A Validated Risk Prediction Model for Breast Cancer in US Black Women.


Journal

Journal of clinical oncology : official journal of the American Society of Clinical Oncology
ISSN: 1527-7755
Titre abrégé: J Clin Oncol
Pays: United States
ID NLM: 8309333

Informations de publication

Date de publication:
01 12 2021
Historique:
pubmed: 9 10 2021
medline: 29 12 2021
entrez: 8 10 2021
Statut: ppublish

Résumé

Breast cancer risk prediction models are used to identify high-risk women for early detection, targeted interventions, and enrollment into prevention trials. We sought to develop and evaluate a risk prediction model for breast cancer in US Black women, suitable for use in primary care settings. Breast cancer relative risks and attributable risks were estimated using data from Black women in three US population-based case-control studies (3,468 breast cancer cases; 3,578 controls age 30-69 years) and combined with SEER age- and race-specific incidence rates, with incorporation of competing mortality, to develop an absolute risk model. The model was validated in prospective data among 51,798 participants of the Black Women's Health Study, including 1,515 who developed invasive breast cancer. A second risk prediction model was developed on the basis of estrogen receptor (ER)-specific relative risks and attributable risks. Model performance was assessed by calibration (expected/observed cases) and discriminatory accuracy (C-statistic). The expected/observed ratio was 1.01 (95% CI, 0.95 to 1.07). Age-adjusted C-statistics were 0.58 (95% CI, 0.56 to 0.59) overall and 0.63 (95% CI, 0.58 to 0.68) among women younger than 40 years. These measures were almost identical in the model based on estrogen receptor-specific relative risks and attributable risks. Discriminatory accuracy of the new model was similar to that of the most frequently used questionnaire-based breast cancer risk prediction models in White women, suggesting that effective risk stratification for Black women is now possible. This model may be especially valuable for risk stratification of young Black women, who are below the ages at which breast cancer screening is typically begun.

Identifiants

pubmed: 34623926
doi: 10.1200/JCO.21.01236
pmc: PMC8608262
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3866-3877

Subventions

Organisme : NCI NIH HHS
ID : U01 CA164974
Pays : United States
Organisme : NCI NIH HHS
ID : P50 CA058223
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA058420
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA228357
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA100598
Pays : United States

Auteurs

Julie R Palmer (JR)

Slone Epidemiology Center at Boston University, Boston, MA.
Boston University School of Medicine, Boston, MA.

Gary Zirpoli (G)

Slone Epidemiology Center at Boston University, Boston, MA.

Kimberly A Bertrand (KA)

Slone Epidemiology Center at Boston University, Boston, MA.
Boston University School of Medicine, Boston, MA.

Tracy Battaglia (T)

Boston University School of Medicine, Boston, MA.

Leslie Bernstein (L)

City of Hope Comprehensive Cancer Center, Duarte, CA.

Christine B Ambrosone (CB)

Roswell Park Comprehensive Cancer Center, Buffalo, NY.

Elisa V Bandera (EV)

Rutgers Cancer Institute of New Jersey, New Brunswick, NJ.

Melissa A Troester (MA)

University of North Carolina Lineberger Comprehensive Cancer Center, Chapel Hill, NC.

Lynn Rosenberg (L)

Slone Epidemiology Center at Boston University, Boston, MA.

Ruth M Pfeiffer (RM)

National Cancer Institute, Division of Cancer Epidemiology and Genetics, Bethesda, MD.

Ludovic Trinquart (L)

Boston University School of Public Health, Boston, MA.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH