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◆ European journal of nuclear medicine and molecular imaging2026-09-15

Development and validation of a preoperative 18F-PSMA-1007 PET/MR prognostic model for predicting biochemical recurrence in prostate cancer: a multicentre study.

Jiajia Hu, Hangxing Chunyu, Yihong Yang, Yanyan Song, Chao Cheng, Hailang Tang, Xiaoyue Chen, Ran Cheng, Jun Dai, Hongping Meng, Changjing Zuo, Jun Zhao, Biao Li

一句话结论

The 18F-PSMA-1007 PET/MR model provided externally validated prognostic information. It also showed incremental value beyond CAPRA-S at 3 years. Prospective validation is required before it can guide secondary-treatment decisions.

原始摘要(原文)
PURPOSE: To develop and externally validate a preoperative 18F-PSMA-1007 PET/MR model for biochemical recurrence (BCR) after radical prostatectomy and assess its incremental prognostic value beyond clinical risk scores. METHODS: This multicentre retrospective study included 210 patients from three centres (training, n = 150; external validation, n = 60). Predictors were selected by 10-fold cross-validated LASSO-Cox regression using the one-standard-error criterion and entered into a multivariable Cox model. Performance at 1-3 years was assessed using time-dependent AUCs, calibration, IPCW Brier scores, and decision-curve analysis. Incremental value beyond CAPRA-S was evaluated using likelihood-ratio tests (LRTs). Sensitivity analyses assessed the potential influence of persistent postoperative PSA and secondary treatment initiated before BCR. RESULTS: Seventy-five patients experienced the study endpoint of biochemical recurrence. The final model included ADCmin-TBR, TMR, and PET/MR T-stage. Time-dependent AUCs were 0.703-0.858 in the training cohort and 0.766-0.846 in the validation cohort. DeLong tests showed no significant AUC differences from CAPRA-S; however, adding the PET/MR model improved fit at 2 and 3 years in the derivation cohort (both LRT p < 0.001) and at 3 years in the external validation cohort (LRT p = 0.031). DCA showed positive net benefit across most clinically relevant thresholds. ADCmin-TBR and TMR remained directionally stable across sensitivity analyses, whereas the T-stage effect was attenuated after treatment censoring. CONCLUSIONS: The 18F-PSMA-1007 PET/MR model provided externally validated prognostic information. It also showed incremental value beyond CAPRA-S at 3 years. Prospective validation is required before it can guide secondary-treatment decisions. TRIAL REGISTRATION: ClinicalTrials.gov (NCT06604377) retrospectively registered on September 17, 2024.
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Development and validation of a preoperative 18F-PSMA-1007 PET/MR prognostic model for predicting biochemical recurrence in prostate cancer: a multicentre study. — 科研速览 Science Skim