Effect of an artificial intelligence-assisted system on endoscopic diagnosis of superficial oesophageal squamous cell carcinoma and precancerous lesions: a multicentre, tandem, double-blind, randomised controlled trial.

IF 5.5 2区 化学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Biomacromolecules Pub Date : 2024-01-01 Epub Date: 2023-11-10 DOI:10.1016/S2468-1253(23)00276-5
Xiang-Lei Yuan, Wei Liu, Yi-Xiu Lin, Qian-Yi Deng, Yuan-Ping Gao, Ling Wan, Bin Zhang, Tao Zhang, Wan-Hong Zhang, Xiao-Gang Bi, Guo-Dong Yang, Bi-Hui Zhu, Fan Zhang, Xiao-Bo Qin, Feng Pan, Xian-Hui Zeng, Hunza Chaudhry, Mao-Yin Pang, Juliana Yang, Jing-Yu Zhang, Bing Hu
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引用次数: 0

Abstract

Background: Despite the usefulness of white light endoscopy (WLE) and non-magnified narrow-band imaging (NBI) for screening for superficial oesophageal squamous cell carcinoma and precancerous lesions, these lesions might be missed due to their subtle features and interpretation variations among endoscopists. Our team has developed an artificial intelligence (AI) system to detect superficial oesophageal squamous cell carcinoma and precancerous lesions using WLE and non-magnified NBI. We aimed to evaluate the auxiliary diagnostic performance of the AI system in a real clinical setting.

Methods: We did a multicentre, tandem, double-blind, randomised controlled trial at 12 hospitals in China. Eligible patients were aged 18 years or older and underwent sedated upper gastrointestinal endoscopy for screening, investigation of gastrointestinal symptoms, or surveillance. Patients were randomly assigned (1:1) to either the AI-first group or the routine-first group using a computerised random number generator. Patients, pathologists, and statistical analysts were masked to group assignment, whereas endoscopists and research assistants were not. The same endoscopist at each centre did tandem upper gastrointestinal endoscopy for each eligible patient on the same day. In the AI-first group, the endoscopist did the first examination with the assistance of the AI system and the second examination without it. In the routine-first group, the order of examinations was reversed. The primary outcome was the miss rate of superficial oesophageal squamous cell carcinoma and precancerous lesions, calculated on a per-lesion and per-patient basis. All analyses were done on a per-protocol basis. This trial is registered with the Chinese Clinical Trial Registry (ChiCTR2100052116) and is completed.

Findings: Between Oct 19, 2021, and June 8, 2022, 5934 patients were randomly assigned to the AI-first group and 5912 to the routine-first group, of whom 5865 and 5850 were eligible for analysis. Per-lesion miss rates were 1·7% (2/118; 95% CI 0·0-4·0) in the AI-first group versus 6·7% (6/90; 1·5-11·8) in the routine-first group (risk ratio 0·25, 95% CI 0·06-1·08; p=0·079). Per-patient miss rates were 1·9% (2/106; 0·0-4·5) in AI-first group versus 5·1% (4/79; 0·2-9·9) in the routine-first group (0·37, 0·08-1·71; p=0·40). Bleeding after biopsy of oesophageal lesions was observed in 13 (0·2%) patients in the AI-first group and 11 (0·2%) patients in the routine-first group. No serious adverse events were reported by patients in either group.

Interpretation: The observed effect of AI-assisted endoscopy on the per-lesion and per-patient miss rates of superficial oesophageal squamous cell carcinoma and precancerous lesions under WLE and non-magnified NBI was consistent with substantial benefit through to a neutral or small negative effect. The effectiveness and cost-benefit of this AI system in real-world clinical settings remain to be further assessed.

Funding: National Natural Science Foundation of China, 1·3·5 project for disciplines of excellence, West China Hospital, Sichuan University, and Chengdu Science and Technology Project.

Translation: For the Chinese translation of the abstract see Supplementary Materials section.

