2021
DOI: 10.1016/j.biopha.2020.111013
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Incorporating SULF1 polymorphisms in a pretreatment CT-based radiomic model for predicting platinum resistance in ovarian cancer treatment

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Cited by 28 publications
(22 citation statements)
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“…Though the majority patients with BRCA1/2 and/or HRD are platinum-sensitive, the overlap is still limited (15). Other genetic features, including gene expression, gene variants, single nucleotide polymorphism and copy number changes, have been studied in the value of predicting of platinum sensitivity in ovarian cancer (16)(17)(18). Based on the large TCGA dataset (The Cancer Genome Atlas), Yin et al devised a 131-gene signature associated with platinum resistance, but was still not applicable to clinical use (19).…”
Section: Introductionmentioning
confidence: 99%
“…Though the majority patients with BRCA1/2 and/or HRD are platinum-sensitive, the overlap is still limited (15). Other genetic features, including gene expression, gene variants, single nucleotide polymorphism and copy number changes, have been studied in the value of predicting of platinum sensitivity in ovarian cancer (16)(17)(18). Based on the large TCGA dataset (The Cancer Genome Atlas), Yin et al devised a 131-gene signature associated with platinum resistance, but was still not applicable to clinical use (19).…”
Section: Introductionmentioning
confidence: 99%
“…The results showed that the best test accuracy and AUC for predicting chemotherapy response with KI67 and EZRIN were 0.85 and 0.89, respectively. In recent research for predicting platinum resistance of ovarian cancer (OC), Yi et al [93] generated an ML model incorporating radiomics data based on pretreatment CT images, clinicopathological data, and genomic data of single-nucleotide polymorphisms (SNPs) of human sulfatase 1 (SULF1). This combined model showed better classification efficiency, high calibration, and promising clinical utility, with AUC values of 0.993 (95% CI 0.83-0.98) in the training dataset (n = 71) and 0.967 (95% CI 0.83-0.98) in the validation dataset (n = 31).…”
Section: Predicting Treatment Responsesmentioning
confidence: 99%
“…Yi et al [45] selected 12 Single-Nucleotide Polymorphisms (SNPs) of Human Sulfatase 1 (SULF1) for genotyping and combined it with radiomic and clinical features to build a combination model. They used LASSO and RF as weak regressors, then combined them with SVM to build the algorithm.…”
Section: Clinical Correlationsmentioning
confidence: 99%