Skip to content
DraconiticResearch
Search Sources API
201,818 studies31 sourcesUpdated 50 min ago
Peer-reviewedCC BY-NC-NDBMC cancer

Differentiating Xp11.2/TFE3 translocation renal cell carcinoma from clear cell carcinoma: performance of a radiomics model.

5 affiliations
  1. 1Department of Radiology, Peking University First Hospital, No. 8 Xishiku Street, Xicheng District, Beijing, 100034, China.
  2. 2Beijing Smart Tree Medical Technology Co., Ltd, 24, Huangsi Avenue, Xicheng District, Beijing, 100035, China.
  3. 3Department of Urology, Peking University First Hospital, No. 8 Xishiku Street, Xicheng District, Beijing, 100034, China.
  4. 4Institute of Urology, Beijing Key Laboratory of Urogenital Diseases (Male) Molecular Diagnosis and Treatment Center, Peking University, National Urological Cancer Center, No. 8 Xishiku Street., Xicheng District, Beijing, 100034, China.
  5. 5Department of Radiology, Peking University First Hospital, No. 8 Xishiku Street, Xicheng District, Beijing, 100034, China. [email protected].

Abstract

Purpose

This study aims to assess the computed tomography (CT) features of transcription factor E3 gene fusion renal cell carcinoma (TFE3-RCC) and develop a radiomics-based model for preoperative discrimination between TFE3-RCCs and clear cell renal cell carcinomas (ccRCCs).Methods

A total of 34 pathologically confirmed TFE3-RCC and 98 ccRCC cases with preoperative renal CT were enrolled. Subjective image analysis was performed to determine the CT parameters that can distinguish TFE3-RCCs from ccRCCs. A random forest classifier was evaluated through 5-fold cross-validation to establish the radiomics model. Diagnostic performance was assessed using receiver operating characteristic (ROC) curve analysis.Results

Patients with TFE3-RCC were significantly younger (36.2 ± 14.4 vs. 56.8 ± 13.5 years, P < 0.001). Ten of the 34 TFE3-RCCs had calcification, whereas only four in the ccRCC group did (29.4% vs. 4.1%, P < 0.001). Additionally, the TOC enhancement ratio in the corticomedullary phase were significantly lower in the TFE3-RCC group compared with the ccRCC group (0.61 ± 0.11 vs. 0.90 ± 0.13, p < 0.001). The random forest classifier achieved stable performance with robust cross-validation metrics (AUC = 0.82 ± 0.17, accuracy = 85% ± 13%).Conclusion

The CT radiomics model exhibits favorable diagnostic performance for noninvasively differentiating TFE3-RCC from ccRCC, supporting its potential utility in preoperative personalized management of renal masses.

Related

  1. A multimodal MRI radiomics sonata for differentiating small renal masses: a two-center retrospective study.
    Chao Fang, Li Tian, Ming Gao +10
    Clinics (Sao Paulo, Brazil)Peer-reviewedCC BYFull textMedical imaging & radiologyEurope PMC
  2. TFE3 fusions drive expression of CD44 and SPP1 in Translocation Renal Cell Carcinoma
    K. Asrani, J. Woo, T. Vidotto +26
    bioRxivPreprintAll rights reservedFull textOncologybioRxiv
  3. Development and validation of a multiphase CT radiomics-based machine learning model for prognostic prediction in sarcomatoid renal cell carcinoma
    Tongpeng Liu, Yu Yao, Zhijian Zhou +3
    Frontiers in OncologyPeer-reviewedCC BY 4.0OncologyFrontiersCrossref
  4. Multimodal CT radiomics and 2.5D deep learning for preoperative grading of clear cell renal cell carcinoma in older patients: a multicenter study
    Zhengkun Wang, Zixin Liang, Dingyang Lv +9
    Frontiers in OncologyPeer-reviewedCC BY 4.0OncologyFrontiersCrossref
  5. Multiparametric MRI-based radiomics for differentiating HER2-negative, HER2-low, and HER2-positive breast cancer
    Lulu Gai, Shubin Luo, Yudong Yan +9
    Frontiers in medicinePeer-reviewedCC BYFull textGeneral medicineEurope PMC
BibTeX
@article{liu2026differentiating,
  title = {{Differentiating Xp11.2/TFE3 translocation renal cell carcinoma from clear cell carcinoma: performance of a radiomics model.}},
  author = {Yi Liu and Kexin Wang and Yaofeng Zhang and Jiangtao Liu and Zuqiang Xi and Xiangpeng Wang and Yanfei Yu and Xiaoying Wang},
  journal = {BMC cancer},
  year = {2026},
  month = jul,
  doi = {10.1186/s12885-026-16463-8},
  url = {https://europepmc.org/article/MED/42894154},
  note = {CC BY-NC-ND},
}
RIS
TY  - JOUR
TI  - Differentiating Xp11.2/TFE3 translocation renal cell carcinoma from clear cell carcinoma: performance of a radiomics model.
AU  - Yi Liu
AU  - Kexin Wang
AU  - Yaofeng Zhang
AU  - Jiangtao Liu
AU  - Zuqiang Xi
AU  - Xiangpeng Wang
AU  - Yanfei Yu
AU  - Xiaoying Wang
PY  - 2026
DA  - 2026/07/01
JO  - BMC cancer
DO  - 10.1186/s12885-026-16463-8
UR  - https://europepmc.org/article/MED/42894154
AB  - Purpose  This study aims to assess the computed tomography (CT) features of transcription factor E3 gene fusion renal cell carcinoma (TFE3-RCC) and develop a radiomics-based model for preoperative discrimination between TFE3-RCCs and clear cell renal cell carcinomas (ccRCCs).Methods  A total of 34 pathologically confirmed TFE3-RCC and 98 ccRCC cases with preoperative renal CT were enrolled. Subjective image analysis was performed to determine the CT parameters that can distinguish TFE3-RCCs from ccRCCs. A random forest classifier was evaluated through 5-fold cross-validation to establish the radiomics model. Diagnostic performance was assessed using receiver operating characteristic (ROC) curve analysis.Results  Patients with TFE3-RCC were significantly younger (36.2 ± 14.4 vs. 56.8 ± 13.5 years, P < 0.001). Ten of the 34 TFE3-RCCs had calcification, whereas only four in the ccRCC group did (29.4% vs. 4.1%, P < 0.001). Additionally, the TOC enhancement ratio in the corticomedullary phase were significantly lower in the TFE3-RCC group compared with the ccRCC group (0.61 ± 0.11 vs. 0.90 ± 0.13, p < 0.001). The random forest classifier achieved stable performance with robust cross-validation metrics (AUC = 0.82 ± 0.17, accuracy = 85% ± 13%).Conclusion  The CT radiomics model exhibits favorable diagnostic performance for noninvasively differentiating TFE3-RCC from ccRCC, supporting its potential utility in preoperative personalized management of renal masses.
SN  - 1471-2407
ER  -