Trends and variations in breast and colorectal cancer incidence from 1995 to 2011: A comparative study between Texas Cancer Registry and National Cancer Institute's Surveillance, Epidemiology and End Results data

  • Authors:
    • Zheyu Liu
    • Yefei Zhang
    • Luisa Franzin
    • Janice N. Cormier
    • Wenyaw Chan
    • Hua Xu
    • Xianglin L. Du
  • View Affiliations

  • Published online on: February 6, 2015     https://doi.org/10.3892/ijo.2015.2881
  • Pages: 1819-1826
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Abstract

Few studies have examined the cancer incidence trends in the state of Texas, and no study has ever been conducted to compare the temporal trends of breast and colorectal cancer incidence in Texas with those of the National Cancer Institute's Surveillance, Epidemiology and End Results (SEER) in the United States. This study aimed to conduct a parallel comparison between the Texas Cancer Registry and the National Cancer Institute's SEER on cancer incidence from 1995 to 2011. A total of 951,899 breast and colorectal cancer patients were included. Age-adjusted breast cancer incidence was 134.74 per 100,000 in Texas and 131.78 per 100,000 in SEER in 1995-2011, whereas age-adjusted colorectal cancer incidence was 50.52 per 100,000 in Texas and 49.44 per 100,000 in SEER. Breast cancer incidence increased from 1995 to 2001, decreased from 2002 to 2006, and then remained relatively stable from 2007 to 2011. For colorectal cancer, the incidence increased in 1995‑1997, and then decreased continuously from 1998 to 2011 in Texas and SEER areas. Incidence rates and relative risks by age, gender and ethnicity were identical between Texas and SEER.

Introduction

Breast cancer is the most commonly diagnosed cancer in women in the United States, while colorectal cancer is one of the top three most commonly diagnosed cancers among men and women (13). It is estimated that there will be 136,830 new colorectal cancer cases and 235,030 new breast cancer cases in 2014 in the USA (46). The incidence rates for breast and colorectal cancer have been declining consistently in recent years among all age groups and ethnicities (79). The decreasing incidence trends in breast and colorectal cancer have been attributed to earlier detection and more advanced treatment (1014). Although cancer incidence rates have declined since the early 1990’s, the burden of cancer and its complications remains high and has a significant impact on human health (1517).

A number of studies have examined Surveillance, Epidemiology and End Results (SEER) data for national cancer incidence trends and variations by age, ethnicity, cancer stage and other factors in the USA (1823). However, the SEER data do not include Texas, a large and diverse state. The Texas Cancer Registry collects data on cancer in Texas. Few studies have examined the cancer incidence trends in the state of Texas (2426), and no study has ever been conducted to compare the temporal trends of breast and colorectal cancer incidence in Texas with those of SEER. Therefore, in this study, we used the National Cancer Institute’s SEER data and Texas Cancer Registry (TCR) data to examine whether the overall incidence trends for both breast and colorectal cancer have similar patterns in the TCR and in SEER areas over the past 17 years from 1995 to 2011 (2,27). We also examined the variations in cancer incidence rates by age, gender, ethnicity, tumor stage and tumor grade in the TCR and SEER areas. The findings from this parallel comparison are expected to provide a significant overview of cancer incidence trends at the state and national level, and also to identify important factors associated with a decreasing risk of cancer, which are critical to enhance cancer prevention and control.

Materials and methods

Data sources

The SEER (Surveillance, Epidemiology and End Results) public-use dataset and the TCR (Texas Cancer Registry) limited-use dataset were utilized for this study (2,27). The SEER program, supported by the National Cancer Institute, includes population-based tumor registries in selected geographic areas in the USA. Because of our study comparison between the TCR and SEER for cancer cases in 1995 through 2011, we selected the following 9 SEER areas: Atlanta, Connecticut, Detroit, Hawaii, Iowa, New Mexico, San Francisco-Oakland, Seattle-Puget Sound and Utah, accounting for ~9.4% of the USA population (2). By the year of 2010, there were 18 SEER registries that covered 26.2% of the USA population (2). Because our study aimed to compare the incidence trends in breast and colorectal cancer from 1995 to 2011, only these nine registries, which had complete records on tumor stage and tumor grade in the study period, were included. The SEER registries ascertain all newly diagnosed (incident) cancer cases from multiple reporting sources such as hospitals, outpatient clinics, laboratories, private medical practitioners, nursing/convalescent homes/hospices, autopsy reports and death certificates (2). The TCR is a statewide and population-based cancer registry and is Gold Certified by the North American Association of Central Cancer Registries (27). The TCR dataset was determined to cover at least 95% statewide data for all cancer cases diagnosed from 1995 through 2011 in Texas. The denominator of population data used to calculate incidence rates were acquired from the U.S. Census Bureau’s Population Estimates Program (28). The Committee for the Protection of Human Subjects at the University of Texas Health Science Center in Houston approved this study.

