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. Author manuscript; available in PMC: 2012 Jun 1.
Published in final edited form as: Breast Cancer Res Treat. 2010 Oct 7;127(3):729–738. doi: 10.1007/s10549-010-1191-6

Disparities in Breast Cancer Characteristics and Outcomes by Race/Ethnicity

Siew Loon Ooi 1,2, Maria Elena Martinez 3,4, Christopher I Li 1,2
PMCID: PMC3081535  NIHMSID: NIHMS262866  PMID: 21076864

Abstract

Purpose

Disparities in breast cancer stage and mortality by race/ethnicity in the United States are persistent and well known. However, few studies have assessed differences across racial/ethnic subgroups of women broadly defined as Hispanic, Asian, or Pacific Islander, particularly using more recent data.

Methods

Using data from 17 population-based cancer registries in the Surveillance, Epidemiology, and End Results (SEER) Program, we evaluated the relationships between race/ethnicity and breast cancer stage, hormone receptor status, treatment, and mortality. The cohort consisted of 229,594 women 40-79 years of age diagnosed with invasive breast carcinoma between January 2000 and December 2006, including 176,094 non-Hispanic whites, 20,486 blacks, 15,835 Hispanic whites, 14,951 Asians, 1,224 Pacific Islanders and 1,004 American Indians/Alaska Natives.

Results

With respect to statistically significant findings, American Indian/Alaska Native, Asian Indian/Pakistani, black, Filipino, Hawaiian, Mexican, Puerto Rican, and Samoan women had 1.3 to 7.1-fold higher odds of presenting with stage IV breast cancer compared to non-Hispanic white women. Almost all groups were more likely to be diagnosed with estrogen receptor-negative/progesterone receptor-negative (ER-/PR-) disease with black and Puerto Rican women having the highest odds ratios (2.4 and 1.9-fold increases, respectively) compared to non-Hispanic whites. Lastly, black, Hawaiian, Puerto Rican, and Samoan patients had 1.5 to 1.8-fold elevated risks of breast cancer specific mortality.

Conclusions

Breast cancer disparities persist by race/ethnicity, though there is substantial variation within subgroups of women broadly defined as Hispanic or Asian. Targeted, multi-pronged interventions that are culturally appropriate may be important means of reducing the magnitudes of these disparities.

Keywords: Breast cancer, disparities, race, ethnicity, stage, estrogen receptor, progesterone receptor, mortality

INTRODUCTION

It is well established that compared to non-Hispanic whites, several racial/ethnic groups, including blacks, Hispanic whites, and American Indians, are more likely to be diagnosed with advanced stage breast cancer and have poorer disease specific survival rates [10]. These same groups of women are also more likely to be diagnosed with hormone receptor negative tumors [14], which are more aggressive than hormone receptor positive tumors and have a poorer prognosis regardless of factors such as stage of disease [6]. There is clear evidence that over the past two decades the proportion of breast cancers diagnosed at an advanced stage has fallen and survival rates have increased across women of all racial/ethnic groups [10, 23]. However, the relative disparities with respect to stage and mortality have held essentially constant by race/ethnicity [10, 17].

Few studies have assessed breast cancer disparities related to stage or mortality across subgroups of broadly defined racial/ethnic groups, such as Asians, Hispanic whites, and Pacific Islanders. Here we assess these disparities among six distinct Asian populations, four distinct Hispanic populations, and two distinct Pacific Islander populations. We have previously reported on some of these differences based on Surveillance, Epidemiology and End Results (SEER) Program data from 1992-1998, which was the first to document differences in these disparities across many of these subgroups [3, 15]. An update of this report to both confirm the disparities and to evaluate how they have changed is warranted, particularly since the SEER Program was substantially expanded in 2000 and now includes 26% of the United States population. Identification of the types of disparities experienced by each racial/ethnic subgroup can help identify needs specific to different communities and facilitate the development of culturally appropriate strategies to reduce these disparities.

METHODS

Women 40-79 years of age without a prior history of any type of cancer who were diagnosed with invasive breast cancer between January 2000 and December 2006 were identified through 17 population-based cancer registries in the United States that participate in the National Cancer Institute's SEER Program. Women less than 40 years of age and 80 years of age and older were excluded. This is because one of the primary outcomes of interest was cancer stage, and stage is influenced by mammographic screening and routine screening is not recommended for women <40 and is less common among women ≥80 years of age. 2000 was chosen as the starting point for this analysis because this was the year when several registries were added to the SEER program. The SEER registries that were included serve the states of California (through the participation of four distinct SEER registries), Connecticut, Hawaii, Iowa, Kentucky, Louisiana, New Jersey, New Mexico, and Utah, the areas surrounding Atlanta, Georgia; Detroit, Michigan, and Seattle, Washington; a rural area of Georgia; and the population of Alaskan Natives living in Alaska. It is estimated that more than 95% of all incident cases in the populations under surveillance are ascertained. The primary source of data used by SEER is patient medical records, and further operational details regarding the methodology employed by the SEER Program are provided elsewhere [28].

A total of 242,056 women were potentially eligible for this study. To make our race/ethnicity categories mutually exclusive, 195 black women, 27 American Indian/Alaska Native women, 60 Asian women, and 25 Pacific Islanders who were also categorized as being Hispanic were excluded, as were the 1,610 with an unknown race/ethnicity. Of the remaining 240,139 cases, 10,545 with an unknown AJCC were excluded leaving a total of 229,594 cases.

Our primary exposure of interest was race/ethnicity. Based on SEER data, race/ethnicity was categorized into six broad groups: non-Hispanic white, black, Hispanic white, Asian, Pacific Islander, and American Indian/Alaska Native. SEER also collects more detailed data on Hispanic, Asian, and Pacific Islander subgroups. Analyses were conducted on the following subgroups: Hispanics – Mexican, South/Central American, Puerto Rican, and Cuban women; Asians – Filipino, Chinese, Japanese, Asian Indian/Pakistani, Korean, and Vietnamese women; and Pacific Islanders – Hawaiian and Samoan women.