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人工智能辅助系统对食管浅表鳞状细胞癌和癌前病变内镜诊断的影响:一项多中心、串联、双盲、随机对照试验。
背景:尽管白光内镜(WLE)和非放大窄带成像(NBI)在筛查浅表食管鳞状细胞癌和癌前病变方面很有用,但由于这些病变的细微特征和内镜医师对其解释的差异,这些病变可能会被遗漏。我们的团队开发了一种人工智能(AI)系统,可以使用WLE和非放大NBI检测浅表食管鳞状细胞癌和癌前病变。我们旨在评估人工智能系统在真实临床环境中的辅助诊断性能。方法:我们在中国12家医院进行了多中心、串联、双盲、随机对照试验。符合条件的患者年龄在18岁或以上,并接受了镇静的上消化道内窥镜检查,以进行筛查、胃肠道症状调查或监测。使用计算机化随机数发生器将患者随机(1:1)分配到人工智能优先组或常规优先组。患者、病理学家和统计分析人员被分组分配,而内窥镜医师和研究助理则没有。每个中心的同一位内窥镜医师在同一天为每位符合条件的患者进行串联上消化道内窥镜检查。在AI-first组中,内镜医师在AI系统的帮助下进行第一次检查,第二次检查没有AI系统的帮助。在常规第一组中,检查顺序颠倒。主要结果是浅表食管鳞状细胞癌和癌前病变的漏报率,以每个病变和每个患者为基础计算。所有的分析都是在每个方案的基础上完成的。该试验已在中国临床试验注册中心注册(ChiCTR2100052116),并已完成。研究结果:在2021年10月19日至2022年6月8日期间,5934名患者被随机分配到人工智能优先组,5912名患者被随机分配到常规优先组,其中5865名和5850名患者符合分析条件。单个病灶漏诊率为1.7% (2/118;AI-first组的95% CI为0- 4.0,而AI-first组为6.7% (6/90;(风险比0.25,95% CI 0.06 - 1.08;p = 0·079)。每例漏诊率为1.9% (2/106;AI-first组为0·0-4·5),而AI-first组为5.1% (4/79;常规第一组(0.37,0.08 - 1.71;p = 0·40)。AI-first组有13例(0.2%)食管病变活检后出血,而常规-first组有11例(0.2%)。两组患者均未报告严重不良事件。解释:观察到人工智能辅助内镜对WLE和非放大NBI下浅表食管鳞状细胞癌和癌前病变的每个病变和每个患者的漏检率的影响,从实质性的获益到中性或小的负面影响都是一致的。这种人工智能系统在现实世界临床环境中的有效性和成本效益仍有待进一步评估。资助项目:国家自然科学基金、1·3·5优秀学科专项、四川大学华西医院、成都科技项目。翻译:摘要的中文翻译见补充资料部分。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biomacromolecules
Biomacromolecules 化学-高分子科学
CiteScore
10.60
自引率
4.80%
发文量
417
审稿时长
1.6 months
期刊介绍: Biomacromolecules is a leading forum for the dissemination of cutting-edge research at the interface of polymer science and biology. Submissions to Biomacromolecules should contain strong elements of innovation in terms of macromolecular design, synthesis and characterization, or in the application of polymer materials to biology and medicine. Topics covered by Biomacromolecules include, but are not exclusively limited to: sustainable polymers, polymers based on natural and renewable resources, degradable polymers, polymer conjugates, polymeric drugs, polymers in biocatalysis, biomacromolecular assembly, biomimetic polymers, polymer-biomineral hybrids, biomimetic-polymer processing, polymer recycling, bioactive polymer surfaces, original polymer design for biomedical applications such as immunotherapy, drug delivery, gene delivery, antimicrobial applications, diagnostic imaging and biosensing, polymers in tissue engineering and regenerative medicine, polymeric scaffolds and hydrogels for cell culture and delivery.
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