Study population

We identified all women diagnosed with breast cancer and men and women diagnosed with colorectal cancer as their primary tumor in 1995–2011 from both SEER and TCR. In the 9 SEER registries, 328,142 patients with breast cancer and 224,511 patients with colorectal cancer were included. In Texas, 243,695 women with breast cancer and 155,551 patients with colorectal cancer were included.

Study variables

The primary outcome of interest was the incidence rates of breast and colorectal cancer from 1995 to 2011. Incidence rates were defined as the number of new cases in one calendar year divided by the total population at risk in the same year (29). Breast cancer cases were identified using the ‘Primary Site’ variable in both SEER and TCR, coded as C500–C509 according to ‘International Classification of Diseases for Oncology, Third Edition (ICD-O-3), and Topography Section (2,7)’. Colorectal cancer cases were coded as C180–C189, C199, C209, and C260 (2). According to the methods by Wu et al in counting total colorectal cancer cases, colon included the cecum (C180), appendix (C181), ascending colon (C182), hepatic flexure (C183), transverse colon (C184), splenic flexure (C185), descending colon (C186), sigmoid colon (C187), and large intestine, NOS(C188–C189,C260) (30). The rectum included the rectosigmoid junction (C199) and the rectum-not otherwise specified (C209).

The independent variables of interest in this study included age, gender, ethnicity, tumor stage and tumor grade. Age was classified according to five categories with <50, 50–59, 60–69, 70–79 and ≥80 years. Gender was a binary variable with male and female, but for breast cancer, only women were included because of the rarity of diagnosis in men. Ethnicity was categorized as white, black and other. Tumor stage was classified as localized, regional, distant and unknown. Localized stage was confined within the breast and colon. Regional stage was defined as tumor involvement of the regional lymph nodes, primarily those in the axilla, to be involved. Distant stage was defined as the cancer metastatic to other parts of the body as well. The unknown stage was defined as having missing information of cancer status (31). Tumor grade represented the level of differentiation, in which poorly differentiated cancer cells usually divide more quickly and therefore represent more aggressive malignancies (32). Tumor grade at diagnosis was stratified into four categories: differentiated, moderately differentiated, poorly differentiated and undetermined.

Statistical analysis

Annual incidence rates of breast and colorectal cancer cases per 100,000 persons were age-adjusted to the 2000 US standard population stratified by five age groups. The incidence rates were computed by age-group, gender, race, tumor stage, and tumor grade for breast and colorectal cancer separately. We used the SEER*Stat software to calculate incidence rates by dividing the number of new cancer cases in each category over the total population at risk (33). The SAS statistical software was used to calculate incidence rates with 95% confidence intervals for TCR data. Poisson regression model with population size specific to demographic groups as offset variable were used to determine the association between incidence rates and potential risk factors. Covariates included age-group, gender, race, tumor stage and tumor grade. In order to determine the temporal relationship, risk ratios between two cancer incidence rates were calculated and adjusted by potential confounders. The assumption of the Poisson model were examined by examining constant variance plots of the variables. No specific pattern was detected in the outputs indicating that the constant variance was valid.

Results

Table I presents the total number of patients diagnosed with breast and colorectal cancer in Texas and in 9 SEER areas. From 1995 to 2011, there were 243,695 new breast cancer cases and 155,551 colorectal cancer cases in Texas, and 328,142 breast cancer cases and 224,511 colorectal cancer cases in 9 SEER areas. The mean age for breast cancer was 60.5 years in the TCR and 61.7 years in SEER, and the mean age for colorectal cancer was 67.2 years in the TCR and 69.2 years in SEER. The age distribution of these cancer cases was similar overall in the TCR and SEER, although the proportion of younger patients appeared to be slightly higher in Texas. Over 50% of new breast cancer cases occurred in those aged ≥60 years, while >70% of new colorectal cancer cases occurred in those aged ≥60 years. There were a slightly more male colorectal cancer cases in the TCR and SEER, and >80% of patients were white. The overall distribution by tumor stage and tumor grade was similar between Texas and SEER, but the proportion of cancer cases with unknown tumor stage and undetermined tumor grade was higher in the TCR than that in SEER.

Table I

Number (proportion) of patients with breast and CRC in the Texas Cancer Registry (TCR) and SEER, 1995–2011, stratified by patient and tumor factors.

Table I

Number (proportion) of patients with breast and CRC in the Texas Cancer Registry (TCR) and SEER, 1995–2011, stratified by patient and tumor factors.