Our primary outcomes of interest were AJCC stage, joint estrogen receptor (ER)/progesterone receptor (PR) status, receipt of appropriate treatment, and breast cancer specific mortality. Data on AJCC stage and ER/PR status are directly available in the SEER data. The 14,444 women with missing stage data and the additional 40,182 women missing ER/PR status were excluded leaving a final total of 229,594 women included in our analyses. We were also interested in assessing whether or not the primary surgical and radiation treatments given to women of different races/ethnicities with stage I and II breast carcinomas less than 2.0 cm in size met current standards of care outlined by National Comprehensive Cancer Network using methodology consistent with previous reports [2, 20]. Women were categorized as having received an appropriate first course of treatment if they either received a total mastectomy or had breast conserving surgery (BCS) with axillary node dissection and radiation. Women who had BCS but did not receive axillary node dissection and/or radiation were categorized as having received inappropriate treatment. This analysis was limited to women with tumors <2.0 cm because of the potential benefit those with larger tumors experience with neoadjuvant chemotherapy. Our final outcome of interest was breast cancer specific mortality. Information on vital status and survival time is obtained annually by each registry through a variety of data sources. SEER calculates survival time in months beginning with the month and year of diagnosis, and in this study the outcome of interest was death due to breast cancer. So women were followed until whichever of the following occurred first: 1) date of death due to breast cancer, 2) date of death due to a cause other than breast cancer (censored) 3) date last known to be alive, or 4) December 31, 2006, the follow-up cutoff date used in this analysis.

Associations between race/ethnicity and AJCC stage, ER/PR status, and treatment were estimated using polytomous logistic regression. Risks of mortality by race/ethnicity were calculated using the Cox proportional hazards model. In all analyses non-Hispanic white women served as the reference race/ethnicity, and risk estimates were adjusted for age at diagnosis, year of diagnosis, SEER registry, and county level measures of poverty and education according to how they are categorized in Table 1. Analyses of ER/PR status and treatment were additionally adjusted for AJCC stage. For risk of mortality we conducted analyses additionally adjusted for AJCC stage, surgical and radiation treatments, and ER/PR status. All analyses were conducted using Stata/SE 10.1 for Windows (Stata Corp, College Station, TX) statistical software.

Table 1.

Characteristics of the 229,594 breast cancer cases by race/ethnicity

Non-Hispanic
whites
(n=176,094)
Blacks
(n=20,486)
Hispanic
whites
(n=15,835)
Asians
(n=14,951)
Pacific
Islanders
(n=1,224)
American Indians/
Alaska Natives
(n=1,004)
n % n % n % n % n % n %
Age at diagnosis, years
40-49 37,015 21.0 5,816 28.4 5,157 32.6 4,503 30.1 323 26.4 307 30.6
50-59 52,288 29.7 6,457 31.5 4,783 30.2 4,826 32.3 412 33.7 331 33.0
60-69 46,260 26.3 4,805 23.5 3,525 22.3 3,318 22.2 315 25.7 225 22.4
70-79 40,531 23.0 3,408 16.6 2,370 15.0 2,304 15.4 174 14.2 141 14.0
Mean±standard deviation 59.7±10.8 57.3±10.6 56.4±10.6 56.7±10.5 57.2±10.1 56.5±10.2
Year of diagnosis
2000 26,581 15.1 2,833 13.8 1,904 12.0 1,879 12.6 138 11.3 131 13.0
2001 26,916 15.3 2,850 13.9 2,020 12.8 1,993 13.3 190 15.5 132 13.1
2002 26,354 15.0 2,986 14.6 2,257 14.3 2,210 14.8 176 14.4 125 12.5
2003 24,549 13.9 2,983 14.6 2,249 14.2 2,061 13.8 193 15.8 162 16.1
2004 24,064 13.7 3,006 14.7 2,341 14.8 2,197 14.7 178 14.5 147 14.6
2005 23,651 13.4 2,740 13.4 2,563 16.2 2,281 15.3 186 15.2 157 15.6
2006 23,979 13.6 3,088 15.1 2,501 15.8 2,330 15.6 163 13.3 150 14.9
SEER Registry
Alaska Natives 0 0.0 0 0.0 0 0.0 0 0.0 0 0.0 282 28.1
Atlanta 5,479 3.1 2,522 12.3 146 0.9 200 1.3 3 0.2 5 0.5
Connecticut 11,164 6.3 766 3.7 454 2.9 135 0.9 6 0.5 10 1.0
Detroit 10,131 5.8 2,870 14.0 110 0.7 136 0.9 1 0.1 8 0.8
Greater California 43,538 24.7 2,038 9.9 5,726 36.2 3,354 22.4 131 10.7 201 20.0
Hawaii 1,135 0.6 20 0.1 62 0.4 2,138 14.3 828 67.6 18 1.8
Iowa 9,372 5.3 117 0.6 58 0.4 27 0.2 2 0.2 17 1.7
Kentucky 12,176 6.9 834 4.1 41 0.3 43 0.3 4 0.3 1 0.1
Los Angeles 14,546 8.3 2,787 13.6 4,746 30.0 3,484 23.3 66 5.4 30 3.0
Louisiana 9,058 5.1 3,591 17.5 94 0.6 73 0.5 3 0.2 9 0.9
New Jersey 23,073 13.1 3,039 14.8 1,485 9.4 1,047 7.0 29 2.4 13 1.3
New Mexico 3,665 2.1 54 0.3 1,021 6.4 44 0.3 0 0.0 184 18.3
Rural Georgia 258 0.1 124 0.6 1 0.0 0 0.0 0 0.0 0 0.0
San Francisco-Oakland 9,547 5.4 1,194 5.8 895 5.7 2,330 15.6 73 6.0 22 2.2
San Jose-Monterey 5,002 2.8 124 0.6 678 4.3 1,070 7.2 19 1.6 12 1.2
Seattle-Puget Sound 13,183 7.5 386 1.9 170 1.1 798 5.3 39 3.2 174 17.3
Utah 4,767 2.7 20 0.1 148 0.9 72 0.5 20 1.6 18 1.8
% of population in county living below 200% of the federal poverty level in the year 2000, quartiles
≥36.74% 38,927 22.1 6,193 30.2 7,800 49.3 4,215 28.2 97 7.9 282 28.1
28.36-36.73% 42,292 24.0 7,222 35.3 3,662 23.1 2,040 13.6 218 17.8 179 17.8
19.74-28.35% 45,222 25.7 4,221 20.6 2,497 15.8 5,315 35.5 807 65.9 413 41.1
≤19.73% 49,653 28.2 2,850 13.9 1,876 11.8 3,381 22.6 102 8.3 130 12.9
% of population in county with less than a high school education in the year 2000, quartiles
≥25.06% 36,970 21.0 6,163 30.1 8,151 51.5 4,378 29.3 108 8.8 155 15.4
17.64-25.05% 45,606 25.9 7,671 37.4 3,324 21.0 3,231 21.6 80 6.5 161 16.0
14.73-17.63% 41,906 23.8 4,160 20.3 2,996 18.9 4,908 32.8 909 74.3 170 16.9
≤14.72% 51,612 29.3 2,492 12.2 1,364 8.6 2,434 16.3 127 10.4 518 51.6

