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Socioeconomic and Racial Disparities in Cancer Stage at Diagnosis, Tumor Size, and Clinical Outcomes in a Large Cohort of Women with Breast Cancer, 2007-2016

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Background: Socioeconomic and treatment factors contribute to diagnosis of early-stage (local-stage) breast cancer, as well as excess deaths among African American women. Objectives: We evaluated socioeconomic and treatment predictive factors for early-stage breast cancer among African American women compared to Caucasian women. A secondary aim evaluated predictors and overall risks associated with all-cause and breast cancer-specific mortality. Methods: We used retrospective cohort population-based study data from the Surveillance, Epidemiology, and End Results (SEER) Program on 547,703 women aged ≥ 20 years diagnosed with breast cancer primary tumors from 2007 to 2016. Statistical analysis used logistic regression to assess predictors of early-stage breast cancer and Cox proportional hazards regression for mortality risks. Results: African American women were more likely to be diagnosed at advanced-stage, had larger tumor size at diagnosis, and received less cancer-directed surgery, but more chemotherapy than Caucasian women. Insured women (> 50%) were more likely to be diagnosed at early-stage and to have smaller tumors (p < 0.05). Education level, poverty level, and household income had no impact on racial disparities or socioeconomic disparities in women diagnosed at early stage. We found increased risks for all-cause mortality (hazard ratio = 1.18; 95% confidence interval, 1.16-1.21) and breast cancer-specific mortality (HR = 1.22; 95% CI, 1.19-1.25) among African American women compared to Caucasian women after adjusting for demographic, socioeconomic, and treatment factors. Conclusions: In this population-based study using the most recent SEER data, African American women with breast cancer continued to exhibit higher all-cause mortality and breast cancer-specific mortality compared to Caucasian women.
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1 23
Journal of Racial and Ethnic Health
Disparities
ISSN 2197-3792
J. Racial and Ethnic Health Disparities
DOI 10.1007/s40615-020-00855-y
Socioeconomic and Racial Disparities in
Cancer Stage at Diagnosis, Tumor Size,
and Clinical Outcomes in a Large Cohort of
Women with Breast Cancer, 2007–2016
Dale Hardy & Daniel Y.Du
1 23
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Socioeconomic and Racial Disparities in Cancer Stage at Diagnosis,
Tumor Size, and Clinical Outcomes in a Large Cohort of Women
with Breast Cancer, 20072016
Dale Hardy
1
&Daniel Y. Du
2
Received: 7 April 2020 /Revised: 19 August 2020 /Accepted: 24 August 2020
#W. Montague Cobb-NMA Health Institute 2020
Abstract
Background Socioeconomic and treatment factors contribute to diagnosis of early-stage (local-stage) breast cancer, as well as
excess deaths among African American women.
Objectives We evaluated socioeconomic and treatment predictive factors for early-stage breast cancer among African American
women compared to Caucasian women. A secondary aim evaluated predictors and overall risks associated with all-cause and
breast cancerspecific mortality.
Methods We used retrospective cohort population-based study data from the Surveillance, Epidemiology, and End Results
(SEER) Program on 547,703 women aged 20 years diagnosed with breast cancer primary tumors from 2007 to 2016.
Statistical analysis used logistic regression to assess predictors of early-stage breast cancer and Cox proportional hazards
regression for mortality risks.
Results African American women were more likely to be diagnosed at advanced-stage, had larger tumor size at diagnosis, and
received less cancer-directed surgery, but more chemotherapy than Caucasian women. Insured women (> 50%) were more likely
to be diagnosed at early-stage and to have smaller tumors (p< 0.05). Education level, poverty level, and household income had no
impact on racial disparities or socioeconomic disparities in women diagnosed at early stage. We found increased risks for all-
cause mortality (hazard ratio = 1.18; 95% confidence interval, 1.161.21) and breast cancerspecific mortality (HR = 1.22; 95%
CI, 1.191.25) among African American women compared to Caucasian women after adjusting for demographic, socioeconom-
ic, and treatment factors.
Conclusions In this population-based study using the most recent SEER data, African American women with breast cancer
continued to exhibit higher all-cause mortality and breast cancerspecific mortality compared to Caucasian women.
Keywords Breast cancer .Early stage .Racial disparities .Treatment .Surgery .Chemotherapy .Race/ethnicity .African
American women
Introduction
Despite continual efforts to reduce the burden of inequalities
in socioeconomic levels and among ethnic minority races
compared to Caucasians, disparities in health care utilization
and clinical outcomes continue to persist [111]. Reports by
the Institute of Medicine [1] and other studies [211]have
consistently demonstrated disparities observed in cancer care
and treatment among ethnic minority populations compared to
Caucasians. Although outcomes on racial disparities in cancer
care utilization are relatively consistent, there are conflicting
reports on racial differences in survival even after adjustment
for dissimilarities in treatment [1227]. Some studies showed
that racial disparities no longer existed after adjusting for treat-
ment rendered [1216], while other studies demonstrated that
differences persisted in survival and mortality despite
adjusting for dissimilarities in health care and treatment
[1727]. These inconsistent findings could be due to different
study designs, analytical methods, and biases and
*Dale Hardy
dhardy@msm.edu
1
Department of Internal Medicine, Morehouse School of Medicine,
Research Wing, Rm 339, 720 Westview Drive, Atlanta, GA 30310,
USA
2
Department of Natural Sciences, University of Houston,
Houston, TX 77030, USA
Journal of Racial and Ethnic Health Disparities
https://doi.org/10.1007/s40615-020-00855-y
Author's personal copy
confounding in information and measurements [1227].
Moreover, many previous reports did not have information
on treatment received [1719]. Because health insurance and
access to health care are fundamentally important for early
detection of cancer and timely treatment [11,2832], it is
critical to incorporate this information in the analysis. The
aim of this study was to evaluate socioeconomic and treatment
predictive factors associated with early-stage breast cancer
among African American compared to Caucasian women. A
secondary aim evaluated risk factors and overall risks associ-
ated with all-cause mortality and breast cancerspecific mor-
tality. In this study, we used the most recent data from the
National Cancer Institutes Surveillance, Epidemiology, and
End Results (SEER) data released in November 2018. These
data sources enabled us to examine socioeconomic and racial
disparities in cancer stage at diagnosis, as well as tumor size
and clinical outcomes on survival in a large cohort of African
American and Caucasian women with breast cancer. Our
study findings may help inform interventions and policies
for cancer prevention and control.
Patients and Methods
Data Sources
We used data from the National Cancer Institutes SEER
Public Use Data Set released in November 2018 [34]. SEER
data is an authoritative source of data on cancer incidence and
has high accuracy and completeness [33]. The SEER program
supports population-based tumor registries in nine areas (San
Francisco/Oakland, San Jose-Monterey, Los Angeles, Greater
California, Detroit, Seattle, Atlanta, Rural Georgia, and
Greater Georgia) and 8 states (Connecticut, Iowa, New
Mexico, Utah, Hawaii, Louisiana, Kentucky, and New
Jersey), covering 28% of the US population. The registries
ascertain all newly diagnosed (incident) breast cancer cases
from multiple reporting sources such as hospitals, outpatient
clinics, laboratories, private medical practitioners, nursing/
convalescent homes/hospices, autopsy reports, and death cer-
tificates. The SEER public use data set includes information
on types of cancer-directed surgical procedures received, re-
ceipt of radiation therapy, and chemotherapy. These treat-
ments were provided in the first course of therapy (within
4 months of initial therapy after diagnosis).
Information on SEER data also includes data on health
insurance coverage at the time of cancer diagnosis from
2007 through 2016, as well as information on tumor stage at
diagnosis, tumor location and size, lymph node and distant
organ metastases, histologic type, tumor grade, and demo-
graphic characteristics such as age, race/ethnicity, and marital
status. Additional variables included socioeconomic variables
such as education level, poverty level, and household income
at the county level. Our research received approval from
SEER after signing the SEER Research Data Agreement.
We received additional approval for using data on treatment
information for radiation therapy and chemotherapy. The
study was considered exempt for Institutional Review Board
(IRB) review because it did not involve any patient contact
and only contained review of de-identified SEER Public Use
Data.
Study Population
Our initial sample included 559,113 African American and
Caucasian women who were diagnosed with incident breast
cancer at age 20 or older between 2007 and 2016 in 17 SEER
registries. Patients of other race/ethnicity were not included in
the study. We studied cases diagnosed withbreastcancerfrom
2007 through 2016 because health insurance status informa-
tion was only available during these years. From our initial
sample (559,113 women), we excluded women with missing
information on tumor stage (n= 11,285) and socioeconomic
variables (education level, poverty level, and household in-
come) at the county level (n= 125). Our final sample for
analysis included 547,703 women of which 66,703 (11.6%)
were African American women and 481,000 (87%) were
Caucasian women.
Study Variables
Race/Ethnicity and Patient Characteristics
Tumor and patient characteristics included tumor size (cate-
gorized as < 1.0, 1.0< 2.0, 2.0< 3.0, 3.0< 4.0, 4.0 cm,
and unknown tumor size); histological stage (local, regional,
or distant stage); tumor grade (well, moderately, poorly dif-
ferentiated, undifferentiated, or unknown); hormone receptor
status (estrogen or progesterone receptor positive, negative, or
unknown); age at diagnosis (< 45, 4554, 5564, 6574, 75
79, 80 years); marital status (married, unmarried, and un-
known marital status); race/ethnicity (African American and
Caucasians women); time period (2007 to 2016); and geo-
graphic areas (17 SEER registries) [34].
