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. 2020 Apr 19;21(8):2856. doi: 10.3390/ijms21082856

Table 6.

Prediction of clinical outcome by radiomics in cancer patients undergoing immune-checkpoint blockade.

Reference Author Tumor Entity Findings
[187] Sun et al. solid tumors OS prediction based on radiomics CD8+ cell score
[195] Bensch et al. bladder cancer, NSCLC, TNBC ↑ ORR/PFS/OS prediction by PET evaluation with zirconium-89-labeled atezolizumab compared to IHC or RNA-sequencing based PD-L1 assessment
[196] Khorrami et al. NSCLC ORR and OS prediction based on changes in radiomic texture (“DelRADx”)
[197] Trebeschi et al. melanoma, NSCLC Response prediction of individual metastases and OS prediction based on multiple radiomic features
[198] Himoto et al. ovarian cancer Prediction of clinical benefit by intratumoral heterogeneity (radiomic feature) and by number of disease sites
[199] Ligero et al. solid tumors ↑ ORR prediction by clinical-radiomics signature score
[200] Tunali et al. NSCLC Prediction of hyperprogressive disease based on clinical-radiomic models
[201] Dercle et al. non-squamous NSCLC PFS prediction based on tumor volume reduction, infiltration of tumor boundaries or spatial heterogeneity
[202] Korpics et al. solid tumors Prediction of local tumor failure, PFS and OS in cancer patients receiving SBRT and anti-PD-1 Tx based on a radiomics score

PET: positron emission tomography; PFS: progression-free survival; SBRT: stereotactic body radiotherapy, Tx: therapy; NSCLC: non-small cell lung cancer; TNBC: triple negative breast cancer; OS: overall survival; ORR: overall response rate; IHC: immunohistochemistry; PD-L1: programmed cell death-ligand 1.