Society: ASGE

Introduction: Adenoma per colonoscopy (APC) has recently been proposed as a quality measure for colonoscopy. We evaluated the impact of a novel AI system, compared to standard HD colonoscopy, for APC measurement.
Methods: This was a U.S. based, multi-center, prospective randomized trial (NCT04979962) investigating a novel AI detection system - EW10-EC02 that enables a real-time colorectal polyp detection enabled with the colonoscope (CAD-EYE™); Figure 1. Eligible average risk subjects (45 and older) undergoing screening or surveillance colonoscopy were randomized to undergo either computer-assisted colonoscopy (CAC) or conventional colonoscopy (CC). Primary outcomes were APC and positive predictive value (PPV, total number of adenomas divided by total polyps removed). Secondary outcomes were withdrawal time, ADR, sessile serrated lesion detection rate, polyp detection rate and polyp per colonoscopy.
Results: Of 1033 subjects (age: 59.1+/-9.8; 49.9% male) randomized, 510 underwent CAC vs. 523 underwent CC with no significant differences in age, gender, ethnicity, or colonoscopy indication between the 2 groups. For the primary aim, CAC led to a significantly higher APC compared to CC: 0.99± 1.6 vs. 0.85±1.5, p=0.02, Incident Rate Ratio 1.17 (1.03-1.33, p=0.02) with no significant difference in the withdrawal time: 11.28±4.59 min vs. 10.8±4.81 min; p=0.11 between the 2 groups. For the co-primary end point, the positive predictive value of a polyp being adenoma (or non-adenoma) was not inferior (<10%). There were no significant differences in ADR (46.9% vs. 42.8%), advanced adenoma (6.5% vs. 6.3%), sessile serrated lesion detection rate (12.9% vs. 10.1%) and polyp detection rate (63.9% vs 59.3%) between the 2 groups. There was a higher polyp per colonoscopy with CAC compared to CC: 1.67 ± 2.1 vs. 1.33 ± 1.8 (incidence rate ratio 1.27; 1.15-1.4; p<0.01).
Conclusion: Use of a novel AI detection system leads to a significantly higher number of adenomas per colonoscopy compared to conventional HD colonoscopy without any increase in colonoscopy withdrawal time, thus supporting use of AI-assisted colonoscopy to improve colonoscopy quality.

Figure 1. (a and b) Polyp is detected by the CADEYE system with rectangular blue box

Figure 1a

Figure 1b

Introduction: Randomized controlled trials have shown that computer-assisted detection (CAD) can improve adenoma detection rate (ADR). Up to 20% of lesions were still missed by CAD due to “non-visibility” on screen. This study aims to determine whether the combined use of device that increase mucosal exposure (Endocuff) and CAD could further increase the ADR,as compared to CAD alone and white light (WLI) colonoscopy. This is an on-going three-arm prospective randomized trial comparing the use of CAD (with or without endocuff) and conventional WLI colonsocopy on colorectal adenoma detection.

Method: Consecutive patients aged 40 or above undergoing elective colonoscopy were recruited. Patients with history of colonic resection or cancer, familial colorectal cancer syndrome, bleeding tendency, severe comorbid illness, pregnancy women or unable to provide written informed consent were excluded. Eligible patients were randomized in a 1:1:1 ratio to receive CAD (OIP-1, Olympus) with Endocuff (CAD-Endocuff; both by Olympus), CAD alone (CAD) or WLI under high definition colonoscope. Procedures were performed by either experienced endoscopist or trainees with more than 2 years of colonoscopy experience as well as hands-on training on CAD. Analysis was based on per-protocol analysis with ADR as primary outcome.

Result: This is the planned interim analysis of the first 300 patients with complete colonsocopy (Table 1). The mean age of patients was 64.7 (SD 10.3) years and there was 169 (56.3%) male. 58 (19.3%) patients underwent colonoscopy for screening. Among the three groups, the CAD-Endocuff group had the highest ADR (65.7%), PDR (80.8%), SDR (41.4%) and AADR (14.1%). The WLI group had the lowest ADR (46.8%), PDR (59.6%), SDR (23.4%) and AADR (10.5%), with the CAD group in the intermediate (Table 1 and Figure 1). The mean number of adenoma, polyp and advanced adenoma detected per patient followed the same trend and was highest in the CAD-Endocuff group and lowest in the WLI group (Figure 1). On this interim analysis, there was already a significant difference in the ADR (ANOVA; P=0.03), PDR (P<0.01) and SDR (P=0.02) among the three groups. Specficially, CAD-Endocuff group was significantly better than than WLI group in ADR (P=0.01; after Bonferrini correction), PDR (P<0.01), SDR (P=0.01) and the mean number of adenoma (P=0.01) or polyp (P<0.01) detected per patient. CAD alone, however, was only better than WLI in PDR (P=0.02) and mean number of polyp detected (P=0.01).

Conclusion: Interim analysis of this ongoing randomized trial already showed a promising effect of the combined use of CAD and endocuff on enhancing colonic lesions detection, including adenoma and serrated lesions. Further patient enrollment are ongoing to delineate the the potential incremental benefits of adding mucosal exposure device to CAD on colorectal lesion detection.

Table 1: Summary of demographic and clinical outcomes among three groups

Table 1: Summary of demographic and clinical outcomes among three groups

Figure 1: The endoscopic outcomes of three groups

Figure 1: The endoscopic outcomes of three groups

Vivien Tsui

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