Project Summary

Breast cancer heterogeneity presents significant challenges for prognosis and management. This project reclassifies breast tumors using molecular subtypes, including Ki-67, to examine associations with patient survival and clinical outcomes. The study leverages a large institutional cohort with long-term follow-up and detailed clinical and pathological data. By applying advanced statistical models, we aim to generate refined prognostic insights, identify subtype-specific disparities in outcomes, and inform personalized treatment strategies. Results will provide evidence for integrating molecular subtyping into clinical decision-making and national breast cancer management guidelines.

Collaborator

Oncology Center KFSHRC.

Figure

Figure01 Association of Breast Cancer Molecular Subtypes with Patient Survival and Clinical Outcomes
Figure. Molecular Subtype Distribution in Global vs. Saudi Cohorts and Regional Ki-67 Scoring Practices. Panel A: Comparison of molecular subtype distribution between Saudi women diagnosed with breast cancer (2015–2019) and U.S. SEER estimates. Luminal A tumors accounted for only 24% in the Saudi cohort compared to 50% in SEER data, while luminal B and aggressive subtypes (HER2-enriched, TNBC) were more prevalent. Panel B: Regional variation in Ki-67 scoring methods. Percentage-based scoring dominates in Europe and North America, whereas ordinal scales are still commonly used in Saudi Arabia and other GCC countries.
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