RESULTS

Non-Hispanic white women were somewhat older at diagnosis compared to women in each of the other racial/ethnic groups (Table 1). The proportions of patients that were non-Hispanic white generally decreased from 2000-2006, while they increased somewhat among blacks, Hispanic whites, Asians, and American Indians/Alaska Natives. Non-Hispanic white women most frequently came from the Greater California and New Jersey registries; black women from Atlanta, Detroit, Los Angeles, Louisiana and New Jersey; Hispanic whites from Greater California and Los Angeles, Asians from Greater California, Hawaii, Los Angeles and San Francisco-Oakland; Pacific Islanders from Hawaii and Greater California; and American Indians/Alaska Natives from the Alaska Natives, Greater California, New Mexico and Seattle-Puget Sound registries. Higher proportions of blacks, Hispanic whites, Asians, and American Indians/Alaska Natives lived in counties where higher proportions of the population were living below 200% of the federal poverty level based on 2000 census data. Higher proportions of Hispanic whites, blacks and Asians lived in counties where higher proportions of the population had less than a high school education.

With respect to statistically significant findings (p<0.05), compared with non-Hispanic white women, black, Hispanic white, Pacific Islander and American Indian/Alaska Native women had 1.5 to 2.5-fold higher odds of presenting with stage IV tumors (Table 2). Among Hispanic whites, Mexican and Puerto Rican women had the highest odds of presenting with stage IV disease (OR=1.8, 95% CI: 1.6-2.1 and OR=1.5, 95% CI: 1.1-2.1, respectively). Among Asians, both Chinese and Japanese women were 30% less likely while Filipino and Asian Indian/Pakistani women were 30% and 50%, respectively, more likely to be diagnosed with stage IV disease. Samoan women had the highest odds of having stage IV breast cancer of any of the women studied (OR=7.1, 95% CI: 3.6-14.0), though both Hawaiian and other Pacific Islander women were also more likely to present with stage IV disease.

Table 2.

Risk of advanced stage breast cancer by race/ethnicity

Stage I
Stage II
Stage III
Stage IV
Race/ethnicity n % n % OR 95% CI n % OR 95% CI n % OR 95% CI
Non-Hispanic white 88,505 50.3 65,922 37.4 1.0 ref 14,228 8.1 1.0 ref 7,439 4.2 1.0 ref
Black 7,257 35.4 8,836 43.1 1.5 1.5-1.6* 2,726 13.3 2.1 2.0-2.2* 1,667 8.1 2.5 2.4-2.7*
Hispanic white 6,060 38.3 6,914 43.7 1.4 1.3-1.5* 2,114 13.4 1.8 1.7-1.9* 747 4.7 1.5 1.3-1.6*
Asian 7,096 47.5 6,001 40.1 1.1 1.1-1.2* 1,326 8.9 1.1 1.1-1.2* 528 3.5 1.0 0.9-1.1
Pacific Islander 508 41.5 511 41.7 1.6 1.4-1.8* 132 10.8 2.0 1.6-2.5* 73 6.0 2.4 1.8-3.1*
American Indian/Alaska Native 448 44.6 403 40.1 1.2 1.0-1.4* 89 8.9 1.3 1.0-1.8* 64 6.4 2.3 1.7-3.0*

Hispanic Subgroups
Mexican 1,569 33.8 2,090 45.0 1.6 1.5-1.7* 751 16.2 2.4 2.2-2.7* 232 5.0 1.8 1.6-2.1*
South or Central American 902 41.2 925 42.3 1.2 1.1-1.4* 271 12.4 1.6 1.4-1.8* 89 4.1 1.1 0.9-1.4
Puerto Rican 250 38.3 280 42.9 1.5 1.2-1..7* 86 13.2 2.1 1.6-2.7* 37 5.7 1.5 1.1-2.1*
Cuban 159 43.2 144 39.1 1.2 1.0-1.5 42 11.4 1.6 1.1-2.3* 23 6.3 1.4 0.9-2.2
Other Hispanics 3,324 39.8 3,627 43.4 1.4 1.3-1.4* 1,011 12.1 1.6 1.5-1.7* 386 4.6 1.4 1.2-1.5*

Asian Subgroups
Filipino 1,892 43.6 1,812 41.7 1.2 1.2-1.3* 451 10.4 1.4 1.3-1.6* 189 4.4 1.3 1.1-1.5*
Chinese 1,451 50.2 1,134 39.2 1.0 0.9-1.1 225 7.8 0.9 0.8-1.0 83 2.9 0.7 0.6-0.9*
Japanese 1,503 56.5 919 34.6 0.9 0.8-1.0* 165 6.2 0.8 0.7-1.0* 71 2.7 0.7 0.5-0.9*
Asian Indian/Pakastani 436 41.3 447 42.3 1.3 1.2-1.5* 118 11.2 1.5 1.2-1.8* 55 5.2 1.5 1.1-1.9*
Korean 444 43.8 442 43.6 1.2 1.1-1.4* 97 9.6 1.2 0.9-1.5 31 3.1 0.9 0.6-1.2
Vietnamese 397 45.5 351 40.3 1.1 0.9-1.3 93 10.7 1.3 1.0-1.6* 31 3.6 1.0 0.7-1.5
Other Asians 1,002 46.1 921 42.4 1.2 1.1-1.3* 182 8.4 1.0 0.9-1.2 69 3.2 0.9 0.7-1.1

Pacific Islander Subgroups
Hawaiian 390 44.1 368 41.6 1.5 1.2-1.7* 83 9.4 1.7 1.3-2.2* 44 5.0 1.8 1.3-2.6*
Samoan 26 21.7 59 49.2 3.1 1.9-4.9* 22 18.3 5.5 3.1-9.8* 13 10.8 7.1 3.6-14.0*
Other Pacific Islanders 106 43.4 91 37.3 1.1 0.9-1.5 31 12.7 1.7 1.1-2.6* 16 6.6 2.9 2.0-4.4*
*

p<0.05.

