TY - JOUR
T1 - Associations between sociodemographic and clinicopathological factors and breast cancer subtypes in a population-based study
AU - Llanos, Adana A.M.
AU - Chandwani, Sheenu
AU - Bandera, Elisa V.
AU - Hirshfield, Kim M.
AU - Lin, Yong
AU - Ambrosone, Christine B.
AU - Demissie, Kitaw
N1 - Funding Information:
This work was supported by grants from the National Cancer Institute (R01 CA133264, R01 CA100598, P01 CA151135, and Cancer Center Support Grants P30 CA072720 [Rutgers Cancer Institute of New Jersey] and P30 CA016056 [Roswell Park Cancer Institute]), the American Cancer Society (RSGT-07-291-01-CPHPS), the Susan G. Komen Breast Cancer Foundation (POP131006), the US Army Medical Research and Material Command (DAMD-17-01-1-0334), the Breast Cancer Research Foundation, a gift from the Philip L. Hubbell family, and a gift from the Buckingham Foundation. We sincerely thank our research personnel at the Rutgers Cancer Institute of New Jersey, Roswell Park Cancer Institute, Rutgers School of Public Health, and the New Jersey State Cancer Registry, as well as our African-American breast cancer advocates and community partners, and all the women who generously donated their time and participation to the study.
Publisher Copyright:
© 2015, Springer International Publishing Switzerland.
PY - 2015/9/16
Y1 - 2015/9/16
N2 - Purpose: This study examines the factors distinguishing breast cancer (BC) subtypes. Methods: We examined subtypes in 629 women with invasive BC, diagnosed from 2006 to 2012, and enrolled in an epidemiological study in New Jersey. Using molecular characteristics from pathology reports, BCs were categorized as luminal A, luminal B, non-luminal HER2-expressing, or triple-negative breast cancer (TNBC) subtypes. Multinomial logistic models (luminal A as referent) were used to describe BC subtype associations. Results: Women with luminal B tumors were more likely to be younger at diagnosis [odds ratio (OR) 1.8, 95 % confidence interval (CI) 1.0–3.4] and to have higher-grade (OR 2.6, 95 % CI 1.5–4.7), larger (OR 1.9, 95 % CI 1.0–3.6), and Ki67-positive tumors (OR 2.1, 95 % CI 1.1–4.0). Women with non-luminal HER2-expressing BCs were more likely to have higher-grade tumors (OR 14.5, 95 % CI 5.3–39.7). Women with TNBCs were more likely to be African-American (OR 1.9, 95 % CI 1.0–3.4) and to have higher-grade (OR 9.7, 95 % CI 5.1–18.4), larger (OR 2.2, 95 % CI 1.0–4.8), and Ki67-positive (OR 2.9, 95 % CI 1.6–5.2) tumors. Notably, compared to the luminal A subtype, luminal B, non-luminal HER2-expressing, and triple-negative subtypes were more frequently self-detected; however, these associations were attenuated in multivariable models. Conclusions: These findings suggest that some BC subtypes were associated with features denoting more aggressive phenotypes, namely higher grade, larger size, and Ki67 positivity, and possibly patient self-detection among some women. These findings highlight a need for enhanced screening, particularly among younger women, racial/ethnic minorities, and lower socioeconomic subgroups.
AB - Purpose: This study examines the factors distinguishing breast cancer (BC) subtypes. Methods: We examined subtypes in 629 women with invasive BC, diagnosed from 2006 to 2012, and enrolled in an epidemiological study in New Jersey. Using molecular characteristics from pathology reports, BCs were categorized as luminal A, luminal B, non-luminal HER2-expressing, or triple-negative breast cancer (TNBC) subtypes. Multinomial logistic models (luminal A as referent) were used to describe BC subtype associations. Results: Women with luminal B tumors were more likely to be younger at diagnosis [odds ratio (OR) 1.8, 95 % confidence interval (CI) 1.0–3.4] and to have higher-grade (OR 2.6, 95 % CI 1.5–4.7), larger (OR 1.9, 95 % CI 1.0–3.6), and Ki67-positive tumors (OR 2.1, 95 % CI 1.1–4.0). Women with non-luminal HER2-expressing BCs were more likely to have higher-grade tumors (OR 14.5, 95 % CI 5.3–39.7). Women with TNBCs were more likely to be African-American (OR 1.9, 95 % CI 1.0–3.4) and to have higher-grade (OR 9.7, 95 % CI 5.1–18.4), larger (OR 2.2, 95 % CI 1.0–4.8), and Ki67-positive (OR 2.9, 95 % CI 1.6–5.2) tumors. Notably, compared to the luminal A subtype, luminal B, non-luminal HER2-expressing, and triple-negative subtypes were more frequently self-detected; however, these associations were attenuated in multivariable models. Conclusions: These findings suggest that some BC subtypes were associated with features denoting more aggressive phenotypes, namely higher grade, larger size, and Ki67 positivity, and possibly patient self-detection among some women. These findings highlight a need for enhanced screening, particularly among younger women, racial/ethnic minorities, and lower socioeconomic subgroups.
KW - African-American women
KW - Aggressive phenotypes
KW - Breast cancer
KW - Clinicopathological factors
KW - Subtypes
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U2 - 10.1007/s10552-015-0667-4
DO - 10.1007/s10552-015-0667-4
M3 - Article
C2 - 26376894
AN - SCOPUS:84945487584
SN - 0957-5243
VL - 26
SP - 1737
EP - 1750
JO - Cancer Causes and Control
JF - Cancer Causes and Control
IS - 12
ER -