TY - JOUR
T1 - Integrated noninvasive diagnostics for prediction of survival in immunotherapy
AU - Yeghaian, M.
AU - Bodalal, Z.
AU - Tareco Bucho, T. M.
AU - Kurilova, I.
AU - Blank, C. U.
AU - Smit, E. F.
AU - van der Heijden, M. S.
AU - Nguyen-Kim, T. D.L.
AU - van den Broek, D.
AU - Beets-Tan, R. G.H.
AU - Trebeschi, S.
N1 - Funding Information:
The computational infrastructure used in this study was made possible by generous grants from the Maurits en Anna de Kock Stichting (2019-8) and the NVIDIA Academic GPU program. The authors acknowledge the Research High Performance Computing (RHPC) facility of the Netherlands Cancer Institute - AVL Hospital. None declared. The authors have declared no conflicts of interest.
Publisher Copyright:
© 2024 The Author(s)
PY - 2024/12/1
Y1 - 2024/12/1
N2 - Background: Integrating complementary diagnostic data sources promises enhanced robustness in the predictive performance of artificial intelligence (AI) models, a crucial requirement for future clinical validation/implementation. In this study, we investigate the potential value of integrating data from noninvasive diagnostic modalities, including chest computed tomography (CT) imaging, routine laboratory blood tests, and clinical parameters, to retrospectively predict 1-year survival in a cohort of patients with advanced non-small-cell lung cancer, melanoma, and urothelial cancer treated with immunotherapy. Patients and methods: The study included 475 patients, of whom 444 had longitudinal CT scans and 475 had longitudinal laboratory data. An ensemble of AI models was trained on data from each diagnostic modality, and subsequently, a model-agnostic integration approach was adopted for combining the prediction probabilities of each modality and producing an integrated decision. Results: Integrating different diagnostic data demonstrated a modest increase in predictive performance. The highest area under the curve (AUC) was achieved by CT and laboratory data integration (AUC of 0.83, 95% confidence interval 0.81-0.85, P < 0.001), whereas the performance of individual models trained on laboratory and CT data independently yielded AUCs of 0.81 and 0.73, respectively. Conclusions: In our retrospective cohort, integrating different noninvasive data modalities improved performance.
AB - Background: Integrating complementary diagnostic data sources promises enhanced robustness in the predictive performance of artificial intelligence (AI) models, a crucial requirement for future clinical validation/implementation. In this study, we investigate the potential value of integrating data from noninvasive diagnostic modalities, including chest computed tomography (CT) imaging, routine laboratory blood tests, and clinical parameters, to retrospectively predict 1-year survival in a cohort of patients with advanced non-small-cell lung cancer, melanoma, and urothelial cancer treated with immunotherapy. Patients and methods: The study included 475 patients, of whom 444 had longitudinal CT scans and 475 had longitudinal laboratory data. An ensemble of AI models was trained on data from each diagnostic modality, and subsequently, a model-agnostic integration approach was adopted for combining the prediction probabilities of each modality and producing an integrated decision. Results: Integrating different diagnostic data demonstrated a modest increase in predictive performance. The highest area under the curve (AUC) was achieved by CT and laboratory data integration (AUC of 0.83, 95% confidence interval 0.81-0.85, P < 0.001), whereas the performance of individual models trained on laboratory and CT data independently yielded AUCs of 0.81 and 0.73, respectively. Conclusions: In our retrospective cohort, integrating different noninvasive data modalities improved performance.
KW - artificial intelligence
KW - cancer survival prediction
KW - immunotherapy
KW - integrated diagnostics
KW - longitudinal data
KW - machine learning
U2 - 10.1016/j.iotech.2024.100723
DO - 10.1016/j.iotech.2024.100723
M3 - Article
SN - 2590-0188
VL - 24
JO - Immuno-Oncology and Technology
JF - Immuno-Oncology and Technology
M1 - 100723
ER -