Health Insurance and Socioeconomic Status (SES)
Table 2gives a summary of the following variables in the first
column. Health Insurance at an individual level available from
2007 to 2017 was coded as uninsured, any Medicaid, insured,
insured but without specifics, and unknown. There were three
socioeconomic variables at the county level available in the
SEER*Stat program including education level, poverty level,
and household income. Counties were divided into quartiles
based on percentages of the patients in the given county with
the specific criteria for each of these 3 variables. Education
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level divided into quartiles for patients with less than high
school education was coded as follows: first quartile (2.1<
9.8%), second (9.8< 12.8%), third (12.8<17.8%), and
fourth quartile (17.8%). For people living under poverty
levels, the countiesquartiles were defined as 4.0<10.7%,
10.7< 14.0%, 14.017.9%, and 17.9% percentage. For
household income, counties were classified based on the me-
dian annual household income grouped into quartiles:
$68,650, $57,580< 68,650, $49,000< 57,580, and
< $49,000. Education, poverty, and household income vari-
ables were first recoded to ensure that lower values represent-
ed lower quartiles of socioeconomic status.
Treatment for Breast Cancer
Cancer-directed surgery was coded as 1089 in SEER data
and included total mastectomy and breast-conserving surgery
that was defined as receiving segmental mastectomy, lumpec-
tomy, quadrantectomy, tylectomy, wedge resection, nipple
resection, excisional biopsy, or partial mastectomy unspeci-
fied [34]. SEER records radiation therapy provided within
4 months after diagnosis that was coded as either yes or no/
unknown. Radiation therapy included beam radiation, radio-
active implants, brachytherapy, radioisotopes or other radia-
tion [33]. Chemotherapy was also coded as either yes or no/
unknown. Treatments were coded separately, but it was un-
known if radiation therapy or chemotherapy was given before
surgery or as adjuvant therapy after surgery, or stand-alone
treatment.
Survival and Mortality Variables
The vital status (dead or alive), cause of death, date of death,
and survival time in months from the date of diagnosis to the
date of death or the date of last follow-up (December 31, 2016)
were available from the SEER*Stat data [34]. All-cause mor-
tality was defined as death from any cause that was the under-
lying cause of death indicated in the SEER registries. Patients
who were alive at the last date of follow-up were censored.
Breast cancerspecific mortality was defined as breast cancer
as the underlying cause of death. In this specific analysis, pa-
tients who died of causes other than breast cancer or who were
still alive at the date of last follow-up were censored.
Statistical Analysis
Differences in the distribution of baseline characteristics among
the two race/ethnic groups were tested using Pearsonschi-
square statistic. Logistic regression models were used to assess
the odds ratio of being diagnosed at early tumor stage (local
stage), having smaller tumor size, and receiving cancer-directed
treatment (surgery, radiation therapy, and chemotherapy) after
adjusting for other risk factors and confounders, including age,
marital status, tumor grade, hormone receptor status, year of
diagnosis, SEER geographic areas, and socioeconomic factors
(health insurance, education level, poverty level, and household
income at the county level). Kaplan-Meier curves for survival
curves and log-rank tests were conducted between comparison
groups. Cox proportional hazard regression model was used in
survival analysis using the PHREG procedure available in the
SAS system (Cary, NC: SAS Institute, Inc.). The proportional-
ity assumption was satisfied when the log-log Kaplan-Meier
curves for survival functions by race/ethnicity or socioeconom-
ic status were parallel and did not intersect. In these Cox pro-
portional hazard regression analyses, four models were ana-
lyzed; however only the third and fourth models were present-
ed. The first model was an unadjusted model on the hazard ratio
of mortality between African American and Caucasian women.
The second model adjusted for patient demographic character-
istics (including age and marital status), tumor factors (such as
tumor stage, tumor grade, tumor size, and hormone receptor
status), year of diagnosis, and SEER geographic areas. The
third model adjusted for health insurance, education level, pov-
erty level, and household income, in addition to the factors in
the second model. The fourth model adjusted additionally for
cancer-directed treatment received (surgery, radiation therapy,
and chemotherapy).
Results
Table 1presents the distribution of demographic characteris-
tics, tumor characteristics, and treatment between the two
race/ethnic groups of women diagnosed with breast cancer
at age 20 over the past 10 years from 2007 to 2016.
Compared to Caucasian women, a higher percentage of
African American women were diagnosed with breast cancer
at younger ages, were unmarried at diagnosis, were diagnosed
at advanced stage, had larger tumor size, had less differentiat-
ed grade, and had negative hormone receptor status. These
differences were statistically significant at p<0.001.
Table 2presents the distribution of health insurance and
socioeconomic status by race/ethnicity. A larger percentage
of African American women with breast cancer were unin-
sured or on Medicaid and were in the lowest quartiles (3rd
and 4th quartiles) of socioeconomic status (education level,
poverty level, and household income atthe county level) com-
pared to Caucasians. For example, 74.7% of African
American women vs. 86% of Caucasians women were in-
sured, while 69.6% of African American women vs. 46.7%
Caucasian women were in the last two lowest quartiles of
socioeconomic status.
Table 3presents the percentage of patients diagnosed with
early tumor stage (local stage), having tumor size < 1 cm, and
receiving cancer-directed treatment (surgery, radiation thera-
py, and chemotherapy) by race/ethnicity, health insurance,
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and other socioeconomic factors. A higher percentage of
Caucasian women were diagnosed at an early stage, had
smaller tumor size at diagnosis, and received cancer-directed
surgery than African American women. However, a higher
percentage of African American women with breast cancer
received less radiation therapy, but more chemotherapy than
Caucasian women. In addition, a higher percentage of women
with breast cancer were diagnosed at an early stage and re-
ceived cancer-directed surgery. Moreover, a higher percent-
age of women without health insurance or who had Medicaid
coverage received chemotherapy. This was likely due to
detection of late-stage tumor at diagnosis. In addition, there
were statistically significant differences in early-stage diagno-
sis, tumor size, and treatment by socioeconomic status factors
(education level, poverty level, and household income) at the
county level.
Table 4presents the adjusted odds ratio of having been diag-
nosed at early tumor stage (local stage), having tumor size <
1 cm, and receiving cancer-directed treatment (surgery, radiation
therapy, and chemotherapy) by race/ethnicity, health insurance,
and other socioeconomic factors after adjusting for differences
in age, marital status, other tumor characteristics, year of
Table 1 Comparison of patient
and tumor characteristics between
African American and Caucasian
and women diagnosed with breast
cancer, 20072016
Patient and tumor African Americans Caucasians pvalue
Characteristics n%n%
Age (years) <0.001
<45 (2044) 9419 14.1 46,865 9.7
4554 15,957 23.9 96,876 20.1
5564 18,223 27.3 123,113 25.6
6574 13,489 20.2 115,857 24.1
7584 7186 10.8 71,263 14.8
85 2429 3.6 27,026 5.6
Marital Status <0.001
Married 22,373 33.5 267,486 55.6
Unmarried 40,531 60.8 189,404 39.1
Unknown 3799 5.7 24,110 5.0
Tumor stage <0.001
Local stage 37,631 56.4 314,183 65.8
Regional stage 23,235 34.8 137,661 28.6
Distant stage 5837 8.8 26,787 5.6
Tumor size (cm) <0.001
< 1.0 10,262 15.4 101,283 21.1
1.0< 2.0 19,103 28.6 163,395 34.0
2.0< 3.0 13,023 19.5 88,957 18.5
3.0< 4.0 7378 11.1 41,538 8.6
4.0 13,709 20.6 67,769 14.1
Unknown size 3228 4.8 18,058 3.8
Tumor grade <0.001
Well differentiated (I) 9054 13.6 109,317 22.7
Moderately differentiated(II) 23,232 34.8 202,340 40.1
Poorly differentiated (III) 28,694 43.0 136,706 28.4
Undifferentiated (IV) 380 0.6 2303 0.5
Unknown 5343 8.0 30,334 6.3
Hormone receptor status < 0.001
Positive 46,217 69.3 392,978 81.7
Negative 17,775 26.7 70,362 14.6
Unknown 2711 4.1 17,660 3.7
Total 66,703 100.0 481,000 100.0
pvalues for proportions of categorical variables among patient and tumor characteristics were calculated using
Pearsons chi-square tests of hypothesis for independence
J. Racial and Ethnic Health Disparities
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diagnosis, and SEER geographic areas. Similar to our findings
in Table 3, African American women were more likely to be
diagnosed at advanced stage, more likely to have larger tumor
size at diagnosis, and more likely to receive chemotherapy, but
less likely to receive cancer-directed surgery than Caucasian
women. In addition, insured women were more likely to receive
cancer-directed surgery, but were less likely to receive chemo-
therapy as compared to uninsured patients, after adjusting for
age, marital status, tumor stage, tumor grade, hormone receptor
status, year of diagnosis, and SEER geographic areas. There
were no significant differences in early-stage diagnosis for so-
cioeconomic factors (education level, poverty level, and house-
hold income at the county level). However, there were varying
effects of socioeconomic factors for tumor size < 1 cm and treat-
ment by the quartiles of education level, poverty level, and
household income at the county level. For example, patients in
the lowest quartile (4th quartile) compared to those in the highest
quartile (1st quartile) of education were 8% less likely to have a
smaller tumor size < 1 cm (odds ratio = 0.92; 95% confidence
interval, 0.880.95), unlike those in the 2nd quartile of education
whowere7%morelikelytohaveatumorsize<1cm(OR=
1.07; 95% CI, 1.051.10).