No. (%) of cancer cases

Patient and tumor characteristicsTCR (%)SEER (%)TCR (%)SEER (%)
Mean age60.4661.7367.1569.16
Age (years)
 <5060017 (24.63)74066 (22.57)17359 (11.16)20190 (8.99)
 50–5959481 (24.41)76676 (23.37)28088 (18.06)35423 (15.78)
 60–6955660 (22.84)72686 (22.15)37406 (24.05)48532 (21.62)
 70–7943744 (17.95)62866 (19.16)40976 (26.34)62987 (28.06)
 ≥8024793 (10.17)41848 (12.75)31722 (20.39)57379 (25.56)
Gender
 Male82571 (53.08)113388 (50.50)
 Female243695 (100)328142 (100)72980 (46.92)111123 (49.50)
Race/ethnicity
 White210903 (86.54)269958 (82.65)132793 (85.37)181261 (81.14)
 Black26161 (10.74)30525 (9.35)19428 (12.49)22513 (10.08)
 Other (American Indian/Asian/Pacific Islander)6631 (2.72)26135 (8.00)3330 (2.14)19609 (8.78)
Tumor stage
 Localized149999 (61.55)207998 (63.39)57800 (37.16)88825 (39.56)
 Regional61325 (25.16)96063 (29.27)52374 (33.67)81824 (36.45)
 Distant11567 (4.75)15808 (4.82)26594 (17.10)41776 (18.61)
 Unknown20804 (8.54)8273 (2.52)18783 (12.08)12086 (5.38)
Tumor grade
 I: Well differentiated34324 (14.08)63902 (19.47)11562 (7.43)18962 (8.45)
 II: Moderately differentiated77260 (31.70)123943 (37.77)84543 (54.35)128657 (57.31)
 III: Poorly differentiated75475 (30.97)100962 (30.77)23173 (14.90)36499 (16.26)
 IV: Undetermined56636 (23.24)39335 (11.99)36273 (23.32)40393 (17.99)
Total243695328142155551224511

Fig. 1 presents parallel comparisons of age-adjusted incidence trends from 1995 to 2011 for breast cancer between the TCR and SEER areas, whereas Fig. 2 presents the age-adjusted incidence trends from 1995 to 2011 for colorectal cancer in the TCR as compared to SEER. The overall incidence trends and changing patterns over the 17-year periods for breast and colorectal cancer were almost identical between the TCR and SEER areas. Specifically, breast cancer incidence increased from 1995 to 2001, decreased from 2002 to 2006, and then remained relatively stable from 2007 to 2011 (Fig. 1). The increased breast cancer incidence in 1995–2001 was consistent with the time period when the widespread use of screening program was implemented (34). For colorectal cancer, the incidence increased in the first three years between 1995 and 1997, and then decreased continuously from 1998 to 2011 in both Texas and SEER areas.

Figs. 3 and 4 present the age-adjusted tumor stage-specific incidence rates for breast and colorectal cancer in the TCR and SEER. For breast cancer, tumor stage-specific incidence rates were similar between the TCR (Fig. 3A) and SEER (Fig. 3B), in which incidence for localized breast cancer increased early on and then decreased, while the incidence for distant stage breast cancer was stable with a slight increase over time. For colorectal cancer, the incidence for all stages decreased over time in the TCR (Fig. 4A) and in SEER (Fig. 4B) except for an increase for unknown stage colorectal cancer in the TCR from 2008 to 2011.

Table II presents the age-adjusted incidence rates of breast cancer and the relative risks of cancer incidence by patient and tumor characteristics in the TCR and SEER. The overall age-adjusted breast cancer incidence in 1995–2011 was 134.74 per 100,000 in the TCR and 131.78 per 100,000 in SEER. The specific incidence rates and relative risks by age, gender and ethnicity were also similar between in the TCR and SEER after adjusting for tumor stage and grade. For example, as compared to those <50 years of age, women ≥60 were >9 times more likely to develop breast cancer, whereas American Indians and Asian-Pacific Islanders were significantly less likely to develop breast cancer and African Americans had a marginally lower risk of developing breast cancer as compared to whites.

Table II

Age-adjusted incidence rates of breast cancer in the Texas Cancer Registry (TCR) and in SEER, 1995–2011.

Table II

Age-adjusted incidence rates of breast cancer in the Texas Cancer Registry (TCR) and in SEER, 1995–2011.

