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Evaluating the Accuracy of Privacy-Preserving Large Language Models in Calculating the Spinal Instability Neoplastic
Li Yi Tammy Chan1, Ding Zhou Matthew Chan1, Yi Liang Tan1
1Department of Diagnostic Imaging, National University Hospital, Singapore 119074, Singapore.
Abstract:
Background: Large language models (LLMs) have emerged as powerful tools in healthcare. In diagnostic radiology, LLMs can assist in the computation of the Spine Instability Neoplastic Score (SINS), which is a critical tool for assessing spinal metastases. However, the accuracy of LLMs in calculating the SINS based on radiological reports remains underexplored. Objective: This study evaluates the accuracy of two institutional privacy-preserving LLMs-Claude 3.5 and Llama 3.1-in computing the SINS from radiology reports and electronic medical records, comparing their performance against clinician readers. Methods: A retrospective analysis was conducted on 124 radiology reports from patients with spinal metastases. Three expert readers established a reference standard for the SINS calculation. Two orthopaedic surgery residents and two LLMs (Claude 3.5 and Llama 3.1) independently calculated the SINS. The intraclass correlation coefficient (ICC) was used to measure the inter-rater agreement for the total SINS, while Gwet's Kappa was used to measure the inter-rater agreement for the individual SINS components. Results: Both LLMs and clinicians demonstrated almost perfect agreement with the reference standard for the total SINS. Between the two LLMs, Claude 3.5 (ICC = 0.984) outperformed Llama 3.1 (ICC = 0.829). Claude 3.5 was also comparable to the clinician readers with ICCs of 0.926 and 0.986, exhibiting a near-perfect agreement across all individual SINS components [0.919-0.990]. Conclusions: Claude 3.5 demonstrated high accuracy in calculating the SINS and may serve as a valuable adjunct in clinical workflows, potentially reducing clinician workload while maintaining diagnostic reliability. However, variations in LLM performance highlight the need for further validation and optimisation before clinical integration.