Finally, we investigated the risk of all-cause mortality as
well as breast cancerspecific mortality using four different
statistical models for African American women compared to
Caucasian women (Table 5). For all-cause mortality, in model
1 (not presented), the unadjusted hazard ratio (HR) showed a
1.50-fold increased risk (HR = 1.50; 95% CI, 1.481.53) in
African American women as compared to Caucasian women
with breast cancer. However, this effect estimate decreased in
model 2 (not presented) to 1.27-fold increased risk (HR =
1.27; 95% CI, 1.251.30) for all-cause mortality after
adjusting for patient and tumor characteristics as well as year
of diagnosis, and SEER geographic areas. In model 3 in
Table 5, we further adjusted for health insurance and other
socioeconomic factors (education level, poverty level, and
household income at the county level), and the hazard ratio
was reduced to 1.22-fold increased risk (HR = 1.22; 95% CI,
1.191.24) for all-cause mortalityfor African American wom-
en as compared to Caucasian women. Model 4 in Table 5
further adjusted for cancer-directed treatment rendered (sur-
gery, radiation therapy, and chemotherapy), and the hazard
ratio for all-cause mortality was reduced to 1.18-fold in-
creased risk (HR = 1.18; 95% CI, 1.161.21) for all-cause
Table 2 Comparison of
socioeconomic factors between
African American and Caucasian
women diagnosed with breast
cancer, 20072016
Socioeconomic Factors African Americans Caucasians pvalue
N%n%
Health insurance <0.001
Uninsured 2180 3.3 6556 1.4
Any Medicaid 13,301 19.9 46,028 9.6
Insured 49,828 74.7 417,880 86.9
Insured with no specifics 9685 14.5 66,201 13.8
Unknown 1394 21. 10,536 2.2
Education (% with less than high school) at county level < 0.001
1st quartile (2.1< 9.8%) 9894 14.8 126,198 26.2
2nd quartile (9.8< 12.8%) 17,984 27.0 120,094 25.0
3rd quartile (12.8< 17.8%) 22,789 34.2 113,748 23.7
4th quartile (17.8%) 16,036 24.0 120,960 25.2
Poverty (% with poverty line) at county level < 0.001
1st quartile (4.0< 10.7%) 8085 12.1 127,361 26.5
2nd quartile (10.7< 14.0%) 12,216 18.3 129,123 26.8
3rd quartile (14.017.9%) 18,913 28.4 118,644 24.7
4th quartile (17.9%) 27,489 41.2 105,872 22.0
Household income ($) at county level < 0.001
1st quartile ($19,340< $49,000) 25,189 37.8 111,713 23.2
2nd quartile ($49,000< $57,580) 18,039 27.0 117,426 24.4
3rd quartile ($57,580< $68,650) 13,451 20.2 125,192 26.0
4th quartile ($68,650) 10,024 15.0 126,669 26.3
Total 66,703 100.0 481,000 100.0
pvalues for proportions of categorical variables for patient and tumor characteristics were calculated using
Pearsons chi-square tests of hypothesis for independence
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mortality, and remained significantly higher in African
American women compared to in Caucasian women. We then
investigated the risk of breast cancerspecific mortality for
African American women compared to Caucasian women.
Model 1 (not presented) had an unadjusted hazard ratio of
1.83-fold increased risk (HR = 1.83; 95% CI, 1.791.88) in
African American women compared to Caucasian women.
Model 2 (not presented) had a substantially reduced hazard
ratio (HR = 1.29; 95% CI, 1261.32) after adjusting for pa-
tient and tumor characteristics as well as year of diagnosis, and
SEER geographic areas in African American women com-
pared to Caucasian women. Model 3 and model 4 in Table 5
showed a small decrease in risk for breast cancerspecific
mortality for African American women compared to
Caucasian women, after adjusting for health insurance and
other socioeconomic status factors at the county level (HR =
1.25; 95% CI, 1.221.28) and treatment rendered (HR = 1.22;
95% CI, 1.191.25).
Among all women with breast cancer in 20072016 with the
last follow-up of December 31, 2016, mean survival time was
49.4 months for Caucasian women and 45.2 months for
African American women with breast cancer. Figure 1presents
the Kaplan-Meier survival curves for overall survival and
breast cancerspecific survival, in which survival rates were
higher in Caucasian women than in African American women
with breast cancer (log-rank tests were significant at p<0.001).
Discussion
In this study, we examined socioeconomic and treatment pre-
dictive factors for early-stage breast cancer among African
American women compared to Caucasian women. In addi-
tion, we evaluated predictors and overall risks associated with
all-cause mortality and breast cancerspecific mortality. We
found that more Caucasian women were diagnosed at early
stage compared to African American women. African
American women had larger tumors at diagnosis and received
less cancer-directed surgery but received more chemotherapy
treatment than Caucasian women. Being insured was impor-
tant for being diagnosed at early stage with smaller tumors.
For patients diagnosed at early stage, education level, poverty
Table 3 Percentage of patients who were diagnosed at early stage, small tumor size, and treatment received including race/ethnicity and socioeconomic
factors in women with breast cancer
Percent (%)
Race and socioeconomic factors Early-stage diagnosis Tumor size < 1 cm Cancer-directed surgery Radiation therapy Chemotherapy
Race (%)
African Americans 56.4* 15.4* 86.6* 46.0* 50.1*
Caucasians 65.8 21.1 91.6 47.7 37.5
Health insurance (%)
Uninsured 47.6* 11.3* 78.2* 42.9* 55.9*
Any Medicaid 52.6 12.8 85.6 42.4 48.2
Insured 66.8 21.8 92.3 49.2 38.5
Insured with no specifics 64.8 20.1 89.2 45.3 34.2
Unknown 65.6 19.1 76.3 31.8 27.0
Education (% with less than high school) at county level
1st quartile (2.1< 9.8%) 66.5* 22.5* 91.6* 52.3* 38.2*
2nd quartile (9.8< 12.8%) 65.9 21.7 91.2 50.5 38.7
3rd quartile (12.8< 17.8%) 63.7 19.7 90.7 46.7 39.9
4th quartile (17.8%) 62.5 17.6 90.4 40.4 39.1
Poverty (% with poverty line) at county level
1st quartile (4.0< 10.7%) 67.1* 22.8* 91.8* 51.9* 37.9*
2nd quartile (10.7< 14.0%) 65.4 21.1 91.2 48.7 38.5
3rd quartile (14.017.9%) 63.6 19.2 90.2 42.9 38.0
4th quartile (17.9%) 62.6 18.4 90.6 46.4 41.7
Household income ($) at county level (%)
1st quartile ($19,340< 49,000) 63.2* 19.1* 90.9* 47.2* 41.0*
2nd quartile ($49,000< 57,580) 63.4 18.9 90.5 43.2 38.8
3rd quartile ($57,580< 68,650) 65.1 21.3 91.2 50.2 39.1
4th quartile ($68,650) 67.0 22.1 91.2 49.1 37.2
*Indicates significance at p< 0.05 from chi-square crude comparisons by race, insurance, education, poverty, and income
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level, and household income had no impact on racial dispar-
ities or socioeconomic health disparities in breast cancer be-
tween African American and Caucasian women. There were
significant disparities in mortality between African American
women compared to Caucasian women with breast cancer.
However, these differences were reduced substantially after
adjusting for patient and tumor characteristics, health insur-
ance, socioeconomic factors, and treatment received.
Nevertheless, African American women had increased risks
for all-cause mortality and breast cancerspecific mortality
compared to Caucasian women.
Other studies have investigated early-stage breast
cancerspecific mortality in African American compared
to Caucasian women [3541]. Komenaka et al. [35]report-
ed that in their study of mostly uninsured women, the effect
of race on survival was no longer significant after adjusting
for demographic and treatment factors. Yedjou et al. [39]
reported in their review that the disparity in mortality for
African American women compared to Caucasian women
may be due to many clinical and non-clinical risk factors,
such as lack of health insurance, barriers to early detection
and screening, more advanced stage of disease at diagnosis,
and lack of access to better cancer treatment. In our study,
we found that African American women were diagnosed at
later stages and subsequently had larger-sized tumors than
Caucasian women. Furthermore, after we controlled for
confounders and risk factors, there were significant differ-
ences in early stage at diagnosis, and varying effects for
predictors of tumor size < 1 cm and treatment, education
level, poverty level, and household income at the county
level. In addition, African American women with breast
cancer received less cancer-directed surgery but were more
likely to receive chemotherapy than their Caucasian coun-
terparts after adjusting for risk factors.
