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Poster Display session

553P - Risk of newly incident diabetes mellitus and its treatment risk factor in breast cancer survivors: Landmark analyses of nationwide data

Date

07 Dec 2024

Session

Poster Display session

Presenters

Hyeongjin Shim

Citation

Annals of Oncology (2024) 35 (suppl_4): S1595-S1615. 10.1016/annonc/annonc1695

Authors

H. Shim1, K. Han2, B. Kim2, H.Y. Koo3, S. Kim4, D. Lee5, W. Jung6, D.W. Shin7

Author affiliations

  • 1 Family Medicine, Samsung Medical Center (SMC), 06351 - Seoul/KR
  • 2 Statistics And Actuarial Science, Soongsil University, 06978 - Seoul/KR
  • 3 Family Medicine, Seoul National University Bundang Hospital, 463-707 - Seongnam/KR
  • 4 Family Medicine, Samsung Medical Center (SMC), 135-710 - Seoul/KR
  • 5 Family Medicine, Hallym University Medical Center (HUMC)-Dongtan Sacred Heart Hospital, 18450 - Hwaseong/KR
  • 6 Division Of Cardiology, Perelman School of Medicine, 19104 - PA/US
  • 7 Family Medicine, Samsung Medical Center (SMC) - Sungkyunkwan University School of Medicine, 135-710 - Seoul/KR

Resources

This content is available to ESMO members and event participants.

Abstract 553P

Background

Breast cancer survivors are at increased risk of diabetes mellitus (DM), particularly in the early years post-treatment. This study examines short- and long-term DM risk by treatment methods and lifestyle factors.

Methods

Using Korean Health Insurance Service data, the study included 65,982 women newly diagnosed with invasive breast cancer (2010-2016). The primary outcome was DM, defined as individuals receiving diabetic medications. Sub-distribution hazard ratios (sHR) and 95% confidence intervals (CI) were estimated using competing risk analysis considering death.

Results

I In patients under 50, DM risk was significantly higher in the first year (sHR 3.742, 95% CI 3.078-4.548). The 1-year landmark analysis showed a smaller increase (sHR 1.106, 95% CI 1.032-1.186), but no significant increase after three years. Patients over 50 had increased DM risk during the first year (sHR 1.711, 95% CI 1.921-2.352), with no significant increase in later years. BMI ≥ 25 (sHR 1.449, 95% CI 1.318-1.594), current smoking (sHR 1.715, 95% CI 1.492-1.972), hypertension (sHR 1.476, 95% CI 1.367-1.593), and dyslipidemia (sHR 1.49, 95% CI 1.377-1.612) were all associated with increased DM risk across all age groups. Patients receiving taxane had higher DM risk regardless of age (sHR 1.148, 95% CI 1.062-1.242). Among those on endocrine therapy, only patients under 50 treated with tamoxifen had a significant DM risk increase (sHR 1.217, 95% CI 1.061-1.395).

Conclusions

DM risk increased in patients under 50 during the first three years, while patients over 50 showed increased risk only in the first year. Higher DM risk was also observed in those with high BMI, smoking, hypertension, dyslipidemia, or treated with taxane or tamoxifen.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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