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Review

Artificial Intelligence-Aided Endoscopy and Colorectal Cancer Screening

1
Department of Biomedical Sciences, Humanitas University, 20090 Rozzano, Italy
2
Endoscopy Unit, Humanitas Clinical and Research Center, IRCCS, 20090 Rozzano, Italy
3
Clinical Effectiveness Research Group, Institute of Health and Society, Faculty of Medicine, University of Oslo, 0315 Oslo, Norway
4
Digestive Disease Center, Showa University Northern Yokohama Hospital, Yokohama 224-0032, Japan
5
Division of Gastroenterology and Hepatology, Veterans Affairs Medical Center, Kansas City, MO 64128, USA
*
Author to whom correspondence should be addressed.
Diagnostics 2023, 13(6), 1102; https://doi.org/10.3390/diagnostics13061102
Submission received: 2 February 2023 / Revised: 19 February 2023 / Accepted: 11 March 2023 / Published: 14 March 2023
(This article belongs to the Special Issue Advancements in Colonoscopy 2nd Edition)

Abstract

:
Colorectal cancer (CRC) is the third most common cancer worldwide, with the highest incidence reported in high-income countries. However, because of the slow progression of neoplastic precursors, along with the opportunity for their endoscopic detection and resection, a well-designed endoscopic screening program is expected to strongly decrease colorectal cancer incidence and mortality. In this regard, quality of colonoscopy has been clearly related with the risk of post-colonoscopy colorectal cancer. Recently, the development of artificial intelligence (AI) applications in the medical field has been growing in interest. Through machine learning processes, and, more recently, deep learning, if a very high numbers of learning samples are available, AI systems may automatically extract specific features from endoscopic images/videos without human intervention, helping the endoscopists in different aspects of their daily practice. The aim of this review is to summarize the current knowledge on AI-aided endoscopy, and to outline its potential role in colorectal cancer prevention.

1. Introduction

Colorectal cancer (CRC) is the third most common cancer worldwide [1,2,3], with the highest incidence reported in high-income countries in Europe, North America and Oceania [4]. Although the overall prognosis has been improving in the last decades, with a 5-year survival rate of almost 65% [4], colorectal cancer still ranks as the second most common cause of cancer-related mortality [1,2,3]. However, because of the slow progression of neoplastic precursors (i.e., adenomas and serrated lesions) [5], along with the opportunity for their endoscopic detection and resection [6,7], a well-designed endoscopic screening program is expected to strongly decrease colorectal cancer incidence and mortality [7].
In this regard, quality of colonoscopy has been clearly related with the risk of post-colonoscopy colorectal cancer. The Adenoma Detection Rate (ADR), defined as the percentage of patients undergoing colonoscopy with at least one adenoma resected, is currently considered as the most relevant quality indicator correlating with the incidence of interval colorectal cancer (defined as a colorectal cancer diagnosed within 60 months following a negative colonoscopy screening). In detail, a suboptimal endoscopist Adenoma Detection Rate has been associated with a substantial increase in the risk of post-colonoscopy colorectal cancer incidence, whereas an Adenoma Detection Rate increase was effective in reversing such a detrimental effect, offering additional prevention to the patients [8,9,10,11,12].
Nevertheless, a recent systematic review with meta-analysis reported that about 25% of colorectal neoplasms are missed at screening colonoscopy, resulting in an unacceptable variability in the key quality indicator among endoscopists [13]. The most plausible reasons for such variability are both the inability to detect colonic adenomas due to their subtle appearance, especially for small and flat lesions, and the incomplete inspection of the colorectal mucosa due to blind areas at the flexures or behind folds. In particular, unrecognised lesions within the visual field are considered as the most important issue, as several proof-of-concept studies showed an increased detection when a second observer (i.e., nurse or trainee) assisted the first operator [14,15,16]. Innovations such as virtual and dye-spray chromoendoscopy may enhance mucosal contrast, helping to improve the Adenoma Detection Rate; however, all these strategies are operator-dependent and require a learning curve. As a matter of fact, apart from the advent of high definition (HD) imaging, none of such innovations has revolutionized endoscopists’ daily practice.
Recently, interest in the development of artificial intelligence (AI) applications in the medical field has been growing. Through machine learning processes, and, more recently, deep learning, if a very high number of learning samples are available, artificial intelligence systems may automatically extract specific features from endoscopic images/videos without human intervention [17,18,19], helping the endoscopists in different aspects of their daily practice.
The aim of this review is to summarize the current knowledge on artificial intelligence-aided endoscopy, and to outline its potential role in colorectal cancer prevention.

2. Principles of Artificial Intelligence

Artificial intelligence is an evolution of general software systems generating an output from an input through an algorithm [17]. The ability of the artificial intelligence software to develop the most adequate algorithm for a specific aim, after an appropriate training, is called Machine Learning (ML). In the endoscopic field, two principal ML methods have been used: handcrafted knowledge and deep learning. The first one represents the first attempt to develop artificial intelligence, characterized by a preset of rules describing knowledge in a well-defined field. Unfortunately, this system doesn’t have the ability to dynamically improve its algorithm (“to learn”), showing poor ability in conditions of uncertainty. Deep learning can be considered as an evolution of handcrafted knowledge. In particular, this method utilizes a convolutional neural network (CNN) that automatically extracts specific features from data without human intervention after an adequate training with a very high number of learning samples. These large artificial convolutional neural networks enhance the ability to “think” and “learn” and improve performance proportionally to the depth of the network. For this goal, deep learning sets neural connections in motion in order to improve its performance through continuous learning. This network is characterized by a layer of input nodes, connected by numerous internal nodes, organized in different levels (Figure 1).

3. Artificial Intelligence in Colonoscopy

Computer-Aided Diagnosis (CAD) systems are expected to have at least two major roles in endoscopy practice, mitigating inherent human errors accompanying colonoscopy procedures. Computer-Aided Detection (CADe) systems have the potential to decrease the polyp miss rate [20], contributing to improved adenoma detection [21] (Figure 2).
Computer-Aided Characterization (CADx) systems may improve the accuracy of colorectal polyp optical diagnosis [22], leading to the reduction of unnecessary removal of non-neoplastic lesions, potential implementation of a resect-and-discard and leave-in-situ strategy, and the proper application of advanced resection techniques (Figure 3).
Moreover, the possible role of artificial intelligence systems as a computer-aided quality assurance during colonoscopy (i.e., cecum detector; speedometer; blind spot detector; bowel preparation identifier) is taking place in the artificial intelligence research field.

