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. Author manuscript; available in PMC: 2020 Aug 1.
Published in final edited form as: Cancer Epidemiol Biomarkers Prev. 2019 May 30;28(8):1353–1363. doi: 10.1158/1055-9965.EPI-18-0872

Disaggregating Hispanic American cancer mortality burden by detailed ethnicity

Steven M Zamora 1, Paulo S Pinheiro 2, Scarlett Lin Gomez 3,4,5, Katherine G Hastings 6, Latha P Palaniappan 6, Jiaqi Hu 6, Caroline A Thompson 1,7
PMCID: PMC6771432  NIHMSID: NIHMS1530565  PMID: 31147314

Abstract

Background:

Hispanics are the largest minority population in the United States (18%). They represent a heterogeneous and growing population. Cancer is the leading cause of death among Hispanics, yet few studies have described cancer mortality burden by specific Hispanic group nationwide.

Methods:

Cancer-related deaths from U.S. death certificates for the years 2003-2012 were analyzed for decedents identifying as Mexican, Puerto Rican, Cuban, and Central or South American. We calculated descriptive statistics including potential years of lives lost (PYLL), age-adjusted rates, standardized mortality ratios, and fitted JoinPoint regression models to evaluate annual trends by Hispanic group, using non-Hispanic Whites (NHWs) as the reference population.

Results:

We identified 287,218 cancer deaths among Hispanics and 4,570,559 among NHWs. Mortality trends were heterogeneous across Hispanic groups. Female NHWs and male Puerto Ricans had the greatest rates of adjusted PYLL per 1000 (NHWs, 19.6; Puerto Ricans, 16.5). Liver cancer was ranked among the top 5 cancer-related deaths for every Hispanic group, but not for NHWs. Stomach cancer mortality was twice as high for most Hispanic groups when compared to NHWs and especially high for Mexicans (male SMR, 2.07; 95% CI, 2.01-2.13; female SMR, 2.62; 95% CI, 2.53-2.71)

Conclusion:

We observed marked heterogeneity in cancer mortality across Hispanic groups. Several cancers affect Hispanics disproportionately compared to NHWs. Screening programs in Hispanics should be considered for stomach and liver cancer.

Impact:

Disaggregated analysis of Hispanics is needed to fully understand cancer burden among the diverse Hispanic population and is critical for cancer prevention and control efforts.

Keywords: epidemiology, cancer, vital statistics, Hispanic American, ethnic disparities

INTRODUCTION

The Hispanic population is the largest minority group in the United States and is rapidly growing[1]. 18% of the U.S. identified as Hispanic in 2016 and the population increased by 57% between 2000 and 2014[1, 2]. The rapid growth of the Hispanic population makes it essential to accurately assess health problems and uncover health disparities that affect this population. Cancer incidence and mortality appear to be steadily decreasing among the Hispanic population[3]. Factors such as acculturation, diet, physical activity, alcohol consumption, and smoking all affect the cancer burden in Hispanics[3]. Relative to the non-Hispanic white population, the Hispanic population in the U.S. is also disproportionately affected by lower income, education, and access to health care[4]. Language barriers, low health insurance coverage, low income, and unfamiliarity with dealing with insurance providers have all been shown to be obstacles of cancer screenings in the U.S.[4] In most studies, Hispanics are aggregated into a single group because Hispanics share a similar migration history, have a common language, and share many values[5]. However, specific Hispanic groups can vary significantly via genetic, cultural, behavioral, geographic, and socioeconomic factors[6-9]. For example, the poverty rate for aggregated Hispanics is 25%, but ranges from 27% for Mexicans to 18% in Cubans[10]. Behaviors such as alcohol intake also differ by Hispanic group. A recent survey found that Cuban males report drinking 8.4 drinks a week while Puerto Rican males drink 16.9 drinks a week[11]. Due to this heterogeneity in health behaviors among Hispanics, aggregation may mask important differences among specific Hispanic groups. Furthermore, studies in Asian populations have shown that disaggregated cancer statistics are essential to understanding cancer burden in a population[9, 12].

The Hispanic population presents a unique opportunity to study cancer burden because they share similar immigration experiences and have cultural commonalities, but also have key behavioral differences between them that can highlight the severity of important cancer risk factors[5]. While few studies of this kind have been done, they have shown that cancer burden is heterogeneous across Hispanic groups in specific states such as Florida[13], and California[25]. However, none of the existing studies report mortality trends over time by disaggregated Hispanic ethnicity. The goal of this paper is to report specific Hispanic cancer mortality rates and 10-year mortality trends for the first time at a national level.

MATERIALS AND METHODS

We obtained death certificate information (cause of death, age of death, sex, and race/ethnicity) from the National Center for Health Statistic (NCHS) from 2003–2012. All cancer deaths from this time period, for all ages, were identified by the “Underlying cause of death” which was coded by NCHS using International Classification of Diseases, 10th revision (ICD-10; specific codes provided in Supplementary Table 1). We chose 10 cancer sites based on their overall contribution to Hispanic mortality burden: lung, female breast, liver, colorectal, prostate, pancreas, ovary, stomach, leukemia, and Non-Hodgkin Lymphoma (NHL)[3] . Statistics for “all cancer sites” include all other cancer sites in addition to the top 10.

