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Breast Cancer Risk Assessment Tool (BCRAT) and long-term breast cancer mortality in the Women's Health Initiative.
Nelson, Rebecca A; Chlebowski, Rowan T; Pan, Kathy; Rohan, Thomas E; Mortimer, Joanne; Wactawski-Wende, Jean; Lane, Dorothy S; Kruper, Laura.
Affiliation
  • Nelson RA; Division of Medical Oncology & Experimental Therapeutics, City of Hope Comprehensive Cancer Center, Duarte, CA, USA.
  • Chlebowski RT; The Lundquist Institute, 1124 W. Carson Street, Torrance, CA, 90502, USA. rowanchlebowski@gmail.com.
  • Pan K; Kaiser Permanente Southern California, Downey, CA, USA.
  • Rohan TE; Department of Epidemiology & Population Health, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Mortimer J; Division of Medical Oncology & Experimental Therapeutics, City of Hope Comprehensive Cancer Center, Duarte, CA, USA.
  • Wactawski-Wende J; Department of Epidemiology & Population Health, University at Buffalo, Buffalo, NY, USA.
  • Lane DS; Department of Family, Population and Preventive Medicine, Stony Brook University School of Medicine, Stony Brook, NY, USA.
  • Kruper L; Division of Medical Oncology & Experimental Therapeutics, City of Hope Comprehensive Cancer Center, Duarte, CA, USA.
Article in En | MEDLINE | ID: mdl-39254768
ABSTRACT

BACKGROUND:

While the Breast Cancer Risk Assessment Tool (BCRAT) predicts breast cancer incidence, the model's performance, re-purposed to predict breast cancer mortality, is uncertain. Therefore, we examined whether the BCRAT model predicts breast cancer mortality in postmenopausal women in the Women's Health Initiative (WHI).

METHODS:

BCRAT 5-year breast cancer incidence risk estimates were calculated for 145,408 women (aged 50-79 years) enrolled in the WHI at 40 US clinical centers to examine associations of BCRAT risk groups (< 1%, 1-< 3%, ≥ 3%) with breast cancer mortality using Cox proportional regression modeling in all participants and in those with incident breast cancer.

RESULTS:

Women with BCRAT ≥ 3% risk, compared to women with BCRAT < 1% risk, were older (age 70-79 years 38.3% versus 5.3%), less commonly Black (1.1% versus 40.2%), and had stronger breast cancer family history. With 20-years follow-up, considering all participants, with 8,849 breast cancers and 1,076 breast cancer deaths, breast cancer mortality in BCRAT group ≥ 3% was not higher versus BCRAT group < 1% (Hazard Ratio [HR] 1.06 95% Confidence Interval [CI] 0.80-1.40) percent without 20-year breast cancer mortality; 99.4% [group < 1%] and 98.8% [group ≥ 3%]. Considering women with incident breast cancer, breast cancer mortality was also not higher in BCRAT group ≥ 3% versus BCRAT group < 1% (HR 1.07 95% CI 0.79-1.45).

CONCLUSIONS:

The BCRAT model, at ≥ 3% 5-year incidence risk (US guideline threshold for chemoprevention), does not identify women with higher breast cancer mortality risk, with implications for breast cancer prevention strategies.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Breast Cancer Res Treat Year: 2024 Document type: Article Affiliation country: United States Country of publication: Netherlands

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Breast Cancer Res Treat Year: 2024 Document type: Article Affiliation country: United States Country of publication: Netherlands