3.1. Artificial Intelligence-Assisted Detection (CADe)

Initial experiences with Computer-Aided Detection systems were reported in the early 2000s [23,24,25]. However, those systems were designed with handcrafted algorithms, limited in real practice application due to both low specificity and low sensitivity, coupled with long processing times. Recently, deep learning-based algorithms have been developed aiming to assist in adenoma detection. After showing promising results in ex vivo studies [26,27,28], the use of artificial intelligence algorithms has been claimed to improve detection of colorectal lesions in several randomized controlled trials [29,30,31,32,33,34,35,36,37,38,39,40,41] (Table 1).
In a recent standard pairwise meta-analysis that pooled data of such randomized trials, artificial intelligence showed a significantly higher detection performance compared to standard colonoscopy, independently from adenoma location, size and morphology [21], providing a 44% Adenoma Detection Rate increase. Moreover, artificial intelligence systems ranked first in an Adenoma Detection Rate increase, showing a significant improvement when compared to other advanced endoscopy techniques (i.e., chromoendoscopy, systems that increase mucosal visualisation) in a network meta-analysis [42].
In more recent randomized tandem trials [20,43,44,45], Computer-Aided Detection colonoscopy reduced the overall adenoma miss rate when compared to standard colonoscopy (Table 2).
However, it is important to underline that the improvement in detection due to AI systems is only related to the increased capacity for detecting lesions within the visual field, that is, dependent on the amount of mucosa exposed by the endoscopist during the scope withdrawal. To tackle this issue, different add-on devices (e.g., Endocuff Vision) have been developed with the aim of improving mucosal exposure [46]. These tools combined with Computer-Aided Detection systems may theoretically maximize the Computer-Aided Detection performances. A proof-of-concept randomized controlled trial is currently assessing the additional diagnostic yield obtained from Endocuff Vision + artificial intelligence-assisted colonoscopy when compared with the yield obtained with artificial intelligence-assisted colonoscopy alone (NCT04676308) [47].
A Computer-Aided Detection system should be thus only considered as a tool for the endoscopist, since his/her skills and experience remain fundamental in order to perform high-quality colonoscopy, and thus to take advantage of the AI support [48,49].
However, it may be argued that a further increase the performance in adenoma detection of expert endoscopists, such as the ones involved in the first trials [29,30,31,32,33,34,35,36,37,38,39,40,41], may provide only little additional benefit.
In this regard, Repici and colleagues [35] recently investigated the role of a novel artificial intelligence Computer-Aided Detection system (GI-Genius, Medtronic Corp., USA) among non-expert endoscopists, reporting promising results, thus showing the opportunity to reduce once and for all the unwanted variation among endoscopists who are involved in screening programs. With this in mind, when applied to large-scale screening programs, AI systems were modelled to avoid colorectal cancer cases and deaths among the screening population [50].
In addition, a recent population-based cohort [51] study on a Dutch fecal immunochemical testing (FIT)-based colorectal cancer screening program showed that the Adenoma Detection Rate of endoscopists is inversely associated with the risk for interval PCCRC (post-colonoscopy colorectal cancers) in FIT-positive colonoscopies. This study showed that for every 1000 patients undergoing colonoscopy, the expected number of interval PCCRC diagnoses after five years was approximately 2 for endoscopists with Adenoma Detection Rates of 70%, compared with more than 2.5, almost 3.5, and more than 4.5 for endoscopists with Adenoma Detection Rates of 65%, 60%, and 55%, respectively. Endoscopists performing colonoscopy in FIT-based screening should thus aim for markedly higher Adenoma Detection Rates compared with primary colonoscopy, and AI could help filling the gap.
High-quality clinical data confirming this model are needed to suggest that AI-assisted endoscopy, by increasing the detection rate and subsequently the Adenoma Detection Rate, may reduce the risk of post-colonoscopy colorectal cancer, and that AI could be particularly helpful in both settings of non-expert endoscopists and FIT-based colorectal cancer screening.
Nevertheless, in recent years, colorectal lesions with a serrated pattern, namely sessile serrated lesions (SSLs) with or without dysplasia, or traditional serrated lesions, have also been identified as precursors of up to 30% of all colorectal cancers [52]. In particular, advanced serrated lesions, defined as either serrated lesions ≥ 10 mm in size, or one of the two serrated polyp subtypes, namely sessile serrated lesions with dysplasia, or traditional serrated lesions, and considered as colorectal lesions that have a high risk of developing into colorectal cancer, have been recently proposed as a possible target for designing an optimal colonoscopy-based colorectal cancer screening program [53].
These lesions are often flat and subtle, being sessile serrated lesions typically located in the proximal colon, and the rarer traditional serrated lesions, often found distally. These features make such lesions difficult to detect, on one hand explaining the wide difference in serrated detection performances among different operators [54], and on the other hand explaining the higher risk of metachronous colorectal cancer after the resection of these lesions when compared with individuals without any significant lesions in baseline colonoscopy [55].
As for colorectal adenomas, the initial experience with Computer-Aided Detection systems showed promising results in improving the detection of serrated lesions, as reported by the comprehensive meta-analysis of Hassan and colleagues [21]. Whereas individual studies did not detect any significant differences in serrated lesions detection performance, pooling their data together increased the diagnostic yield. Then, the benefits of artificial intelligence-assisted colonoscopy appeared clear even in detecting such subtle lesions when compared to standard high-definition colonoscopy.
On the other hand, implementation of AI could increase medical costs in various ways (higher polypectomy, pathological assessment, and surveillance costs, etc.) [56]; however, the savings related to colorectal cancer reduction may mitigate such additional costs [50]. All these models have been thought through considering actual evidence and guidelines in term of endoscopy surveillance after the index colonoscopy [57,58,59]. Even in this case, the relevant impact on adenoma detection due to Computer-Aided Diagnosis systems, and, eventually, the reduction of missed adenomas, may change the paradigm of endoscopy surveillance itself, as we move from planning our strategy based on what we may have left behind to what we have actually detected (and resected). This may allow us to provide a personalized and dynamic AI-driven surveillance strategy for each patient.

3.2. Artificial Intelligence-Assisted Characterization (CADx)

Although the benefits of increasing the Adenoma Detection Rate are well known, there is also risk of overdiagnosis as well. As a matter of fact, most of the polyps detected during colonoscopy are diminutive in size (<5 mm) and of low malignant potential. Furthermore, in AI-aided endoscopy, this proportion may be higher, considering that Computer-Aided Detection systems would particularly improve the detection of such subtle lesions [21,29,30,31,32,33,34,35]. Among specifically trained endoscopists, the accuracy in characterizing these small lesions is reported to be <80% [60], with even lower performances reported for non-expert endoscopists. Thus, the diffusion of Computer-Aided Detection systems would lead to a consistent increase in the resection of hyperplastic polyps, which almost never evolve in a malignant lesion. The observation and/or the resection of these polyps would represent an unnecessary waste of time, and an unnecessary financial burden. In this regard, CADx systems may improve the accuracy of colorectal polyp optical diagnosis, leading to the reduction of unnecessary removal of hyperplastic polyps, with the potential implementation of resect-and-discard (when polyps are resected and discarded without histological evaluation) and leave-in-situ (when non-neoplastic lesions located in the rectum and sigmoid are left in situ without resection, as they have no malignant potential) strategies.
The Preservation and Incorporation of Valuable Endoscopic Innovations (PIVI) performance thresholds have been outlined by the American Society for Gastrointestinal Endoscopy (ASGE) [61]. To fulfil the ASGE PIVI thresholds, such a strategy should achieve (1) >90% agreement in assignment of post-polypectomy surveillance intervals compared to pathology-based decisions, and (2) a negative predictive value (NPV) > 90% when used with high confidence.
More recently, the European Society of Gastrointestinal Endoscopy (ESGE) also published an official Position Statement aiming to define simple, safe, and easy-to-measure competence standards for endoscopists and artificial intelligence systems performing optical diagnosis of diminutive colorectal polyps [62]. Thus, according to a panel of experts, in order to implement the leave-in-situ strategy for diminutive colorectal lesions (1–5 mm), it is clinically acceptable if, during real-time colonoscopy, at least 90% sensitivity and 80% specificity is achieved for high-confidence endoscopic characterization of colorectal neoplasia of diminutive polyps in the rectosigmoid. Considering the resect-and-discard strategy, it is clinically acceptable if, during real-time colonoscopy, at least 80% sensitivity and 80% specificity is achieved for high-confidence endoscopic characterization of colorectal neoplasia of diminutive lesions.
The initial CADx systems were developed for magnifying scopes using narrow-band imaging (NBI) based on support vector machine (SVM) models [63,64,65]. More recently, deep learning algorithms based on convolutional neural networks have been used for CADx systems as well, resulting in both higher diagnostic accuracy and faster processing time. An important advantage of such algorithms was the ability to use raw and unprocessed videos, therefore allowing a real-time integration of the AI system during endoscopy.
Mori et al. [66] assessed the performance of a real-time CADx system providing microvascular and cellular visualization of colorectal polyps after application of NBI and methylene blue staining, with high accuracy; in this case, the system could meet required thresholds.
In order to improve the reproducibility in a real-life clinical scenario, Byrne et al. used white light imaging (WLI) and non-magnified NBI videos to test their CADx system [67]. With sensitivity, specificity, PPV, NPV, and accuracy for differentiating diminutive adenomas and hyperplastic polyps of 98%, 83%, 90%, 97%, and 94%, respectively, this resulted in the first CADx study to reach the ASGE PIVI thresholds with a not-magnified NBI setting in real-time clinical practice. Further, equal prediction performance across two different imaging technologies (NBI and Blue Light Imaging (BLI)) has been reported. It is of note that the BLI was not part of the training set [68], suggesting the potential to have a CADx trained and used with different technologies.
More recently, two CADx systems were shown to exceed the PIVI thresholds for implementation of cost-saving strategies when applied to unmagnified imaging in clinical practice [69,70,71].
Further studies have also evaluated the benefit of integrating CADx systems in clinical practice [72,73], underlying the role of AI systems in significantly improving the performance of all endoscopists, with the greatest benefit achieved in trainees (from 63.8–72% to 82.7–84.2%, p > 0.001), thus minimizing the differences with expert endoscopists [72]. Interestingly, these results may lead to a relevant cost saving [74].
However, so far only conflictual and not definitive data are available for most of the commercially available AI tools for characterization [75]. On top of that, for reliable data, the performance of CADx systems should be further evaluated in prospective randomized controlled trials, conducted among both expert endoscopists and trainees in academic and community centers.