Breast cancer in TCRBreast cancer in SEER


CharacteristicsIncidence (95% CI)aRR (95% CI)bIncidence (95% CI)aRR (95% CI)b
Age (years)
 <5043.03 (42.24–43.82)1.00 (Reference)44.17 (43.85–44.49)1.00 (Reference)
 50–59287.02 (274.65–299.38)6.58 (6.50–6.65)267.75 (265.86–269.66)6.16 (6.10–6.23)
 60–69405.00 (392.57–417.44)9.34 (9.23–9.45)394.61 (391.75–397.50)9.29 (9.20–9.39)
 70–79461.24 (444.70–477.78)10.63 (10.50–10.76)463.28 (459.66–466.92)11.74 (11.62–11.87)
 ≥80404.07 (389.27–418.87)9.27 (9.14–9.41)419.42 (415.40–423.46)12.06 (11.91–12.20)
Race/ethnicity
 White136.14 (131.91–140.37)1.00136.45 (135.93–136.97)1.00
 Black131.90 (129.40–134.40)0.98 (0.97–0.99)123.33 (121.93–124.75)0.93 (0.92–0.94)
 Other (American Indian/Asian/Pacific Islander)98.51 (89.74–107.27)0.77 (0.75–0.79)96.75 (95.58–97.94)0.72 (0.71–0.73)
Total134.74 (130.88–138.60)131.78 (131.32–132.23)

a Incidence rate was number of cases per 100,000 population and was age adjusted to the 2000 US population (28).

b Incidence ratio (relative risk) was adjusted for age, race, tumor stage and tumor grade.

Similarly, Table III presents the age-adjusted incidence rates of colorectal cancer and relative risks of cancer incidence stratified by patient characteristics in the TCR and SEER after adjusting for tumor stage and grade. Overall age adjusted colorectal cancer incidence rate from 1995 to 2011 was 50.52 per 100,000 in the TCR and 49.44 per 100,000 in SEER. Because the mean age for developing colorectal cancer was older than that for breast cancer, those aged 60–69 years were >23 times more likely to develop colorectal cancer and those aged ≥80 years were >58 times more likely to develop this disease than those <50 years of age. The risk of developing colorectal cancer was noted to be significantly lower in women than in men. African Americans had a higher risk of developing colorectal cancer as compared to whites.

Table III

Age-adjusted incidence rates of CRC in the Texas Cancer Registry (TCR) and in SEER, 1995–2011.

Table III

Age-adjusted incidence rates of CRC in the Texas Cancer Registry (TCR) and in SEER, 1995–2011.

Colorectal cancer in TCRColorectal cancer in SEER


CharacteristicsIncidence (95% CI)aRR (95% CI)bIncidence (95% CI)aRR (95% CI)b
Age (years)
 <506.11 (5.92–6.30)1.00 (Reference)6.03 (5.95–6.12)1.00 (Reference)
 50–5968.46 (67.00–69.92)11.29 (11.07–11.50)63.13 (62.47–63.79)10.60 (10.42–10.79)
 60–69145.38 (137.06–153.69)23.76 (23.33–24.19)139.91 (138.67–141.16)23.37 (22.98–23.76)
 70–79245.37 (225.95–264.79)41.05 (40.33–41.79)262.84 (260.79–264.90)45.09 (44.38–45.82)
 ≥80342.33 (314.44–370.23)58.68 (57.60–59.78)371.32 (368.29–374.37)65.51 (64.46–66.59)
Gender
 Male60.78 (57.26–64.29)1.0057.49 (57.15–57.83)1.00
 Female42.70 (40.18–45.21)0.70 (0.69–0.71)43.12 (42.87–43.38)0.75 (0.74–0.76)
Race/ethnicity
 White49.37 (46.52–52.22)1.0048.87 (48.65–49.10)1.00
 Black64.84 (61.68–67.99)1.35 (1.33–1.37)58.43 (57.65–59.22)1.21 (1.19–1.22)
 Other (American Indian/Asian/Pacific Islander)36.69 (33.71–39.67)0.75 (0.72–0.77)42.67 (42.07–43.27)0.88 (0.86–0.89)
Total50.52 (47.67–53.38)49.44 (49.23–49.64)

a Incidence rate was number of cases per 100,000 population and was age adjusted to the 2000 US population (28).

b Incidence ratio (relative risk) was adjusted for age, gender, race, tumor stage and tumor grade.

Discussion

This parallel comparison study between the TCR and SEER reported a number of significant findings. The overall incidence trends for both breast and colorectal cancer were noted to have similar patterns from 1995 to 2011. The breast and colorectal cancer incidence rates by age, gender, ethnicity, tumor stage and tumor grade in the TCR were also similar to those in SEER areas. These cancer incidence trends over time and variations by other factors are important findings when monitoring cancer progress, assessing the success of cancer prevention and control, and identifying high-risk populations for additional intervention. Furthermore, the identical cancer incidence trends reported in this comparative study can also be viewed as important evidence of the validity of the TCR’s incidence data. This is because the National Cancer Institute’s SEER has been established since 1973 and is often considered the gold standard in cancer registries (2).