Note: Non-Hispanic white women served as the reference race/ethnicity and all odds ratios (OR) are adjusted for age at diagnosis, year of diagnosis, SEER registry, and county level measures of poverty and education.

Compared with non-Hispanic white women, black, Hispanic white, Asian and American Indian/Alaska Native women had 1.2 to 2.4-fold higher odds of being diagnosed with ER-/PR- breast cancer (Table 3). Among Hispanic whites, Mexican, South or Central American and Puerto Rican women had higher likelihood of being diagnosed with ER-/PR- breast cancer (OR=1.5, 95% CI: 1.4-1.6, OR=1.4, 95% CI: 1.2-1.5 and OR=1.9, 95% CI: 1.6-2.3, respectively). Among Asians, Japanese women had a 20% lower odds of having ER-/PR- breast cancer, while Korean women had the highest OR (1.5, 95% CI: 1.3-1.7). Black women had the highest odds of being diagnosed with ER-/PR- breast cancer of any of the racial/ethnic groups studied (OR=2.4, 95% CI: 2.3-2.5).

Table 3.

Risk of breast cancer by estrogen and progesterone status by race/ethnicity

ER+/PR+
ER+/PR−
ER−/PR−
Race/ethnicity n % n % OR 95% CI n % OR 95% CI
Non-Hispanic white 102,537 68.4 19,528 13.0 1.0 ref 27,824 18.6 1.0 ref
Black 8,214 49.4 2,175 13.1 1.3 1.3-1.4* 6,230 37.5 2.4 2.3-2.5*
Hispanic white 7,868 61.4 1,634 12.8 1.1 1.0-1.2* 3,310 25.8 1.4 1.3-1.5*
Asian 8,417 66.2 1,606 12.6 1.1 1.0-1.2* 2,682 21.1 1.2 1.2-1.3*
Pacific Islander 783 70.9 114 10.3 0.9 0.7-1.1 208 18.8 1.1 0.9-1.2
American Indian/Alaska Native 571 65.3 96 11.0 0.8 0.6-1.1 208 23.8 1.3 1.1-1.6*

Hispanic Subgroups
Mexican 2,239 60.1 440 11.8 1.0 0.9-1.2 1,048 28.1 1.5 1.4-1.6*
South or Central American 1,089 61.8 233 13.2 1.1 1.0-1.3 441 25.0 1.4 1.2-1.5*
Puerto Rican 290 54.9 73 13.8 1.2 0.9-1.6 165 31.3 1.9 1.6-2.3*
Cuban 203 70.7 34 11.8 0.8 0.5-1.1 50 17.4 0.9 0.7-1.2
Other Hispanics 4,237 62.2 892 13.1 1.1 1.0-1.2* 1,686 24.7 1.3 1.3-1.4*

Asian Subgroups
Filipino 2,343 64.0 484 13.2 1.1 1.0-1.3* 834 22.8 1.3 1.2-1.4*
Chinese 1,633 66.6 317 12.9 1.1 1.0-1.3* 501 20.4 1.2 1.0-1.2*
Japanese 1,699 73.5 280 12.1 1.0 0.8-1.1 332 14.4 0.8 0.7-0.9*
Asian Indian/Pakastani 558 62.3 108 12.1 1.0 0.8-1.3 229 25.6 1.4 1.2-1.6*
Korean 544 62.5 100 11.5 1.1 0.9-1.3 227 26.1 1.5 1.3-1.7*
Vietnamese 448 62.9 82 11.5 1.1 0.8-1.4 182 25.6 1.4 1.2-1.7*
Other Asians 1,228 66.3 240 13.0 1.1 1.0-1.3 385 20.8 1.2 1.0-1.3*

Pacific Islander Subgroups
Hawaiian 582 72.5 85 10.6 0.9 0.7-1.2 136 16.9 0.9 0.7-1.1
Samoan 75 70.1 9 8.4 0.7 0.3-1.3 23 21.5 0.9 0.6-1.5
Other Pacific Islanders 143 65.6 23 10.6 0.9 0.6-1.4 52 23.9 1.3 0.9-1.8
*

p<0.05.

Note: Non-Hispanic white women served as the reference race/ethnicity and all odds ratios (OR) are adjusted for age at diagnosis, year of diagnosis, AJCC stage, SEER registry, and county level measures of poverty and education.

Among women with stage I or II breast carcinomas less than 2.0 cm in size, compared with non-Hispanic white women, black and Hispanic white women had increased odds of receiving inappropriate primary surgical and radiation breast cancer treatment (OR=1.5, 95% CI: 1.3-1.6 and OR=1.2, 95% CI: 1.1-1.3, respectively) (Table 4). Among Hispanic whites, Mexican and South or Central American women had the highest likelihood of receiving inappropriate treatment (OR=1.2, 95% CI: 1.0-1.5 and OR=1.3, 95% CI: 1.0-1.7, respectively). Samoan women had the highest OR of receiving inappropriate treatment of any of the racial/ethnic subgroups studied (OR=5.1, 95% CI: 2.0-13.0).

Table 4.

