Abstract 1255P
Background
Artificial Intelligence (AI) and Natural Language Processing (NLP) advancements have led to sophisticated tools like GPT-4.0, allowing clinicians to explore its utility as a healthcare management support tool. Our study aimed to assess GPT-4's ability to suggest the definitive diagnosis and the most appropriate work-up to minimize unnecessary procedures.
Methods
We conducted a retrospective comparative analysis, extracting relevant clinical data from 10 cases published at NEJM after 2022 and inputting it into GPT-4 to generate diagnostic and workup recommendations. Primary endpoint: the ability to correctly identify the final diagnosis. Secondary endpoints: its ability to list the definitive diagnosis in the five most likely differential diagnoses and determine an adequate workup.
Results
The AI could not identify the definitive diagnosis in 2 out of the 10 cases (20% inaccuracy). Among the 8 cases correctly identified by the AI, 5 (63%) had the definitive diagnosis as the top differential diagnosis list. Regarding the suggested diagnostic tests and exams, requests for exams that would not aid in the patient's final diagnosis were made in 2 cases, representing 40% of the patients whose final diagnosis was not correctly identified by the AI. Moreover, the AI could not suggest adequate treatment for 7 cases (70%). Among them, the AI suggested inappropriate management for 2 cases, and the remaining 5 received incomplete or non-specific advice, such as chemotherapy, without specifying the best regimen.
Conclusions
Our study demonstrated GPT-4's potential as an academic support tool, although it cannot correctly identify the final diagnosis in 20% of the cases. There is also a limitation regarding the management suggested by AI. In cases where the main diagnostic hypothesis was incorrectly identified or not listed as the top differential diagnosis, the AI requested unnecessary additional diagnostic tests for 40% of the patients. Future research should focus on evaluating the performance of GPT-4 using a more extensive and diverse sample, incorporating prospective assessments, and investigating its ability to optimize diagnostic and therapeutic procedures to optimize healthcare utilization.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
1229P - Selective phenotypic and genotypic evaluation of circulating glial cells for improved diagnosis of glial malignancies
Presenter: Sewanti Limaye
Session: Poster session 14
1230P - hPG80 (circulating progastrin) is a new blood-based biomarker for diagnosis of early-stage non-small cell lung cancers
Presenter: Paul Hofman
Session: Poster session 14
1231P - Machine learning prediction of the case-fatality of COVID-19 and risk factors for adverse outcomes in patients with non-small cell lung cancer
Presenter: Yeji Jung
Session: Poster session 14
1232P - Analytic analysis of PanSeer7, a targeted bisulfite sequencing assay for blood-based multi-cancer detection for cancer early detection and tissue-of-origin identification
Presenter: Xinrong Yang
Session: Poster session 14
1233P - Accurate prediction of gastrointestinal cancer tissue of origin using comprehensive plasma cell-free DNA fragmentomics features
Presenter: Xinrong Yang
Session: Poster session 14
1234P - HistoMate: Automated preprocessing software for digital histopathology image to enhance deep learning
Presenter: Jinok Lee
Session: Poster session 14
1235P - Enrichment of rare cancers in pragmatic precision cancer medicine trial: Experience from IMPRESS-Norway
Presenter: Aaslaug Helland
Session: Poster session 14
1236P - Feasibility of online symptom monitoring to detect lung cancer relapse in Poland
Presenter: Ewa Pawlowska
Session: Poster session 14
1237P - Design and validation of a custom next-generation sequencing panel in melanoma, glioma and gastrointestinal stromal tumor
Presenter: Xiaoyan Zhou
Session: Poster session 14
1238P - Detecting driver mutations by AmoyDx 11-gene PCR with high concordance with next-generation sequencing in Chinese non-small cell lung cancer patients
Presenter: Dongmei Lin
Session: Poster session 14