This study demonstrated that breast cancer incidence increased from 1995 to 2001, decreased from 2002 to 2006, and then was relatively stable from 2007 to 2011. The interval of increased breast cancer incidence was consistent with the time period when widespread use of early detection for breast cancer such as screening mammography programs were implemented. According to a study by Swan et al, the increased use of mammography during the late 1990’s resulted in a dramatically increased number of breast cancer cases among females in the USA (35). Many other studies also supported this finding (36,37). After the peak time increase in 2001, breast cancer incidence continued to decline and became relatively stable over the past several years. A number of studies have suggested that the decreased incidence rates may be attributable to reduction in the use of peri-menopausal hormone therapy, decreases in utilization of mammography and decreases in the number of preclinical cases detected by screening in recent years (3844).

Similarly, we found that colorectal cancer incidence increased from 1995 to 1997 and then continued to decrease from 1998 to 2011 in both the TCR and SEER areas. We did not observe any dramatically increasing trend period associated with colorectal cancer screening. Several previous studies have reported similar findings and conclusions (7,8,29). This may be related to the nature and gradual adoption of screening tools for colorectal cancer over time (13,14). The U.S. Preventive Service Task Force has recommended that fecal occult blood testing and sigmoidoscopy be used for colorectal cancer screening since the 1990s for persons aged ≥50 (45). The federal Medicare program began covering the cost of colonoscopy screening for colorectal cancer since 2001 for individuals with an average-risk of developing colorectal cancer (46). Colorectal cancer is known to occur later in life with a mean age at 70 years (68 for men and 72 for women) (47,48). We found that men had a higher risk of developing colorectal cancer than women in both the TCR and SEER. Our finding is consistent with the study by Cook et al who concluded that males had much higher risk (RR, 1.36) for colorectal cancer than females from 1995 to 2004 (49). Differences in colorectal cancer incidence rates stratified by ethnicity can largely be explained by differences in education level, smoking status and health insurance status (5055). In our analysis, the black population had highest colorectal cancer incidence rates. Possible explanations include a larger percentage of the smoking population in blacks; the highest prevalence of cigarette smoking is also known to occur among individuals with high school or lower education (5658).

Although TCR and SEER datasets are known to be comprehensive and of high quality, a number of factors may have affected the findings. First, we were unable to verify specific populations by year in each registry, which might have resulted in biased calculations for the annual incidence rates. Second, we studied the 9 SEER areas that accounted for ~9% of the USA population, and therefore the results may not be generalizable to all SEER areas or to the entire USA population. Furthermore, a number of important known risk factors for breast and colorectal cancer such as smoking, family history, physical exercise and environmental factors are not included in these datasets and cannot be studied. The differences in these factors may have affected the cancer incidence comparisons.

In conclusion, breast and colorectal cancer incidence trends from 1995 to 2011 were almost identical between the TCR and SEER areas. Breast cancer incidence increased in 1995–2001 and decreased afterwards, while colorectal cancer incidence decreased continuously from 1998 to 2011. Older age was a significant risk factor for the high risk of developing cancer, particularly for colorectal cancer. The cancer risk also varied according to gender and race/ethnicity. Additional studies may be needed to explore smaller geographical areas within these registries and environmental factors associated with the changing incidence trends.

Acknowledgements

This study was supported by a grant from the Cancer Prevention and Research Institute of Texas (RP130051). We acknowledge the efforts of the Texas Cancer Registry and the National Cancer Institute in the creation of these databases. The interpretation and reporting of these data are the sole responsibilities of the authors.

References

1 

Siegel R, Ward E, Brawley O and Jemal A: Cancer statistics, 2011. CA Cancer J Clin. 61:212–236. 2011. View Article : Google Scholar : PubMed/NCBI

2 

National Cancer Institute. Surveillance, Epidemiology, and End Results (SEER): SEER limited-use data, 1973–2011 (9 registries databases). http://seer.cancer.gov. Accessed May 29, 2014

3 

DeSantis C, Siegel R, Bandi P and Jemal A: Breast cancer statistics, 2011. CA Cancer J Clin. 61:408–418. 2011. View Article : Google Scholar

4 

Siegel R, Ma J, Zou Z and Jemal A: Cancer statistics, 2014. CA Cancer J Clin. 64:9–29. 2014. View Article : Google Scholar : PubMed/NCBI

5 

Siegel R, DeSantis C and Jemal A: Colorectal cancer statistics, 2014. CA Cancer J Clin. 64:104–117. 2014. View Article : Google Scholar : PubMed/NCBI

6 

American Cancer Society. Cancer facts and figures. 2014, Atlanta: http://www.cancer.org/. Accessed July 29, 2014

7 

Edwards BK, Ward E, Kohler BA, et al: Annual report to the nation on the status of cancer, 1975–2006, featuring colorectal cancer trends and impact of interventions (risk factors, screening, and treatment) to reduce future rates. Cancer. 116:544–573. 2010. View Article : Google Scholar