Table 4 Multiple regression of being diagnosed at early stage, having small tumor size, and receiving treatment by race and socioeconomic factors in
women with breast cancer
Odds ratio (95% confidence interval)*
Early-stage diagnosis Tumor size < 1 cm Cancer-directed surgery Radiation therapy Chemotherapy
Race/ethnicity
Caucasians 1.00 (ref) 1.00 (ref) 1.00 (ref) 1.00 (ref) 1.00 (ref)
African Americans 0.85 (0.840.87) 0.88 (0.860.90) 0.85 (0.830.88) 1.02 (1.001.04) 1.26 (1.241.29)
Health insurance
Uninsured 1.00 (ref) 1.00 (ref) 1.00 (ref) 1.00 (ref) 1.00 (ref)
Any Medicaid 1.11 (1.051.16) 1.16 (1.081.25) 1.50 (1.401.61) 0.98 (0.931.03) 0.84 (0.800.88)
Insured 1.54 (1.471.61) 1.82 (1.701.95) 1.96 (1.832.09) 1.04 (0.991.09) 0.68 (0.640.71)
Insured with no specifics 1.51 (1.441.59) 1.68 (1.561.80) 1.42 (1.321.52) 0.94 (0.900.98) 0.53 (0.500.55)
Unknown 2.18 (2.042.33) 1.60 (1.471.74) 0.75 (0.690.82) 0.65 (0.610.69) 0.39 (0.360.42)
Education (% with less than high school) at county level
1st quartile (2.1< 9.8%) 1.00 (ref) 1.00 (ref) 1.00 (ref) 1.00 (ref) 1.00 (ref)
2nd quartile (9.8< 12.8%) 0.98 (0.951.00) 1.07 (1.051.10) 1.08 (1.041.13) 1.03 (1.001.05) 0.99 (0.971.02)
3rd quartile (12.8< 17.8%) 0.97 (0.941.00) 0.97 (0.951.01) 1.09 (1.031.14) 0.89 (0.870.92) 1.05 (1.021.08)
4th quartile (17.8%) 0.98 (0.951.02) 0.92 (0.880.95) 1.17 (1.101.24) 0.84 (0.820.87) 1.06 (1.031.10)
Poverty (% with poverty line) at county level
1st quartile (4.0< 10.7%) 1.00 (ref) 1.00 (ref) 1.00 (ref) 1.00 (ref) 1.00 (ref)
2nd quartile (10.7< 14.0%) 1.01 (0.991.04) 0.95 (0.920.97) 0.91 (0.870.95) 0.92 (0.900.94) 0.94 (0.920.96)
3rd quartile (14.017.9%) 0.98 (0.961.02) 0.99 (0.961.03) 0.90 (0.840.95) 1.01 (0.981.04) 0.91 (0.880.95)
4th quartile (17.9%) 0.98 (0.941.02) 0.99 (0.961.04) 0.94 (0.871.01) 1.00 (0.971.04) 0.94 (0.900.98)
Household income ($) at county level
1st quartile ($19,340<49,000) 1.00 (ref) 1.00 (ref) 1.00 (ref) 1.00 (ref) 1.00 (ref)
2nd quartile ($49,000< 57,580) 1.01 (0.961.06) 0.95 (0.901.00) 1.11 (1.021.21) 1.00 (0.971.05) 0.99 (0.941.03)
3rd quartile ($57,580< 68,650) 0.99 (0.951.03) 0.93 (0.890.97) 1.15 (1.071.24) 1.03 (0.991.07) 1.07 (1.021.11)
4th quartile ($68,650) 0.97 (0.951.00) 0.99 (0.961.02) 1.12 (1.061.17) 1.08 (1.051.10) 1.04 (1.011.07)
Italicized values indicate p<0.05
*Odds ratios from multiple logistic regressions models were adjusted for age, marital status, tumor stage, tumor size, tumor grade, hormone receptor
status, SEER areas, year of diagnosis and socioeconomic factors (health insurance, education level, poverty level, and household income at the county
level)
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Table 5 Racial disparities and effects of socioeconomic factors on mortality in women with breast cancer
Hazard ratio (95% confidence interval) of mortality
Race/ethnicity and other factors All-cause mortality Breast cancerspecific mortality
Model 3* Model 4
&
Model 3* Model 4
&
Race/ethnicity
Caucasians 1.00 (ref) 1.00 (ref) 1.00 (ref) 1.00 (ref)
African Americans 1.22 (1.191.24) 1.18 (1.161.21) 1.25 (1.221.28) 1.22 (1.191.25)
Age (years)
<45 (2044) 1.00 (ref) 1.00 (ref) 1.00 (ref) 1.00 (ref)
4554 1.04 (1.011.07) 1.02 (0.991.05) 1.03 (1.001.07) 1.01 (0.981.04)
5564 1.37 (1.341.41) 1.31 (1.271.35) 1.19 (1.151.23) 1.13 (1.091.17)
6574 2.16 (2.102.22) 1.97 (1.922.03) 1.43 (1.381.48) 1.32 (1.271.36)
7584 4.35 (4.234.47) 3.67 (3.573.78) 2.20 (2.122.27) 1.90 (1.841.97)
85 8.92 (8.659.19) 6.48 (6.286.68) 3.82 (3.683.98) 2.90 (2.783.03)
Marital status
Married 1.00 (ref) 1.00 (ref) 1.00 (ref) 1.00 (ref)
Unmarried 1.30 (1.281.32) 1.26 (1.251.28) 1.20 (1.181.22) 1.17 (1.151.19)
Unknown 1.23 (1.191.27) 1.14 (1.111.18) 1.16 (1.111.21) 1.09 (1.041.13)
Tumor stage
Local stage 1.00 (ref) 1.00 (ref) 1.00 (ref) 1.00 (ref)
Regional stage 1.62 (1.60
1.65) 1.72 (1.691.74) 2.69 (2.632.76) 2.77 (2.702.84)
Distant stage 7.49 (7.349.64) 5.02 (4.915.13) 15.63 (15.2216.05) 9.83 (9.5410.13)
Tumor size (cm)
< 1.0 1.00 (ref) 1.00 (ref) 1.00 (ref) 1.00 (ref)
1.0<2.0 1.20 (1.141.20) 1.19 (1.161.22) 1.33 (1.271.39) 1.37 (1.311.43)
2.0<3.0 1.44 (1.411.48) 1.46 (1.421.50) 1.91 (1.821.99) 1.96 (1.872.05)
3.0<4.0 1.77 (1.721.82) 1.72 (1.671.77) 2.50 (2.382.62) 2.48 (2.362.59)
4.0 + 2.13 (2.072.18) 2.06 (2.012.11) 3.20 (3.073.34) 3.14 (3.013.28)
Unknown size 2.45 (2.372.53) 1.90 (1.841.96) 3.64 (3.473.82) 2.88 (2.753.03)
Tumor grade
Well differentiated (I) 1.00 (ref) 1.00 (ref) 1.00 (ref) 1.00 (ref)
Moderately differentiated (II) 1.13 (1.111.16) 1.15 (1.121.17) 1.63 (1.571.69) 1.64 (1.581.71)
Poorly differentiated (III) 1.45 (1.421.49) 1.54 (1.511.58) 2.47 (2.372.57) 2.61 (2.502.71)
Undifferentiated (IV) 1.49 (1.391.59) 1.55 (1.44
1.66) 2.43 (2.222.67) 2.53 (2.312.78)
Unknown 1.40 (1.361.44) 1.21 (1.181.24) 2.27 (2.172.37) 1.92 (1.832.01)
Hormone receptor status
Positive 1.00 (ref) 1.00 (ref) 1.00 (ref) 1.00 (ref)
Negative 1.52 (1.501.55) 1.62 (1.591.65) 1.81 (1.771.85) 1.91 (1.861.95)
Unknown 1.60 (1.561.64) 1.47 (1.431.51) 1.78 (1.721.85) 1.67 (1.621.73)
Health insurance
Uninsured 1.00 (ref) 1.00 (ref) 1.00 (ref) 1.00 (ref)
Any Medicaid 0.91 (0.870.95) 0.95 (0.900.99) 0.89 (0.840.94) 0.93 (0.880.98)
Insured/insured with no specifics 0.61 (0.590.64) 0.67 (0.640.70) 0.67 (0.640.71) 0.74 (0.700.78)
Unknown 0.73 (0.690.78) 0.71 (0.670.75) 0.84 (0.780.90) 0.83 (0.770.89)
Education (% < high school)
1st quartile (2.1< 9.8%) 1.00 (ref) 1.00 (ref) 1.00 (ref) 1.00 (ref)
2nd quartile (9.8< 12.8%) 0.99 (0.961.01) 1.00 (0.971.02) 1.00 (0.971.04) 1.02 (0.981.05)
3rd quartile (12.8< 17.8%) 0.99 (0.961.01) 0.99 (0.961.02) 0.99 (0.951.03) 1.00 (0.961.04)
4th quartile (17.8%) 1.03 (0.991.07) 1.05 (1.021.09) 1.05 (1.001.11) 1.08 (1.031.14)
J. Racial and Ethnic Health Disparities
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Having health insurance was associated with a better like-
lihood of being diagnosed at early stage or to be diagnosed
with a small tumor size < 1 cm, or to receive cancer-directed
surgery, but was associated with less likelihood of receiving
chemotherapy. Green et al. [41] found in their meta-analysis
that African American women were more likely to have de-
lays in treatment over 90 days and were more than likely to
discontinue chemotherapy, which may explain in part the in-
creased risk of mortality.
