Machine learning-driven identification and immunohistochemical validation of an integrated immune-inflammatory phenotype for disease-free survival stratification in breast cancer - Report - MDSpire

Machine learning-driven identification and immunohistochemical validation of an integrated immune-inflammatory phenotype for disease-free survival stratification in breast cancer

  • By

  • Shanshan Han

  • Lin Ran

  • Zhaoan Lian

  • Yong Tian

  • Li Qin

  • Yingchun Xiang

  • Xiaohao Yan

  • Chengyu Shui

  • Cheng Huang

  • June 18, 2026

  • 0 min

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Clinical Report: Identification of Immune-Inflammatory Profile in Breast Cancer

Overview

This study identifies a combined immune-inflammatory profile that enhances disease-free survival (DFS) stratification in breast cancer patients. Machine learning techniques, particularly random survival forest (RSF), demonstrated superior prognostic performance compared to traditional models.

Background

Breast cancer is the most prevalent cancer among women, with significant variability in recurrence risk post-treatment. Traditional prognostic factors often fail to capture the complexity of tumor biology and immune interactions. Understanding immune-related factors, such as tumor-infiltrating lymphocytes (TILs) and systemic immune-inflammation index (SII), is crucial for improving patient outcomes.

Data Highlights

Time (months)AUC
120.867
240.880
360.879
480.893
600.911

Key Findings

  • 107 patients (21.3%) experienced a DFS event during follow-up.
  • RSF model achieved the highest time-dependent AUC of 0.911 at 60 months.
  • Pathological N stage was identified as the most significant predictor of DFS.
  • 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.

Clinical Implications

Incorporating immune-inflammatory markers like TILs and SII into prognostic models may enhance the stratification of recurrence risk in breast cancer. Clinicians should consider these factors when assessing patient prognosis and tailoring treatment strategies.

Conclusion

The integration of machine learning with immune-inflammatory markers offers a promising approach to improve DFS risk stratification in breast cancer. This study underscores the importance of a multifaceted view of tumor biology in clinical practice.

Related Resources & Content

  1. Frontiers in Medicine, 2026 -- Integrating Machine Learning and Clinicopathological Data to Stratify Survival Risk in Young Women with Localized Breast Cancer
  2. asco ai in oncology -- Transcriptomic Classifier for Predicting Neoadjuvant Immunotherapy Response in Triple-Negative Breast Cancer
  3. Integration of Molecular Signatures from Tumor Deposits Using Machine Learning Enhances Prognostic Assessment in Colon Adenocarcinoma
  4. The ASCO Post, 2020 -- Machine Learning Algorithms May Help Predict Response to Immunotherapy in Patients With Advanced Melanoma
  5. Use of Immune Checkpoint Inhibitor Pembrolizumab in the Treatment of High-Risk, Early-Stage Triple-Negative Breast Cancer: ASCO Guideline Rapid Recommendation Update - PubMed
  6. The tale of TILs in breast cancer: A report from The International Immuno-Oncology Biomarker Working Group - PMC
  7. ECTIL: Label-efficient Computational Tumour Infiltrating Lymphocyte (TIL) assessment in breast cancer: Multicentre validation in 2,340 patients with breast cancer
  8. Use of Immune Checkpoint Inhibitor Pembrolizumab in the Treatment of High-Risk, Early-Stage Triple-Negative Breast Cancer: ASCO Guideline Rapid Recommendation Update - PubMed
  9. The tale of TILs in breast cancer: A report from The International Immuno-Oncology Biomarker Working Group - PMC
  10. ECTIL: Label-efficient Computational Tumour Infiltrating Lymphocyte (TIL) assessment in breast cancer: Multicentre validation in 2,340 patients with breast cancer

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