8 

Ries LA, Wingo PA, Miller DS, et al: The annual report to the nation on the status of cancer, 1973–1997, with a special section on colorectal cancer. Cancer. 88:2398–2424. 2000. View Article : Google Scholar : PubMed/NCBI

9 

Bray F, McCarron P and Parkin DM: The changing global patterns of female breast cancer incidence and mortality. Breast Cancer Res. 6:229–239. 2004. View Article : Google Scholar : PubMed/NCBI

10 

Berry DA, Cronin KA, Plevritis SK, et al: Effect of screening and adjuvant therapy on mortality from breast cancer. N Engl J Med. 353:1784–1792. 2005. View Article : Google Scholar : PubMed/NCBI

11 

Coughlin SS, Costanza ME, Fernandez ME, et al: CDC-funded intervention research aimed at promoting colorectal cancer screening in communities. Cancer. 107(Suppl 5): 1196–1204. 2006. View Article : Google Scholar : PubMed/NCBI

12 

Cheng L, Eng C, Nieman LZ, Kapadia AS and Du XL: Trends in colorectal cancer incidence by anatomic site and disease stage in the united states from 1976 to 2005. Am J Clin Oncol. 34:573–580. 2011. View Article : Google Scholar : PubMed/NCBI

13 

Wulfkuhle JD, Liotta LA and Petricoin EF: Proteomic applications for the early detection of cancer. Nat Rev Cancer. 3:267–275. 2003. View Article : Google Scholar : PubMed/NCBI

14 

McKean-Cowdin R, Feigelson HS, Ross RK, Pike MC and Henderson BE: Declining cancer rates in the 1990s. J Clin Oncol. 18:2258–2268. 2000.PubMed/NCBI

15 

Weir HK, Thun MJ, Hankey BF, et al: Annual report to the nation on the status of cancer, 1975–2000, featuring the uses of surveillance data for cancer prevention and control. J Natl Cancer Inst. 95:1276–1299. 2003. View Article : Google Scholar : PubMed/NCBI

16 

Jemal A, Clegg LX, Ward E, et al: Annual report to the nation on the status of cancer, 1975–2001 with a special feature regarding survival. Cancer. 101:3–27. 2004. View Article : Google Scholar : PubMed/NCBI

17 

Ghafoor A, Jemal A, Ward E, Cokkinides V, Smith R and Thun M: Trends in breast cancer by race and ethnicity. CA Cancer J Clin. 53:342–355. 2003. View Article : Google Scholar

18 

Pruitt SL, Shim MJ, Mullen PD, Vernon SW and Amick BC III: Association of area socioeconomic status and breast, cervical, and colorectal cancer screening: a systematic review. Cancer Epidemiol Biomarkers Prev. 18:2579–2599. 2009. View Article : Google Scholar : PubMed/NCBI

19 

Berry J, Bumpers K, Ogunlade V, et al: Examining racial disparities in colorectal cancer care. J Psychosoc Oncol. 27:59–83. 2009. View Article : Google Scholar : PubMed/NCBI

20 

White A, Liu C, Xia R, et al: Racial disparities and treatment trends in a large cohort of elderly african americans and caucasians with colorectal cancer, 1991 to 2002. Cancer. 113:3400–3409. 2008. View Article : Google Scholar : PubMed/NCBI

21 

Fowble BL, Schultz DJ, Overmoyer B, et al: The influence of young age on outcome in early stage breast cancer. Int J Radiat Oncol Biol Phys. 30:23–33. 1994. View Article : Google Scholar : PubMed/NCBI

22 

Chlebowski RT, Chen Z, Anderson GL, et al: Ethnicity and breast cancer: Factors influencing differences in incidence and outcome. J Natl Cancer Inst. 97:439–448. 2005. View Article : Google Scholar : PubMed/NCBI

23 

De Bruijn K, Arends L, Hansen B, Leeflang S, Ruiter R and van Eijck C: Systematic review and meta-analysis of the association between diabetes mellitus and incidence and mortality in breast and colorectal cancer. Br J Surg. 100:1421–1429. 2013. View Article : Google Scholar : PubMed/NCBI

24 

Coyle YM, Hynan LS, Euhus DM and Minhajuddin AT: An ecological study of the association of environmental chemicals on breast cancer incidence in texas. Breast Cancer Res Treat. 92:107–114. 2005. View Article : Google Scholar : PubMed/NCBI

25 

Coyle YM, Minahjuddin AT, Hynan LS and Minna JD: An ecological study of the association of metal air pollutants with lung cancer incidence in texas. J Thorac Oncol. 1:654–661. 2006. View Article : Google Scholar

26 

Whitworth KW, Symanski E and Coker AL: Childhood lympho-hematopoietic cancer incidence and hazardous air pollutants in southeast texas, 1995–2004. Environ Health Perspect. 116:1576–1580. 2008. View Article : Google Scholar : PubMed/NCBI

