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Table 3 This table summarizes the models developed for the prediction of patients’ response to treatment, their inputs and performance

From: Navigating advanced renal cell carcinoma in the era of artificial intelligence

 

Model

Input

Performance/Findings

Limitations

Rossi et al.

CT-based radiomic analysis

Radiomic features from CT scans of 53 mRCC patients

Correlated radiomic features with progression as the best response to ICI therapy

- Small sample size

-Retrospective study

- No validation cohorts

Park et al.

Clinical-CT texture models

Baseline and follow-up CT texture data combined with clinical data in 129 patients

Combined model predicted overall survival (C-index 0.7) and progression-free survival (C-index 0.63), outperforming clinical data alone

- Small sample size

-Retrospective study

- No validation cohorts

-ROI determined by only one radiologist

Khene et al.

Texture analysis for survival prediction

Pre-treatment CT texture features in 48 patients

Identified predictors of overall and progression-free survival in mRCC patients treated with nivolumab.

- Small sample size

-Retrospective study

- No validation cohorts

-Manual ROIs

-Variable CT techniques

Neutrophil to Lymphocyte Ratio Studies

Biomarker analysis

Neutrophil to lymphocyte ratio

Low splenic volume 3 months after ICI treatment linked to improved overall survival

-Retrospective study

- No validation cohorts

Splenic Volume Studies

Automated splenic segmentation

Splenic volume change measured using AI tools

Significant survival improvement associated with low splenic volume

- Small cohorts

- Mixed treatment regimens

- No validation cohorts

Negreros-Osuna et al.

CT-based radiomic model for TKI response prediction

Texture analysis of primary tumors and clinical data in 62 patients

Combined radiomic and clinical model outperformed models using radiomic or clinical data alone.

- Small sample size

-Retrospective study

- No validation cohorts

Chen et al.

CT-based radiomic model for short-term lesion response prediction

Radiomic features from baseline arterial phase (AP) and non-contrast (NC) CT scans in 36 patients with recurrent or mRCC

Delta feature-based model effectively predicted short-term lesion response to first-line TKIs in a small cohort. 0.940 (95% CI, 0.890‒0.990) in the training cohort and 0.916 (95% CI, 0.828‒1.000) in the validation cohort

-Small sample size

-Retrospective study

Udayakumar et al.

Radiogenomic model using DCE-MRI

DCE-MRI, histopathology, and transcriptome correlatives in 49 ccRCC patients

High arterial spin labeling MRI correlated with favorable response to antiangiogenic regimens

-Small sample size

- Cohort included mostly small tumors

-Colocalization between presurgical imaging and postsurgical histologic analysis