Xuanxuan Li1, Yiping Lu1, Pu-Yeh Wu2, Tonggang Yu3, and Bo Yin1
1Huashan Hospital, Fudan University, Shanghai, China, 2GE Healthcare, Beijing, China, 3Shanghai Gamma Hospital, Huashan Hospital, Fudan University, Shanghai, China
Synopsis
The aim
of this study is to adopt machine learning and deep learning methods to predict
the risk of post-GKS edema for meningiomas. 595 multicenter cases were included
to train and validate 38 random survival forest (RSF) and DeepSurv models. The
RSF model incorporating clinical, semantic, and ADC radiomic features achieved
the best performance with a C-index of 0.861 in internal validation, and 0.780
in external validation. The derived nomogram had excellent discrimination and
calibration. The proposed RSF model with a nomogram represents a non-invasive
and cost-effective tool to predict post-GKS edema risks, thus facilitates
personalized decision-making in meningioma treatment.
Introduction
Edema
is a complication after Gamma Knife Radiosurgery (GKS) in meningioma patients
thatleads to a variety of consequences[1]. The
symptoms may necessitate steroid administration and even resection. Potential predictive
factors have been investigated but there are so far no easy-to-use tools to
predict the risks quantificationally The aim of this study is to construct
radiomics-based machine learning (ML) and deep learning (DL) models to predict post-GKS
edema development.
Methods
445
meningioma patients who underwent GKS in our institution were enrolled. All participants underwent pre-treatment MRI examinations, including T1-weighted imaging
(T1WI), T2-weighted imaging (T2WI), diffusion-weighted imaging (DWI), and contrast-enhanced
T1WI. Apparent diffusion coefficient (ADC) maps were automatically calculated
after the DWI acquisition using a mono-exponential fitting method. Data were
partitioned into training and internal validation datasets in a ratio of 8:2.
150 cases from multicenter data were also included as the external validation
dataset. In each case, 1132 radiomic features were extracted from each
pre-treatment MRI sequence (contrast-enhanced T1WI, T2WI, and ADC maps). 9
clinical features and 8 semantic features were also generated. 19 ML (random
survival forest, RSF) and 19 DL (DeepSurv) models with different combination of
radiomic, clinical, and semantic features were developed with the training
dataset, and evaluated with internal and external validation datasets. A
nomogram was derived from the model achieving the highest C-index in external
validation.
Results
All the
models were successfully validated on both validation datasets. The RSF model
incorporating clinical, semantic and ADC radiomic features achieved the best
performance with a C-index of 0.861 (95% CI: 0.748-0.975)
in internal validation, and 0.780 (95% CI: 0.673-0.887) in external validation.
It stratifies high-risk and low-risk cases effectively (Figure 1). The nomogram based on the predicted
risks provided personalized prediction with a C-index of 0.962 (95%CI:
0.951-0.973) and satisfactory calibration (Figure
2).
Discussion
Previous
studies have correlated a variety of risk factors with post-GKS edema in
meningioma patients, including a greater therapeutic dose, greater tumor size,
non-skull base (particularly parasagittal) location, and presence of
pretreatment edema[2]. Our
study incorporated radiomic features for the first time which provided abundant
quantitative image information that was impossible to obtain with human vision.
The radiomic features may predict the post-GKS edema effectively by revealing
heterogeneous vasculature aroused by varying VEGF/VPF distribution[3].
Conclusion
Our RSF
model with the nomogram represents a non-invasive and cost-effective tool to assist
better counselling on the risks, making appropriate treatment decisions
individually, and employ customized follow-up plans. Acknowledgements
No acknowledgement found.References
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