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Retrospective Pathology Foundation Models

Development and Clinical Application of Deep Learning-Based Retrospective Pathology Foundation Models

Status
Enrolling by invitation
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07239297
Enrollment
2000
Registered
2025-11-20
Start date
2025-08-01
Completion date
2028-07-31
Last updated
2025-11-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pancancer

Brief summary

By integrating retrospective multimodal data such as pathology and imaging, AI technologies offer novel solutions for disease classification, tumor grading, histological and molecular subtyping, selection of chemotherapy regimens, risk stratification, and treatment-response prediction. This research direction not only deepens our understanding of tumor biological characteristics but also provides essential support for precision medicine and individualized therapy. It holds significant theoretical and practical value and has important implications for mitigating strained medical resources and improving the accuracy of therapeutic decision-making, representing a cutting-edge application with substantial translational potential.

Interventions

None listed

Sponsors

Nanfang Hospital, Southern Medical University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

1. Aged 18-75 years old. 2. Patients with complete pathological slides and clinical information.

Exclusion criteria

1.Patients with missing data or specimens not meeting quality control requirements for analysis.

Design outcomes

Primary

MeasureTime frameDescription
Area under ROC curve (AUC)Diagnostic evaluation will be performed within 1 week when the WSIs are obtainedArea under the curve

Secondary

MeasureTime frameDescription
SpecificityDiagnostic evaluation will be performed within 1 week when the WSIs are obtainedThe true negative rate (TNR) of the diagnostic platform, which is the ratio between the number of negative individuals correctly categorized by platform and the total number of actual negative individuals (%).
SensitivityDiagnostic evaluation will be performed within 1 week when the WSIs are obtainedThe true positive rate (TPR) of the diagnostic platform, which is the ratio between the number of positive individuals correctly categorized by platform and the total number of actual positive individuals (%).

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026