There were several strengths in this study. A major
strength was the large, retrospective population-based sam-
ple size from 17 SEER geographic areas representing 28%
of the US population. Another unique strength is that we
had sufficient sample size to stratify by race/ethnicity, treat-
ment, and socioeconomic factors. However, our study also
had several limitations. Information on radiation therapy
and chemotherapy was coded yes or no/unknown.
Treatments were coded separately; however, it was un-
known if radiation therapy or chemotherapy was given be-
fore surgery or as adjuvant therapy after surgery, or stand-
alone treatment. Although it is possible to know if multiple
treatments (radiation, chemotherapy, and surgery) were re-
ceived per individual; it may be beyond the scope of this
studys main purpose. In addition, those who did not receive
radiation therapy and chemotherapy might have received
the therapy elsewhere from private clinics outside the reg-
istries; hence, caution should be kept in mind in interpreting
these results. However, several validation studies on these
therapies demonstrated that other sources such as Medicare
or medical chart reviews only enhanced a small percentage
of patients receiving these therapies [42,43]. No evidence
so far showed that the above underreporting of radiation
therapy and chemotherapy was differential by race/
ethnicity and socioeconomic factors, and therefore might
have a minimal effect on the findings and conclusions of
this study. Another important limitation is that we could
not include comorbid conditions for confounder adjustment
in our study and therefore could not assess this effect in our
study. Comorbid conditions may have an important impact
on surgery, chemotherapy, or radiation treatments as well as
on overall mortality. Furthermore, the assessment of socio-
economic status (education, poverty level, and household
income) effects was at the county level but did not reflect
the individual patient level; hence, there could be an eco-
logical bias. However, having health insurance as another
assessment of socioeconomic status was at an individual
Table 5 (continued)
Hazard ratio (95% confidence interval) of mortality
Race/ethnicity and other factors All-cause mortality Breast cancerspecific mortality
Model 3* Model 4
&
Model 3* Model 4
&
Poverty (%) at county level
1st quartile (4.0< 10.7%) 1.00 (ref) 1.00 (ref) 1.00 (ref) 1.00 (ref)
2nd quartile (10.7< 14.0%) 1.03 (1.001.05) 1.01 (0.991.04) 1.03 (0.991.06) 1.01 (0.971.04)
3rd quartile (14.017.9%) 1.03 (0.91.06) 1.01 (0.981.05) 1.04 (0.991.09) 1.02 (0.971.07)
4th quartile (17.9%) 1.03 (0.981.07) 1.01 (0.971.06) 1.02 (0.961.08) 1.01 (0.951.07)
Income at county level
4th quartile ($68,650) 1.00 (ref) 1.00 (ref) 1.00 (ref) 1.00 (ref)
1st quartile ($19,340< 49,000) 1.09 (1.041.14) 1.10 (1.051.16) 1.08 (1.011.15) 1.10 (1.031.17)
2nd quartile ($49,000< 57,580) 1.10 (1.051.14) 1.11 (1.071.16) 1.12 (1.061.18) 1.13 (1.071.20)
3rd quartile ($57,580< 68,650) 1.04 (1.011.07) 1.05 (1.021.08) 1.04 (1.001.09) 1.06 (1.021.10)
Treatment
Surgery (yes vs no/uk) 0.41 (0.400.41) 0.36 (0.350.37)
Radiation therapy (yes vs no/uk) 0.75 (0.740.76) 0.82 (0.810.84)
Chemotherapy (yes vs no/uk) 0.79 (0.780.81) 0.86 (0.840.88)
uk, unknown
Italicized values indicate p<0.05
*Model 3: Hazard ratio adjusted forage, marital status, tumorcharacteristics, SEER areas, yearof diagnosis, and socioeconomic status (health insurance,
education level, poverty level, and household income at county level);
&
Model 4: Hazard ratio further adjusted for treatment received (cancer-directed surgery, radiation therapy, and chemotherapy) in addition to factors
above
Note: In model 3, there are no treatment estimates because these variables were not included in this part of the analysis
J. Racial and Ethnic Health Disparities
Author's personal copy
level, and was found to have a greater impact on stage at
diagnosis and treatment received. Finally, other factors such
as quality of treatment, timeliness of treatment, and patient
adherence were not measured in this study and could have
contributed to the observed results. These factors, in addi-
tion to other factors, could be measured in future studies to
further explore the underlying cause of the observed dispar-
ity between race/ethnic groups.
In summary, African American women tend to be diagnosed
at later stages of breast cancer than Caucasian women. Health
insurance was significantly associated with a higher likelihood
of having an early-stage diagnosis and smaller size tumors <
1 cm and receiving cancer-directed surgery, whereas education
level, poverty level, and household income did not have a sig-
nificant impact on the risk of being diagnosed with early-stage
breast cancer among African American and Caucasian women.
However, African American women with breast cancer remain
at increased risk for all-cause mortality and breast cancer
specific mortality compared to Caucasian women.
Acknowledgments We acknowledge the efforts of the National Cancer
Institute in the creation of the SEER cancer registry data for public use.
We also acknowledge Dr. Xianglin L. Du for his guidance in this study.
Code Availability Code has been addressed in the manuscript and is
given upon request.
AuthorsContributions Dale Hardy and Daniel Du contributed to the
study conception and design.
Dale Hardy and Daniel Du wrote the manuscript.
DSH and DD interpreted the data analysis results.
DSH performed the data analysis.
Data Availability The data is available from SEER.
a. Overall survival.
b. Breast cancer specific survival. -
Fig. 1 Kaplan-Meier survival
curves for overall survival and
breast cancerspecific survival for
African American (Black) and
Caucasian (White) women with
breast cancer. aOverall survival.
bBreast cancerspecific survival.
The log-rank tests were signifi-
cant at p< 0.001 between two
groups
J. Racial and Ethnic Health Disparities
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Compliance with Ethical Standards
Conflict of Interest The authors declare that they have no conflict of
interest.
Ethics Approval Because SEER Public Use Data are de-identified,
existing data without any patient contact and did not involve human
subject participants research, making the study exempt for the
Institutional Review Board (IRB) review.
Consent to Participate See statement above.
Consent for Publication We give our consent to have this manuscript
published.
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... Inequities in breast cancer mortality among Black people have been recognized for decades and yet persist [21,22]. These inequities are partly due to later stage breast cancer diagnosis [21]. ...
... Inequities in breast cancer mortality among Black people have been recognized for decades and yet persist [21,22]. These inequities are partly due to later stage breast cancer diagnosis [21]. Regular interval breast cancer screening with mammography aligned with the United States Preventive Services Task Force (USPSTF) guidelines is an evidence-based intervention to improve earlier diagnosis of and mortality from breast cancer [23]. ...
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Objectives: There is limited evidence regarding the impact of race/racism and its intersection with socioeconomic status (SES) on breast and cervical cancer, the two most common female cancers globally. We investigated racial inequalities in breast and cervical cancer mortality and whether SES (education and household conditions) interacted with race/ethnicity. Design: The 100 Million Brazilian Cohort data were linked to the Brazilian Mortality Database, 2004-2015 (n = 20,665,005 adult women). We analysed the association between self-reported race/ethnicity (White/'Parda'(Brown)/Black/Asian/Indigenous) and cancer mortality using Poisson regression, adjusting for age, calendar year, education, household conditions and area of residence. Additive and multiplicative interactions were assessed. Results: Cervical cancer mortality rates were higher among Indigenous (adjusted Mortality rate ratio = 1.80, 95%CI 1.39-2.33), Asian (1.63, 1.20-2.22), 'Parda'(Brown) (1.27, 1.21-1.33) and Black (1.18, 1.09-1.28) women vs White women. Breast cancer mortality rates were higher among Black (1.10, 1.04-1.17) vs White women. Racial inequalities in cervical cancer mortality were larger among women of poor household conditions, and low education (P for multiplicative interaction <0.001, and 0.02, respectively). Compared to White women living in completely adequate (3-4) household conditions, the risk of cervical cancer mortality in Black women with 3-4, 1-2, and none adequate conditions was 1.10 (1.01-1.21), 1.48 (1.28-1.71), and 2.03 (1.56-2.63), respectively (Relative excess risk due to interaction-RERI = 0.78, 0.18-1.38). Among 'Parda'(Brown) women the risk was 1.18 (1.11-1.25), 1.68 (1.56-1.81), and 1.84 (1.63-2.08), respectively (RERI = 0.52, 0.16-0.87). Compared to high-educated White women, the risk in high-, middle- and low-educated Black women was 1.14 (0.83-1.55), 1.93 (1.57-2.38) and 2.75 (2.33-3.25), respectively (RERI = 0.36, -0.05-0.77). Among 'Parda'(Brown) women the risk was 1.09 (0.91-1.31), 1.99 (1.70-2.33) and 3.03 (2.61-3.52), respectively (RERI = 0.68, 0.48-0.88). No interactions were found for breast cancer. Conclusion: Low SES magnified racial inequalities in cervical cancer mortality. The intersection between race/ethnicity, SES and gender needs to be addressed to reduce racial health inequalities.
