PO.PS01.02 · 人群科学

Sex-specific survival patterns in korean breast cancer: Explainable AI insights from K-CURE Cohort

海报缩略图:Sex-specific survival patterns in korean breast cancer: Explainable AI insights from K-CURE Cohort
编号 3562 展板 12 时间 4/20 02:00–05:00 区域 Section 34 主讲 Seohyun Ahn, MS
分会场 Cancer Surveillance: Emerging Cancer Trends and Population Differences
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作者与单位

Seohyun Ahn1, Juyeon Hwang1, Sun-Young Kong1, Jin Ho Park2, So-Youn Jung1, Hyun-Jin Kim1

1National Cancer Center - Korea, Goyang-si, Korea, Republic of,2Seoul National University Hospital, Seoul, Korea, Republic of

摘要 Abstract

Background: Male breast cancer (MBC) is rare, but its incidence is increasing worldwide. Evidence regarding survival differences compared with female breast cancer (FBC) is limited. This study aimed to characterize sex-specific survival patterns in Korean breast cancer and to identify key contributing factors using explainable artificial intelligence (XAI) methods. Methods: This study utilized data from the Korean Clinical Data Utilization for Research Excellence (K-CURE), a nationwide registry of all breast cancer cases in Korea. Patients diagnosed between 2012 and 2021 were analyzed by sex. Overall survival (OS) and breast cancer-specific survival (BCSS) were assessed using multivariable Cox proportional hazards models. XAI techniques, including SHAP and LIME, were applied to identify sex-specific contributors to survival. Results: Among 200,222 patients (846 males, 199,376 females), males showed significantly poorer OS and BCSS than females ( p <.001). This disparity persisted after adjustment (male OS HR ≈1.30-1.40; BCSS HR ≈1.40-1.50). Distant stage was associated with the highest mortality risk in both sexes (male HR ≈9-12; female HR ≈10-24). Distinct sex-specific patterns were observed. In males, metabolic indicators showed opposite associations with survival: higher hemoglobin was linked to lower mortality (HR ≈0.88), whereas higher fasting blood sugar was associated with increased mortality risk (HR ≈1.04). In females, hormone and targeted therapies were associated with reduced mortality (HR ≈0.30-0.55). XGBoost models achieved moderate predictive performance for both outcomes (OS AUC ≈0.85; BCSS AUC ≈0.87). SHAP and LIME analyses consistently supported these patterns, suggesting that metabolic profiles contributed more to risk estimation in males, whereas tumor stage and treatment factors were relatively more influential in females. Conclusion: These findings indicate that sex differences in breast cancer survival arise not only from differences in overall risk profiles but also from distinct prognostic factors specific to each sex. In males, metabolic indicators were more closely associated with survival, whereas in females, tumor stage and treatment factors had greater relevance. Overall, these results reflect differing underlying mechanisms by sex and highlight the need for tailored, sex-specific management strategies in breast cancer care.
利益披露 Disclosure
S. Ahn, None.. J. Hwang, None.. S. Kong, None.. J. Park, None.. S. Jung, None.. H. Kim, None.

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