Risk of inappropriate treatment for early stage breast cancer by race/ethnicity

Standard
Treatment
Inappropriate
Treatment
Race/ethnicity n % n % OR 95% CI
Non-Hispanic white 94,779 94.2 5,876 5.8 1.0 ref
Black 7,716 92.0 672 8.0 1.5 1.3-1.6*
Hispanic white 6,549 93.6 451 6.4 1.2 1.1-1.3*
Asian 7,564 94.6 431 5.4 1.0 0.9-1.2
Pacific Islander 539 92.9 41 7.1 1.4 1.0-1.9
American Indian/Alaska Native 476 93.9 31 6.1 1.3 0.8-2.0

Hispanic Subgroups
Mexican 1,743 94.3 106 5.7 1.2 1.0-1.5*
South or Central American 961 92.8 75 7.2 1.3 1.0-1.7*
Puerto Rican 273 91.6 25 8.4 1.2 0.8-1.8
Cuban 159 92.4 13 7.6 1.0 0.6-1.8
Other Hispanics 3,573 93.5 247 6.5 1.2 1.1-1.4*

Asian Subgroups
Filipino 1,991 94.7 112 5.3 1.0 0.9-1.3
Chinese 1,572 94.6 90 5.4 1.0 0.8-1.3
Japanese 1,585 94.0 102 6.0 0.9 0.7-1.1
Asian Indian/Pakastani 461 95.4 22 4.6 0.9 0.6-1.3
Korean 485 94.2 30 5.8 1.3 0.9-1.8
Vietnamese 412 95.2 21 4.8 1.1 0.7-1.8
Other Asians 1,093 95.0 57 5.0 1.1 0.9-1.5

Pacific Islander Subgroups
Hawaiian 418 93.3 30 6.7 1.2 0.8-1.8
Samoan 21 77.8 6 22.2 5.1 2.0-13.0*
Other Pacific Islanders 113 95.0 6 5.0 1.1 0.5-2.4
*

p<0.05.

Note: Non-Hispanic white women served as the reference race/ethnicity and all odds ratios (OR) are adjusted for age at diagnosis, year of diagnosis, AJCC stage, SEER registry, and county level measures of poverty and education.

Compared with non-Hispanic white women, black, Hispanic white, Pacific Islander and American Indian/Alaska Native women had 1.4 to 2.4-fold greater risks of breast cancer specific mortality, adjusting for diagnosis age, year, and SEER registry (Table 5). Elevations in risk of mortality were still observed, though attenuated, in black, Hispanic white and Pacific Islander women, after additionally adjusting for stage, ER/PR status, surgical and radiation treatments, and county level measures of poverty and education. Among Hispanic whites, Puerto Rican women had the highest risk of breast cancer specific mortality in our multivariate adjusted model (OR=1.7, 95% CI: 1.3-2.1). Among Asians, Japanese women had 20% lower breast cancer specific mortality risks, after multivariate adjustment (OR=0.8, 95% CI: 0.6-1.0). Among Pacific Islanders, both Hawaiian and Samoan women had increased risk of mortality (multivariate adjusted OR=1.5, 95% CI: 1.1-2.0 and OR=1.8, 95% CI: 1.1-3.0, respectively).

Table 5.

Risk of breast cancer specific mortality by race/ethnicity

Adjusted for
age and registry
Multivariate
adjusted
Alive Dead HR 95% CI HR 95% CI
Non-Hispanic white 165,271 10,823 1.0 ref 1.0 ref
Black 17,678 2,808 2.4 2.3-2.5* 1.5 1.4-1.6*
Hispanic white 14,647 1,188 1.4 1.3-1.5* 1.1 1.0-1.2*
Asian 1,407 744 1.0 0.9-1.1 0.9 0.8-1.0
Pacific Islander 1,125 99 1.8 1.5-2.3* 1.5 1.2-1.9-
American Indian/Alaska Native 925 79 1.6 1.3-2.1* 1.1 0.8-1.4

Hispanic Subgroups
Mexican 4,259 383 1.7 1.5-1.8* 1.1 0.9-1.2
South or Central American 2,052 135 1.1 1.0-1.4 1.0 0.8-1.2
Puerto Rican 570 83 2.2 1.8-2.8* 1.7 1.3-2.1*
Cuban 328 40 1.8 1.3-2.5* 1.4 0.9-2.1
Other Hispanics 7,770 578 1.3 1.2-1.4* 1.1 0.9-1.2

Asian Subgroups
Filipino 4,063 281 1.2 1.1-1.4* 1.1 0.9-1.2
Chinese 2,761 132 0.9 0.7-1.0 1.0 0.8-1.2
Japanese 2,553 105 0.7 0.6-0.9* 0.8 0.6-1.0*
Asian Indian/Pakastani 1,002 54 1.0 0.8-1.3 0.7 0.5-1.0*
Korean 958 53 1.1 0.9-1.5 1.0 0.8-1.4
Vietnamese 827 45 1.1 0.8-1.4 1.0 0.7-1.4
Other Asians 2,100 74 0.7 0.6-0.9* 0.6 0.5-0.8*

Pacific Islander Subgroups
Hawaiian 817 68 1.6 1.2-2.0* 1.5 1.1-2.0*
Samoan 101 19 3.7 2.4-5.9* 1.8 1.1-3.0*
Other Pacific Islanders 228 16 1.5 0.9-2.4 1.2 0.7-2.0
*

p<0.05.

Note: Non-Hispanic white women served as the reference race/ethnicity and all odds ratios (OR) are adjusted for age at diagnosis, year of diagnosis, SEER registry, AJCC stage, ER/PR status, surgical and radiation treatments, and county level measures of poverty and education.