3.3. Artificial Intelligence-Assisted Quality Control

Although most of the studies on AI-assisted endoscopy have focused on adenoma detection and characterization, improving the quality of the endoscopic examination process itself has been recently becoming a more and more travelled path. In this regard, because of the established correlation between the quality of bowel preparation and Adenoma Detection Rate, along with a certain inter-observer variability in quality assessment, different convolutional neural network-based systems have been developed in order to obtain a standardized report [76,77], achieving a rate of accuracy higher than 90%, thus outperforming the endoscopists consulted for the study, according to Zhou et al. [76]. The same system (ENDOANGEL) was also tested for the monitoring of cecal intubation, withdrawal time and exit speed, alerting the endoscopist in case of blind spots caused due to scope sliding [32]. Thus far, automated blind spots identification systems have been initially investigated in upper GI endoscopy [78,79]; however, it may be even more relevant as a quality metric for colonoscopy, as preliminarily reported by McGill et al. [80].
Polyp size measurements are important for treatment selection and the establishment of monitoring intervals; however, currently used subjective methods are flawed. Indeed, Requa et al. [81] developed a highly accurate convolutional neural network to estimate the size of polyps in colonoscopy, dividing them into three size-based groups of ≤5, 6–9, and ≥10 mm (model accuracy: 97%, 97%, and 98%, respectively). More recently, Abdelrahim et al. [82] developed a deep learning model based on convolutional neural networks (CNN) with an 80% accuracy in real-time polyp sizing. Such systems when integrated to CADx could improve polyp management strategies.

4. Limitations

Artificial intelligence is a strong focus of interest for health care. In particular, diagnostic endoscopy is an attractive field for the definitive affirmation of AI as an adjunct weapon against colorectal cancer, with a real potential to improve patient care, principally through standardisation of endoscopy quality. As discussed, the integration of Computer-Aided Diagnosis modules in real-time colonoscopy has shown promising results in increasing adenoma detection while improving optical biopsy accuracy. Yet, several issues need to be addressed before AI can be successfully implemented in daily practice.
First, in considering data coming from RCTs supporting the efficacy of Computer-Aided Detection systems in improving the Adenoma Detection Rate, it could be argued that the fact that all but two of the AI studies were performed in China mitigates the generalizability of the results. In this regard, the promising magnitude of the Adenoma Detection Rate increase may be somewhat facilitated by the low baseline Adenoma Detection Rate across the control groups of the Chinese studies. This is to be related with the relatively young age of the enrolled patients; however, the possible impact of a suboptimal endoscopic quality in the first place cannot be excluded. However, the benefit observed in the two Western trials [30,35], with much higher baseline Adenoma Detection Rate values, seems to exclude such a possibility, as the gradient of increase is very similar to what is estimated in Eastern studies [29,31,32,33,34] and meta-analysis [21]. On the other hand, further studies conducted among both Eastern and Western endoscopists with different endoscopic skills would be of paramount importance in order to corroborate present data.
Secondly, because Computer-Aided Detection systems are based on deep learning architectures in which there is no human control on the final algorithm, their outcomes incorporate some unpredictability, and the endoscopist may be presented with false positive (FP) images which should be never considered as suspicious [83,84,85]. Such FPs may potentially hamper the efficiency of Computer-Aided Detection-assisted colonoscopy due to increased withdrawal time, unneeded polypectomies, and higher endoscopist’s fatigue and distraction [86,87,88]. However, despite a relevant number of FPs per colonoscopy (27.3 ± 13.1), only a minority of them (5.7%) required additional exploration, resulting in a negligible 1% increase in the total withdrawal time [89] in a post hoc analysis of an RCT [30], and confirmed by a following comparative study [90] (Figure 4).
Moreover, considering the lack of high-quality clinical data on AI-assisted optical biopsy, further studies would be even more relevant to confirm the accuracy of the different CADx systems, showing how they might impact both endoscopist behaviour and costs in real life through the implementation of “resect and discard” and/or “leave in situ” strategies. As a matter of fact, one of the major concerns about AI-assisted colonoscopy is the over-expectation of the benefits of Computer-Aided Detection in cancer prevention. Although promising, we must not be satisfied with present evidences. Only a properly powered RCT may confirm the benefit in term of cancer incidence and death.

5. Conclusions

In conclusion, the burden of missed preneoplastic lesions during colonoscopy is far from being negligible, resulting in still unacceptable cases of colorectal cancer. Artificial intelligence is set to go on stage with regard to different health care fields, and endoscopy may be a fertile terrain for its development and refinement [91,92]. Further studies have the task of both confirming the promising results of first experiences and redesigning the optimal screening setting considering the new technological opportunity. Regarding Computer-Aided Detection systems, to improve their reliability and minimize bias, the performance of Computer-Aided Diagnosis systems should be corroborated in prospective RCTs, conducted in both community and academic centers, and among endoscopists with different levels of experience. Then, the actual impact of adenoma detection improvement on colorectal cancer prevention needs to be assessed in large-scale population-based studies. Preliminary data on both CADx and AI-assisted quality-control systems are promising; however, the lack of high-quality clinical studies prevents any reliable conclusion. Thus, such studies should be considered as a priority in future research agendas. The steps to be done are still many, but the path does not seem so steep anymore.

Author Contributions

All authors contributed to this paper with conception, literature review, drafting, critical revision and editing, and approval of the final version. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Conflicts of Interest

M.S.: none. D.M.: none. Y.M.: consulting for Olympus Corp.; ownership interest in Cybernet Corp. L.A.: none. A.F.: none. R.M.: consulting fees for Fuji. P.S.: consulting fees for Fuji. C.H.: consulting fees for Fuji and Medtronic. A.R.: consulting fees for Fuji, Olympus, and Medtronic.