The study population included 243,777 Hispanic decedents, of all races, who were identified on their death certificate as Mexican, Puerto Rican, Cuban, and Central or South American and 4,579,559 non-Hispanic White (NHW) decedents who were included as the reference group. Statistics calculated for the “All Hispanic” group (N=287,218) are an aggregate of the four specific Hispanic groups as well as those who identified as “Other Hispanic”.

Statistical Analysis

Annual population denominator counts were estimated using linear interpolation and extrapolation based on age-specific population data from the 2000 and 2010 U.S. Census. Annual counts were then summed to determine total person-years for 10-year study period. Using decedent counts by sex, Hispanic group and cancer site, we estimated potential years of lives lost (PYLL), proportional cancer mortality, and age-adjusted mortality rates (AMRs). We then fitted regression models for trends in annual cancer-related mortality over the 10-year period also by sex, Hispanic group, and cancer site.

PYLL measures the impact of cancer on the potential duration of life that individuals of the given population should have, on average, in absence of death from the index cause (i.e., site-specific cancer). We calculated PYLL with respect to a fixed age limit, based on benchmarks for life expectancy of NHWs and Hispanics obtained from a report from the Center for Disease Control (CDC)[14]. For NHWs, age 81 was used as a benchmark for females, and age 76 for males. For Hispanics, age 83 was used for females, and 78 for males. The PYLL per sex and Hispanic group (for all cancer deaths) was calculated as:

PYLL=ax<hdx(hax)

where h is the fixed age limit (as defined above) and ax is the average age of death in each 5-year age group, and dx is the total number of deaths in the 5-year age group [15]. We report the crude PYLL as a rate per 1,000 person-years, where the denominator is the size of the underlying population that gave rise to the premature deaths and we also standardized this rate to the 2000 U.S. population age distribution to account for differing age distributions of the study populations.

Proportional cancer mortality, AMR, and SMR were calculated and stratified by cancer site, sex, and Hispanic group. The site-specific proportion of all cancer deaths was used to determine proportional cancer mortality. AMRs and 95% confidence intervals were calculated as deaths per 100,000 for the duration of the study period and directly standardized to the age distribution of the 2000 U.S. population. AMRs are comparable across Hispanic groups and cancer sites. SMRs were indirectly standardized by dividing the stratum-specific deaths in by the expected number of deaths (i.e., the death count for the NHW reference population). SMRs can only be compared within groups, not across groups, because they are not re-weighted by a standard distribution.

We used Joinpoint regression analysis to model cancer-related mortality trends [16]. Joinpoint analysis is used to determine if multiple “best fit” line segments of differing rates, created utilizing a Monte Carlo permutation method, are better at describing a trend rather than a single-best fit line segment. If a significant change in trend is detected (P≤0.05) a “joinpoint” is created that connects the segments of differing rates and signifies the year that the change in trend occurred. A maximum of one joinpoint was allowed due to the limited time period examined in this analysis, meaning one cancer mortality trend is limited to two-line segments if a significant change in trend occurred over the 10-year period. The estimated annual percent change (APC) was used to test the statistical significance of trends after line segments were established. PROC STDRATE in SAS version 9.4 (SAS Institute) were used to calculate direct AMRs, indirect SMRs, and adjusted PYLL rates. Trend models were fit using SEER JoinPoint software [17] and all figures were created using Microsoft Excel.

RESULTS

Top Cancer Sites

The top sites of cancer deaths ranked as proportion of all cancers (Table 1; Figure 1) among NHW males were: lung (30.8%), prostrate (9.2%), colorectal (8.9%), pancreas (5.9%), and leukemia (4.4%). Our disaggregated analysis of Hispanic cancer mortality revealed heterogeneity among Hispanic males after lung cancer, which was found to be the leading cause of cancer death in all groups. For Mexican males, these rankings were: lung (19.3%), colorectal (10.5%), liver (10.1%), prostate (9.4%), and pancreas (6.4%). For Cuban males: lung (28.6%), prostate (11.6%), colorectal (10.9%), pancreas (6.4%), and liver (4.3%). For Puerto Rican males: lung (20.9%), liver (11.2%), colorectal (10.7%), prostate (8.7%), and pancreas (5.7%). And for Central or South American males: lung (14.7%), prostate (9.9%) colorectal (9.2%), stomach (9.1%), and liver (7.2%).

Table 1:

Male and Female Top 5 cancer mortality sites ranked1 by proportion to all cancers- by ethnicity (2003-2012)

MALE
(RANK)
NHW
(n=2,389,032)
ALL HISPANIC
(N= 151,385)
MEXICAN
(n=83,236)
CUBAN
(N=16,570)
PUERTO RICAN
(N=19,034)
CENTRAL OR
SOUTH AMERICAN
(N=10,521)
1 Lung
30.8%
Prostate
9.2%
Lung
19.3%
Colon
10.5%
Lung
17.6%
Colon
10.4%
Lung
28.6%
Prostate
11.6%
Lung
20.9%
Liver
11.2%
Lung
14.7%
Prostate
9.9%
2
3 Colon
8.9%
Prostate
9.4%
Liver
10.1%
Colon
10.9%
Colon
10.7%
Colon
9.2%
4 Pancreas
5.9%
Liver
9.1%
Prostate
8.8%
Pancreas
6.4%
Prostate
8.7%
Stomach
9.1%
5 Leukemia
4.4%
Pancreas
6.4%
Pancreas
6.4%
Liver
4.3%
Pancreas
5.7%
Liver
7.2%
FEMALE
(RANK)
NHW
(N=2,190,527)
ALL HISPANIC
(n=135,833)
MEXICAN
(N=72,657)
CUBAN
(N=12,559)
PUERTO RICAN
(N=16,327)
CENTRAL OR
SOUTH AMERICAN
(N=12,873)
1 Lung
27.3%
Breast
15.9%
Breast
15.9%
Breast
16.0%
Breast
16.4%
Breast
15.1%
2 Breast
14.6%
Lung
13%
Lung
11.9%
Lung
15.5%
Lung
15.3%
Lung
10.6%
3 Colon
9.4%
Colon
9.6%
Colon
8.6%
Colon
13.4%
Colon
11.5%
Colon
8.4%
4 Pancreas
6.3%
Pancreas
7.0%
Pancreas
7.0%
Pancreas
7.8%
Pancreas
6.3%
Pancreas
7.2%
5 Ovary
5.5%
Ovary
5.8%
Ovary
5.9%
Ovary
5.4%
Ovary
5.0%
Stomach
7.1%
1.