... Many studies have postulated that the racial disparities among breast cancer patients and their mortality trends vary due to different receptor expressions and stages of disease at the time of diagnosis [3][4][5][6]. Furthermore, socioeconomic variables and lifestyle are also plausible explanations for this discrepancy [7][8][9][10]. Even in clinical trials, there remains an underrepresentation of all ethnic minorities [11][12][13][14]. ...
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Breast cancer is the second most diagnosed malignancy in American women with a lifetime occurrence of 1 in 8 women in the United States. There has been a dearth of research focusing on regional differences in breast cancer mortality with respect to race in the US. It is crucial to identify regions that are lagging to uplift the outreach of breast cancer care to certain races. Data for this study were obtained from the 2016–2018 Nationwide Inpatient Sample. In-hospital mortality, race and hospital regions for the patients with the primary diagnosis of Malignant Neoplasms of Breast were studied. Baseline characteristics of participants were summarized using descriptive statistics. The patient population was stratified as per race, hospital region, gender, therapy received and family history. Logistic regression was performed to derive the odds ratio while adjusting for different variables. 99, 543 patients with metastatic breast cancer were identified. African Americans (AAs) were found to have the highest reported deaths at 5.54%, followed by Asians and Pacific Islanders at 4.80% and Caucasians 4.09% (p < 0.0001). The odds of dying were significantly higher in the AA population when compared to Caucasian population (OR 1.391 (1.286–1.504)), and the odds were consistently higher across all regions of the US. In terms of regional disparities with respect to race, AA’s had highest mortality in the south whereas all other races had the highest mortality in the west. It was seen that races identifying as “others” had significantly higher odds of dying in the Northeast. It is crucial to identify racial differences in the various regions across the US in order to implement appropriate outreach strategies to tackle these disparities.
... 1 Multiple structural barriers to healthcare access have been linked to this racial disparity. Relative to White women, Black women are less likely to receive highquality screening, [2][3][4] be diagnosed at an early stage, [5][6][7][8] receive a diagnosis and begin treatment without delay, [9][10][11][12] and receive guideline-concordant care. [13][14][15][16] However, access to care does not fully account for the racial disparity in breast cancer mortality. ...
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Background: Despite similar incidence rates among Black and White women, breast cancer mortality rates are 40% higher among Black women. More than half of the racial difference in breast cancer mortality can be attributed to triple negative breast cancer (TNBC), an aggressive subtype of invasive breast cancer that disproportionately affects Black women. Recent research has implicated neighborhood conditions in the etiology of TNBC. This study investigated the relationship between cumulative neighborhood-level exposures and TNBC risk. Methods: This single-institution retrospective study was conducted on a cohort of 3316 breast cancer cases from New Castle County, Delaware (from 2012 to 2020), an area of the country with elevated TNBC rates. Cases were stratified into TNBC and "Non-TNBC" diagnosis and geocoded by residential address. Neighborhood exposures included census tract-level measures of unhealthy alcohol use, metabolic dysfunction, breastfeeding, and environmental hazards. An overall cumulative risk score was calculated based on tract-level exposures. Results: Univariate analyses showed each tract-level exposure was associated with greater TNBC odds. In multivariate analyses that controlled for patient-level race and age, tract-level exposures were not associated with TNBC odds. However, in a second multivariate model that included patient-level variables and considered tract-level risk factors as a cumulative exposure risk score, each one unit increase in cumulative exposure was significantly associated with a 10% increase in TNBC odds. Higher cumulative exposure risk scores were found in census tracts with relatively high proportions of Black residents. Conclusions: Cumulative exposure to neighborhood-level risk factors that disproportionately affect Black communities was associated with greater TNBC risk.
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1.1 Objectives Biases inherent in electronic health records (EHRs), and therefore in medical artificial intelligence (AI) models may significantly exacerbate health inequities and challenge the adoption of ethical and responsible AI in healthcare. Biases arise from multiple sources, some of which are not as documented in the literature. Biases are encoded in how the data has been collected and labeled, by implicit and unconscious biases of clinicians, or by the tools used for data processing. These biases and their encoding in healthcare records undermine the reliability of such data and bias clinical judgments and medical outcomes. Moreover, when healthcare records are used to build data-driven solutions, the biases are further exacerbated, resulting in systems that perpetuate biases and induce healthcare disparities. This literature scoping review aims to categorize the main sources of biases inherent in EHRs. 1.2 Methods We queried PubMed and Web of Science on January 19th, 2023, for peer-reviewed sources in English, published between 2016 and 2023, using the PRISMA approach to stepwise scoping of the literature. To select the papers that empirically analyze bias in EHR, from the initial yield of 430 papers, 27 duplicates were removed, and 403 studies were screened for eligibility. 196 articles were removed after the title and abstract screening, and 96 articles were excluded after the full-text review resulting in a final selection of 116 articles. 1.3 Results Systematic categorizations of diverse sources of bias are scarce in the literature, while the effects of separate studies are often convoluted and methodologically contestable. Our categorization of published empirical evidence identified the six main sources of bias: a) bias arising from past clinical trials ; b) data-related biases arising from missing, incomplete information or poor labeling of data; human-related bias induced by c) implicit clinician bias, d) referral and admission bias; e) diagnosis or risk disparities bias and finally, (f) biases in machinery and algorithms. 1.4 Conclusions Machine learning and data-driven solutions can potentially transform healthcare delivery, but not without limitations. The core inputs in the systems (data and human factors) currently contain several sources of bias that are poorly documented and analyzed for remedies. The current evidence heavily focuses on data-related biases, while other sources are less often analyzed or anecdotal. However, these different sources of biases add to one another exponentially. Therefore, to understand the issues holistically we need to explore these diverse sources of bias. While racial biases in EHR have been often documented, other sources of biases have been less frequently investigated and documented (e.g. gender-related biases, sexual orientation discrimination, socially induced biases, and implicit, often unconscious, human-related cognitive biases). Moreover, some existing studies lack causal evidence, illustrating the different prevalences of disease across groups, which does not per se prove the causality. Our review shows that data-, human- and machine biases are prevalent in healthcare and they significantly impact healthcare outcomes and judgments and exacerbate disparities and differential treatment. Understanding how diverse biases affect AI systems and recommendations is critical. We suggest that researchers and medical personnel should develop safeguards and adopt data-driven solutions with a “bias-in-mind” approach. More empirical evidence is needed to tease out the effects of different sources of bias on health outcomes. CCS Concepts • Computing methodologies → Machine learning ; Machine learning approaches ; • Applied computing → Health care information systems ; Health informatics ; • Social and professional topics → Personal health records ; Medical records . ACM Reference Format Oriel Perets, Emanuela Stagno, Eyal Ben Yehuda, Megan McNichol, Leo Anthony Celi, Nadav Rappoport, and Matilda Dorotic. 2024. Inherent Bias in Electronic Health Records: A Scoping Review of Sources of Bias. 1, 1 (April 2024), 24 pages. https://doi.org/XXXXXXX.XXXXXXX
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Background The U.S. Preventive Services Task Force recently issued an updated draft recommendation statement to initiate breast cancer screening at age 40, reflecting well-documented disparities in breast cancer–related mortality that disproportionately impact younger Black women. This study applied a novel approach to identify hotspots of breast cancer diagnosed before age 50 and/or at an advanced stage to improve breast cancer detection within these communities. Methods Cancer registry data for 3,497 women with invasive breast cancer diagnosed or treated between 2012 and 2020 at the Helen F. Graham Cancer Center and Research Institute (HFGCCRI) and who resided in the HFGCCRI catchment area, defined as New Castle County, Delaware, were geocoded and analyzed with spatial intensity. Standardized incidence ratios stratified by age and race were calculated for each hotspot. Results Four hotspots were identified, two for breast cancer diagnosed before age 50, one for advanced breast cancer, and one for advanced breast cancer diagnosed before age 50. Younger Black women were overrepresented in these hotspots relative to the full-catchment area. Conclusions The novel use of spatial methods to analyze a community cancer center catchment area identified geographic areas with higher rates of breast cancer with poor prognostic factors and evidence that these areas made an outsized contribution to racial disparities in breast cancer. Impact Identifying and prioritizing hotspot breast cancer communities for community outreach and engagement activities designed to improve breast cancer detection have the potential to reduce the overall burden of breast cancer and narrow racial disparities in breast cancer.
Article
Background: We aimed to develop a nomogram to predict the overall survival of elderly patients with Triple-negative invasive ductal breast carcinoma (TNIDC). Research design and methods: 12165 elderly patients with nonmetastatic TNIDC were retrieved from the SEER database from 2010 to 2019 and were randomly assigned to training and validation cohorts. Stepwise Cox regression analysis was used to select variables for the nomogram based on the training cohort. Univariate and multivariate Cox analyses were used to calculate the correlation between variables and prognosis of the patients. Survival analysis was performed for high- and low-risk subgroups based on risk score. Results: Eleven predictive factors were identified to construct our nomograms. Compared with the TNM stage, the discrimination of the nomogram revealed good prognostic accuracy and clinical applicability as indicated by C-index values of 0.741 (95% CI 0.728-0.754) against 0.708 (95% CI 0.694-0.721) and 0.765 (95% CI 0.747-0.783) against 0.725 (95% CI 0.705-0.744) for the training and validation cohorts, respectively. Differences in OS were also observed between the high- and low-risk groups (p < 0.001). Conclusion: The proposed nomogram provides a convenient and reliable tool for individual evaluations for elderly patients with M0_stage TNIDC. However, the model may only for Americans.
