Goal: After radical prostatectomy, integrate whole-slide images from the prostatectomy specimen, biopsy findings, preoperative MRI, and longitudinal PSA kinetics to estimate time-dependent biochemical recurrence (BCR) risk. Cases may include multiple MRIs and/or biopsies over time, and missing modalities are intentionally present.

Input modalities

  • Report of prostatectomy H&E whole-slide images
  • Report of preoperative biopsy WSI
  • Report of multiparametric MRI
  • Longitudinal PSA measurements (prior to surgery)
  • Clinical variables: age, Gleason Grade Group, surgical margins, extracapsular extension, pT stage, and T stage

Output required

  • Quantitative BCR risk estimates at 1, 2, and 5 years
  • Structured prognostic reasoning identifying dominant factors contributing to recurrence risk and handling of missing or conflicting data

Ground truth: BCR defined as confirmed PSA rise >= 0.2 ng/mL post-prostatectomy. Patients without recurrence at last follow-up, as well as those who received salvage treatment, migrated, died, or were otherwise lost to follow-up, are treated as censored observations.

Dataset

Split Cases Notes
Training 75 Radboudumc; real-world class distribution
Validation 75 Radboudumc; up to 5 submissions allowed
Test 250 100 cases from Karolinska Institute (external); 1 submission allowed

Input data: JSON file with structured input modalities.

Expected output per case: JSON file (~5 KB) containing BCR risk estimates at 1, 2, and 5 years, and a structured reasoning trace.

Primary metric: Time-dependent AUC

Provided tools: Standardized preprocessing and feature extraction for prostatectomy WSI; automated Gleason grading for biopsy and prostatectomy specimens; MRI-based cancer detection tool