Proportional mortality was determined by dividing site specific cancer deaths by total cancer deaths, by sex and ethnic group.

Figure 1:

Figure 1:

Cancer proportional mortality by detailed ethnicity and sex, 2003-2012. Proportional mortality was determined by dividing site specific cancer deaths by total cancer deaths, by sex and ethnicity.

The rankings of top five sites of cancer mortality for NWH females were lung (27.3%), breast (14.6%), colorectal (9.4%), pancreas (6.3%), and ovary (5.5%). In contrast to the male findings, the top 5 sites among Hispanic females were mostly homogenous. The ranking (ranges) were breast (15.1%−16.4%), lung (10.6%−15.5%), colorectal (8.4%−13.4%), pancreas (6.3%−7.8%) and ovary (5.0%−5.8%). One exception was for Central or South American females who had stomach cancer (7.1%) in the fifth ranking rather than ovarian cancer.

Potential Years of Life Lost

Crude and adjusted PYLL’s by sex and Hispanic group are provided in Table 2. NHWs had the highest count of premature cancer deaths and age-adjusted PYLL rates (Male 16.5, Female 19.6). Puerto Ricans and Mexicans had the highest rate of age-adjusted PYLL among female Hispanics (15.7 and 15.1, respectively). Among male Hispanics, Puerto Ricans and Cubans had the highest age-adjusted PYLL rates (Puerto Rican, 16.5; Cuban 15.0).

Table 2:

Potential Years of Lives Lost (PYLL) based on a fixed life expectancy for all cancer deaths by Hispanic group and sex, 2003-2012

Sex Group Premature Cancer
Deaths1
Crude PYLL Rate per 1,000
person-years2
Age-Adjusted PYLL Rate
per 1,000 person-years3
Average Age of Cancer Death4
Female Non-Hispanic White 1,444,0801 24.7 19.6 71
Female Mexican 64,999 10.0 15.1 64
Female Cuban 9,968 17.5 14.5 72
Female Puerto Rican 14,425 12.8 15.7 66
Female Central or South American 11,420 8.5 9.6 64
Male Non-Hispanic White 1,321,012 20.3 16.5 71
Male Mexican 66,384 8.0 12.6 65
Male Cuban 11,594 17.3 15.0 71
Male Puerto Rican 15,702 12.3 16.5 65
Male Central or South American 8,806 5.9 7.6 62
1.

Count of “premature” cancer deaths is the total number of decedents who died before reaching the age of the fixed life expectancy.

2.

The crude PYLL was determined by using a fixed life expectancy limit to find the difference between age of cancer death and expected age of death. For NHWs, age 81 was used as a benchmark for females, and age 76 for males. For Hispanics, age 83 was used for females, and 78 for males. PYLL’s are calculated as the difference between the age of death and the fixed age expectancy, summed across all age groups and reported as a rate per 1,000 person-years.

3.

Age-adjusted PYLL was determined by directly standardizing the crude PYLL to the age distribution of the 2000 U.S. population.

4.

The average age of cancer death was calculated for each sex within each Hispanic group by summing the product of category median age and age-specific death counts and then dividing by the total death count in that group.

Age-Adjusted Rates and Trend Models

Rates of cancer mortality from any site for NHWs was 220.42/100,000 person-years (males) and 157.33/100,000 person-years (females). Hispanics (as an aggregated group) die from cancer of any site at about 70% the rate of NHWs (Table 3). Among Hispanics, Puerto Ricans (male AMR: 179.73/100,000 person-years 95% CI: 176.92–182.54; female AMR: 111.41/100,000 person-years 95% CI: 109.64–113.17) had the highest overall cancer mortality. Central and South Americans have the lowest overall cancer mortality rates (male AMR: 91.19/100,000 person-years 95% CI: 89.09–93.29; female AMR: 69.72/100,000 person years 95% CI: 68.42–71.01). Trend analyses (Figure 2a-i and Figure 3a-j) revealed that all ethnicity-specific Hispanic mortality rates of cancer at any site are stable or decreasing, but rates of liver cancer are increasing for Hispanics (overall, males and females). Annual percentage change results for the trend models are included in the Supplementary Tables 2 and 3.

Table 3:

Male and Female Hispanic Cancer Statistics by cancer site: age-adjusted average annual mortality rate (AMR) per 100,000 person-years and standardized mortality ratios (SMRs), 2003-2012.