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Objective: Presently, there is a lack of research examining gendered racial disparities in psycho-oncology referral rates for Black women with cancer. Informed by intersectionality, gendered racism, and the Strong Black Woman framework, this study sought to examine the possibility that Black women are adversely affected by such phenomena as evidenced by lower probability of being referred to psycho-oncology services compared to Black men, White women and White men. Methods: Data for this study consisted of 1598 cancer patients who received psychosocial distress screening at a comprehensive cancer center in a large Midwest teaching hospital. Multilevel logistic modeling was used to examine the probability of referral to psycho-oncology services for Black women, Black men, White women, and White men while controlling for patient-reported emotional and practical problems and psychosocial distress. Results: Results indicated that Black women had the lowest probability of being referred to psycho-oncology services (2%). In comparison, the probability of being referred to psycho-oncology were 10% for White women, 9% for Black men, and 5% for White men. Additionally, as nurses' patient caseload decreased, the probability of being referred to psycho-oncology increased for Black men, White men, and White women. In contrast, nurses' patient caseload had little effect on the probability of being referred to psycho-oncology for Black women. Conclusions: These findings suggest unique factors influence psycho-oncology referral rates for Black women. Findings are discussed with particular focus on how to enhance equitable care for Black women with cancer.
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Background: We investigated trends in incidence rates, stage at diagnosis and relative survival rates among adults with oral cancer in relation to race in the context of previously uncovered cancer-specific health disparities. Methods: We analyzed 2000—2017 SEER data among adults with oral cancer from 18 registries. We used SEER*Stat to compute proportions for each oral cancer site by stage at diagnosis and race and five-year relative survival rates by sex, cancer site, stage at diagnosis, age and race and explored trends over time. Results: Among 95,040 oral cancer cases reported to SEER, the most prevalent site was the tongue. While the rate among Black men decreased from 12.9 to 8/100,000, Blacks had significantly higher proportions of oral cancer that had spread at diagnosis than whites. Survival rates were substantially lower among Blacks than whites. Conclusions: The steep decline in oral cancer incidence rates in Black men is encouraging, although the persistent racial disparity with respect to late diagnosis and poor survival is alarming, requiring targeted interventions. Practical implications: Highlighting racial disparities with respect to oral cancer to increase awareness is the first step in developing interventions to address these disparities.
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Importance Compared with non-Hispanic white women, racial/ethnic minority women receive a diagnosis of breast cancer at a more advanced stage and have higher morbidity and mortality with breast cancer diagnosis. Access to care with adequate insurance may be associated with earlier diagnosis, expedited treatment, and improved prognosis. Objective To examine the extent to which insurance is associated with access to timely breast cancer diagnosis and breast cancer stage differences among a large, diverse population of US patients with breast cancer. Design, Setting, and Participants This retrospective, cross-sectional population-based study used data from the Surveillance, Epidemiology, and End Results Program on 177 075 women aged 40 to 64 years who received a diagnosis of stage I to III breast cancer between January 1, 2010, and December 31, 2016. Statistical analysis was performed from August 1, 2017, to October 1, 2019. Main Outcomes and Measures The primary outcome was the risk of having a more advanced stage of breast cancer at diagnosis (ie, stage III vs stages I and II). Mediation analyses were conducted to determine associations of race/ethnicity and proportion of observed differences mediated by health insurance status with earlier stage of diagnosis. Results A total of 177 075 women (mean [SD] age, 53.5 [6.8] years; 148 124 insured and 28 951 uninsured or receiving Medicaid) were included in the study. A higher proportion of women either receiving Medicaid or who were uninsured received a diagnosis of locally advanced breast cancer (stage III) compared with women with health insurance (20% vs 11%). In multivariable models, non-Hispanic black (odds ratio [OR], 1.46 [95% CI, 1.40-1.53]), American Indian or Alaskan Native (OR, 1.31 [95% CI, 1.07-1.61]) and Hispanic (OR, 1.35 [95% CI, 1.30-1.42]) women had higher odds of receiving a diagnosis of locally advanced disease (stage III) compared with non-Hispanic white women. When adjusting for health insurance and other socioeconomic factors, associations between race/ethnicity and risk of locally advanced breast cancer were attenuated (non-Hispanic black: OR, 1.29 [95% CI, 1.23-1.35]; American Indian or Alaskan Native: OR, 1.11 [95% CI, 0.91-1.35]; Hispanic: OR, 1.17 [95% CI, 1.12-1.22]). Nearly half (45%-47%) of racial differences in the risk of locally advanced disease were mediated by health insurance. Conclusions and Relevance This study’s findings suggest that nearly half of the observed racial/ethnic disparities in higher stage at breast cancer diagnosis are mediated by health insurance coverage.
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Purpose: We conducted a systematic review and meta-analysis to measure the extent to which race is associated with delayed initiation or receipt of inadequate chemotherapy among women with early-stage breast cancer. Methods: We performed a systematic search of all articles published from January 1987 until June 2017 within four databases: PubMed/Medline, EMBASE, CINAHL, and Cochrane CENTRAL. Eligible studies were US-based and examined the influence of race on chemotherapy delays, cessation, or dose reductions among women with stage I, II, or III breast cancer. Data were pooled using a random effects model. Results: A total of twelve studies were included in the quantitative analysis. Blacks were significantly more likely than whites to have delays to initiation of adjuvant therapy of 90 days or more (OR 1.41, 95% CI 1.06-1.87; X² = 31.05, p < 0.00001; I² = 90%). There was no significant association between race and chemotherapy dosing. Due to overlap between studies assessing the relationship between race and completion of chemotherapy, we conducted two separate analyses. Black patients were significantly more likely to discontinue chemotherapy, however, this was no longer statistically significant when larger numbers of patients with more advanced (stage III) breast cancer were included. Conclusions: These results suggest that black breast cancer patients experience clinically relevant delays in the initiation of adjuvant chemotherapy more often than white patients, which may in part explain the increased mortality observed among black patients.
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Breast cancer is the second leading cause of cancer related deaths among women aged 40–55 in the United States and currently affects more than one in ten women worldwide. It is also one of the most diagnosed cancers in women both in wealthy and poor countries. Fortunately, the mortality rate from breast cancer has decreased in recent years due to increased emphasis on early detection and more effective treatments in White population. Although the mortality rates have declined in some ethnic populations, the overall cancer incidence among African American and Hispanic populations has continued to grow. The goal of the present review article was to highlight similarities and differences in breast cancer morbidity and mortality rates primarily among African American women compared to White women in the United States. To reach our goal, we conducted a search of articles in journals with a primary focus on minority health, and authors who had published articles on racial/ethnic disparity related to breast cancer patients. A systematic search of original research was conducted using MEDLINE, PUBMED and Google Scholar databases. We found that racial/ethnic disparities in breast cancer may be attributed to a large number of clinical and non-clinical risk factors including lack of medical coverage, barriers to early detection and screening, more advanced stage of disease at diagnosis among minorities, and unequal access to improvements in cancer treatment. Many African American women have frequent unknown or unstaged breast cancers than White women. These risk factors may explain the differences in breast cancer treatment and survival rate between African American women and White women. New strategies and approaches are needed to promote breast cancer prevention, improve survival rate, reduce breast cancer mortality, and ultimately improve the health outcomes of racial/ethnic minorities
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Background . This paper presents data on breast cancer prevalence and mortality among US Hispanics and Hispanic subgroups, including Cuban, Mexican, Puerto Rican, Central American, and South American. Methods . Five-year average annual female breast cancer prevalence and mortality rates for 2009–2013 were examined using data from the National Health Interview Survey (prevalence) and the National Center for Health Statistics and the American Community Survey (mortality rates). Results . Overall breast cancer prevalence among US Hispanic women was 1.03%. Although the estimates varied slightly by Hispanic subgroup, these differences were not statistically significant. The breast cancer mortality rate for Hispanics overall was 17.71 per 100,000 women. Higher rates were observed among Cubans (17.89), Mexicans (18.78), and Puerto Ricans (19.04), and a lower rate was observed among Central and South Americans (10.15). With the exception of the rate for Cubans, all Hispanic subgroup rates were statistically significantly different from the overall Hispanic rate. Additionally, all Hispanic subgroups rates were statistically significantly higher than the Central and South American rate. Conclusion . The data reveal significant differences in mortality across Hispanic subgroups. These data enable public health officials to develop targeted interventions to help lower breast cancer mortality among the highest risk populations.