27 

Texas Cancer Registry. Epidemiology and Surveillance branch, Texas Department of State Health Services, 211 E. 7th street, suite 325, Austin, TX 78701. http://www.dshs.state.tx.us/tcr/default.shtm/. Accessed May 28, 2014

28 

U.S. Census Bureau. American community survey (ACS), 2014. http://www.census.gov/topics/population/. Accessed June 11, 2014

29 

Ries L, Melbert D, Krapcho M, et al: SEER cancer statistics review, 1975–2005. Bethesda, MD: National Cancer Institute; pp. 1975–2005. 2008

30 

Wu XC, Chen VW, Steele B, et al: Subsite-specific incidence rate and stage of disease in colorectal cancer by race, gender, and age group in the united states, 1992–1997. Cancer. 92:2547–2554. 2001. View Article : Google Scholar

31 

Ries LAG, Fritz AG and Hurlbut A: SEER summary staging manual-2000: codes and coding instructions. National Cancer Institute, SEER Program, NIH Pub. 62-84. 2007

32 

Klassen AC, Curriero F, Kulldorff M, Alberg AJ, Platz EA and Neloms ST: Missing stage and grade in Maryland prostate cancer surveillance data, 1992–1997. Am J Prev Med. 30:S77–S87. 2006. View Article : Google Scholar : PubMed/NCBI

33 

National Cancer Institute. Surveillance epidemiology and end results (SEER). surveillance research program, National Cancer Institute SEER*Stat software. Updated version 8.1.5. 2014

34 

Smith RA, Saslow D, Sawyer KA, et al: American Cancer Society guidelines for breast cancer screening: update 2003. CA Cancer J Clin. 53:141–169. 2003. View Article : Google Scholar : PubMed/NCBI

35 

Swan J, Breen N, Coates RJ, Rimer BK and Lee NC: Progress in cancer screening practices in the United States. Cancer. 97:1528–1540. 2003. View Article : Google Scholar : PubMed/NCBI

36 

Jorgensen KJ and Gotzsche PC: Overdiagnosis in publicly organised mammography screening programmes: systematic review of incidence trends. BMJ. 339:b25872009. View Article : Google Scholar : PubMed/NCBI

37 

Miller BA, Feuer EJ and Hankey BF: Recent incidence trends for breast cancer in women and the relevance of early detection: an update. CA Cancer J Clin. 43:27–41. 1993. View Article : Google Scholar : PubMed/NCBI

38 

Althuis MD, Dozier JM, Anderson WF, Devesa SS and Brinton LA: Global trends in breast cancer incidence and mortality 1973–1997. Int J Epidemiol. 34:405–412. 2005. View Article : Google Scholar : PubMed/NCBI

39 

Ravdin PM, Cronin KA, Howlader N, et al: The decrease in breast-cancer incidence in 2003 in the United States. N Engl J Med. 356:1670–1674. 2007. View Article : Google Scholar : PubMed/NCBI

40 

Cronin KA, Ravdin PM and Edwards BK: Sustained lower rates of breast cancer in the united states. Breast Cancer Res Treat. 117:223–224. 2009. View Article : Google Scholar

41 

Glass AG, Lacey JV Jr, Carreon JD and Hoover RN: Breast cancer incidence, 1980–2006 combined roles of menopausal hormone therapy, screening mammography, and estrogen receptor status. J Natl Cancer Inst. 99:1152–1161. 2007. View Article : Google Scholar : PubMed/NCBI

42 

Breen N, Cronin AK, Meissner HI, et al: Reported drop in mammography. Cancer. 109:2405–2409. 2007. View Article : Google Scholar : PubMed/NCBI

43 

Jemal A, Ward E and Thun MJ: Recent trends in breast cancer incidence rates by age and tumor characteristics among U.S. women. Breast Cancer Res. 9:R282007. View Article : Google Scholar : PubMed/NCBI

44 

Pelucchi C, Levi F and La Vecchia C: The rise and fall in menopausal hormone therapy and breast cancer incidence. Breast. 19:198–201. 2010. View Article : Google Scholar : PubMed/NCBI

45 

U.S. Preventive Services Task Force. Screening for colorectal cancer: U.S. preventive services task force recommendation statement. Ann Intern Med. 149:627–637. 2008. View Article : Google Scholar : PubMed/NCBI

46 

Gross CP, Andersen MS, Krumholz HM, McAvay GJ, Proctor D and Tinetti ME: Relation between medicare screening reimbursement and stage at diagnosis for older patients with colon cancer. JAMA. 296:2815–2822. 2006. View Article : Google Scholar : PubMed/NCBI

47 

Slater G, Papatestas AE, Tartter PI, Mulvihill M and Aufses AH Jr: Age distribution of right- and left-sided colorectal cancers. Am J Gastroenterol. 77:63–66. 1982.PubMed/NCBI

