Evidence map›Paper›PMID 39630238›Full record

ArticleSkeletal radiology2025

Predicting progression-free survival in sarcoma using MRI-based automatic segmentation models and radiomics nomograms: a preliminary multicenter study.

Nana Zhu, Feige Niu, Shuxuan Fan, Xianghong Meng, Yongcheng Hu, Jun Han, Zhi Wang

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Skeletal radiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

  1. Observational
4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Nana ZhuGraduate School, Tianjin Medical University, Tianjin, China.
Feige NiuGraduate School, Tianjin Medical University, Tianjin, China.
Shuxuan FanThe Department of Radiology, Tianjin Medical University Cancer Hospital, Tianjin, China.
Xianghong MengThe Department of Radiology, Tianjin University Tianjin Hospital, 406 Jiefang Southern Road, Tianjin, 300211, China.
Yongcheng HuThe Department of Radiology, Tianjin University Tianjin Hospital, 406 Jiefang Southern Road, Tianjin, 300211, China.
Jun HanThe Department of Radiology, Tianjin University Tianjin Hospital, 406 Jiefang Southern Road, Tianjin, 300211, China.
Zhi WangThe Department of Radiology, Tianjin University Tianjin Hospital, 406 Jiefang Southern Road, Tianjin, 300211, China. 15002213919@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesSome sarcomas are highly malignant, associated with high recurrence despite treatment. This multicenter study aimed to develop and validate a radiomics signature to estimate sarcoma progression-free survival (PFS). MATERIALS AND

methodsThe study retrospectively enrolled 202 consecutive patients with pathologically diagnosed sarcoma, who had pre-treatment axial fat-suppressed T2-weighted images (FS-T2WI), and included them in the ROI-Net model for training. Among them, 120 patients were included in the radiomics analysis, all of whom had pre-treatment axial T1-weighted and transverse FS-T2WI images, and were randomly divided into a development group (n = 96) and a validation group (n = 24). In the development cohort, Least Absolute Shrinkage and Selection Operator (LASSO) Cox regression was used to develop the radiomics features for PFS prediction. By combining significant clinical features with radiomics features, a nomogram was constructed using Cox regression.

resultsThe proposed ROI-Net framework achieved a Dice coefficient of 0.820 (0.791-0.848). The radiomics signature based on 21 features could distinguish high-risk patients with poor PFS. Univariate Cox analysis revealed that peritumoral edema, metastases, and the radiomics score were associated with poor PFS and were included in the construction of the nomogram. The Radiomics-T1WI-Clinical model exhibited the best performance, with AUC values of 0.947, 0.907, and 0.924 at 300 days, 600 days, and 900 days, respectively.

conclusionThe proposed ROI-Net framework demonstrated high consistency between its segmentation results and expert annotations. The radiomics features and the combined nomogram have the potential to aid in predicting PFS for patients with sarcoma.

Indexed as

Magnetic Resonance ImagingNomogramsSarcomaAdolescentAdultAgedFemaleHumansMaleMiddle AgedProgression-Free SurvivalRadiomicsRetrospective StudiesDeep learningRadiomicsRecurrenceSarcomaTumor segmentation

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.