ArticleScientific reports2019
Development and Validation of Nomograms for Malignancy Prediction in Soft Tissue Tumors Using Magnetic Resonance Imaging Measurements.
Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed, 10 citations in OpenAlex.
- Soft tissue and juxtaarticular tumors of the knee.Skeletal radiology · 2026Review
- Clinical and radiologic features of soft tissue sarcoma in trunk and extremities that underwent unplanned excision.PloS one · 2024Article
- Diagnostic Performance of US and MRI in Predicting Malignancy of Soft Tissue Masses: Using a Scoring System.Frontiers in oncology · 2022Article
- The safety of primary surgical excision of small deep indeterminate musculoskeletal soft tissue masses.The British journal of radiology · 2021Article
- The value of bi-exponential and non-Gaussian distribution diffusion-weighted imaging in the differentiation of recurrent soft tissue neoplasms and post-surgical changes.Annals of translational medicine · 2020Article
- Soft tissue sarcoma: DWI and DCE-MRI parameters correlate with Ki-67 labeling index.European radiology · 2020Observational
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5 authors at 3 institutions in 1 country.
Funding
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Abstract
The objective of this study was to develop, validate, and compare nomograms for malignancy prediction in soft tissue tumors (STTs) using conventional and diffusion-weighted magnetic resonance imaging (MRI) measurements. Between May 2011 and December 2016, 239 MRI examinations from 236 patients with pathologically proven STTs were included retrospectively and assigned randomly to training (n = 100) and validation (n = 139) cohorts. MRI of each lesion was reviewed to assess conventional and diffusion-weighted imaging (DWI) measurements. Multivariate nomograms based on logistic regression analyses were built using conventional measurements with and without DWI measurements. Predictive accuracy was measured using the concordance index (C-index) and calibration plots. Statistical differences between the C-indexes of the two models were analyzed. Models were validated by leave-one-out cross-validation and by using a validation cohort. The mean lesion size, presence of infiltration, edema, and the absence of the split fat sign were significant and independent predictors of malignancy and included in the conventional model. In addition to these measurements, the mean and minimum apparent diffusion coefficient values were included in the DWI model. The DWI model exhibited significantly higher diagnostic performance only in the validation cohort (training cohort, 0.899 vs. 0.886, P = 0.284; validation cohort, 0.791 vs. 0.757, P = 0.020). Calibration plots showed fair agreements between the nomogram predictions and actual observations in both cohorts. In conclusion, nomograms using MRI features as variables can be utilized to predict the malignancy probability in patients with STTs. There was no definite gain in diagnostic accuracy when additional DWI features were used.
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