References

  1. Bray, F.; Ferlay, J.; Soerjomataram, I.; Siegel, R.L.; Torre, L.A.; Jemal, A. Global Cancer Statistics 2018: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA Cancer J. Clin. 2018, 68, 394–424. [Google Scholar] [CrossRef] [Green Version]
  2. Siegel, R.L.; Miller, K.D.; Jemal, A. Cancer Statistics, 2018. CA Cancer J. Clin. 2018, 68, 7–30. [Google Scholar] [CrossRef]
  3. Arnold, M.; Sierra, M.S.; Laversanne, M.; Soerjomataram, I.; Jemal, A.; Bray, F. Global Patterns and Trends in Colorectal Cancer Incidence and Mortality. Gut 2017, 66, 683–691. [Google Scholar] [CrossRef] [Green Version]
  4. Brenner, H.; Kloor, M.; Pox, C.P. Colorectal Cancer. Lancet 2014, 383, 1490–1502. [Google Scholar] [CrossRef]
  5. Nishihara, R.; Wu, K.; Lochhead, P.; Morikawa, T.; Liao, X.; Qian, Z.R.; Inamura, K.; Kim, S.A.; Kuchiba, A.; Yamauchi, M.; et al. Long-Term Colorectal-Cancer Incidence and Mortality after Lower Endoscopy. N. Engl. J. Med. 2013, 369, 1095–1105. [Google Scholar] [CrossRef] [Green Version]
  6. Schoen, R.E.; Pinsky, P.F.; Weissfeld, J.L.; Yokochi, L.A.; Church, T.; Laiyemo, A.O.; Bresalier, R.; Andriole, G.L.; Buys, S.S.; Crawford, E.D.; et al. Colorectal-Cancer Incidence and Mortality with Screening Flexible Sigmoidoscopy. N. Engl. J. Med. 2012, 366, 2345–2357. [Google Scholar] [CrossRef] [Green Version]
  7. Brenner, H.; Bouvier, A.M.; Foschi, R.; Hackl, M.; Larsen, I.K.; Lemmens, V.; Mangone, L.; Francisci, S.; EUROCARE Working Group. Progress in Colorectal Cancer Survival in Europe from the Late 1980s to the Early 21st Century: The EUROCARE Study. Int. J. Cancer 2012, 131, 1649–1658. [Google Scholar] [CrossRef]
  8. Kaminski, M.F.; Regula, J.; Kraszewska, E.; Polkowski, M.; Wojciechowska, U.; Didkowska, J.; Zwierko, M.; Rupinski, M.; Nowacki, M.P.; Butruk, E. Quality Indicators for Colonoscopy and the Risk of Interval Cancer. N. Engl. J. Med. 2010, 362, 1795–1803. [Google Scholar] [CrossRef] [Green Version]
  9. Corley, D.A.; Levin, T.R.; Doubeni, C.A. Adenoma Detection Rate and Risk of Colorectal Cancer and Death. N. Engl. J. Med. 2014, 370, 2541. [Google Scholar] [CrossRef] [Green Version]
  10. Robertson, D.J.; Lieberman, D.A.; Winawer, S.J.; Ahnen, D.J.; Baron, J.A.; Schatzkin, A.; Cross, A.J.; Zauber, A.G.; Church, T.R.; Lance, P.; et al. Colorectal Cancers Soon after Colonoscopy: A Pooled Multicohort Analysis. Gut 2014, 63, 949–956. [Google Scholar] [CrossRef] [Green Version]
  11. Anderson, R.; Burr, N.E.; Valori, R. Causes of Post-Colonoscopy Colorectal Cancers Based on World Endoscopy Organization System of Analysis. Gastroenterology 2020, 158, 1287–1299.e2. [Google Scholar] [CrossRef]
  12. Hassan, C.; Piovani, D.; Spadaccini, M.; Parigi, T.; Khalaf, K.; Facciorusso, A.; Fugazza, A.; Rösch, T.; Bretthauer, M.; Mori, Y.; et al. Variability in Adenoma Detection Rate in Control Groups of Randomized Colonoscopy Trials. Gastrointest. Endosc. 2022, 97, 212–225.e7. [Google Scholar] [CrossRef]
  13. Zhao, S.; Wang, S.; Pan, P.; Xia, T.; Chang, X.; Yang, X.; Guo, L.; Meng, Q.; Yang, F.; Qian, W.; et al. Magnitude, Risk Factors, and Factors Associated With Adenoma Miss Rate of Tandem Colonoscopy: A Systematic Review and Meta-Analysis. Gastroenterology 2019, 156, 1661–1674.e11. [Google Scholar] [CrossRef]
  14. Aslanian, H.R.; Shieh, F.K.; Chan, F.W.; Ciarleglio, M.M.; Deng, Y.; Rogart, J.N.; Jamidar, P.A.; Siddiqui, U.D. Nurse Observation during Colonoscopy Increases Polyp Detection: A Randomized Prospective Study. Am. J. Gastroenterol. 2013, 108, 166–172. [Google Scholar] [CrossRef] [PubMed]
  15. Lee, C.K.; Park, D.I.; Lee, S.-H.; Hwangbo, Y.; Eun, C.S.; Han, D.S.; Cha, J.M.; Lee, B.-I.; Shin, J.E. Participation by Experienced Endoscopy Nurses Increases the Detection Rate of Colon Polyps during a Screening Colonoscopy: A Multicenter, Prospective, Randomized Study. Gastrointest. Endosc. 2011, 74, 1094–1102. [Google Scholar] [CrossRef]
  16. Buchner, A.M.; Shahid, M.W.; Heckman, M.G.; Diehl, N.N.; McNeil, R.B.; Cleveland, P.; Gill, K.R.; Schore, A.; Ghabril, M.; Raimondo, M.; et al. Trainee Participation Is Associated with Increased Small Adenoma Detection. Gastrointest. Endosc. 2011, 73, 1223–1231. [Google Scholar] [CrossRef]
  17. Attardo, S.; Chandrasekar, V.T.; Spadaccini, M.; Maselli, R.; Patel, H.K.; Desai, M.; Capogreco, A.; Badalamenti, M.; Galtieri, P.A.; Pellegatta, G.; et al. Artificial Intelligence Technologies for the Detection of Colorectal Lesions: The Future Is Now. World J. Gastroenterol. 2020, 26, 5606–5616. [Google Scholar] [CrossRef]
  18. Sinagra, E.; Badalamenti, M.; Maida, M.; Spadaccini, M.; Maselli, R.; Rossi, F.; Conoscenti, G.; Raimondo, D.; Pallio, S.; Repici, A.; et al. Use of Artificial Intelligence in Improving Adenoma Detection Rate during Colonoscopy: Might Both Endoscopists and Pathologists Be Further Helped. World J. Gastroenterol. 2020, 26, 5911–5918. [Google Scholar] [CrossRef]
  19. Spadaccini, M.; Koleth, G.; Emmanuel, J.; Khalaf, K.; Facciorusso, A.; Grizzi, F.; Hassan, C.; Colombo, M.; Mangiavillano, B.; Fugazza, A.; et al. Enhanced Endoscopic Ultrasound Imaging for Pancreatic Lesions: The Road to Artificial Intelligence. World J. Gastroenterol. 2022, 28, 3814–3824. [Google Scholar] [CrossRef]
  20. Wang, P.; Liu, P.; Glissen Brown, J.R.; Berzin, T.M.; Zhou, G.; Lei, S.; Liu, X.; Li, L.; Xiao, X. Lower Adenoma Miss Rate of Computer-Aided Detection-Assisted Colonoscopy vs Routine White-Light Colonoscopy in a Prospective Tandem Study. Gastroenterology 2020, 159, 1252–1261.e5. [Google Scholar] [CrossRef]
  21. Hassan, C.; Spadaccini, M.; Iannone, A.; Maselli, R.; Jovani, M.; Chandrasekar, V.T.; Antonelli, G.; Yu, H.; Areia, M.; Dinis-Ribeiro, M.; 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. [Google Scholar] [CrossRef]
  22. Neumann, H.; Kreft, A.; Sivanathan, V.; Rahman, F.; Galle, P.R. Evaluation of Novel LCI CAD EYE System for Real Time Detection of Colon Polyps. PLoS ONE 2021, 16, e0255955. [Google Scholar] [CrossRef] [PubMed]
  23. Karkanis, S.A.; Iakovidis, D.K.; Maroulis, D.E.; Karras, D.A.; Tzivras, M. Computer-Aided Tumor Detection in Endoscopic Video Using Color Wavelet Features. IEEE Trans. Inf. Technol. Biomed. 2003, 7, 141–152. [Google Scholar] [CrossRef] [Green Version]