MALES NON-HISPANIC WHITE ALL HISPANIC MEXICAN CUBAN PUERTO RICAN CENTRAL or SOUTH AMERICAN
Cancer Site n AMR1 (95% CI) SMR2 n AMR1 (95% CI) SMR2 n AMR1 (95% CI) SMR2 n AMR1 (95% CI) SMR2 n AMR1 (95% CI) SMR2 n AMR1 (95% CI) SMR2
All Sites 2389032 220.42 (220.14-220.71) 1 151385 153.68 (152.84-154.53) 0.69 (0.69-0.69) 83236 154.72 (153.55-155.89) 0.69 (0.69-0.69) 16570 178.62 (175.89-181.36) 0.81 (0.8-0.82) 19034 179.73 (176.92-182.54) 0.84 (0.82-0.85) 10521 91.19 (89.09-93.29) 0.4 (0.39-0.41)
Lung 736913 66.69 (66.54-66.85) 1 29246 31.73 (31.34-32.12) 0.44 (0.44-0.45) 14634 30.51 (29.98-31.04) 0.41 (0.4-0.41) 4737 50.26 (48.82-51.69) 0.75 (0.73-0.78) 3969 37.59 (36.32-38.85) 0.57 (0.55-0.59) 1546 14.63 (13.79-15.47) 0.20 (0.10-0.21)
Prostate 218687 21.68 (21.59-21.77) 1 14212 19.1 (18.77-19.43) 0.89 (0.88-0.91) 7361 18.69 (18.25-19.14) 0.87 (0.85-0.89) 1929 21.51 (20.54-22.47) 1 (0.95-1.04) 1651 21.32 (20.23-22.42) 1 (0.95-1.05) 1038 13.95 (13.02-14.88) 0.64 (0.60-0.68)
Colon and rectum 213040 19.74 (19.65-19.82) 1 15892 16.06 (15.79-16.34) 0.81 (0.79-0.82) 8670 15.86 (15.49-16.23) 0.8 (0.79-0.82) 1813 19.54 (18.64-20.44) 1 (0.95-1.04) 2033 19.8 (18.85-20.75) 1 (0.96-1.05) 969 7.81 (7.22-8.41) 0.41 (0.38-0.44)
Pancreas 139941 12.66 (12.59-12.73) 1 9714 9.72 (9.51-9.93) 0.75 (0.74-0.77) 5355 9.81 (9.52-10.1) 0.76 (0.74-0.78) 1057 11.28 (10.6-11.96) 0.89 (0.84-0.95) 1092 10.01 (9.36-10.66) 0.81 (0.76-0.86) 711 6.3 (5.75-6.84) 0.46 (0.42-0.49)
Liver 81255 7.17 (7.12-7.22) 1 13850 12.45 (12.22-12.68) 1.7 (1.67-1.73) 8397 14.01 (13.68-14.34) 1.86 (1.82-1.9) 720 7.68 (7.12-8.25) 1.07 (0.99-1.15) 2123 16.71 (15.94-17.48) 2.51 (2.41-2.62) 763 6.13 (5.62-6.65) 0.75 (0.69-0.8)
Stomach 43192 4 (3.96-4.04) 1 7996 7.79 (7.6-7.98) 1.97 (1.93-2.02) 4610 8.15 (7.89-8.42) 2.07 (2.01-2.13) 429 4.67 (4.22-5.11) 1.16 (1.05-1.27) 834 8.41 (7.78-9.03) 2 (1.86-2.14) 965 7.58 (7-8.16) 1.97 (1.84-2.09)
Leukemia 105913 10.09 (10.03-10.16) 1 7615 6.28 (6.12-6.44) 0.74 (0.72-0.76) 4462 6.19 (5.97-6.41) 0.78 (0.75-0.8) 645 7.07 (6.52-7.62) 0.7 (0.65-0.75) 764 6.7 (6.16-7.24) 0.74 (0.68-0.79) 712 4.81 (4.36-5.27) 0.6 (0.55-0.64)
NHL 94053 8.84 (8.78-8.9) 1 6725 6.54 (6.36-6.71) 0.78 (0.76-0.8) 3769 6.77 (6.52-7.01) 0.79 (0.77-0.82) 619 6.72 (6.19-7.25) 0.76 (0.7-0.82) 817 7.31 (6.75-7.86) 0.92 (0.86-0.99) 632 4.97 (4.49-5.45) 0.62 (0.57-0.67)
FEMALES NHW ALL HISPANIC MEXICAN CUBAN PUERTO RICAN CENTRAL or SOUTH AMERICAN
Site n AMR1 (95% CI) SMR2 n AMR1 (95% CI) SMR2 n AMR1 (95% CI) SMR2 n AMR1 (95% CI) SMR2 n AMR1 (95% CI) SMR2 n AMR1 (95% CI) SMR2
All Sites 183994 157.33 (156.59-158.07) 1 38978 106.49 (105.39-107.59) 0.69 (0.68-0.69) 72657 107.33 (106.51-108.15) 0.7 (0.69-0.7) 12559 103.87 (102.01-105.73) 0.67 (0.66-0.68) 16327 111.41 (109.64-113.17) 0.72 (0.71-0.73) 12873 69.715 (68.42-71.01) 0.44 (0.44-0.45)
Breast 597825 23.11 (23.02-23.19) 1 21651 15.05 (14.84-15.26) 0.67 (0.66-0.68) 11572 15.28 (14.99-15.58) 0.69 (0.68-0.7) 2026 17.56 (16.78-18.34) 0.76 (0.73-0.79) 2684 17.02 (16.36-17.69) 0.75 (0.72-0.78) 1947 9.11 (8.67-9.54) 0.41 (0.39-0.43)
Lung 319254 23.11 (23.02-23.19) 1 17662 14.32 (14.1-14.53) 0.32 (0.32-0.33) 8647 14.35 (14.03-14.66) 0.31 (0.31-0.32) 1947 16.05 (15.32-16.78) 0.38 (0.36-0.39) 2498 17.49 (16.78-18.19) 0.4 (0.39-0.42) 1366 8.12 (7.66-8.57) 0.17 (0.16-0.18)
Colon and rectum 206599 14.06 (14-14.12) 1 13088 10.34 (10.16-10.52) 0.74 (0.72-0.75) 6252 9.7 (9.45-9.95) 0.7 (0.68-0.72) 1680 13.36 (12.71-14.01) 0.95 (0.91-1) 1880 13.34 (12.72-13.96) 0.96 (0.91-1) 1077 6.16 (5.77-6.56) 0.44 (0.41-0.46)
Pancreas 137154 9.46 (9.41-9.52) 1 9560 7.82 (7.65-7.98) 0.81 (0.79-0.82) 5075 8.34 (8.1-8.57) 0.86 (0.83-0.88) 982 7.68 (7.19-8.17) 0.83 (0.78-0.88) 1022 7.41 (6.94-7.87) 0.77 (0.72-0.82) 931 5.7 (5.32-6.09) 0.56 (0.53-0.6)
Ovary 42249 2.97 (2.94-3) 1 7933 5.87 (5.74-6.01) 0.67 (0.66-0.69) 4311 6.24 (6.04-6.44) 0.72 (0.69-0.74) 683 5.86 (5.41-6.31) 0.66 (0.61-0.71) 810 5.5 (5.11-5.89) 0.62 (0.57-0.66) 818 4.1 (3.79-4.4) 0.48 (0.45-0.51)
Liver 29096 2.01 (1.99-2.03) 1 6877 5.52 (5.38-5.65) 1.78 (1.74-1.83) 4122 6.65 (6.44-6.87) 2.11 (2.05-2.17) 458 3.6 (3.26-3.93) 1.27 (1.15-1.38) 713 4.95 (4.58-5.32) 1.67 (1.54-1.79) 639 3.84 (3.53-4.16) 1.18 (1.09-1.27)
Stomach 79045 5.56 (5.52-5.6) 1 6015 4.46 (4.34-4.58) 2.33 (2.28-2.39) 3415 4.92 (4.74-5.09) 2.62 (2.53-2.71) 260 2.1 (1.84-2.36) 1.04 (0.91-1.17) 565 4.04 (3.69-4.38) 1.99 (1.83-2.16) 922 4.73 (4.4-5.06) 2.57 (2.4-2.73)
Leukemia 121526 8.72 (8.67-8.77) 1 5999 4.03 (3.92-4.14) 0.8 (0.78-0.82) 3308 3.99 (3.84-4.14) 0.85 (0.82-0.88) 547 4.54 (4.15-4.94) 0.8 (0.73-0.87) 641 4.17 (3.83-4.5) 0.79 (0.73-0.86) 622 3.12 (2.86-3.39) 0.62 (0.57-0.67)
NHL 80204 5.47 (5.43-5.51) 1 5599 4.44 (4.32-4.56) 0.83 (0.81-0.85) 3007 4.75 (4.57-4.93) 0.89 (0.86-0.92) 556 4.51 (4.12-4.89) 0.8 (0.73-0.86) 617 4.33 (3.98-4.69) 0.83 (0.76-0.89) 585 3.49 (3.19-3.79) 0.64 (0.59-0.69)
1.

