Evaluating artificial intelligence (AI) as a clinical decision support tool for lung cancer treatment recommendations.

R Roupen Odabashian (Department of Hematology and Oncology, Karmanos Cancer Institute, Wayne State University, Detroit, MI) J Jeffrey Karson (Department of Supportive Oncology, Karmanos Cancer Institute, Wayne State University, Detroit, MI) G Gregory Dyson (Karmanos Cancer Institute/Department of Oncology, Detroit, MI) A Asmita Shukla (1Karmanos Cancer Institute, Detroit, United States) S Sushmitha Nanja Reddy (1Karmanos Cancer Institute, Detroit, United States) N Nagasai Yalavarthi (1Karmanos Cancer Institute, Detroit, United States) P Padmapriya Muthu (Mayo Clinic Arizona, Scottsdale, Arizona, United States) S Suha Soni (Department of Medicine, Division of Cardiology, The University of Texas Health Science Center, San Antonio, TX) T Tarik Hadid (Department of Hematology and Oncology, Barbara Ann Karmanos Cancer Institute, Wayne State University School of Medicine, Detroit, MI) R Rami Manochakian (Mayo Clinic Florida, Jacksonville, FL) A Anastasios Dimou A Aakash Desai (Allegheny Health Network, Pittsburgh, PA) H Hirva Mamdani

Abstract

e20011 Background: The therapeutic landscape of lung cancer is rapidly evolving, presenting oncologists with the challenge of staying updated amidst an overwhelming influx of data. Clinical decision support (CDS) tools, including artificial intelligence (AI) and large language models (LLMs), may help bridge this gap. Evaluating the accuracy of LLMs in complex, real-world oncology scenarios is crucial to understanding their potential. Methods: Twenty-five de-identified lung cancer cases from the fellows’ clinic at Karmanos Cancer Institute, Detroit, MI, were analyzed. Two LLMs, GPT-4 (OpenAI) and Claude Opus (Anthropic), were assessed using advanced prompting techniques like persona-based and chain-of-thought prompting. Five board-certified lung cancer oncologists from NCI-designated centers evaluated LLM-generated responses based on accuracy, treatment recommendation comprehensiveness, and supportive care planning, using a 1–5 scale. Novel insights, the presence of fabricated information, and harmful recommendations were flagged as binary outcomes. Oncologists were blinded to the LLM source and actual treatment decisions. Results: Table 1 presents patient characteristics. GPT-4 achieved an average accuracy score of 4.2 (95% CI, 3.9–4.4), with 3.7 for comprehensiveness of medical/surgical treatment recommendations and 3.7 for supportive care planning. Six responses (32%) were flagged as potentially harmful, and two (8%) contained inaccuracies. Sixteen GPT-4 responses (64%) were rated trustworthy as a CDS tool. Claude Opus had an average accuracy score of 3.6 (95% CI, 3.1–4.1), scoring 3.6 for treatment recommendation comprehensiveness and 3.5 for supportive care planning. Nine responses (36%) were flagged for potential harm, and five (20%) included inaccuracies. Eleven Claude responses (44%) were deemed trustworthy. Significant differences were observed in accuracy (p=0.04) and trustworthiness (p=0.03) between models using McNemar's test. Other factors showed no statistical significance. Conclusions: GPT-4 outperformed Claude Opus in accuracy and trustworthiness, but both models demonstrated limitations, including harmful recommendations and inaccuracies. These findings highlight the need for improved LLM refinement before routine use as CDS tools in lung cancer treatment. Patient demographics and clinical characteristics. Category subcategory Number Median Age (range)- Yr 65 (26-78) Female 7 Male 18 Histology Adenocarcinoma 10 Squamous Cell Carcinoma (SCC) 7 Small Cell Carcinoma 6 Poorly Differentiated 2 Total 25 Stage NSCLC Stage 3 7 NSCLC Stage 4 13 Small Cell limited stage 3 Small Cell Extensive Stage 2

Article Details

Volume / Issue Vol. 43, Issue 16_suppl
Published June 01, 2025
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (13)

R

Roupen Odabashian

Department of Hematology and Oncology, Karmanos Cancer Institute, Wayne State University, Detroit, MI

J

Jeffrey Karson

Department of Supportive Oncology, Karmanos Cancer Institute, Wayne State University, Detroit, MI

G

Gregory Dyson

Karmanos Cancer Institute/Department of Oncology, Detroit, MI

A

Asmita Shukla

1Karmanos Cancer Institute, Detroit, United States

S

Sushmitha Nanja Reddy

1Karmanos Cancer Institute, Detroit, United States

N

Nagasai Yalavarthi

1Karmanos Cancer Institute, Detroit, United States

P

Padmapriya Muthu

Mayo Clinic Arizona, Scottsdale, Arizona, United States

S

Suha Soni

Department of Medicine, Division of Cardiology, The University of Texas Health Science Center, San Antonio, TX

T

Tarik Hadid

Department of Hematology and Oncology, Barbara Ann Karmanos Cancer Institute, Wayne State University School of Medicine, Detroit, MI

R

Rami Manochakian

Mayo Clinic Florida, Jacksonville, FL

A

Anastasios Dimou

A

Aakash Desai

Allegheny Health Network, Pittsburgh, PA

H

Hirva Mamdani