  24. Maroulis, D.E.; Iakovidis, D.K.; Karkanis, S.A.; Karras, D.A. CoLD: A Versatile Detection System for Colorectal Lesions in Endoscopy Video-Frames. Comput. Methods Programs Biomed. 2003, 70, 151–166. [Google Scholar] [CrossRef] [PubMed]
  25. Jerebko, A.; Lakare, S.; Cathier, P.; Periaswamy, S.; Bogoni, L. Symmetric Curvature Patterns for Colonic Polyp Detection. Med. Image Comput. Comput. Assist. Interv. 2006, 9, 169–176. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  26. Misawa, M.; Kudo, S.-E.; Mori, Y.; Cho, T.; Kataoka, S.; Yamauchi, A.; Ogawa, Y.; Maeda, Y.; Takeda, K.; Ichimasa, K.; et al. Artificial Intelligence-Assisted Polyp Detection for Colonoscopy: Initial Experience. Gastroenterology 2018, 154, 2027–2029.e3. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  27. Urban, G.; Tripathi, P.; Alkayali, T.; Mittal, M.; Jalali, F.; Karnes, W.; Baldi, P. Deep Learning Localizes and Identifies Polyps in Real Time With 96% Accuracy in Screening Colonoscopy. Gastroenterology 2018, 155, 1069–1078.e8. [Google Scholar] [CrossRef]
  28. Hassan, C.; Wallace, M.B.; Sharma, P.; Maselli, R.; Craviotto, V.; Spadaccini, M.; Repici, A. New Artificial Intelligence System: First Validation Study versus Experienced Endoscopists for Colorectal Polyp Detection. Gut 2020, 69, 799–800. [Google Scholar] [CrossRef]
  29. Su, J.-R.; Li, Z.; Shao, X.-J.; Ji, C.-R.; Ji, R.; Zhou, R.-C.; Li, G.-C.; Liu, G.-Q.; He, Y.-S.; Zuo, X.-L.; et al. Impact of a Real-Time Automatic Quality Control System on Colorectal Polyp and Adenoma Detection: A Prospective Randomized Controlled Study (with Videos). Gastrointest. Endosc. 2020, 91, 415–424.e4. [Google Scholar] [CrossRef]
  30. Repici, A.; Badalamenti, M.; Maselli, R.; Correale, L.; Radaelli, F.; Rondonotti, E.; Ferrara, E.; Spadaccini, M.; Alkandari, A.; Fugazza, A.; et al. Efficacy of Real-Time Computer-Aided Detection of Colorectal Neoplasia in a Randomized Trial. Gastroenterology 2020, 159, 512–520.e7. [Google Scholar] [CrossRef]
  31. Wang, P.; Berzin, T.M.; Glissen Brown, J.R.; Bharadwaj, S.; Becq, A.; Xiao, X.; Liu, P.; Li, L.; Song, Y.; Zhang, D.; et al. Real-Time Automatic Detection System Increases Colonoscopic Polyp and Adenoma Detection Rates: A Prospective Randomised Controlled Study. Gut 2019, 68, 1813–1819. [Google Scholar] [CrossRef] [Green Version]
  32. Gong, D.; Wu, L.; Zhang, J.; Mu, G.; Shen, L.; Liu, J.; Wang, Z.; Zhou, W.; An, P.; Huang, X.; et al. Detection of Colorectal Adenomas with a Real-Time Computer-Aided System (ENDOANGEL): A Randomised Controlled Study. Lancet Gastroenterol. Hepatol. 2020, 5, 352–361. [Google Scholar] [CrossRef] [PubMed]
  33. Wang, P.; Liu, X.; Berzin, T.M.; Glissen Brown, J.R.; Liu, P.; Zhou, C.; Lei, L.; Li, L.; Guo, Z.; Lei, S.; et al. Effect of a Deep-Learning Computer-Aided Detection System on Adenoma Detection during Colonoscopy (CADe-DB Trial): A Double-Blind Randomised Study. Lancet Gastroenterol. Hepatol. 2020, 5, 343–351. [Google Scholar] [CrossRef]
  34. Liu, W.-N.; Zhang, Y.-Y.; Bian, X.-Q.; Wang, L.-J.; Yang, Q.; Zhang, X.-D.; Huang, J. Study on Detection Rate of Polyps and Adenomas in Artificial-Intelligence-Aided Colonoscopy. Saudi J. Gastroenterol. 2020, 26, 13–19. [Google Scholar] [CrossRef]
  35. Repici, A.; Spadaccini, M.; Antonelli, G.; Correale, L.; Maselli, R.; Galtieri, P.A.; Pellegatta, G.; Capogreco, A.; Milluzzo, S.M.; Lollo, G.; et al. Artificial Intelligence and Colonoscopy Experience: Lessons from Two Randomised Trials. Gut 2022, 71, 757–765. [Google Scholar] [CrossRef]
  36. Yao, L.; Zhang, L.; Liu, J.; Zhou, W.; He, C.; Zhang, J.; Wu, L.; Wang, H.; Xu, Y.; Gong, D.; et al. Effect of an Artificial Intelligence-Based Quality Improvement System on Efficacy of a Computer-Aided Detection System in Colonoscopy: A Four-Group Parallel Study. Endoscopy 2022, 54, 757–768. [Google Scholar] [CrossRef]
  37. Liu, P.; Wang, P.; Glissen Brown, J.R.; Berzin, T.M.; Zhou, G.; Liu, W.; Xiao, X.; Chen, Z.; Zhang, Z.; Zhou, C.; et al. The Single-Monitor Trial: An Embedded CADe System Increased Adenoma Detection during Colonoscopy: A Prospective Randomized Study. Therap. Adv. Gastroenterol. 2020, 13, 1756284820979165. [Google Scholar] [CrossRef]
  38. Rondonotti, E.; Di Paolo, D.; Rizzotto, E.R.; Alvisi, C.; Buscarini, E.; Spadaccini, M.; Tamanini, G.; Paggi, S.; Amato, A.; Scardino, G.; et al. Efficacy of a Computer-Aided Detection System in a Fecal Immunochemical Test-Based Organized Colorectal Cancer Screening Program: A Randomized Controlled Trial (AIFIT Study). Endoscopy 2022, 54, 1171–1179. [Google Scholar] [CrossRef]
  39. Shaukat, A.; Lichtenstein, D.R.; Somers, S.C.; Chung, D.C.; Perdue, D.G.; Gopal, M.; Colucci, D.R.; Phillips, S.A.; Marka, N.A.; Church, T.R.; et al. Computer-Aided Detection Improves Adenomas per Colonoscopy for Screening and Surveillance Colonoscopy: A Randomized Trial. Gastroenterology 2022, 163, 732–741. [Google Scholar] [CrossRef]
  40. Aniwan, S.; Mekritthikrai, K.; Kerr, S.J.; Tiankanon, K.; Vandaungden, K.; Sritunyarat, Y.; Piyachaturawat, P.; Luangsukrerk, T.; Kulpatcharapong, S.; Wisedopas, N.; et al. Computer-Aided Detection, Mucosal Exposure Device, Their Combination, and Standard Colonoscopy for Adenoma Detection: A Randomized Controlled Trial. Gastrointest. Endosc. 2023, 97, 507–516. [Google Scholar] [CrossRef]
  41. Gimeno-García, A.Z.; Negrin, D.H.; Hernández, A.; Nicolás-Pérez, D.; Rodríguez, E.; Montesdeoca, C.; Alarcon, O.; Romero, R.; Baute Dorta, J.L.; Cedrés, Y.; et al. Usefulness of a Novel Computer-Aided Detection System for Colorectal Neoplasia: A Randomized Controlled Trial. Gastrointest. Endosc. 2022. [Google Scholar] [CrossRef]
  42. Spadaccini, M.; Iannone, A.; Maselli, R.; Badalamenti, M.; Desai, M.; Chandrasekar, V.T.; Patel, H.K.; Fugazza, A.; Pellegatta, G.; Galtieri, P.A.; et al. Computer-Aided Detection versus Advanced Imaging for Detection of Colorectal Neoplasia: A Systematic Review and Network Meta-Analysis. Lancet Gastroenterol. Hepatol. 2021, 6, 793–802. [Google Scholar] [CrossRef] [PubMed]
  43. Kamba, S.; Tamai, N.; Saitoh, I.; Matsui, H.; Horiuchi, H.; Kobayashi, M.; Sakamoto, T.; Ego, M.; Fukuda, A.; Tonouchi, A.; et al. Reducing Adenoma Miss Rate of Colonoscopy Assisted by Artificial Intelligence: A Multicenter Randomized Controlled Trial. J. Gastroenterol. 2021, 56, 746–757. [Google Scholar] [CrossRef] [PubMed]
