Machine learning-driven identification and immunohistochemical validation of an integrated immune-inflammatory phenotype for disease-free survival stratification in breast cancer - Scorecard - MDSpire
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Machine learning-driven identification and immunohistochemical validation of an integrated immune-inflammatory phenotype for disease-free survival stratification in breast cancer
Clinical Scorecard: Identification and Immunohistochemical Confirmation of a Combined Immune-Inflammatory Profile for Stratifying Disease-Free Survival in Breast Cancer Using Machine Learning Techniques
At a Glance
Category
Detail
Condition
Breast Cancer
Key Mechanisms
Stromal tumor-infiltrating lymphocytes (TILs) and systemic immune-inflammation index (SII)
Target Population
Patients with surgically treated breast cancer
Care Setting
Single-center retrospective cohort study
Key Highlights
RSF model achieved the best prognostic performance with time-dependent AUCs reaching 0.911 at 60 months.
21.3% of patients experienced a disease-free survival (DFS) event during follow-up.
The poor integrated immune phenotype was independently associated with worse DFS (hazard ratio 2.53).
Immunohistochemical validation showed significant differences in CD8 and CD163 cell densities between phenotypes.
Combining machine learning with immune-inflammatory markers may enhance recurrence risk stratification.
Guideline-Based Recommendations
Diagnosis
Assessment of stromal tumor-infiltrating lymphocytes (TILs) and systemic immune-inflammation index (SII) for prognostic evaluation.
Management
Utilization of machine learning models like RSF for improved DFS prediction.
Monitoring & Follow-up
Regular follow-up and assessment of immune-related factors in breast cancer patients.
Risks
Higher SII and poor integrated immune phenotype associated with increased risk of recurrence.
Patient & Prescribing Data
503 patients with surgically treated breast cancer
Integration of immune markers with clinical data may inform treatment decisions.
Clinical Best Practices
Incorporate immune-inflammatory markers in routine prognostic assessments.
Utilize advanced survival modeling techniques for better risk stratification.