Bi-parametric MRI-based quantification radiomics model for the noninvasive prediction of histopathology and biochemical recurrence after prostate cancer surgery: a multicenter study.
[RATIONALE AND OBJECTIVES] To develop and evaluate the performance of a noninvasive radiomics combined model based on preoperative bi-parametric MRI to assess biochemical recurrence (BCR) risk factors
- p-value p = 0.028
- p-value p = 0.044
- 95% CI 0.750-0.925
APA
Wu SY, Wang Y, et al. (2025). Bi-parametric MRI-based quantification radiomics model for the noninvasive prediction of histopathology and biochemical recurrence after prostate cancer surgery: a multicenter study.. Abdominal radiology (New York), 50(9), 4320-4330. https://doi.org/10.1007/s00261-025-04873-4
MLA
Wu SY, et al.. "Bi-parametric MRI-based quantification radiomics model for the noninvasive prediction of histopathology and biochemical recurrence after prostate cancer surgery: a multicenter study.." Abdominal radiology (New York), vol. 50, no. 9, 2025, pp. 4320-4330.
PMID
40095016
Abstract
[RATIONALE AND OBJECTIVES] To develop and evaluate the performance of a noninvasive radiomics combined model based on preoperative bi-parametric MRI to assess biochemical recurrence (BCR) risk factors and to predict biochemical recurrence free survival in PCa patients.
[MATERIALS AND METHODS] Pretreatment bp-MRI and clinicopathology data of 666 (discovery cohort, 545; test cohort, 121) PCa patients from four centers between January 2015 to March 2023 were retrospectively included. To predict BCR, extracapsular extension (ECE), pelvic lymph node metastasis (PLNM), and Gleason Grade group (GG), the pred-BCR, pred-ECE, pred-PLNM, and pred-GG models were developed, respectively. Subsequently, a logistic regression algorithm was used to combine one or more radiomics models and clinicopathology variables into radiomics-clinicopathology combined models (M1, M2) and radiomics-clinical combined model without pathology results (M3) for predicting BCR.
[RESULTS] In the test cohort, the AUCs for the pred-BCR, pred-ECE, pred-PLNM, and pred-GG models were 0.841, 0.764, 0.896, and 0.698. Of the three combined models, M3 has the best prediction performance with an AUC of 0.884, M2 is the following with an AUC of 0.863, and M1 has the lowest performance with an AUC of 0.838 (95% CI 0.750-0.925) in the test cohort. Delong's test showed that the M3 was significantly higher (M1 vs. M3, p = 0.028; M2 vs. M3, p = 0.044).
[CONCLUSION] The combined model developed in this study, which is not dependent on pathologic biopsies, can noninvasively predict postoperative histopathology and BCR after PCa, therefore may provide decision support for follow-up and treatment strategies for patients in the postoperative period.
[MATERIALS AND METHODS] Pretreatment bp-MRI and clinicopathology data of 666 (discovery cohort, 545; test cohort, 121) PCa patients from four centers between January 2015 to March 2023 were retrospectively included. To predict BCR, extracapsular extension (ECE), pelvic lymph node metastasis (PLNM), and Gleason Grade group (GG), the pred-BCR, pred-ECE, pred-PLNM, and pred-GG models were developed, respectively. Subsequently, a logistic regression algorithm was used to combine one or more radiomics models and clinicopathology variables into radiomics-clinicopathology combined models (M1, M2) and radiomics-clinical combined model without pathology results (M3) for predicting BCR.
[RESULTS] In the test cohort, the AUCs for the pred-BCR, pred-ECE, pred-PLNM, and pred-GG models were 0.841, 0.764, 0.896, and 0.698. Of the three combined models, M3 has the best prediction performance with an AUC of 0.884, M2 is the following with an AUC of 0.863, and M1 has the lowest performance with an AUC of 0.838 (95% CI 0.750-0.925) in the test cohort. Delong's test showed that the M3 was significantly higher (M1 vs. M3, p = 0.028; M2 vs. M3, p = 0.044).
[CONCLUSION] The combined model developed in this study, which is not dependent on pathologic biopsies, can noninvasively predict postoperative histopathology and BCR after PCa, therefore may provide decision support for follow-up and treatment strategies for patients in the postoperative period.
MeSH Terms
Humans; Male; Prostatic Neoplasms; Retrospective Studies; Neoplasm Recurrence, Local; Magnetic Resonance Imaging; Aged; Middle Aged; Neoplasm Grading; Predictive Value of Tests; Prostatectomy; Radiomics
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