  44. Glissen Brown, J.R.; Mansour, N.M.; Wang, P.; Chuchuca, M.A.; Minchenberg, S.B.; Chandnani, M.; Liu, L.; Gross, S.A.; Sengupta, N.; Berzin, T.M. Deep Learning Computer-Aided Polyp Detection Reduces Adenoma Miss Rate: A United States Multi-Center Randomized Tandem Colonoscopy Study (CADeT-CS Trial). Clin. Gastroenterol. Hepatol. 2022, 20, 1499–1507.e4. [Google Scholar] [CrossRef]
  45. Wallace, M.B.; Sharma, P.; Bhandari, P.; East, J.; Antonelli, G.; Lorenzetti, R.; Vieth, M.; Speranza, I.; Spadaccini, M.; Desai, M.; et al. Impact of Artificial Intelligence on Miss Rate of Colorectal Neoplasia. Gastroenterology 2022, 163, 295–304.e5. [Google Scholar] [CrossRef] [PubMed]
  46. Gubbiotti, A.; Spadaccini, M.; Badalamenti, M.; Hassan, C.; Repici, A. Key Factors for Improving Adenoma Detection Rate. Expert Rev. Gastroenterol. Hepatol. 2022, 16, 819–833. [Google Scholar] [CrossRef] [PubMed]
  47. Istituto Clinico Humanitas. The CERTAIN Study: Combining Endo-Cuff in a Randomized Trial for Artificial Intelligence Navigation; U.S. National Library of Medicine: Rozzano, Italy, 2022. [Google Scholar]
  48. Spadaccini, M.; Mönkemüller, K. Commentary. Endoscopy 2022, 54, 1124. [Google Scholar] [CrossRef] [PubMed]
  49. Hassan, C.; Mori, Y.; Sharma, P.; Spadaccini, M.; Repici, A. Detrimental Detection of Advanced Lesions With AI: False Confidence or Prevalence Bias? Am. J. Gastroenterol. 2022, 117, 2088–2089. [Google Scholar] [CrossRef]
  50. Areia, M.; Mori, Y.; Correale, L.; Repici, A.; Bretthauer, M.; Sharma, P.; Taveira, F.; Spadaccini, M.; Antonelli, G.; Ebigbo, A.; et al. Cost-Effectiveness of Artificial Intelligence for Screening Colonoscopy: A Modelling Study. Lancet Digit. Health 2022, 4, e436–e444. [Google Scholar] [CrossRef]
  51. Wisse, P.H.A.; Erler, N.S.; de Boer, S.Y.; den Hartog, B.; Oudkerk Pool, M.; Terhaar Sive Droste, J.S.; Verveer, C.; Meijer, G.A.; Lansdorp-Vogelaar, I.; Kuipers, E.J.; et al. Adenoma Detection Rate and Risk for Interval Postcolonoscopy Colorectal Cancer in Fecal Immunochemical Test-Based Screening: A Population-Based Cohort Study. Ann. Intern. Med. 2022, 175, 1366–1373. [Google Scholar] [CrossRef]
  52. Van Toledo, D.E.F.W.M.; IJspeert, J.E.G.; Dekker, E. Current Approaches in Managing Colonic Serrated Polyps and Serrated Polyposis. Annu. Rev. Med. 2022, 73, 293–306. [Google Scholar] [CrossRef] [PubMed]
  53. Van Toledo, D.E.F.W.M.; Breekveldt, E.C.H.; IJspeert, J.E.G.; van Vuuren, A.J.; van Kemenade, F.J.; Ramakers, C.; Nagtegaal, I.D.; van Leerdam, M.E.; Spaander, M.C.W.; Lansdorp-Vogelaar, I.; et al. Advanced Serrated Polyps as a Target of Screening: Detection Rate and Positive Predictive Value within a Fecal Immunochemical Test-Based Colorectal Cancer Screening Population. Endoscopy 2023. online ahead of print. [Google Scholar] [CrossRef] [PubMed]
  54. Hetzel, J.T.; Huang, C.S.; Coukos, J.A.; Omstead, K.; Cerda, S.R.; Yang, S.; O’Brien, M.J.; Farraye, F.A. Variation in the Detection of Serrated Polyps in an Average Risk Colorectal Cancer Screening Cohort. Am. J. Gastroenterol. 2010, 105, 2656–2664. [Google Scholar] [CrossRef] [PubMed]
  55. Zessner-Spitzenberg, J.; Waldmann, E.; Jiricka, L.; Rockenbauer, L.-M.; Hinterberger, A.; Cook, J.; Asaturi, A.; Szymanska, A.; Majcher, B.; Trauner, M.; et al. Comparison of Adenoma Detection Rate and Proximal Serrated Polyp Detection Rate and Their Effect on Post-Colonoscopy Colorectal Cancer Mortality in Screening Patients. Endoscopy 2022. online ahead of print. [Google Scholar] [CrossRef] [PubMed]
  56. Mori, Y.; Wang, P.; Løberg, M.; Misawa, M.; Repici, A.; Spadaccini, M.; Correale, L.; Antonelli, G.; Yu, H.; Gong, D.; et al. Impact of Artificial Intelligence on Colonoscopy Surveillance After Polyp Removal: A Pooled Analysis of Randomized Trials. Clin. Gastroenterol. Hepatol. 2022. [Google Scholar] [CrossRef] [PubMed]
  57. Duvvuri, A.; Chandrasekar, V.T.; Srinivasan, S.; Narimiti, A.; Dasari, C.; Nutalapati, V.; Kennedy, K.F.; Spadaccini, M.; Antonelli, G.; Desai, M.; et al. Risk of Colorectal Cancer and Cancer Related Mortality After Detection of Low-Risk or High-Risk Adenomas, Compared With No Adenoma, at Index Colonoscopy: A Systematic Review and Meta-Analysis. Gastroenterology 2021, 160, 1986–1996.e3. [Google Scholar] [CrossRef] [PubMed]
  58. Abu-Freha, N.; Katz, L.H.; Kariv, R.; Vainer, E.; Laish, I.; Gluck, N.; Half, E.E.; Levi, Z. Post-Polypectomy Surveillance Colonoscopy: Comparison of the Updated Guidelines. United Eur. Gastroenterol. J. 2021, 9, 681–687. [Google Scholar] [CrossRef] [PubMed]
  59. Hassan, C.; Antonelli, G.; Dumonceau, J.-M.; Regula, J.; Bretthauer, M.; Chaussade, S.; Dekker, E.; Ferlitsch, M.; Gimeno-Garcia, A.; Jover, R.; et al. Post-Polypectomy Colonoscopy Surveillance: European Society of Gastrointestinal Endoscopy (ESGE) Guideline—Update 2020. Endoscopy 2020, 52, 687–700. [Google Scholar] [CrossRef] [PubMed]
  60. Rees, C.J.; Rajasekhar, P.T.; Wilson, A.; Close, H.; Rutter, M.D.; Saunders, B.P.; East, J.E.; Maier, R.; Moorghen, M.; Muhammad, U.; et al. Narrow Band Imaging Optical Diagnosis of Small Colorectal Polyps in Routine Clinical Practice: The Detect Inspect Characterise Resect and Discard 2 (DISCARD 2) Study. Gut 2017, 66, 887–895. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  61. Rex, D.K.; Kahi, C.; O’Brien, M.; Levin, T.R.; Pohl, H.; Rastogi, A.; Burgart, L.; Imperiale, T.; Ladabaum, U.; Cohen, J.; et al. The American Society for Gastrointestinal Endoscopy PIVI (Preservation and Incorporation of Valuable Endoscopic Innovations) on Real-Time Endoscopic Assessment of the Histology of Diminutive Colorectal Polyps. Gastrointest. Endosc. 2011, 73, 419–422. [Google Scholar] [CrossRef] [PubMed]
  62. Houwen, B.B.S.L.; Hassan, C.; Coupé, V.M.H.; Greuter, M.J.E.; Hazewinkel, Y.; Vleugels, J.L.A.; Antonelli, G.; Bustamante-Balén, M.; Coron, E.; Cortas, G.A.; et al. Definition of Competence Standards for Optical Diagnosis of Diminutive Colorectal Polyps: European Society of Gastrointestinal Endoscopy (ESGE) Position Statement. Endoscopy 2022, 54, 88–99. [Google Scholar] [CrossRef]
  63. Tischendorf, J.J.W.; Gross, S.; Winograd, R.; Hecker, H.; Auer, R.; Behrens, A.; Trautwein, C.; Aach, T.; Stehle, T. Computer-Aided Classification of Colorectal Polyps Based on Vascular Patterns: A Pilot Study. Endoscopy 2010, 42, 203–207. [Google Scholar] [CrossRef]