DISCUSSION

The results of our study (summarized in Table 6) are consistent with multiple prior studies that have evaluated various aspects of breast cancer disparities by race/ethnicity. Specifically, it is consistent with the literature demonstrating that compared to non-Hispanic white women, black [3, 15, 18, 22], Hispanic white [13, 15, 16, 18, 22], Hawaiian [4, 7, 15], and American Indian [15, 26, 27] women present with more advanced stages of breast cancer and have greater risks of mortality after a breast cancer diagnosis. It has also been previously reported that Japanese women have better breast cancer survival rates compared to non-Hispanic white women [4, 19]; that black and Hispanic white women are more likely to receive inappropriate treatments [3, 15]; and that black, Hispanic white and American Indian women are more likely to present with tumors that were ER- or PR- [11, 14, 16, 21]. Beyond confirming that all of these disparities persist in the United States through 2006, a unique contribution is the characterization of breast cancer disparities impacting Pacific Islander women. These women, and in particular Samoan women, were among those experiencing disparities with the highest magnitudes. Specifically, Samoan women had substantially higher odds of presenting with Stage IV disease (OR=7.1) and receiving inappropriate treatment for early stage breast cancer (OR=5.1), and the highest risk of any group of breast cancer mortality (HR=1.8) despite being one of the only groups to have a similar risk of ER-/PR- disease compared to non-Hispanic whites. This suggests that the disparities these women experience are primarily related to issues of access to care with respect to both screening and follow-up after a breast cancer diagnosis rather than differences in tumor biology. These disparities have not been previously well characterized as most prior studies have combined Pacific Islander women with Asian women in their analyses despite the fact that they are a racially diverse group of people with respect to genetics, socioeconomic status (SES), and culture.

Table 6.

Summary of Breast Cancer Disparities by Race/Ethnicity

Race/ethnicity Stage IV ER−/PR− Inappropriate
treatment
Multivariate adjusted
risk of breast cancer
specific mortality
Non-Hispanic white ref ref ref ref
Black ↑ ↑ ↑ ↑
Hispanic
Asian
Pacific Islander ↑ ↑
American Indian/Alaska Native ↑ ↑

Hispanic Subgroups
Mexican
South or Central American
Puerto Rican
Cuban

Asian Subgroups
Filipino
Chinese
Japanese
Asian Indian/Pakistani
Korean
Vietnamese

Pacific Islander Subgroups
Hawaiian
Samoan ↑ ↑ ↑ ↑

↑ denotes a statistically significant increase ≤2.0 in magnitude

↑↑ denotes a statistically significant increase >2.0 in magnitude

↓ denotes a statistically significant decrease

– denotes not statistically different from non-Hispanic whites

Black breast cancer patients continue to fare quite poorly as they had elevated likelihood of having all four adverse breast outcomes assessed here. This suggests that disparities are impacting black women across the breast cancer spectrum with respect to access and utilization of screening and preventive services, clinical care subsequent to breast cancer diagnosis, and long term follow-up care and clinical management for black breast cancer survivors. These results support continued multi-pronged efforts to address these disparities in black communities throughout the U.S.

We observed distinct differences with respect to breast cancer stage, treatment and mortality risks within the broadly defined racial/ethnic group of Hispanic whites, Asians and Pacific Islanders. With respect to Hispanic white women of the four subgroups assessed, Mexican women had the highest likelihood of presenting with stage III and IV breast cancer, Puerto Rican women were the most frequently diagnosed with ER-/PR- disease, only Mexican and South/Central American women had higher likelihood of receiving inappropriate treatment, and only Puerto Rican women had an increased risk of mortality in the multivariate adjusted model. As each outcome measured is an indicator of different types of disparities, this information could be potentially useful in designing public health strategies. For example, the high likelihood of advanced stage cancer among Mexican women suggests that efforts to promote breast cancer screening and/or timely access to care after an abnormal mammogram may be of particular importance in this population, while the high risk of mortality among Puerto Rican women indicates that efforts to ensure that Puerto Rican breast cancer survivors get adequate treatment and follow-up care may be needed.

Even greater heterogeneity was observed among Asian subgroups. Japanese women consistently had better outcomes than non-Hispanic white women in several respects including lower odds of having stage IV breast cancer, ER-/PR- disease, and lower mortality risk. The picture was more mixed for other Asian subgroups as Chinese women also had lower likelihood of presenting with stage IV disease but more likely to have ER-/PR- disease and Asian Indian/Pakistani women had odds of having stage III and IV breast cancer but had a lower risk of mortality. With the exception of higher odds of ER-/PR- disease, Korean and Vietnamese women were similar to non-Hispanic whites in other respects. Lastly, of all the Asian subgroups, Filipino women in general had the poorest outcomes compared to the other Asian subgroups in that they were more likely to present with advanced stage and with ER-/PR- breast cancer. Again, consideration of the nature of the disparities each subgroup experienced could be useful in developing strategies to address them.

We also found that Alaska Native/American Indian women are more likely to be diagnosed with advanced stage and ER-/PR- breast cancer. Our results agree with previous studies that show that American Indian/Alaska Native women are more likely to be diagnosed with late stage breast cancer. Prior studies also suggest that these women are more likely to die of breast cancer [27], even after adjustment for definitive therapy [26]; however, results of our study did not show differences in mortality. While it is possible that relative mortality rates for these women have improved, there is also considerable heterogeneity across American Indian/Alaska Native populations, which could contribute to this difference.

While many of the relative disparities persist, including with respect to receipt of appropriate treatment for early stage breast cancer, one encouraging difference we found is in the higher proportions of women with early stage disease who do receive appropriate treatment across all races/ethnicities. While our study that included data from 1992-1998 found that the percentage of women receiving appropriate therapy ranged from 77.1-86.3% across races/ethnicities, the more recent 2000-2006 data shown here indicate that with the exception of Samoan women, 91.6-95.4% of women across races/ethnicities received appropriate treatment.

One potential limitation of our study was that race/ethnicity was determined via medical record reviews only, and is also subjected to misclassification of race/ethnicity, which has been shown to vary by race/ethnicity [8]. Consequently, a sizable proportion of Asian, Pacific Islander and Hispanic white women were classified as “other” or “not-otherwise-specified” (NOS) (14.5%, 19.5% and 51.5%, respectively). Precisely how our point estimates would have changed if these women, and particularly the large number of Hispanic whites, NOS, could have been correctly classified into a subgroup is unknown. In general though, the point estimates for the “other” groups were consistent with those for the broader classifications. Another potential limitation is misclassification of our various outcomes. For example, ER/PR data also came from medical record data and so variation in the methods used to evaluate and interpret ER and PR status across hospitals and geographic regions could contribute to this misclassification. Lastly, a lack of data on individual level socioeconomic variables as well as other factors such as family history of breast cancer, lifestyle factors, anthropometric characteristics, and treatment with hormonal therapy and chemotherapy precludes us from evaluating these exposures as potential confounders or effect modifiers of the relationships observed.

