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Multicenter prospective in vivo study of an endocytoscope system (ECS) for superficial esophageal cancer

BACKGROUND: Endocytoscope systems (ECS) can visualize cellular nuclei of the mucosa of the gastrointestinal tract and are predicted to provide real-time microscopic diagnosis. However, their practical diagnostic performance remains unclear. Therefore, we conducted a multicenter prospective study to...

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Detalles Bibliográficos
Autores principales: Morita, Shuko, Goda, Kenichi, Yano, Tomonori, Kaise, Mitsuru, Kato, Mototsugu, Inoue, Haruhiro, Niwa, Yasumasa, Kodashima, Shinya, Miyahara, Ryoji, Ochiai, Atsushi, Ikegami, Masahiro, Hamatani, Shigeharu, Shimoda, Tadakazu, Ohkura, Yasuo, Aida, Junko, Nakanishi, Yukihiro, Yoshimura, Kenichi, Ishikawa, Hideki, Takubo, Kaiyo, Muto, Manabu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Singapore 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8370913/
https://www.ncbi.nlm.nih.gov/pubmed/34304331
http://dx.doi.org/10.1007/s00535-021-01810-2
Descripción
Sumario:BACKGROUND: Endocytoscope systems (ECS) can visualize cellular nuclei of the mucosa of the gastrointestinal tract and are predicted to provide real-time microscopic diagnosis. However, their practical diagnostic performance remains unclear. Therefore, we conducted a multicenter prospective study to evaluate the visualization of superficial esophageal neoplasm in vivo using an ECS, and its diagnostic capability. METHODS: The study target was histologically confirmed squamous cell carcinoma (SCC) and high-grade intraepithelial neoplasia (HGIN). An integrated ECS was used to obtain ECS images. In each patient, three ECS images of cancerous and corresponding noncancerous regions were selected for evaluation. A pathological review board of five certified pathologists made the final diagnosis of the images. The primary endpoint was the sensitivity of ECS diagnosis by pathologists. RESULTS: ECS images of 68 patients were assessed: 42 lesions were mucosal SCC, 13 were submucosal SCC, and 13 were HGIN. The rate of assessable images was 96% (95% CI 87.6–99.1). The sensitivity of ECS diagnosis by pathologists was 88% (95% CI 77.2–94.5). CONCLUSIONS: ECS can provide high-quality images of cancerous lesions and a high diagnostic accuracy by pathologists, and could be useful for real-time endoscopic histological diagnosis of SCC and HGIN. TRIAL REGISTRATION: The UMIN Clinical Trials Registry Identification Number: 000004218 SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00535-021-01810-2.