  64. Gross, S.; Trautwein, C.; Behrens, A.; Winograd, R.; Palm, S.; Lutz, H.H.; Schirin-Sokhan, R.; Hecker, H.; Aach, T.; Tischendorf, J.J.W. Computer-Based Classification of Small Colorectal Polyps by Using Narrow-Band Imaging with Optical Magnification. Gastrointest. Endosc. 2011, 74, 1354–1359. [Google Scholar] [CrossRef]
  65. Kominami, Y.; Yoshida, S.; Tanaka, S.; Sanomura, Y.; Hirakawa, T.; Raytchev, B.; Tamaki, T.; Koide, T.; Kaneda, K.; Chayama, K. Computer-Aided Diagnosis of Colorectal Polyp Histology by Using a Real-Time Image Recognition System and Narrow-Band Imaging Magnifying Colonoscopy. Gastrointest. Endosc. 2016, 83, 643–649. [Google Scholar] [CrossRef]
  66. Mori, Y.; Kudo, S.-E.; Misawa, M.; Saito, Y.; Ikematsu, H.; Hotta, K.; Ohtsuka, K.; Urushibara, F.; Kataoka, S.; Ogawa, Y.; et al. Real-Time Use of Artificial Intelligence in Identification of Diminutive Polyps During Colonoscopy: A Prospective Study. Ann. Intern. Med. 2018, 169, 357–366. [Google Scholar] [CrossRef] [PubMed]
  67. Byrne, M.F.; Chapados, N.; Soudan, F.; Oertel, C.; Linares Pérez, M.; Kelly, R.; Iqbal, N.; Chandelier, F.; Rex, D.K. Real-Time Differentiation of Adenomatous and Hyperplastic Diminutive Colorectal Polyps during Analysis of Unaltered Videos of Standard Colonoscopy Using a Deep Learning Model. Gut 2019, 68, 94–100. [Google Scholar] [CrossRef] [Green Version]
  68. Zorron Cheng Tao Pu, L.; Maicas, G.; Tian, Y.; Yamamura, T.; Nakamura, M.; Suzuki, H.; Singh, G.; Rana, K.; Hirooka, Y.; Burt, A.D.; et al. Computer-Aided Diagnosis for Characterization of Colorectal Lesions: Comprehensive Software That Includes Differentiation of Serrated Lesions. Gastrointest. Endosc. 2020, 92, 891–899. [Google Scholar] [CrossRef] [PubMed]
  69. Hassan, C.; Balsamo, G.; Lorenzetti, R.; Zullo, A.; Antonelli, G. Artificial Intelligence Allows Leaving-In-Situ Colorectal Polyps. Clin. Gastroenterol. Hepatol. 2022, 20, 2505–2513.e4. [Google Scholar] [CrossRef] [PubMed]
  70. Rondonotti, E.; Hassan, C.; Tamanini, G.; Antonelli, G.; Andrisani, G.; Leonetti, G.; Paggi, S.; Amato, A.; Scardino, G.; Di Paolo, D.; et al. Artificial Intelligence-Assisted Optical Diagnosis for the Resect-and-Discard Strategy in Clinical Practice: The Artificial Intelligence BLI Characterization (ABC) Study. Endoscopy 2023, 55, 14–22. [Google Scholar] [CrossRef]
  71. Hassan, C.; Sharma, P.; Mori, Y.; Bretthauer, M.; Rex, D.K.; EUROCARE Working Group; Repici, A. Comparative Performance of Artificial Intelligence Optical Diagnosis Systems for Leaving in Situ Colorectal Polyps. Gastroenterology 2022, 164, 467–469. [Google Scholar] [CrossRef]
  72. Song, E.M.; Park, B.; Ha, C.-A.; Hwang, S.W.; Park, S.H.; Yang, D.-H.; Ye, B.D.; Myung, S.-J.; Yang, S.-K.; Kim, N.; et al. Endoscopic Diagnosis and Treatment Planning for Colorectal Polyps Using a Deep-Learning Model. Sci. Rep. 2020, 10, 30. [Google Scholar] [CrossRef] [Green Version]
  73. Jin, E.H.; Lee, D.; Bae, J.H.; Kang, H.Y.; Kwak, M.-S.; Seo, J.Y.; Yang, J.I.; Yang, S.Y.; Lim, S.H.; Yim, J.Y.; et al. Improved Accuracy in Optical Diagnosis of Colorectal Polyps Using Convolutional Neural Networks with Visual Explanations. Gastroenterology 2020, 158, 2169–2179.e8. [Google Scholar] [CrossRef] [PubMed]
  74. Mori, Y.; Kudo, S.-E.; East, J.E.; Rastogi, A.; Bretthauer, M.; Misawa, M.; Sekiguchi, M.; Matsuda, T.; Saito, Y.; Ikematsu, H.; et al. Cost Savings in Colonoscopy with Artificial Intelligence-Aided Polyp Diagnosis: An Add-on Analysis of a Clinical Trial (with Video). Gastrointest. Endosc. 2020, 92, 905–911.e1. [Google Scholar] [CrossRef]
  75. Mori, Y.; Neumann, H.; Misawa, M.; Kudo, S.-E.; Bretthauer, M. Artificial Intelligence in Colonoscopy—Now on the Market. What’s Next? J. Gastroenterol. Hepatol. 2021, 36, 7–11. [Google Scholar] [CrossRef]
  76. Zhou, J.; Wu, L.; Wan, X.; Shen, L.; Liu, J.; Zhang, J.; Jiang, X.; Wang, Z.; Yu, S.; Kang, J.; et al. A Novel Artificial Intelligence System for the Assessment of Bowel Preparation (with Video). Gastrointest. Endosc. 2020, 91, 428–435.e2. [Google Scholar] [CrossRef]
  77. Karnes, W.E.; Ninh, A.; Dao, T.; Requa, J.; Samarasena, J.B. Sa1940 Unambiguous real-time scoring of bowel preparation using artificial intelligence. Gastrointest. Endosc. 2018, 87, AB258. [Google Scholar] [CrossRef]
  78. Wu, L.; Zhang, J.; Zhou, W.; An, P.; Shen, L.; Liu, J.; Jiang, X.; Huang, X.; Mu, G.; Wan, X.; et al. Randomised Controlled Trial of WISENSE, a Real-Time Quality Improving System for Monitoring Blind Spots during Esophagogastroduodenoscopy. Gut 2019, 68, 2161–2169. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  79. Chen, D.; Wu, L.; Li, Y.; Zhang, J.; Liu, J.; Huang, L.; Jiang, X.; Huang, X.; Mu, G.; Hu, S.; et al. Comparing Blind Spots of Unsedated Ultrafine, Sedated, and Unsedated Conventional Gastroscopy with and without Artificial Intelligence: A Prospective, Single-Blind, 3-Parallel-Group, Randomized, Single-Center Trial. Gastrointest. Endosc. 2020, 91, 332–339.e3. [Google Scholar] [CrossRef] [PubMed]
  80. McGill, S.K.; Rosenman, J.; Wang, R.; Ma, R.; Frahm, J.-M.; Pizer, S. Artificial Intelligence Identifies and Quantifies Colonoscopy Blind Spots. Endoscopy 2021, 53, 1284–1286. [Google Scholar] [CrossRef] [PubMed]
  81. Requa, J.; Dao, T.; Ninh, A.; Karnes, W. Can a Convolutional Neural Network Solve the Polyp Size Dilemma? Category Award (Colorectal Cancer Prevention) Presidential Poster Award: 282. Off. J. Am. Coll. Gastroenterol.|ACG 2018, 113, S158. [Google Scholar] [CrossRef]
  82. Abdelrahim, M.; Saiga, H.; Maeda, N.; Hossain, E.; Ikeda, H.; Bhandari, P. Automated Sizing of Colorectal Polyps Using Computer Vision. Gut 2022, 71, 7–9. [Google Scholar] [CrossRef]
  83. Van der Sommen, F.; de Groof, J.; Struyvenberg, M.; van der Putten, J.; Boers, T.; Fockens, K.; Schoon, E.J.; Curvers, W.; de With, P.; Mori, Y.; et al. Machine Learning in GI Endoscopy: Practical Guidance in How to Interpret a Novel Field. Gut 2020, 69, 2035–2045. [Google Scholar] [CrossRef]
  84. Hoogenboom, S.A.; Bagci, U.; Wallace, M.B. Artificial Intelligence in Gastroenterology. The Current State of Play and the Potential. How Will It Affect Our Practice and When? Tech. Innov. Gastrointest. Endosc. 2020, 22, 42–47. [Google Scholar] [CrossRef]