Average annual mortality rates (AMRs) are reported per 100,000 person-years. The numerator of the rate was determined by the total number of cancer deaths over the 10-year period in each sex-, Hispanic group- and site-specific stratum. The denominator is the 10-year sum of the sex- and Hispanic group-specific U.S population based on census data. Rates were directly standardized to the 2000 U.S. population age distribution to render them comparable across stratum.

2.

Standardized mortality ratios (SMRs) were created by dividing the sum of the 10-year sex-, Hispanic group- and site-specific deaths by the “expected” number of deaths, as defined by the sum of the 10-year deaths for the sex- and site-specific NHW population (the reference population).

Figure 2:

Figure 2:

Cancer mortality trends (men, 2003-2012). These trends were modeled using Joinpoint regression of the age-adjusted annual morality rates by cancer site and ethnic group. A maximum of two segments were allowed per stratum. Corresponding annual percentage change results from the JoinPoint models are included in the Supplementary Tables 2 and 3.

Figure 3:

Figure 3:

Cancer mortality trends (women, 2003-2012). These trends were modeled using Joinpoint regression of the age-adjusted annual morality rates by cancer site and ethnic group. A maximum of two segments were allowed per stratum. Corresponding annual percentage change results from the JoinPoint models are included in the Supplementary Tables 2 and 3.