The disparities identified here are multifactorial and due to a combination of several factors including those related to socioeconomic status, access to health care, lifestyle and cultural differences, and cancer biology. These factors all have the potential to influence disparities at several points along the spectrum of breast cancer clinical care from prevention and screening services, to diagnosis and treatment, and to long-term follow-up and survivorship. We demonstrate here that many breast cancer disparities persist after adjusting for various aspects of these disparities. Other studies with more detailed individual level data have shown that some disparities are attenuated or disappear after adjusting for certain factors, while other show that they persist [5, 9, 12, 24, 25]. For example, one study compared breast cancer outcomes among underinsured black and non-Hispanic white patients treated in an equal healthcare access setting over a ten year period (1997-2006) [12]. It found that black patients had a poorer breast cancer-specific survival rate compared to non-Hispanic white patients, but that after adjustment for clinical and sociodemographic factors this difference was no longer statistically significant. Similar attenuation was seen in another study that evaluated breast cancer outcomes in a population with low SES and similar access to health care [5]. 60% of the patients in the two hospitals studied were blacks and over two-thirds of patients had either Medicaid coverage or no insurance, and here 5-year overall survival rates for black and Caucasian patients were similar. In contrast, a study of breast cancer incidence observed that even after adjusting for factors associated with SES, a disparity in breast cancer incidence persisted among blacks [24]. The authors utilized several studies (published between 1990 and 2007) that addressed disparities in breast cancer incidence across racial and socioeconomic strata to calculate incidence rate ratios (IRRs) comparing the highest to the lowest strata of SES for white, black, Hispanic and Asian/Pacific Islander populations. They found that the magnitude of the disparity in breast cancer incidence between races decreased as SES increased. However, when adjusted for factors closely associated with SES, disparities in breast cancer incidence between white, Hispanic, and Asian/Pacific-Islander were no longer seen, but did persist in the comparison between white and black women. With respect to disparities in breast cancer diagnosis and treatment delay by race/ethnicity, in a study of 49,865 female Medicare recipients 65 years and older diagnosed with breast cancer during a seven-year period (1992-1999), black women most frequently experienced delays in both initial diagnosis and initiation of breast cancer treatment relative to women of other races/ethnicities in a multivariate adjusted model that included access to healthcare [9, 25]. Diagnostic and therapeutic delays were also found to contribute to breast and cervical cancer disparity in a population-based sampling and cross sectional design study, which showed that Hispanic whites are more likely to report diagnostic delays while blacks are more likely to report therapeutic delays [1]. However, breast cancer disparities by race/ethnicity seem to be less affected by mammography usage during our study time period. Mammography usage based on Behavioral Risk Factor Surveillance System (BRFSS) data indicate that from 1993 to 2003 mammography utilization has been similar among Black and non-Hispanic women [23].

While many other studies have also addressed these issues, the studies described above are illustrative of the complexity and multifactorial nature of racial/ethnic disparities in breast cancer. Our study shows that despite ongoing efforts, breast cancer disparities by race and ethnicity persist in the United States and in particular quantitates disparities present in smaller racial/ethnic subgroups that have not been previously well studied. Importantly, our study identifies the types of disparities faced by distinct racial/ethnic subgroups and can potentially help inform further development and implementation of specific strategies to address them.

ACKNOWLEDGEMENTS

This work was supported by the National Cancer Institute [grant number R25-CA94880].

