Validation of a commercially available CAD-system for lung nodule detection and characterization using CT-scans
- PMID: 39042303
- PMCID: PMC11782423
- DOI: 10.1007/s00330-024-10969-0
Validation of a commercially available CAD-system for lung nodule detection and characterization using CT-scans
Abstract
Objectives: This study aims to externally validate a commercially available Computer-Aided Detection (CAD)-system for the automatic detection and characterization of solid, part-solid, and ground-glass lung nodules (LN) on CT scans.
Methods: This retrospective study encompasses 263 chest CT scans performed between January 2020 and December 2021 at a Dutch university hospital. All scans were read by a radiologist (R1) and compared with the initial radiology report. Conflicting scans were assessed by an adjudicating radiologist (R2). All scans were also processed by CAD. The standalone performance of CAD in terms of sensitivity and false-positive (FP)-rate for detection was calculated together with the sensitivity for characterization, including texture, calcification, speculation, and location. The R1's detection sensitivity was also assessed.
Results: A total of 183 true nodules were identified in 121 nodule-containing scans (142 non-nodule-containing scans), of which R1 identified 165/183 (90.2%). CAD detected 149 nodules, of which 12 were not identified by R1, achieving a sensitivity of 149/183 (81.4%) with an FP-rate of 49/121 (0.405). CAD's detection sensitivity for solid, part-solid, and ground-glass LNs was 82/94 (87.2%), 42/47 (89.4%), and 25/42 (59.5%), respectively. The classification accuracy for solid, part-solid, and ground-glass LNs was 81/82 (98.8%), 16/42 (38.1%), and 18/25 (72.0%), respectively. Additionally, CAD demonstrated overall classification accuracies of 137/149 (91.9%), 123/149 (82.6%), and 141/149 (94.6%) for calcification, spiculation, and location, respectively.
Conclusions: Although the overall detection rate of this system slightly lags behind that of a radiologist, CAD is capable of detecting different LNs and thereby has the potential to enhance a reader's detection rate. While promising characterization performances are obtained, the tool's performance in terms of texture classification remains a subject of concern.
Clinical relevance statement: Numerous lung nodule computer-aided detection-systems are commercially available, with some of them solely being externally validated based on their detection performance on solid nodules. We encourage researchers to assess performances by incorporating all relevant characteristics, including part-solid and ground-glass nodules.
Key points: Few computer-aided detection (CAD) systems are externally validated for automatic detection and characterization of lung nodules. A detection sensitivity of 81.4% and an overall texture classification sensitivity of 77.2% were measured utilizing CAD. CAD has the potential to increase single reader detection rate, however, improvement in texture classification is required.
Keywords: Computer-assisted detection; Early detection of cancer; Lung; Lung cancer; Validation study.
© 2024. The Author(s).
Conflict of interest statement
Compliance with ethical standards. Guarantor: The scientific guarantor of this publication is Jacob J. Visser, MD, PhD. Conflict of interest: The authors of this manuscript declare relationships with the following companies: Souvik Mandal, Prakash Vanapalli, Vikash Challa, Saigopal Sathyamurthy, Ranjana Devi, and Ritvik Jain are full-time paid employees of Qure.ai. Jacob J. Visser, MD, PhD: Grant to institution from Qure.ai; consulting fees from Tegus; payment to institution for lectures from Roche; travel grant from Qure.ai; participation on a data safety monitoring board or advisory board from Quibim, Contextflow, Noaber Foundation, and NLC Ventures; leadership or fiduciary role on the steering committee of the PINPOINT Project (payment to institution from AstraZeneca) and RSNA Common Data Elements Steering Committee (unpaid); phantom shares in Contextflow and Quibim. The remaining authors declare no conflicts of interest. Statistics and biometry: Daniel Bos, MD, PhD and Saigopal Sathyamurthy kindly provided statistical advice for this manuscript. Informed consent: Written informed consent was waived by the Institutional Review Board because of the retrospective nature of the study and the analysis only used anonymous data. Ethical approval: The study protocol was reviewed and approved by the Medical Ethics Review Committee Erasmus Medical Centre Rotterdam (2022-0465). Study subjects or cohorts overlap: No overlaps. Methodology: Retrospective Diagnostic or prognostic study Performed at one institution
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