[摘要]LB015:基于Paris系统的人工智能尿细胞病理报告算法的临床评价

Wei-Lei Yang, Jen-Fan Hang, Chi-Bin Li, Ching-Ming Lee, Yi-Sheng Lin, T. Tsao, M. Chang, Y. Ou, Tien-Jen Liu
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METHODS: A total of 131 urine cytology slides from bladder cancer patients, either first diagnosis or post-treatment follow-up, were retrieved and digitized as whole slide images (WSIs). A deep learning-based computational model was used to analyze these WSIs. Candidate urothelial cells were automatically highlighted and classified into high-risk and low-risk atypia categories in each sample based on TPS criteria. Slide-wide statistical data, including a total number of high-risk and low-risk cells, nuclear-cytoplasmic ratio (N:C ratio) and nuclear area for each cell, and the distribution and mean values of these variables, were also provided. In a blind study, a cytotechnologist and a cytopathologist parallelly reviewed the AI-annotated images and quantitative data for each WSI sample. Suspicious for HUGC and HGUC were considered to be \"positive\" and the other diagnostic categories were considered to be \"negative\" according to whether trigger cystoscopy. The results were compared with the final diagnosis reviewed by a senior cytopathologist via microscopy to evaluate the performance of the AI-assisted model. RESULTS: There were 35 positive and 96 negative urine cytology samples based on the final diagnosis. The AI algorithm annotated a total of 26,502 cells and a mean of 757.2 cells at cancer risk from all positive samples and a total of 950 cells and a mean of 9.9 cells at cancer risk from all negative samples. The mean N:C ratio was 0.68 for high-risk atypical cells and 0.56 for low-risk atypical cells. The performance of the AI-assisted reports of the cytotechnologist was 88.6% sensitivity, 97.9% specificity, 93.9% positive prediction value (PPV), and 95.9% negative prediction value (NPV) and the cytopathologist was 91.4% sensitivity, 95.8% specificity, 88.9% PPV, and 96.8% NPV. CONCLUSIONS: We demonstrated an AI algorithm that can effectively assist the reporting of urine cytology by classifying urothelial cells at cancer risk and calculating quantitative data using WSI analysis. Integrating this AI model into clinical urine cytology workflow supported TPS for reporting urinary cytopathology, reduced the interobserver variations, and may potentially reduce the human labor for screening. Citation Format: Wei-Lei Yang, Jen-Fan Hang, Chi-Bin Li, Ching-Ming Lee, Yi-Sheng Lin, Tang-Yi Tsao, Ming-Chen Chang, Yen-Chuan Ou, Tien-Jen Liu. Clinical evaluation of The Paris System-based artificial intelligence algorithm for reporting urinary cytopathology [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2021; 2021 Apr 10-15 and May 17-21. 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引用次数: 1