Footnotes

Potential conflicts of interest: None

REFERENCES

  • 1.Ashing-Giwa KT, Gonzalez P, Lim JW, Chung C, Paz B, Somlo G, Wakabayashi MT. Diagnostic and therapeutic delays among a multiethnic sample of breast and cervical cancer survivors. Cancer. 2010;116:3195–3204. doi: 10.1002/cncr.25060. [DOI] [PubMed] [Google Scholar]
  • 2.Ballard-Barbash R, Potosky AL, Harlan LC, Nayfield SG, Kessler LG. Factors associated with surgical and radiation therapy for early stage breast cancer in older women. J Natl Cancer Inst. 1996;88:716–726. doi: 10.1093/jnci/88.11.716. [DOI] [PubMed] [Google Scholar]
  • 3.Berz JP, Johnston K, Backus B, Doros G, Rose AJ, Pierre S, Battaglia TA. The influence of black race on treatment and mortality for early-stage breast cancer. Med Care. 2009;47:986–992. doi: 10.1097/MLR.0b013e31819e1f2b. [DOI] [PubMed] [Google Scholar]
  • 4.Braun KL, Fong M, Gotay CC, Chong CD. Ethnic differences in breast cancer in Hawai'i: age, stage, hormone receptor status, and survival. Pac Health Dialog. 2004;11:146–153. [PubMed] [Google Scholar]
  • 5.Chu QD, Smith MH, Williams M, Panu L, Johnson LW, Shi R, Li BD, Glass J. Race/Ethnicity has no effect on outcome for breast cancer patients treated at an academic center with a public hospital. Cancer Epidemiol Biomarkers Prev. 2009;18:2157–2161. doi: 10.1158/1055-9965.EPI-09-0232. [DOI] [PubMed] [Google Scholar]
  • 6.Dunnwald LK, Rossing MA, Li CI. Hormone receptor status, tumor characteristics, and prognosis: a prospective cohort of breast cancer patients. Breast Cancer Res. 2007;9:R6. doi: 10.1186/bcr1639. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Goggins WB, Wong GK. Poor survival for US Pacific Islander cancer patients: evidence from the Surveillance, Epidemiology, and End Results database: 1991 to 2004. J Clin Oncol. 2007;25:5738–5741. doi: 10.1200/JCO.2007.13.8271. [DOI] [PubMed] [Google Scholar]
  • 8.Gomez SL, Glaser SL. Misclassification of race/ethnicity in a population-based cancer registry (United States) Cancer Causes Control. 2006;17:771–781. doi: 10.1007/s10552-006-0013-y. [DOI] [PubMed] [Google Scholar]
  • 9.Gorin SS, Heck JE, Cheng B, Smith SJ. Delays in breast cancer diagnosis and treatment by racial/ethnic group. Arch Intern Med. 2006;166:2244–2252. doi: 10.1001/archinte.166.20.2244. [DOI] [PubMed] [Google Scholar]
  • 10.Harper S, Lynch J, Meersman SC, Breen N, Davis WW, Reichman MC. Trends in area-socioeconomic and race-ethnic disparities in breast cancer incidence, stage at diagnosis, screening, mortality, and survival among women ages 50 years and over (1987-2005) Cancer Epidemiol Biomarkers Prev. 2009;18:121–131. doi: 10.1158/1055-9965.EPI-08-0679. [DOI] [PubMed] [Google Scholar]
  • 11.Hausauer AK, Keegan TH, Chang ET, Clarke CA. Recent breast cancer trends among Asian/Pacific Islander, Hispanic, and African-American women in the US: changes by tumor subtype. Breast Cancer Res. 2007;9:R90. doi: 10.1186/bcr1839. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Komenaka IK, Martinez ME, Pennington RE, Jr., Hsu CH, Clare SE, Thompson PA, Murphy C, Zork NM, Goulet RJ., Jr. Race and Ethnicity and Breast Cancer Outcomes in an Underinsured Population. J Natl Cancer Inst. 2010 doi: 10.1093/jnci/djq215. [DOI] [PubMed] [Google Scholar]
  • 13.Kouri EM, He Y, Winer EP, Keating NL. Influence of birthplace on breast cancer diagnosis and treatment for Hispanic women. Breast Cancer Res Treat. 2010;121:743–751. doi: 10.1007/s10549-009-0643-3. [DOI] [PubMed] [Google Scholar]
  • 14.Li CI, Malone KE, Daling JR. Differences in breast cancer hormone receptor status and histology by race and ethnicity among women 50 years of age and older. Cancer Epidemiol Biomarkers Prev. 2002;11:601–607. [PubMed] [Google Scholar]
  • 15.Li CI, Malone KE, Daling JR. Differences in breast cancer stage, treatment, and survival by race and ethnicity. Arch Intern Med. 2003;163:49–56. doi: 10.1001/archinte.163.1.49. [DOI] [PubMed] [Google Scholar]
  • 16.Martinez ME, Nielson CM, Nagle R, Lopez AM, Kim C, Thompson P. Breast cancer among Hispanic and non-Hispanic White women in Arizona. J Health Care Poor Underserved. 2007;18:130–145. doi: 10.1353/hpu.2007.0112. [DOI] [PubMed] [Google Scholar]
  • 17.McDougall JA, Li CI. Trends in distant stage breast, colorectal, and prostate cancer incidence rates from 1992-2004. Hormones and Cancer. 2010;1:55–62. doi: 10.1007/s12672-009-0002-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Menck HR, Mills PK. The influence of urbanization, age, ethnicity, and income on the early diagnosis of breast carcinoma: opportunity for screening improvement. Cancer. 2001;92:1299–1304. doi: 10.1002/1097-0142(20010901)92:5<1299::aid-cncr1451>3.0.co;2-7. [DOI] [PubMed] [Google Scholar]
  • 19.Meng L, Maskarinec G, Lee J. Ethnicity and conditional breast cancer survival in Hawaii. J Clin Epidemiol. 1997;50:1289–1296. doi: 10.1016/s0895-4356(97)00183-2. [DOI] [PubMed] [Google Scholar]
  • 20.Nattinger AB, Hoffmann RG, Kneusel RT, Schapira MM. Relation between appropriateness of primary therapy for early-stage breast carcinoma and increased use of breast-conserving surgery. Lancet. 2000;356:1148–1153. doi: 10.1016/S0140-6736(00)02757-4. [DOI] [PubMed] [Google Scholar]
  • 21.Setiawan VW, Monroe KR, Wilkens LR, Kolonel LN, Pike MC, Henderson BE. Breast cancer risk factors defined by estrogen and progesterone receptor status: the multiethnic cohort study. Am J Epidemiol. 2009;169:1251–1259. doi: 10.1093/aje/kwp036. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Shavers VL, Harlan LC, Stevens JL. Racial/ethnic variation in clinical presentation, treatment, and survival among breast cancer patients under age 35. Cancer. 2003;97:134–147. doi: 10.1002/cncr.11051. [DOI] [PubMed] [Google Scholar]
  • 23.Smigal C, Jemal A, Ward E, Cokkinides V, Smith R, Howe HL, Thun M. Trends in breast cancer by race and ethnicity: update 2006. CA Cancer J Clin. 2006;56:168–183. doi: 10.3322/canjclin.56.3.168. [DOI] [PubMed] [Google Scholar]
  • 24.Vainshtein J. Disparities in breast cancer incidence across racial/ethnic strata and socioeconomic status: a systematic review. J Natl Med Assoc. 2008;100:833–839. doi: 10.1016/s0027-9684(15)31378-x. [DOI] [PubMed] [Google Scholar]
  • 25.Vona-Davis L, Rose DP. The influence of socioeconomic disparities on breast cancer tumor biology and prognosis: a review. J Womens Health (Larchmt) 2009;18:883–893. doi: 10.1089/jwh.2008.1127. [DOI] [PubMed] [Google Scholar]
  • 26.Wampler NS, Lash TL, Silliman RA, Heeren TC. Breast cancer survival of American Indian/Alaska Native women, 1973-1996. Soz Praventivmed. 2005;50:230–237. doi: 10.1007/s00038-004-4020-6. [DOI] [PubMed] [Google Scholar]
  • 27.Wingo PA, King J, Swan J, Coughlin SS, Kaur JS, Erb-Alvarez JA, Jackson-Thompson J, Arambula Solomon TG. Breast cancer incidence among American Indian and Alaska Native women: US, 1999-2004. Cancer. 2008;113:1191–1202. doi: 10.1002/cncr.23725. [DOI] [PubMed] [Google Scholar]
  • 28.Young JL, Jr., Percy CL, Asire AJ, Berg JW, Cusano MM, Gloeckler LA, Horm JW, Lourie WI, Jr., Pollack ES, Shambaugh EM. Cancer incidence and mortality in the United States, 1973-77. Natl Cancer Inst Monogr. 1981:1–187. [PubMed] [Google Scholar]

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