  85. Lui, T.K.L.; Guo, C.-G.; Leung, W.K. Accuracy of Artificial Intelligence on Histology Prediction and Detection of Colorectal Polyps: A Systematic Review and Meta-Analysis. Gastrointest. Endosc. 2020, 92, 11–22.e6. [Google Scholar] [CrossRef]
  86. Greenhill, A.T.; Edmunds, B.R. A Primer of Artificial Intelligence in Medicine. Tech. Innov. Gastrointest. Endosc. 2020, 22, 85–89. [Google Scholar] [CrossRef]
  87. Vinsard, D.G.; Mori, Y.; Misawa, M.; Kudo, S.-E.; Rastogi, A.; Bagci, U.; Rex, D.K.; Wallace, M.B. Quality Assurance of Computer-Aided Detection and Diagnosis in Colonoscopy. Gastrointest. Endosc. 2019, 90, 55–63. [Google Scholar] [CrossRef] [Green Version]
  88. Antonelli, G.; Gkolfakis, P.; Tziatzios, G.; Papanikolaou, I.S.; Triantafyllou, K.; Hassan, C. Artificial Intelligence-Aided Colonoscopy: Recent Developments and Future Perspectives. World J. Gastroenterol. 2020, 26, 7436–7443. [Google Scholar] [CrossRef]
  89. Hassan, C.; Badalamenti, M.; Maselli, R.; Correale, L.; Iannone, A.; Radaelli, F.; Rondonotti, E.; Ferrara, E.; Spadaccini, M.; Alkandari, A.; et al. Computer-Aided Detection-Assisted Colonoscopy: Classification and Relevance of False Positives. Gastrointest. Endosc. 2020, 92, 900–904.e4. [Google Scholar] [CrossRef] [PubMed]
  90. Spadaccini, M.; Hassan, C.; Alfarone, L.; Da Rio, L.; Maselli, R.; Carrara, S.; Galtieri, P.A.; Pellegatta, G.; Fugazza, A.; Koleth, G.; et al. Comparing the Number and Relevance of False Activations between 2 Artificial Intelligence Computer-Aided Detection Systems: The NOISE Study. Gastrointest. Endosc. 2022, 95, 975–981.e1. [Google Scholar] [CrossRef]
  91. Koleth, G.; Emmanue, J.; Spadaccini, M.; Mascagni, P.; Khalaf, K.; Mori, Y.; Antonelli, G.; Maselli, R.; Carrara, S.; Galtieri, P.A.; et al. Artificial Intelligence in Gastroenterology: Where Are We Heading? Endosc. Int. Open 2022, 10, E1474–E1480. [Google Scholar] [CrossRef]
  92. Messmann, H.; Bisschops, R.; Antonelli, G.; Libânio, D.; Sinonquel, P.; Abdelrahim, M.; Ahmad, O.F.; Areia, M.; Bergman, J.J.G.H.M.; Bhandari, P.; et al. Expected Value of Artificial Intelligence in Gastrointestinal Endoscopy: European Society of Gastrointestinal Endoscopy (ESGE) Position Statement. Endoscopy 2022, 54, 1211–1231. [Google Scholar] [CrossRef] [PubMed]
Figure 1. Neural networks and subsets of artificial intelligence.
Figure 1. Neural networks and subsets of artificial intelligence.
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Figure 2. Application of a Computer-Aided Detection (CADe) system (GI-Genius, Medtronic Corp, Minneapolis, MN, USA).
Figure 2. Application of a Computer-Aided Detection (CADe) system (GI-Genius, Medtronic Corp, Minneapolis, MN, USA).
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Figure 3. Application of a Computer-Aided Characterization (CADx) system (CAD-EYE, Fujifilm, Japan).
Figure 3. Application of a Computer-Aided Characterization (CADx) system (CAD-EYE, Fujifilm, Japan).
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Figure 4. Example of false positive activation of two different Computer-Aided Detection systems due to colonic fold and stool residue.
Figure 4. Example of false positive activation of two different Computer-Aided Detection systems due to colonic fold and stool residue.
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Table 1. Parallel Randomized Controlled Trials.
Table 1. Parallel Randomized Controlled Trials.
PublicationCountryStudy TypeNumber of PatientsGenderMean AgeIndicationAdenoma Detection Rate (%)AI System
TotalAI-Assisted
Colonoscopy
Standard
Colonoscopy
MenWomenScreeningNon-ScreeningAI-Assisted
Colonoscopy
Standard
Colonoscopy
Wang, P. 2019ChinaSingle Center105852253651254650849742920EndoScreener
Wang, P. 2020ChinaSingle Center962484478495467491588043428EndoScreener
Liu, P. 2020ChinaSingle Center102650851855147550669603924EndoScreener
Gong, D. 2020ChinaSingle Center7043553493453595036668168ENDOANGEL
Repici, A. 2020ItalyMulti center685341344336348615241615540GI GENIUS
Medtronic
Su, J.-R. 2020ChinaSingle Center623315308307316512164072917Self-Developed
Repici, A. 2021ItalyMulti center660330330330330622454155345GI GENIUS
Medtronic
Yao, L. 2021ChinaSingle Center5392682712353045153452115ENDOANGEL
Liu, P. 2021ChinaSingle Center790393397374416491826082919EndoScreener
Rondonotti, E. 2022ItalyMulti center8004053954093916180005345CAD EYE
FujiFilm
Shaukat, A. 2022USAMulti center135968267772363660135904844SKOUT
device
Aniwan, S. 2022ThailandSingle Center62231231026635662\\5242CAD EYE
FujiFilm
Gimeno-Garcia, A.Z. 2022SpainSingle Center312155157165147642061065745ENDO AID
Olympus
Table 2. Tandem Randomized Controlled Trials.
Table 2. Tandem Randomized Controlled Trials.
PublicationCountryStudy TypeNumber of PatientsGenderMean
Age
IndicationAdenoma Detection Rate (%)AI System
TotalAI-Assisted
Colonoscopy
Standard
Colonoscopy
MenWomenScreeningNon-ScreeningAI-Assisted
Colonoscopy
Standard
Colonoscopy
Wang, P.
2020
ChinaSingle Center369184185179190471132563526EndoScreener
Kamba, S. 2021JapanMulti
center
2951781172722362228676553Self-Developed
Glissen Brown, J.R.
2021
USAMulti
Center
22311311012210161133905044EndoScreener
Wallace, M.B. 2022ItalyMulti
center
230116114157736423006261GI GENIUS
Medtronic
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Spadaccini, M.; Massimi, D.; Mori, Y.; Alfarone, L.; Fugazza, A.; Maselli, R.; Sharma, P.; Facciorusso, A.; Hassan, C.; Repici, A. Artificial Intelligence-Aided Endoscopy and Colorectal Cancer Screening. Diagnostics 2023, 13, 1102. https://doi.org/10.3390/diagnostics13061102

AMA Style

Spadaccini M, Massimi D, Mori Y, Alfarone L, Fugazza A, Maselli R, Sharma P, Facciorusso A, Hassan C, Repici A. Artificial Intelligence-Aided Endoscopy and Colorectal Cancer Screening. Diagnostics. 2023; 13(6):1102. https://doi.org/10.3390/diagnostics13061102

Chicago/Turabian Style

Spadaccini, Marco, Davide Massimi, Yuichi Mori, Ludovico Alfarone, Alessandro Fugazza, Roberta Maselli, Prateek Sharma, Antonio Facciorusso, Cesare Hassan, and Alessandro Repici. 2023. "Artificial Intelligence-Aided Endoscopy and Colorectal Cancer Screening" Diagnostics 13, no. 6: 1102. https://doi.org/10.3390/diagnostics13061102

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