Disparities in receipt of care for high-grade endometrial cancer: A National Cancer Data Base analysis
Introduction
In the United States, endometrial cancer is the most common gynecologic malignancy, with 60,050 new cases estimated in 2016 [1]. While the majority of these cases are early stage and of low-grade endometrioid histology, a proportion of women will be diagnosed with an aggressive histologic subtype that confers a greater risk of disease recurrence and increased mortality [2]. African American women have a higher incidence of high-grade histology [3], [4], [5], [6], [7], which may contribute to the well-documented increase in overall mortality among African American women [8], [9], [10], [11], [12]. While the vast majority of research has focused on the comparison between white and African American women with endometrial cancer, a growing yet limited body of literature has examined differences in disease presentation, treatment patterns and outcomes between Hispanic and non-Hispanic women [7], [13], [14], [15], [16].
“Hispanic or Latino” ethnicity is defined by the federal Office of Management and Budget as “a person of Cuban, Mexican, Puerto Rican, South or Central American, or other Spanish culture or origin, regardless of race” [17]. Hispanics represent the largest ethnic minority group in the United States, and cancer is the leading cause of death among Hispanic women [18]. Hispanic women, similar to African American women, have a higher incidence of high-grade disease [13], [15] and are a vulnerable population disproportionately affected by lower socioeconomic status and barriers to healthcare. While there is substantial racial and cultural diversity within the Hispanic community and significant variation in the literature regarding how Hispanic ethnicity is characterized [19], cancer data are typically presented for Hispanics in aggregate [18]. Despite the heterogeneity within the Hispanic population, there is value in comparing the differences in treatment patterns and clinical outcomes among white women, African American women and Hispanic women with cancer, as such studies are lacking. The objective of this study is to compare the demographics, tumor characteristics, treatment course and overall survival of Hispanic women to non-Hispanic white women and non-Hispanic African American women with high-grade endometrial cancer.
Section snippets
Materials and methods
The National Cancer Data Base (NCDB) was used to identify women with high-grade endometrial cancer diagnosed between 2003 and 2011. The NCDB is a nationwide comprehensive clinical surveillance oncology system established by the American Cancer Society and the Commission on Cancer of the American College of Surgeons. Currently, this database captures approximately 70% of newly diagnosed malignancies in the United States, and receives over one million case reports from over 1500 hospitals
Results
We identified 43,950 women from the NCDB diagnosed with high-grade endometrial cancer between 2003 and 2011 who met inclusion criteria. Table 1 summarizes the demographic and clinical characteristics of the study population. African American women were more frequently in the lowest quartile of income level (41.5% vs. 12.7% vs. 27.3%, p < 0.001) and had a higher comorbidity score of 2 or greater (7.1% vs. 4.7% vs. 4.3%, p < 0.001) when compared to white and Hispanic women. Hispanic women were more
Discussion
In the United States, racial and ethnic disparities in receipt of care, as well as in mortality, are well established for a plethora of conditions. In this study of 43,950 women with high-grade endometrial cancer, after controlling for patient, tumor and treatment-related factors, African American women had lower all-cause overall survival compared to white women. While the root cause of this is undoubtedly multifactorial, unmeasured socioeconomic factors, compounded with measured factors such
Conflict of interest statement
The authors declare that there are no conflicts of interest.
Acknowledgements
This work was supported by The Deborah Kelly Center for Outcomes Research, Massachusetts General Hospital. This work is supported by R25CA092203 from the National Cancer Institute at the National Institutes of Health.
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