Breast cancer detection accuracy of AI in an entire screening population: a retrospective, multicentre study

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  • Mohammad Talal Elhakim
  • Sarah Wordenskjold Stougaard
  • Ole Graumann
  • Nielsen, Mads
  • Kristina Lång
  • Oke Gerke
  • Lisbet Brønsro Larsen
  • Benjamin Schnack Brandt Rasmussen

Background: Artificial intelligence (AI) systems are proposed as a replacement of the first reader in double reading within mammography screening. We aimed to assess cancer detection accuracy of an AI system in a Danish screening population. Methods: We retrieved a consecutive screening cohort from the Region of Southern Denmark including all participating women between Aug 4, 2014, and August 15, 2018. Screening mammograms were processed by a commercial AI system and detection accuracy was evaluated in two scenarios, Standalone AI and AI-integrated screening replacing first reader, with first reader and double reading with arbitration (combined reading) as comparators, respectively. Two AI-score cut-off points were applied by matching at mean first reader sensitivity (AIsens) and specificity (AIspec). Reference standard was histopathology-proven breast cancer or cancer-free follow-up within 24 months. Coprimary endpoints were sensitivity and specificity, and secondary endpoints were positive predictive value (PPV), negative predictive value (NPV), recall rate, and arbitration rate. Accuracy estimates were calculated using McNemar’s test or exact binomial test. Results: Out of 272,008 screening mammograms from 158,732 women, 257,671 (94.7%) with adequate image data were included in the final analyses. Sensitivity and specificity were 63.7% (95% CI 61.6%-65.8%) and 97.8% (97.7-97.8%) for first reader, and 73.9% (72.0-75.8%) and 97.9% (97.9-98.0%) for combined reading, respectively. Standalone AIsens showed a lower specificity (-1.3%) and PPV (-6.1%), and a higher recall rate (+ 1.3%) compared to first reader (p < 0.0001 for all), while Standalone AIspec had a lower sensitivity (-5.1%; p < 0.0001), PPV (-1.3%; p = 0.01) and NPV (-0.04%; p = 0.0002). Compared to combined reading, Integrated AIsens achieved higher sensitivity (+ 2.3%; p = 0.0004), but lower specificity (-0.6%) and PPV (-3.9%) as well as higher recall rate (+ 0.6%) and arbitration rate (+ 2.2%; p < 0.0001 for all). Integrated AIspec showed no significant difference in any outcome measures apart from a slightly higher arbitration rate (p < 0.0001). Subgroup analyses showed higher detection of interval cancers by Standalone AI and Integrated AI at both thresholds (p < 0.0001 for all) with a varying composition of detected cancers across multiple subgroups of tumour characteristics. Conclusions: Replacing first reader in double reading with an AI could be feasible but choosing an appropriate AI threshold is crucial to maintaining cancer detection accuracy and workload.

OriginalsprogEngelsk
Artikelnummer127
TidsskriftCancer Imaging
Vol/bind23
Udgave nummer1
ISSN1740-5025
DOI
StatusUdgivet - 2023

Bibliografisk note

Funding Information:
We are grateful to the Region of Southern Denmark for the funding of this study. We thank ScreenPoint Medical for providing the AI system for this study. We are grateful to the Danish Clinical Quality Program – National Clinical Registries (RKKP), the Danish Breast Cancer Cooperative Group (DBCG) and the Danish Quality Database on Mammography Screening (DKMS) for the provision of data. We thank Henrik Johansen (Regional IT) for technical assistance and data management. We thank all supporting breast radiologists and mammography centres in the Region of Southern Denmark for contributing with their expertise and collaboration during the study conduct. We thank the women and patients for their participation. The authors alone are responsible for the views expressed in this article and they do not necessarily represent the decisions, policies, or view of the Region of Southern Denmark or any other collaborator.

Funding Information:
The study was funded through the Innovation Fund by the Region of Southern Denmark (grant number 10240300). The funder of the study had no role in study design, data collection, data analysis, data interpretation, or writing of the report.

Publisher Copyright:
© 2023, The Author(s).

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