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In this article, the American Cancer Society provides an overview of female breast cancer statistics in the United States, including data on incidence, mortality, survival, and screening. Approximately 252,710 new cases of invasive breast cancer and 40,610 breast cancer deaths are expected to occur among US women in 2017. From 2005 to 2014, overall breast cancer incidence rates increased among Asian/Pacific Islander (1.7% per year), non-Hispanic black (NHB) (0.4% per year), and Hispanic (0.3% per year) women but were stable in non-Hispanic white (NHW) and American Indian/Alaska Native (AI/AN) women. The increasing trends were driven by increases in hormone receptor-positive breast cancer, which increased among all racial/ethnic groups, whereas rates of hormone receptor-negative breast cancers decreased. From 1989 to 2015, breast cancer death rates decreased by 39%, which translates to 322,600 averted breast cancer deaths in the United States. During 2006 to 2015, death rates decreased in all racial/ethnic groups, including AI/ANs. However, NHB women continued to have higher breast cancer death rates than NHW women, with rates 39% higher (mortality rate ratio [MRR], 1.39; 95% confidence interval [CI], 1.35-1.43) in NHB women in 2015, although the disparity has ceased to widen since 2011. By state, excess death rates in black women ranged from 20% in Nevada (MRR, 1.20; 95% CI, 1.01-1.42) to 66% in Louisiana (MRR, 1.66; 95% CI, 1.54, 1.79). Notably, breast cancer death rates were not significantly different in NHB and NHW women in 7 states, perhaps reflecting an elimination of disparities and/or a lack of statistical power. Improving access to care for all populations could eliminate the racial disparity in breast cancer mortality and accelerate the reduction in deaths from this malignancy nationwide. CA Cancer J Clin 2017.
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Purpose To examine change in the percent uninsured and early-stage diagnosis among nonelderly patients with newly diagnosed cancer after the Affordable Care Act (ACA). Patients and Methods By using the National Cancer Data Base, we estimated absolute change (APC) and relative change in percent uninsured among patients with newly diagnosed cancer age 18 to 64 years between 2011 to the third quarter of 2013 (pre-ACA implementation) and the second to fourth quarter of 2014 (post-ACA) in Medicaid expansion and nonexpansion states by family income level. We also examined demographics-adjusted difference in differences in APC between Medicaid expansion and nonexpansion states. We similarly examined changes in insurance and early-stage diagnosis for the 15 leading cancers in men and women (top 17 cancers total). Results Between the pre-ACA and post-ACA periods, percent uninsured among patients with newly diagnosed cancer decreased in all income categories in both Medicaid expansion and nonexpansion states. However, the decrease was largest in low-income patients who resided in expansion states (9.6% to 3.6%; APC, −6.0%; 95% CI, −6.5% to −5.5%) versus their counterparts who resided in nonexpansion states (14.7% to 13.3%; APC, −1.4%; 95% CI, −2.0% to −0.7%), with an adjusted difference in differences of −3.3 (95% CI, −4.0 to −2.5). By cancer type, the largest decrease in percent uninsured occurred in patients with smoking- or infection-related cancers. A small but statistically significant shift was found toward early-stage diagnosis for colorectal, lung, female breast, and pancreatic cancer and melanoma in patients who resided in expansion states. Conclusion Percent uninsured among nonelderly patients with newly diagnosed cancer declined substantially after the ACA, especially among low-income people who resided in Medicaid expansion states. A trend toward early-stage diagnosis for select cancers in expansion states also was found. These results reinforce the importance of policies directed at providing affordable coverage to low-income, vulnerable populations.
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Sizeable disparities exist in breast cancer outcomes, both between Black and White patients in the United States, and between patients in the United States and other high-income countries compared with low- and middle-income countries (LMIC). In both settings, health system factors are key drivers of disparities. In the United States, Black women are more likely to die of breast cancer than Whites and have poorer outcomes, even among patients with similar stage and tumor subtype. Over-representation of higher risk “triple-negative” breast cancers contributes to breast cancer mortality in Black women; however, the greatest survival disparities occur within the good-prognosis hormone receptor–positive (HR⁺) subtypes. Disparities in access to treatment within the complex U.S. health system may be responsible for a substantial portion of these differences in survival. In LMICs, breast cancer mortality rates are substantially higher than in the United States, whereas incidence continues to rise. This mortality burden is largely attributable to health system factors, including late-stage presentation at diagnosis and lack of availability of systemic therapy. This article will review the existing evidence for how health system factors in the United States contribute to breast cancer disparities, discuss methods for studying the relationship of health system factors to racial disparities, and provide examples of health system interventions that show promise for mitigating breast cancer disparities. We will then review evidence of global breast cancer disparities in LMICs, the treatment factors that contribute to these disparities, and actions being taken to combat breast cancer disparities around the world. Clin Cancer Res; 23(11); 2655–64. ©2017 AACR. See all articles in this CCR Focus section, “Breast Cancer Research: From Base Pairs to Populations.”
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Persons living in the United States who lack private medical insurance are less likely to have access to medical care and to take part in cancer screening programs. Regional studies suggest that uninsured and Medicaid-insured individuals are likelier than those who are privately insured to present with advanced-stage cancer, but this has not been confirmed using contemporary national-level information. Complicating the problem is the observation that cancer patients from ethnic minorities are likelier than non-Hispanic whites to be uninsured or Medicaid insured. This study sought relationships between insurance status and disease stage at the time of diagnosis for twelve cancer sites (breast, colorectal, kidney, lung, melanoma, non-Hodgkin lymphoma, ovary, pancreas, prostate, urinary bladder, uterus, thyroid). The study population included 3,742,407 patients whose characteristics resembled those of the U.S. population not included in the analysis. The patients, diagnosed in the years 1998–2004, were enrolled in the U.S. National Cancer Database, a hospital-based registry with patient information from approximately 1430 facilities. Uninsured and Medicaid-insured patients were significantly more likely than privately insured patients to present with advanced-stage (stage III or stage IV) cancer. The relationship was most evident for patients whose cancers can potentially be detected at an early stage by symptom assessment or screening. They include breast and colorectal cancers, lung cancer, and melanoma. Compared with privately insured patients, the odds ratios (ORs) for advanced-stage disease at diagnosis for uninsured and Medicaid-insured patients with colorectal cancer were 2.0 (95% confidence interval, 1.9–2.1) and 1.6 (1.5–1.7), respectively. For advanced-stage melanoma, the OR was 2.3 (2.1–2.5) for uninsured patients and 3.3 (3.0–3.6) for Medicaid-insured patients compared to privately insured patients. Compared with white patients, blacks and Hispanics had an increased risk of advanced-stage disease at diagnosis independently of insurance status. The investigators conclude that cancer patients residing in the United States who are uninsured or have Medicaid insurance are at a considerably increased risk of having more advanced disease when diagnosed than are privately insured patients.
Article
Objectives: Current guidelines support the use of screening for early detection in breast, prostate, colorectal and cervical cancer. The purpose of this study was to evaluate whether insurance status predicts for more advanced disease in these four currently screened cancers. Study design: The Surveillance, Epidemiology, and End Results (SEER) database was queried for breast, prostate, colorectal and cervix in patients aged 18-64 years. The database was queried from 2007 to 2011, with 425,614 patients with known insurance status included. Methods: Multinomial logistic regression was used to evaluate insurance status and cancer presentation. Results: Under multivariate analysis for breast cancer, uninsured patients more often had invasive disease (odds ratio [OR]: 1.55), T- (OR: 2.00), N- (OR: 1.59) stage, and metastatic disease (OR: 3.48), and were more often high-grade (OR: 1.21). For prostate cancer, uninsured patients again presented more commonly with higher T-stage (OR: 1.45), nodal (OR: 2.90) and metastatic (OR: 4.98) disease, in addition to higher prostate-specific antigen (OR: 2.85) and Gleason score (OR: 1.65). Colorectal cancer had similar findings with uninsured individuals presenting with more invasive disease (OR: 1.78), higher T (OR: 1.86), N (OR: 1.22), and M (OR: 1.58) stage, in addition to higher carcinoembryonic antigen levels (OR: 1.66). Similar results were seen for cervical cancer with uninsured having higher T (OR: 2.03), N (OR: 1.21), and M (OR: 1.45) stage. Conclusion: In the four cancers detected by screening exams, those without health insurance present with more advanced disease, with higher stage and grade, and more elevated tumour markers.
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A disproportionate number of cancer deaths occur among racial/ethnic minorities, particularly African Americans, who have a 33% higher risk of dying of cancer than whites. Although differences in incidence and stage of disease at diagnosis may contribute to racial disparities in mortality, evidence of racial disparities in the receipt of treatment of other chronic diseases raises questions about the possible role of inequities in the receipt of cancer treatment. To evaluate racial/ethnic disparities in the receipt of cancer treatment, we examined the published literature that addressed access/use of specific cancer treatment procedures, trends in patterns of use, or survival studies. We found evidence of racial disparities in receipt of definitive primary therapy, conservative therapy, and adjuvant therapy. These treatment differences could not be completely explained by racial/ethnic variation in clinically relevant factors. In many studies, these treatment differences were associated with an adverse impact on the health outcomes of racial/ethnic minorities, including more frequent recurrence, shorter disease-free survival, and higher mortality. Reducing the influence of nonclinical factors on the receipt of cancer treatment may, therefore, provide an important means of reducing racial/ethnic disparities in health. New data resources and improved study methodology are needed to better identify and quantify the full spectrum of nonclinical factors that contribute to the higher cancer mortality among racial/ethnic minorities and to develop strategies to facilitate receipt of appropriate cancer care for all patients.