MSR69 Developing an EHR-based multifeature machine learning model to identify lung cancer subtype

EHR notes from US representative ConcertAI network were accessed for patients with a C34 code. A training set of 7,914 patients was used. For each EHR document, snippets were labeled into NSCLC or SCLC based on exact tumor name or synonyms, stage (extensive, limited for SCLC), or histology (eg: adenocarcinoma for NSCLC). Evidence of subtype is first asserted, then associated temporally and semantically with primary tumor. Then a hybrid rules+ML model is applied at patient level to integrate evidence and resolve contradictions; if unresolved, no prediction is made. A sample of 50 patients predicted as NSCLC and SCLC each (validation set) were compared to expert determined subtype from the EHR. Finally, the model was applied to a larger test cohort and clinical relevance assessed via systemic treatment distribution.

For the training set, the model predicted 67.5% (5,346) NSCLC, 17.7% (1,398) SCLC, and 14.8% (1,170) other patients. Expert validation revealed precision, recall, and specificity of 0.96, 0.87, and 0.93, respectively for NSCLC and 0.92, 0.92, and 0.96, respectively for SCLC. The test set comprised of 432,453 patients, and model predicted 88.8% (375,241) NSCLC, 9.3% (40,324) SCLC, and 3.9% (16,888) other. Top three regimen in first-line advanced setting were platinum-doublet, pembrolizumab+/-chemotherapy, and EGFR TKis for NSCLC and, etoposide+platinum, atezolizumab/durvalumab+platinum+etoposide, and topoisomerase inhibitors for SCLC.

ML-based model that leverages multiple features from structured and unstructured EHR can reliably classify NSCLC and SCLC subtypes validated through alignment with real-world treatment patterns supporting its utility for studying disease phenotype and associated treatment patterns and outcomes.