48 

American Cancer Society. Colorectal cancer facts & figures 2011–2013, Atlanta. http://www.cancer.org/acs/groups/content/@epidemiologysurveilance/documents/document/acspc-028312.pdfacs/groups/content/@epidemiologysurveilance/documents/document/acspc-028312.pdf. Accessed July 8, 2014

49 

Cook MB, Dawsey SM, Freedman ND, et al: Sex disparities in cancer incidence by period and age. Cancer Epidemiol Biomarkers Prev. 18:1174–1182. 2009. View Article : Google Scholar : PubMed/NCBI

50 

Goel MS, Wee CC, McCarthy EP, Davis RB, Ngo-Metzger Q and Phillips RS: Racial and ethnic disparities in cancer screening. J Gen Intern Med. 18:1028–1035. 2003. View Article : Google Scholar : PubMed/NCBI

51 

Belasco EJ, Gong G, Pence B and Wilkes E: The impact of rural health care accessibility on cancer-related behaviors and outcomes. Appl Health Econ Health Policy. 12:461–470. 2014. View Article : Google Scholar : PubMed/NCBI

52 

Leuven E, Plug E and Rønning M: Education and Cancer Risk, IZA Discussion Paper, No. 7956. 2014, http://www.econstor.eu/bitstream/10419/93310/1/dp7956.pdf. Accessed July 8, 2014

53 

Parajuli R, Bjerkaas E, Tverdal A, et al: The increased risk of colon cancer due to cigarette smoking may be greater in women than men. Cancer Epidemiol Biomarkers Prev. 22:862–871. 2013. View Article : Google Scholar : PubMed/NCBI

54 

Hurley S, Goldberg D, Nelson DO, et al: Risk of colorectal cancer associated with active smoking among female teachers. Cancer Causes Control. 24:1291–1304. 2013. View Article : Google Scholar : PubMed/NCBI

55 

Tillmans LS, Vierkant RA, Wang AH, et al: Associations between cigarette smoking, hormone therapy, and folate intake with incident colorectal cancer by TP53 protein expression level in a population-based cohort of older women. Cancer Epidemiol Biomarkers Prev. 23:350–355. 2014. View Article : Google Scholar :

56 

US Department of Health and Human Services. Tobacco use among US racial/ethnic minority groups - African Americans, American indians and Alaska natives, Asian Americans and Pacific islanders, and Hispanics: a report of the surgeon general. National Center for Chronic Disease Prevention and Health Promotion, Office on Smoking and Health. pp. 901998

57 

Fiore MC, Novotny TE, Pierce JP, Hatziandreu EJ, Patel KM and Davis RM: Trends in cigarette smoking in the United States: the changing influence of gender and race. JAMA. 261:49–55. 1989. View Article : Google Scholar : PubMed/NCBI

58 

Novotny TE, Warner KE, Kendrick JS and Remington PL: Smoking by blacks and whites: socioeconomic and demographic differences. Am J Public Health. 78:1187–1189. 1988. View Article : Google Scholar : PubMed/NCBI

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April-2015
Volume 46 Issue 4

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Copy and paste a formatted citation
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Spandidos Publications style
Liu Z, Zhang Y, Franzin L, Cormier JN, Chan W, Xu H and Du XL: Trends and variations in breast and colorectal cancer incidence from 1995 to 2011: A comparative study between Texas Cancer Registry and National Cancer Institute's Surveillance, Epidemiology and End Results data. Int J Oncol 46: 1819-1826, 2015.
APA
Liu, Z., Zhang, Y., Franzin, L., Cormier, J.N., Chan, W., Xu, H., & Du, X.L. (2015). Trends and variations in breast and colorectal cancer incidence from 1995 to 2011: A comparative study between Texas Cancer Registry and National Cancer Institute's Surveillance, Epidemiology and End Results data. International Journal of Oncology, 46, 1819-1826. https://doi.org/10.3892/ijo.2015.2881
MLA
Liu, Z., Zhang, Y., Franzin, L., Cormier, J. N., Chan, W., Xu, H., Du, X. L."Trends and variations in breast and colorectal cancer incidence from 1995 to 2011: A comparative study between Texas Cancer Registry and National Cancer Institute's Surveillance, Epidemiology and End Results data". International Journal of Oncology 46.4 (2015): 1819-1826.
Chicago
Liu, Z., Zhang, Y., Franzin, L., Cormier, J. N., Chan, W., Xu, H., Du, X. L."Trends and variations in breast and colorectal cancer incidence from 1995 to 2011: A comparative study between Texas Cancer Registry and National Cancer Institute's Surveillance, Epidemiology and End Results data". International Journal of Oncology 46, no. 4 (2015): 1819-1826. https://doi.org/10.3892/ijo.2015.2881