Abstract 1266P
Background
Pulmonary nodules (PNs) are frequently detected on CT scans and may indicate early lung cancer. Among PNs, management of ground-glass nodules (GGNs) can be particularly challenging due to their long, often indolent natural course. When malignant, they are usually lepidic adenocarcinomas, for which many targeted therapies exist. Artificial Intelligence (AI)-based malignancy prediction of PNs using CT images has been demonstrated to perform well on solid and part-solid PNs. Here, we aimed to extend one such AI model to GGNs.
Methods
GGN nodules and predominantly-GGN part-solid nodules were collected from 3 sites: two UK, one US. Patients with a 5-30mm nodule on non-contrast CT were included, unless they had a history of cancer in the past 5 years, >5 nodules, or insufficient outcome data from long-term follow-up or histological diagnosis. Scans with >2.5mm slice spacing or significant imaging artifacts were excluded. The most concerning nodule on each CT study was evaluated, giving 169 cancers in 57 patients, and 347 benign nodules in 180 patients. Most patients were enrolled through a text search of radiology reports, and enriched for malignant nodules based on local data. The AI tool is based on a commercial system, further trained using GGNs from an additional UK site. Ability to predict malignancy was evaluated using the Area Under the Receiver Operating Characteristic curve (AUC) and compared to two reference models. The ability to rule benign cases out of follow-up was evaluated by calculating specificity at 100% sensitivity.
Results
The AUC of the AI model was 89.1 [95%CI, 86.3, 91.8], while the AUC of the reference models, Brock and Mayo, were 86.5 95%CI [95% CI, 83.2, 89.6; p=0.39 vs. AI] and 80.9 [95%CI76.9, 84.8; p<0.01 vs. AI] respectively. The percentage of benign GGNs ruled out for cancer at 100% sensitivity were 48.7% for the AI model, 14.1% for Brock, and 16.7% for Mayo.
Conclusions
To our knowledge, this is the first study to demonstrate the potential value of an AI model in predicting the malignancy risk of GGNs. Implementation of such models in clinical practice could lead to more appropriate use of invasive interventions among GGN patients, thereby improving patient outcomes.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Optellum.
Disclosure
A. Vachani: Financial Interests, Institutional, Research Grant: MagArray, Precyte, Optellum. L. Freitag: Financial Interests, Personal, Leadership Role: Optellum. F. Gleeson: Financial Interests, Personal, Stocks/Shares: Optellum. All other authors have declared no conflicts of interest.
Resources from the same session
478P - Germline BRCA1/2 pathogenetic variants (gBRCA1/2 PV) affect outcome of hormone (HR)-positive HER2-negative metastatic breast cancer (MBC) patients (pts) treated with cyclin-dependent kinase 4/6 inhibitor (CDK 4/6i) plus endocrine therapy (ET): The BREAK study
Presenter: Antonella Palazzo
Session: Poster session 04
479P - Radiomics to predict HER2 status in breast cancer brain metastases
Presenter: Gaia Griguolo
Session: Poster session 04
480P - Prognostic significance of somatic DNA gene rearrangement and structural atypia in metastatic breast cancer
Presenter: Hiroshi Tada
Session: Poster session 04
481P - Second generation oral selective estrogen receptor degraders (SERDs) in breast cancer: A systematic review and meta-analysis of clinical trials
Presenter: Maysa Silveira Vilbert
Session: Poster session 04
482P - Precision imaging with human epidermal growth factor receptor 2-positron emission tomography (HER2-PET) for refined treatment selection in patients with HER2-low breast cancer
Presenter: Siri af Burén
Session: Poster session 04
483P - Prognostic value of androgen receptor expression in patients with advanced triple-negative metastatic breast cancer treated with sacituzumab govitecan: A French multicentre retrospective study
Presenter: Monica Arnedos
Session: Poster session 04
484P - Multi-platform characterization of HER2 expression in triple-negative breast cancer
Presenter: Ana C Garrido-Castro
Session: Poster session 04
485P - A novel approach to identify subpopulation of CTCs with metastatic potential using sc-RNA-seq
Presenter: Evgeniya Grigoryeva
Session: Poster session 04
486P - The influence of NF1 germline and somatic mutations on breast cancer patient survival
Presenter: Roope Kallionpää
Session: Poster session 04
487P - Induction of an inflammatory tumor microenvironment with oncolytic virus CF33-hNIS-antiPD-L1 intratumoral injection in patients with metastatic triple-negative breast cancer (mTNBC)
Presenter: Jamie Rand
Session: Poster session 04