Cancers of the Digestive Tract

Liver cancer was ranked among the top 5 causes of cancer-related deaths for Mexican, Puerto Rican, and Central or South American males, but was not a top ranked cancer for NHWs. . In both males and females, the highest liver cancer mortality in comparison to NHWs were among Puerto Ricans (male SMR, 2.51; 95% CI, 2.41–2.62; female SMR, 1.67; 95% CI, 1.54–1.79). Trends in liver cancer death rates among males have been increasing for all Hispanic groups except for Cubans and Central or South Americans with the highest increase in Puerto Ricans (Puerto Rican APC, 3.5; 95% CI, 1.8–5.3; Mexican, 2.2; 95% CI, 1.2–3.2; all Hispanic, 2.5; 95% CI, 1.9–3.1; NHW APC, 3.1; 95% CI, 2.7–3.1;). Among females, increased liver cancer mortality trends were observed in Puerto Ricans and all Hispanics combined (Puerto Rican APC, 2.4; 95% CI, 0.4–4.5; all Hispanic APC, 1.7; 95% CI, 0.6–2.8).

Colorectal cancer ranked among the top 5 causes of cancer deaths for the entire population. However, Hispanics have lower colorectal cancer deaths than NHWs with the lowest rates for Mexican and Central or South Americans (male Mexican AMR, 15.90; 95% CI, 15.49–16.23; male Central or South AMR, 7.81; 95% CI, 7.22–8.41; female Mexican AMR, 9.70; 95% CI, 9.45–9.95; female Central or South AMR, 6.16; 95% CI, 5.77–6.56).

Stomach cancer ranked among the top 5 cancer deaths for Central or South Americans. However, AMRs were at least twice as high in all Hispanic groups apart from Cubans. The highest stomach cancer mortality rates were among Mexicans (male AMR, 8.15; 95% CI, 7.89–8.42; female AMR, 2.62; 95% CI, 2.53–2.71). Cubans had the lowest stomach cancer mortality that largely resembled NHWs (male SMR, 1.16; 95% CI, 1.05–1.27); female SMR, 1.04; 95% CI; 0.91–1.17). Trends in stomach cancer mortality are stable or decreasing for all populations.

Overall, pancreatic cancer mortality is lower in all Hispanic groups compared to NHWs, with the lowest mortality observed in Central or South Americans (male SMR 0.46; 95% CI, 0.42–0.49; female SMR, 0.56; 95% CI, 0.53–0.60). Among males, trends in pancreatic cancer have been increasing for NHWs and Mexicans (NHWs APC, 0.80; 95% CI, 0.50–1.0; Mexican APC, 1.1; 95% CI, 0.0–2.2). Female pancreatic cancer mortality is also increasing for NHWs and all Hispanics combined (NHWs APC, 0.70; 95% CI, 0.50–0.90; all Hispanic APC, 0.70; 95% CI, 0.0–1.4).

Lung Cancer

Lung cancer was the leading cause of cancer-related deaths in male and female NHWs, and for Hispanic males and the second leading cause of cancer-related deaths in Hispanic females. Lung cancer caused about 30% of cancer deaths among male NHWs and male Cubans (Figure 1). With the exception of Cubans, all Hispanic groups have about half the lung cancer mortality compared to NHWs. Among males, Central or South Americans and Mexicans had the lowest lung cancer mortality when compared to NHWs (Central or South SMR, 0.20; 95% CI, 0.10–0.21; Mexican SMR, 0.41; 95% CI, 0.40–0.42). Lung cancer mortality trends for men were significantly decreasing for all populations starting in 2005, but stable or increasing across all years for females.

Female Breast and Ovarian Cancer

Breast cancer was the leading cause of death in Hispanic females accounting for about 16% of all cancer deaths and the second leading cause of death in NHWs (15% of deaths). Overall, female Hispanics had lower cancer deaths than NHWs. Cubans had the highest rates of breast cancer mortality among the Hispanic groups (AMR, 17.56; 95% CI, 16.78–18.34) while Central or South Americans had the lowest (AMR, 9.11; 95% CI, 8.67–9.54). For most groups, breast cancer mortality trends were stable or decreasing.

For all females, ovarian cancer accounted for 5% to 7% of cancer deaths. Hispanic ovarian cancer mortality rates were lower than NHWs for all Hispanic groups with Central or South Americans reporting the lowest ovarian cancer mortality rates (AMR, 4.10; 95 % CI, 3.79–4.40). Ovarian cancer mortality trends were stable or decreasing for all populations.

Non-Hodgkin Lymphoma (NHL) and Leukemia

All Hispanics overall had lower NHL cancer mortality than NHWs (All Hispanic male SMR, 0.78; 95% CI, 0.76–0.80; All Hispanic female SMR, 0.83; 95% CI, 0.81–0.85). Most Hispanic groups reported similar NHL cancer mortality rates, though Central or South Americans had the lowest NHL mortality rates (male AMR, 4.97; 95% CI, 4.49–5.45; female AMR, 3.49; 95% CI, 3.19–3.79).

Leukemia mortality was homogenous across Hispanic groups and compared to NHWs (All Hispanic male SMR, 0.74; 95% CI, 0.72–0.76; All Hispanic female SMR, 0.80; 95% CI, 0.78–0.82). Among Hispanics, Cubans had the highest leukemia mortality rates (male AMR, 7.07; 95% CI, 6.52–7.62; female AMR, 4.54; 95% CI, 4.15–4.94) while Central or South Americans had the lowest (male AMR, 4.81; 95% CI, 4.36–5.27; female AMR, 3.12; 95% CI, 2.86–3.39).

