Paige
Digital pathology AI applications for cancer pathology, including Paige Prostate.
Last updated: June 4, 2026
Back to directoryAI-powered breast cancer prognostic test that combines histology-derived features with clinical factors to help stratify recurrence risk for clinician review.
Breast cancer programs evaluating whether routine H&E pathology can add AI-supported recurrence-risk information alongside pathology, genomic assays, guidelines, and tumor-board review.
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Product-specific review. These product-specific signals summarize what the cited sources imply before treating PreciseDx PreciseBreast as safe for a local clinical, operational, or research workflow.
| Regulatory / FDA | Treat as high-risk oncology prognostic software or laboratory testing until the exact ordering pathway, laboratory status, FDA or local authorization, intended population, and report claims are confirmed. |
|---|---|
| Privacy | Review slide image transfer, clinicopathologic data fields, laboratory ordering, vendor privacy terms, business-associate or data-processing agreements, retention, support access, and whether de-identified data may be used for model improvement. |
| Evidence | Compare published analytical and external validation evidence with local breast cancer subtypes, specimen workflow, scanner diversity, follow-up horizon, recurrence endpoint, calibration, and incremental value over existing assays. |
| Workflow | Best governed as tumor-board decision support where pathologists and oncologists interpret the AI-derived risk score beside standard pathology, biomarkers, genomic tests, treatment guidelines, and patient-specific preferences. |
PreciseDx describes PreciseBreast as an AI digital pathology test that uses OncoIntelligence to combine AI-derived grade with clinical factors and generate a recurrence-risk score for early-stage breast cancer; peer-reviewed records describe analytical validation and external validation of the digital prognostic model, while the company privacy policy should be reviewed for data-handling terms before clinical adoption.
Not for: Autonomous treatment selection, replacing pathology or oncology judgment, use outside the validated breast cancer population, or deployment without local regulatory and laboratory workflow review.
Use these links to confirm current claims, terms, regulatory status, pricing, and deployment requirements.