摘要

背景:尿细胞学Paris系统(TPS)为尿路细胞学标本提供了标准化的诊断标准,重点是检测高级别尿路上皮癌(HGUC)。自2016年发表以来,大量研究报道采用TPS后非典型诊断率下降,HGUC检出率显著提高。然而,主要的挑战包括劳动密集型的筛查和观察者之间的差异。医学影像分析中的人工智能(AI)是一种新兴的辅助诊断工具。为此,我们开发了一种人工智能算法,并进行了回顾性研究,以评估人工智能辅助尿液细胞学报告工作流程。方法:对首次诊断或治疗后随访的131例膀胱癌患者的尿液细胞学切片进行检索,并将其数字化为整张切片图像(WSIs)。使用基于深度学习的计算模型来分析这些wsi。候选尿路上皮细胞自动突出显示,并根据TPS标准在每个样本中分为高风险和低风险异型类别。还提供了全幻灯片的统计数据,包括高危和低危细胞总数、每个细胞的核质比(N:C比)和核面积,以及这些变量的分布和平均值。在一项盲法研究中,一名细胞技术专家和一名细胞病理学家同时审查了每个WSI样本的人工智能注释图像和定量数据。根据是否触发膀胱镜检查,可疑为HUGC和HGUC为“阳性”,其他诊断类别为“阴性”。将结果与高级细胞病理学家通过显微镜检查的最终诊断进行比较,以评估人工智能辅助模型的性能。结果:最终诊断为尿细胞学阳性35例,阴性96例。AI算法在所有阳性样本中总共注释了26,502个细胞,平均注释了757.2个细胞,在所有阴性样本中总共注释了950个细胞,平均注释了9.9个细胞。高危非典型细胞的平均N:C比值为0.68,低危非典型细胞的平均N:C比值为0.56。人工智能辅助下细胞工艺师报告的灵敏度为88.6%,特异性为97.9%,阳性预测值为93.9%,阴性预测值为95.9%;细胞病理学家报告的灵敏度为91.4%,特异性为95.8%,阳性预测值为88.9%,阴性预测值为96.8%。结论:我们展示了一种人工智能算法,该算法可以通过对有癌症风险的尿路上皮细胞进行分类,并使用WSI分析计算定量数据,有效地辅助尿细胞学报告。将该AI模型集成到临床尿细胞学工作流程中,支持TPS报告尿细胞病理学,减少了观察者之间的差异,并可能减少筛查的人工劳动。引用格式:杨伟磊,韩金帆,李志斌,李清明,林义生,曹唐义,张明臣,欧延川,刘天仁。基于Paris系统的尿细胞病理报告人工智能算法的临床评价[摘要]。见:美国癌症研究协会2021年年会论文集;2021年4月10日至15日和5月17日至21日。费城(PA): AACR;癌症杂志,2021;81(13 -增刊):摘要nr LB015。
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Abstract LB015: Clinical evaluation of The Paris System-based artificial intelligence algorithm for reporting urinary cytopathology
BACKGROUND: The Paris System (TPS) for Reporting Urinary Cytology provides standardized diagnostic criteria for urinary tract cytology specimens, focusing on the detection of high-grade urothelial carcinoma (HGUC). Since the publication in 2016, numerous studies have reported a decrease in atypical diagnosis and a significant improvement in the detection of HGUC after adopting TPS. However, the major challenges include labor-intensive screening and interobserver variations. Artificial intelligence (AI) in medical imaging analysis is an emerging tool for ancillary diagnosis. To this end, we have developed an AI algorithm and conducted a retrospective study to evaluate the AI-assisted urine cytology reporting workflow. METHODS: A total of 131 urine cytology slides from bladder cancer patients, either first diagnosis or post-treatment follow-up, were retrieved and digitized as whole slide images (WSIs). A deep learning-based computational model was used to analyze these WSIs. Candidate urothelial cells were automatically highlighted and classified into high-risk and low-risk atypia categories in each sample based on TPS criteria. Slide-wide statistical data, including a total number of high-risk and low-risk cells, nuclear-cytoplasmic ratio (N:C ratio) and nuclear area for each cell, and the distribution and mean values of these variables, were also provided. In a blind study, a cytotechnologist and a cytopathologist parallelly reviewed the AI-annotated images and quantitative data for each WSI sample. Suspicious for HUGC and HGUC were considered to be "positive" and the other diagnostic categories were considered to be "negative" according to whether trigger cystoscopy. The results were compared with the final diagnosis reviewed by a senior cytopathologist via microscopy to evaluate the performance of the AI-assisted model. RESULTS: There were 35 positive and 96 negative urine cytology samples based on the final diagnosis. The AI algorithm annotated a total of 26,502 cells and a mean of 757.2 cells at cancer risk from all positive samples and a total of 950 cells and a mean of 9.9 cells at cancer risk from all negative samples. The mean N:C ratio was 0.68 for high-risk atypical cells and 0.56 for low-risk atypical cells. The performance of the AI-assisted reports of the cytotechnologist was 88.6% sensitivity, 97.9% specificity, 93.9% positive prediction value (PPV), and 95.9% negative prediction value (NPV) and the cytopathologist was 91.4% sensitivity, 95.8% specificity, 88.9% PPV, and 96.8% NPV. CONCLUSIONS: We demonstrated an AI algorithm that can effectively assist the reporting of urine cytology by classifying urothelial cells at cancer risk and calculating quantitative data using WSI analysis. Integrating this AI model into clinical urine cytology workflow supported TPS for reporting urinary cytopathology, reduced the interobserver variations, and may potentially reduce the human labor for screening. Citation Format: Wei-Lei Yang, Jen-Fan Hang, Chi-Bin Li, Ching-Ming Lee, Yi-Sheng Lin, Tang-Yi Tsao, Ming-Chen Chang, Yen-Chuan Ou, Tien-Jen Liu. Clinical evaluation of The Paris System-based artificial intelligence algorithm for reporting urinary cytopathology [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2021; 2021 Apr 10-15 and May 17-21. Philadelphia (PA): AACR; Cancer Res 2021;81(13_Suppl):Abstract nr LB015.
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