Endosc 2021; 54: 488-493
  • 7 Paggi S, Mogavero G, Amato A. et al. Linked color imaging reduces the miss rate of neoplastic lesions in the right colon: a randomized tandem colonoscopy study. Endoscopy 2018; 50: 396-402
  • 8 Oliveira Dos Santos CE, Malaman D, Pereira-Lima JC. et al. Impact of linked-color imaging on colorectal adenoma detection. Gastrointest Endosc 2019; 90: 826-834
  • 9 Shinozaki S, Kobayashi Y, Hayashi Y. et al. Colon polyp detection using linked color imaging compared to white light imaging: systematic review and meta-analysis. Dig Endosc 2020; 32: 874-881
  • 10 Wang A, Mo J, Zhong C. et al. Artificial intelligence-assisted detection and classification of colorectal polyps under colonoscopy: a systematic review and meta-analysis. Ann Transl Med 2021; 9: 1662
  • 11 Barua I, Vinsard DG, Jodal HC. et al. Artificial intelligence for polyp detection during colonoscopy: a systematic review and meta-analysis. Endoscopy 2021; 53: 277-284
  • 12 Zhang Y, Zhang X, Wu Q. et al. Artificial intelligence-aided colonoscopy for polyp detection: a systematic review and meta-analysis of randomized clinical trials. J Laparoendosc Adv Surg Tech A 2021; 31: 1143-1149
  • 13 Huang D, Shen J, Hong J. et al. Effect of artificial intelligence-aided colonoscopy for adenoma and polyp detection: a meta-analysis of randomized clinical trials. Int J Colorectal Dis 2022; 37: 495-506
  • 14 Sakamoto T, Nakashima H, Nakamura K. et al. Performance of computer‑aided detection and diagnosis of colorectal polyps compares to that of experienced endoscopists. Dig Dis Sci 2022; 67: 3976-3983
  • 15 Aronchick CA, Lipshutz WH, Wright SH. et al. Validation of an instrument to assess colon cleansing [abstract]. Am J Gastroenterol 1999; 94: 2667
  • 16 Aronchick CA, Lipshutz WH, Wright SH. et al. A novel tableted purgative for colonoscopic preparation: efficacy and safety comparisons with Colyte and Fleet Phospho-Soda. Gastrointest Endosc 2000; 52: 346-352
  • 17 Barclay RL, Vicari JJ, Doughty AS. et al. Colonoscopic withdrawal times and adenoma detection during screening colonoscopy. N Engl J Med 2006; 355: 2533-2541
  • 18 Takeuchi Y, Sawaya M, Oka S. et al. Efficacy of autofluorescence imaging for flat neoplasm detection: a multicenter randomized controlled trial (A-FLAT trial). Gastrointest Endosc 2019; 89: 460-469
  • 19 Wang P, Berzin TM, Glissen Brown JR. et al. Real-time automatic detection system increases colonoscopic polyp and adenoma detection rates: a prospective randomised controlled study. Gut 2019; 68: 1813-1819
  • 20 Luo Y, Zhang Y, Liu M. et al. Artificial intelligence-assisted colonoscopy for detection of colon polyps: a prospective, randomized cohort study. J Gastrointest Surg 2021; 25: 2011-2018
  • 21 Hassan C, Spadaccini M, Iannone A. et al. Performance of artificial intelligence in colonoscopy for adenoma and polyp detection: a systematic review and meta-analysis. Gastrointest Endosc 2021; 93: 77-85.e6
  • 22 Tholey DM, Shelton CE, Francis G. et al. Adenoma detection in excellent versus good bowel preparation for colonoscopy. J Clin Gastroenterol 2015; 49: 313-319
  • 23 Yoshida N, Naito Y, Yasuda R. et al. Linked color imaging improves the visibility of various featured colorectal polyps in an endoscopist’s visibility and color difference value. Int J Colorectal Dis 2017; 32: 1253-1260
  • 24 Miyaguchi K, Takabayashi K, Saito D. et al. Linked color imaging versus white light imaging colonoscopy for colorectal adenoma detection: a randomized controlled trial. J Gastroenterol Hepatol 2021; 36: 2778-2784
  • 25 Rex DK, Clodfelter R, Rahmani F. et al. Narrow-band imaging versus white light for the detection of proximal colon serrated lesions: a randomized, controlled trial. Gastrointest Endosc 2016; 83: 166-171
  • 26 Suzuki T, Hara T, Kitagawa Y. et al. Linked-color imaging improves endoscopic visibility of colorectal nongranular flat lesions. Gastrointest Endosc 2017; 86: 692-697
  • 27 Murakami T, Kamba E, Nomura K. et al. Linked color imaging improves visibility of colorectal serrated lesion by high color contrast to surrounding mucosa. Dig Endosc 2022; 34: 1422-1432
  • 28 Yoshida N, Inada Y, Yasuda R. et al. Additional thirty seconds observation with linked color imaging improves detection of missed polyps in the right-sided colon. Gastroenterol Res Pract 2018; 2018: 5059834
  • 29 Miyaguchi K, Tsuzuki Y, Hirooka N. et al. Endo-wing versus transparent hood-assisted colonoscopy for colorectal adenoma detection: a randomized controlled trial. J Gastroenterol Hepatol 2022; 37: 766-772
  • 30 Pohl H, Bensen SP, Toor A. et al. Cap-assisted colonoscopy and detection of adenomatous Polyps (CAP) study: a randomized trial. Endoscopy 2015; 47: 891-897
  • 31 González-Fernández C, García-Rangel D, Aguilar-Olivos NE. et al. Higher adenoma detection rate with the Endocuff: a randomized trial. Endoscopy 2017; 49: 1061-1068
  • 32 Ngu WS, Bevan R, Tsiamoulos ZP. et al. Improved adenoma detection with Endocuff Vision: the ADENOMA randomised controlled trial. Gut 2019; 68: 280-288
  • 33 Dik VK, Gralnek IM, Segol O. et al. Multicenter, randomized, tandem evaluation of EndoRings colonoscopy – results of the CLEVER study. Endoscopy 2015; 47: 1151-1158
  • 34 Zorzi M, Hassan C, Battagello J. et al. Adenoma detection by Endocuff-assisted versus standard colonoscopy in an organized screening program: the “ItaVision” randomized controlled trial. Endoscopy 2022; 54: 138-147