Prostate

Prostate cancer mortality rates were homogenous across all Hispanic groups and overall lower than NHWs (All Hispanic SMR, 0.89; 95% CI, 0.88–0.91). Cubans have the highest rates of prostate cancer deaths (AMR, 21.51; 95% CI, 20.54–22.47), though these were still similar to NHWs (SMR, 1.0; 95% CI, 0.95–1.04). Central or South Americans had the lowest prostate cancer mortality rates (AMR, 4.97; 95% CI, 4.49–5.45). Trend analysis shows that prostate cancer was stable or decreasing for all Hispanic populations.

DISCUSSION

This is the first study to describe trends in cancer mortality by specific Hispanic group for the leading 10 causes of cancer deaths nationwide. Consistent with reports from the American Cancer Society and Pinheiro, our results confirmed that for most cancer sites, mortality rates were lower in aggregate Hispanics when compared to NHWs[3, 18] . All-cause cancer mortality rates for aggregate Hispanics were about one-third that of NHWs. We also observed that most cancer mortality trends are declining in both males and females. Liver cancer mortality is a notable exception as mortality trends are increasing for most Hispanic populations. The disaggregation of cancer mortality showed distinct heterogeneity for all cancers and most site-specific cancers across all Hispanic groups.

The decreased cancer burden observed in Hispanics remains surprising due to the increased health disparities Hispanics face in comparison to NHWs. This phenomenon is known as the Hispanic Paradox and has been well characterized in other studies[19, 20] . The phenomenon is not limited to cancer mortality and has also been seen in cardiovascular disease (CVD) mortality as well[21]. Explanations for the Hispanic paradox include the immigration of healthier individuals into the U.S., the out migration of ill individuals to their country of origin, i.e., the Salmon bias, and (for incidence studies) data linkage errors in cancer registries[22] . However, none of these explanations fully account for the cancer mortality advantage seen in Hispanics[23, 24]. A recent study analyzing Hispanic groups in Texas and California suggests that the advantage may be driven by low cancer mortality rates among foreign born Hispanics[25].

In line with other findings, we found that Hispanics were disproportionately affected by cancers related to infectious agents though our study showed that mortality burden of these cancers differ by Hispanic group[26]. Liver cancer mortality disproportionately affects Hispanics and the disaggregated analysis showed that Puerto Ricans and Mexicans drive most of this disproportionality among males. Indeed, Pinheiro, et al. recently reported four-fold increases in Puerto Rican liver cancer mortality compared to NHWs in New York State[27]. This disparity may be driven by lower SES, higher body mass index (BMI) and alcohol consumption seen in these two Hispanic groups[10, 28, 29]. These higher mortality trends may indicate a need for culturally tailored programs for alcohol addiction and weight loss. Previous studies have shown a need for substance abuse research and intervention studies conducted with attention to heterogeneity among Hispanic groups [29-31]. The increases in liver cancer deaths may also indicate a need to prioritize Hepatitis C (HCV) screening and Hepatitis B (HBV) vaccination. HCV is estimated to cause over 50% of all liver cancer incidents and one study reported a 17-fold increase risk for liver cancer among HCV-infected patients[7, 32]. HCV exposure also varies significantly among Hispanic populations, with the highest prevalence in Puerto Ricans, 11.6%, while the exposure among Central or South Americans is as low as 0.4%[33]. Cuba has a high rate of HBV vaccination (99% of children), which may mitigate liver cancer mortality as 15% of liver cancer incidence is attributed to HBV infection [7, 34]. Our trend analyses also show that liver cancer mortality has been significantly increasing for all Puerto Rican and Mexican men, but have remained stable for Mexican women, Cubans, and Central or South Americans.

The higher stomach cancer mortality seen in Central and South Americans, Mexicans, and Puerto Ricans may be associated with increased H. Pylori infection seen in the Hispanic populations[35] . Though male stomach cancer mortality trends are declining in NHWs, the mortality trends for Mexicans, Puerto Ricans, and Cubans are stable. Incident cases of stomach cancer, primarily among young Hispanic men, have also been recently increasing[36]. The combination of stable mortality rates and increasing incident stomach cancer warrant an increased need for screening programs especially among the aforementioned young male populations.

Other studies have confirmed that CRC incidence and mortality have been decreasing since 1998 and this has mainly been attributed to screening guidelines[37, 38]. We found that CRC mortality has been significantly decreasing for NHWs since 2002, but the trends in the Hispanic populations appear to be decreasing at a smaller rate or remaining stable over time. This may be due to a combination of lower CRC screening rates, higher BMI, and higher prevalence of diabetes seen in Hispanics[4, 30, 39]. This is particularly concerning for Puerto Rican and Cuban males as their CRC-related mortality rates appear to have surpassed NHWs as of 2009. Increased CRC mortality in Puerto Rican and Cubans may be associated with their higher acculturation to the U.S[18]. CRC incidence in young Hispanics is also increasing in parts of the U.S.[40]. It is feared that continued adoption of U.S. health behaviors will worsen diet and exercise practices in the Hispanic populations, potentially increasing mortality rates if adherences to CRC screening guidelines are not improved[40,41].

