Accuracy and Efficiency of Deep-Learning–Based Automation of Dual Stain Cytology in Cervical Cancer Screening

Author:

Wentzensen Nicolas1ORCID,Lahrmann Bernd2,Clarke Megan A1ORCID,Kinney Walter3ORCID,Tokugawa Diane4ORCID,Poitras Nancy4,Locke Alex4,Bartels Liam56,Krauthoff Alexandra56,Walker Joan7,Zuna Rosemary7,Grewal Kiranjit K4,Goldhoff Patricia E4,Kingery Julie D4,Castle Philip E8ORCID,Schiffman Mark1,Lorey Thomas S4,Grabe Niels256

Affiliation:

1. Affiliations of authors: Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD, USA

2. Steinbeis Transfer Center for Medical Systems Biology, Heidelberg, Germany

3. Global Coalition Against Cervical Cancer, Arlington, VA, USA

4. Kaiser Permanente TPMG Regional Laboratory, Berkeley, CA, USA

5. Hamamatsu Tissue Imaging and Analysis Center (TIGA), BIOQUANT, University Heidelberg, Heidelberg, Germany

6. National Center of Tumor Diseases, Medical Oncology, University Hospital Heidelberg, Heidelberg, Germany

7. University of Oklahoma, Oklahoma City, OK, USA

8. Albert Einstein College of Medicine, Bronx, NY, USA

Abstract

Abstract Background With the advent of primary human papillomavirus testing followed by cytology for cervical cancer screening, visual interpretation of cytology slides remains the last subjective analysis step and suffers from low sensitivity and reproducibility. Methods We developed a cloud-based whole-slide imaging platform with a deep-learning classifier for p16/Ki-67 dual-stained (DS) slides trained on biopsy-based gold standards. We compared it with conventional Pap and manual DS in 3 epidemiological studies of cervical and anal precancers from Kaiser Permanente Northern California and the University of Oklahoma comprising 4253 patients. All statistical tests were 2-sided. Results In independent validation at Kaiser Permanente Northern California, artificial intelligence (AI)-based DS had lower positivity than cytology (P < .001) and manual DS (P < .001) with equal sensitivity and substantially higher specificity compared with both Pap (P < .001) and manual DS (P < .001), respectively. Compared with Pap, AI-based DS reduced referral to colposcopy by one-third (41.9% vs 60.1%, P < .001). At a higher cutoff, AI-based DS had similar performance to high-grade squamous intraepithelial lesions cytology, indicating a risk high enough to allow for immediate treatment. The classifier was robust, showing comparable performance in 2 cytology systems and in anal cytology. Conclusions Automated DS evaluation removes the remaining subjective component from cervical cancer screening and delivers consistent quality for providers and patients. Moving from Pap to automated DS substantially reduces the number of colposcopies and also achieves excellent performance in a simulated fully vaccinated population. Through cloud-based implementation, this approach is globally accessible. Our results demonstrate that AI not only provides automation and objectivity but also delivers a substantial benefit for women by reduction of unnecessary colposcopies.

Funder

US National Cancer Institute

National Institutes of Health

Department of Health and Human Services

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

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