Artificial intelligence for diagnosing neoplasia on digital cholangioscopy: development and multicenter validation of a convolutional neural network model

Author:

Robles-Medranda Carlos1ORCID,Baquerizo-Burgos Jorge1,Alcivar-Vasquez Juan1,Kahaleh Michel2ORCID,Raijman Isaac34,Kunda Rastislav5ORCID,Puga-Tejada Miguel1,Egas-Izquierdo Maria1,Arevalo-Mora Martha1,Mendez Juan C.6,Tyberg Amy2,Sarkar Avik2,Shahid Haroon2,del Valle-Zavala Raquel1,Rodriguez Jorge1,Merfea Ruxandra C.1,Barreto-Perez Jonathan1,Saldaña-Pazmiño Gabriela7,Calle-Loffredo Daniel1,Alvarado Haydee1,Lukashok Hannah P.1

Affiliation:

1. Gastroenterology, Instituto Ecuatoriano de Enfermedades Digestivas (IECED), Guayaquil, Ecuador

2. Gastroenterology, Robert Wood Johnson Medical School Rutgers University, New Brunswick, New Jersey, United States

3. Houston Methodist Hospital, Houston, Texas, United States

4. Baylor Saint Luke’s Medical Center, Houston, Texas, United States

5. Department of Advanced Interventional Endoscopy, Universitair Ziekenhuis Brussel (UZB)/Vrije Universiteit Brussel (VUB), Brussels, Belgium

6. mdconsgroup, Artificial Intelligence Department, Guayaquil, Ecuador

7. Gastroenterology, Hospital Clínico San Carlos, Madrid, Spain

Abstract

Abstract Background We aimed to develop a convolutional neural network (CNN) model for detecting neoplastic lesions during real-time digital single-operator cholangioscopy (DSOC) and to clinically validate the model through comparisons with DSOC expert and nonexpert endoscopists. Methods In this two-stage study, we first developed and validated CNN1. Then, we performed a multicenter diagnostic trial to compare four DSOC experts and nonexperts against an improved model (CNN2). Lesions were classified into neoplastic and non-neoplastic in accordance with Carlos Robles-Medranda (CRM) and Mendoza disaggregated criteria. The final diagnosis of neoplasia was based on histopathology and 12-month follow-up outcomes. Results In stage I, CNN2 achieved a mean average precision of 0.88, an intersection over the union value of 83.24 %, and a total loss of 0.0975. For clinical validation, a total of 170 videos from newly included patients were analyzed with the CNN2. Half of cases (50 %) had neoplastic lesions. This model achieved significant accuracy values for neoplastic diagnosis, with a 90.5 % sensitivity, 68.2 % specificity, and 74.0 % and 87.8 % positive and negative predictive values, respectively. The CNN2 model outperformed nonexpert #2 (area under the receiver operating characteristic curve [AUC]-CRM 0.657 vs. AUC-CNN2 0.794, P < 0.05; AUC-Mendoza 0.582 vs. AUC-CNN2 0.794, P < 0.05), nonexpert #4 (AUC-CRM 0.683 vs. AUC-CNN2 0.791, P < 0.05), and expert #4 (AUC-CRM 0.755 vs. AUC-CNN2 0.848, P < 0.05; AUC-Mendoza 0.753 vs. AUC-CNN2 0.848, P < 0.05). Conclusions The proposed CNN model distinguished neoplastic bile duct lesions with good accuracy and outperformed two nonexpert and one expert endoscopist.

Publisher

Georg Thieme Verlag KG

Subject

Gastroenterology

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