Breast cancer mortality is lower in Hispanic females than in NHWs. This mortality advantage has been linked to higher parity, earlier age of childbirth, and higher prevalence of breastfeeding seen in Hispanics[3, 41]. However, Hispanics are more likely to be negative for estrogen and progesterone tumor receptors, making breast cancer treatment more difficult than in NHWs[43]. Though this likely worsens survival for Hispanics, it is surprising that mortality is far lower. Nonsignificant differences in tumor receptor status have been reported among Hispanics groups, with Puerto Ricans having the highest risk of being double negative[43]. Nativity also plays a role in burden as foreign born Hispanics have lower breast cancer than U.S born[25, 41]. Cubans and Puerto Ricans have the highest rates of breast cancer mortality among the Hispanic population. This higher mortality has been linked to previously mentioned risks such as acculturation, alcohol consumption, and BMI. In agreement with our findings, a study utilizing the National Health Interview Survey to examine breast cancer risk similarly found heterogeneity by disaggregated Hispanic population [41] .

Patterns of lung cancer mortality are lower in Hispanics overall when compared to NHWs. Cuban males have the highest lung cancer mortality among Hispanics followed by Puerto Ricans though mortality trends for all male groups are declining. Cubans and Puerto Ricans report far higher smoking prevalence and daily cigarette use than the other Hispanic groups[42]. This largely explains the increased lung cancer mortality they experience. Increases use of tobacco and alcohol are indicators of acculturation to the U.S. This may raise caution for the Mexican and Central or South Americans; as these groups increase their time in the U.S. and their level of acculturation, trends in lung cancer mortality may also increase. Our study reinforces that tobacco control efforts should be culturally targeted to particularly reach Hispanics[42]. The variation of lung cancer deaths across the Hispanic population also highlights the importance of disaggregated data. Results for the All Hispanic group may reflect the highest rates, which are among Cubans, who are also among the highest smokers across all Hispanic groups. Indeed, aggregation of Hispanics may hide the true underlying trends and result in misleading interpretation for specific Hispanic groups.

Cancer profiles are also unsurprisingly different by sex, with females showing less cancer mortality than males in all cancer combined and site specific cancers. This is a finding common in most cancer studies and has been attributed to differences in behaviors such as smoking, drinking, BMI, and more[3, 26, 42]. Our study offers a unique look at trends of site specific cancer over the study period. A comparison of lung cancer mortality trends among Hispanics shows that mortality trends for males are rapidly decreasing while mortality trends for females have remained constant. This may be because men picked up smoking behaviors before women so their male trends had time to peak and then decline.

Our PYLL analysis highlights the considerably younger age of cancer-related deaths among the Hispanic groups, which may be worrisome considering that the PYLL is a measure of social and economic loss from premature death[43]. Expressed as an age-adjusted rate, PYLL’s are still higher among NHWs, but the difference is not as dramatic as noted in the AMR calculations, the latter being more heavily impacted by the mortality burden among the elderly, non-working members of society. Since Hispanics are the largest minority population in the U.S. and rapidly increasing in size, these impact measures could have important economic and demographic implications for the U.S. overall.

Limitations

Our study relies on death records which are subject to inaccurate recording race/ethnicity which may lead to misclassification. However, studies have shown the recording of Hispanic origin on death records is valid for mortality studies[13, 44]. Hispanic populations vary geographically. States with fewer Hispanics and a lower Hispanic diversity are subject to more misclassification as state medical officials may not be accustomed to accurately recording the decedent’s specific Hispanic group [23]. Therefore, our statistics of mortality at a national level may not be representative at a state level. There may also be misclassification introduced into the study from the combination of Central or South Americans as these two groups carry their own heterogeneity and carry Dominican misclassification. Denominator counts from census data may suffer from inaccuracies as population counts are only recorded each decade and only account for those who respond [45]. Our use of interpolation methods for estimating the population sizes from 2000–2010 and extrapolation methods after 2010 should improve the precision and accuracy of yearly denominator counts. However, in both numerators (cancer deaths) and denominators (populations), the amount of decedents classified as “other Hispanic” may also impact the rates reported in this study. Nativity status was not considered in this study because the numbers of U.S. born Hispanics are small for Cubans and Central or South Americans. However, studies have shown there are significant differences between foreign-born and U.S. born Hispanic cancer burden for most cancer sites[25, 46, 47]. The study also did not account for racial differences between Hispanic Whites and Hispanic Blacks. Studies have not adequately investigated Hispanic ethnicity due to the underreporting of black and mixed Hispanics making this limitation an opportunity for innovative research. Benchmarks for the calculation of PYLLs use Hispanics as a whole, while unknown differences in life expectancy may exist between the distinct Hispanic groups. Lastly, ten years is a short follow-up time though our trends give substantial insight on the long term trajectories of cancer burden.

Conclusion

The results of our paper highlight the cancer burden of specific Hispanic groups. Future studies are needed to determine the relative importance of the many potential and important risk factors in driving cancer mortality in these specific Hispanic groups. A comprehensive understanding of cancer burden is essential to guide our treatment and prevention strategies, especially in Hispanics as they represent a heterogeneous and growing segment of the U.S. population.

Supplementary Material

1

Acknowledgements:

S.M. Zamora was funded from the Cancer Epidemiology and Education in Special Population (CEESP) program by the National Cancer Institute (R25 CA112383); CT was funded by the National Institute for Advancing Translational Sciences (KL2TR001444) and National Cancer Institute (U54CA132384); KGH, LPP, and JH were funded from the National Institute on Minority Health and Health Disparities (R01 MD007012)

Footnotes

Conflict(s) of interest: The authors declare no potential conflicts of interest.

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