Volume 38, Issue 1 pp. 79-86
Original Article - Gastroenterology (Clinical)

Linked color imaging provides enhanced visibility with a high color difference in upper gastrointestinal neoplasms

Osamu Dohi

Corresponding Author

Osamu Dohi

Molecular Gastroenterology and Hepatology, Kyoto Prefectural University of Medicine Graduate School of Medical Science, Kyoto, Japan

Correspondence Osamu Dohi,Molecular Gastroenterology and Hepatology, Kyoto Prefectural University of Medicine Graduate School of Medical Science, 465 Kawaramachi Hirokoji Kamigyo-ku, Kyoto 602-8566, Japan.

Email: [email protected]

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Shoko Ono

Shoko Ono

Division of Endoscopy, Hokkaido University Hospital, Sapporo, Japan

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Kenro Kawada

Kenro Kawada

Department of Gastrointestinal Surgery, Tokyo Medical and Dental University, Tokyo, Japan

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Shinji Kitamura

Shinji Kitamura

Department of Gastroenterology and Oncology, Tokushima University Graduate School of Biomedical Sciences, Tokushima, Japan

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Waku Hatta

Waku Hatta

Division of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, Japan

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Shinichiro Hori

Shinichiro Hori

Department of Endoscopy, National Hospital Organization Shikoku Cancer Center, Matsuyama, Japan

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Hiromitsu Kanzaki

Hiromitsu Kanzaki

Department of Gastroenterology and Hepatology, Okayama University Hospital, Okayama, Japan

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Takahisa Murao

Takahisa Murao

Department of Health Care Medicine, Kawasaki Medical School General Medical Center, Okayama, Japan

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Nobuaki Yagi

Nobuaki Yagi

Department of Gastroenterology, Asahi University Hospital, Gifu, Japan

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Fumisato Sasaki

Fumisato Sasaki

Digestive and Lifestyle Diseases, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan

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Keiichi Hashiguchi

Keiichi Hashiguchi

Department of Endoscopy, Nagasaki University Hospital, Nagasaki, Japan

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Shiro Oka

Shiro Oka

Department of Endoscopy, Hiroshima University Hospital, Hiroshima, Japan

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Kazuhiro Katada

Kazuhiro Katada

Department of Gastroenterology and Hepatology, North Medical Center, Kyoto Prefectural University of Medicine, Yosa-gun, Kyoto, Japan

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Ryo Shimoda

Ryo Shimoda

Department of Endoscopic Diagnostics and Therapeutics, Saga University Hospital, Saga, Japan

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Kazuhiro Mizukami

Kazuhiro Mizukami

Department of Gastroenterology, Oita University, Yufu, Japan

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Mitsuhiko Suehiro

Mitsuhiko Suehiro

Department of General Internal Medicine 2, Kawasaki Medical School General Medical Center, Okayama, Japan

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Toshihisa Takeuchi

Toshihisa Takeuchi

Endoscopy Center, Osaka Medical and Pharmaceutical University Hospital, Takatsuki, Japan

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Shinichi Katsuki

Shinichi Katsuki

Gastroenterology, Otaru Ekisaikai General Hospital, Otaru, Japan

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Momoko Tsuda

Momoko Tsuda

Department of Gastroenterology, National Hospital Organization Hakodate National Hospital, Hakodate, Japan

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Yuji Naito

Yuji Naito

Molecular Gastroenterology and Hepatology, Kyoto Prefectural University of Medicine Graduate School of Medical Science, Kyoto, Japan

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Tatsuyuki Kawano

Tatsuyuki Kawano

Department of Surgery, Soka Municipal Hospital, Soka, Japan

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Ken Haruma

Ken Haruma

Department of General Internal Medicine 2, Kawasaki Medical School General Medical Center, Okayama, Japan

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Hideki Ishikawa

Hideki Ishikawa

Department of Molecular-Targeting Cancer Prevention, Kyoto Prefectural University of Medicine, Osaka, Japan

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Keita Mori

Keita Mori

Clinical Research Promotion Unit, Clinical Research Center, Shizuoka Cancer Center, Sunto-gun, Shizuoka, Japan

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Mototsugu Kato

Mototsugu Kato

Department of Gastroenterology, National Hospital Organization Hakodate National Hospital, Hakodate, Japan

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LCI-FIND TRIAL Group
First published: 03 October 2022
Citations: 3

Declaration of conflict of interest: Osamu Dohi received a research grant from Fujifilm Co., Ltd. Yuji Naito received scholarship funds from EA Pharma. Co. Ltd. and Taiyo Kagaku Co., Ltd.; a collaboration research fund from Taiyo Kagaku Co., Ltd.; and received lecture fees from EA Pharma. Co. Ltd., Miyarisan Pharma. Co. Ltd., Mochida Pharma. Co. Ltd., Mylan EPD Co., Otsuka Pharma. Co. Ltd., and Takeda Pharma. Co. Ltd. Mototsugu Kato received lecture fees from Takeda Pharmaceutical Co. Ltd., and Otsuka Pharmaceutical Co., Ltd. and received scholarship grants from Fujifilm Co., Ltd. The other authors declare no conflicts of interest. These companies had no role in the design, conduct, data collection, data interpretation, or reporting of this study.

Ethical approval: The study was approved by the Ethical Review Committee of each participating institution and conducted in accordance with the Declaration of Helsinki. The study was registered with the University Hospital Medical Information Network Clinical Trials Registry (UMIN000023863).

Financial support: The authors received a financial support from Fujifilm Co. for the research. However, Fujifilm Co. provided no support for writing or preparing this manuscript.

Abstract

Background and Aim

The aim of this post-hoc analysis in a randomized, controlled, multicenter trial was to evaluate the visibility of upper gastrointestinal (UGI) neoplasms detected using linked color imaging (LCI) compared with those detected using white light imaging (WLI).

Methods

The visibility of the detected UGI neoplasm images obtained using both WLI and LCI was subjectively reviewed, and the median color difference (ΔE) between each lesion and the surrounding mucosa according to the CIE L*a*b* color space was evaluated objectively. Multivariate logistic regression analysis was performed to identify factors associated with neoplasms that were missed under WLI and detected under LCI.

Results

A total of 120 neoplasms, including 10, 32, and 78 neoplasms in the pharynx, esophagus, and stomach, respectively, were analyzed in this study. LCI enhanced the visibility 80.9% and 93.6% of neoplasms in pharynx/esophagus and stomach compared with WLI, respectively. LCI also achieved a higher ΔE of enhanced neoplasms compared with WLI in the pharynx/esophagus and stomach. The median WLI ΔE values for gastric neoplasms missed under WLI and later detected under LCI were significantly lower than those for gastric neoplasms detected under WLI (8.2 vs 9.6, respectively). Furthermore, low levels of WLI ΔE (odds ratio [OR], 7.215) and high levels of LCI ΔE (OR, 22.202) were significantly associated with gastric neoplasms missed under WLI and later detected under LCI.

Conclusion

Color differences were independently associated with missing gastric neoplasms under WLI, suggesting that LCI has an obvious advantage over WLI in enhancing neoplastic visibility.

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