1
Racial/Ethnic Differences in Thyroid Cancer Incidence in the US:2007-2014 Kristin Weeks, BS 1,2 ; Amanda Kahl, MPH 2 ; Charles Lynch, MD, PhD 2 ; Mary Charlton, PhD 2 1 Medical Scientist Training Program, Carver College of Medicine, University of Iowa, Grant: 5 T32 GM007337 2 Department of Epidemiology, College of Public Health, University of Iowa BACKGROUND OBJECTIVE METHODS Thyroid cancer incidence rates are projected to increase by 2030 from the 8 th most common cancer currently to the 4 th most common cancer. TC incidence varies by race in an order opposite to all other head and neck, colorectal, prostate, and lung cancer. Past studies have argued that small tumor diagnostic tools, ultrasound-guided fine-needle aspiration (US-guided FNA) and computed tomography, could be causing rising and racially/ethnically different thyroid cancer incidence rates due to variable overdiagnosis of indolent tumors. Thyroid cancer tumors believed to be overdiagnosed with US-guided FNA have papillary histologies and sizes 20mm at diagnosis. RESULTS CONCLUSION To investigate recent age-adjusted incidence rates (AAIRs) by race/ethnicity across tumor and patient characteristics to determine their likely relationship to diagnostic technology. SEER 18 (Surveillance Epidemiology End Result of the National Cancer Institute Registry) was used to calculate AAIRs from 2007-2014 for five races/ethnicties. SAS (Statistical Analysis System) was used to develop logistic regression model to examine association between race/ethnicity and tumor size/histology at diagnosis. Inclusion: microscopically confirmed malignant thyroid cancer with known ages were included (N= 93,224). Exposure Interest: White, African American, Asian, Native American, Hispanic. Covariates: gender, age, insurance coverage, histology (ICD-O-3), tumor size at diagnosis (AJCC), tumor stage at diagnosis (AJCC), tumor sequence, county level poverty and education. Iowa Seattle/ Puget Sound San Francisco/ San Jose/ Monterey Los Angeles New Mexico Utah Georgia excluding AT/RG Detroit Connecticut Alaska Hawaii Atlanta Oakland Louisiana Kentucky New Jersey SF/SJM/LA California excluding Rural Georgia San Francisco/Oakland, Connecticut, Detroit, Hawaii, Iowa, New Mexico, Seattle/Puget Sound, Utah, Atlanta. SEER 9 is this group. San Jose-Monterey, Los Angeles, Alaska Native Registry, Rural Georgia. SEER 13 is this group plus SEER 9. California excluding SF/SJM/LA, Georgia excluding AT/RG, Kentucky, Louisiana, New Jersey. SEER 18 is this group plus SEER 13. AAIRs increased variably by race/ethnicity for tumors that would be (papillary and 20mm) and should not be (>20mm and non-papillary) overdiagnosed by US-guided FNA. This suggests overdiagnosis is not the sole reason for increasing incidence of thyroid cancer. Insurance coverage affected stage/histology at diagnosis and AAIR trends. Within each race, those privately insured have a 5 to 13-fold greater AAIR than Medicaid, and a 15 to 40-fold greater AAIR then uninsured. Privately insured, Whites had the highest AAIR and African Americans had the lowest. Conversely, Medicaid/uninsured, Whites had the lowest AAIR. Non-White race is associated with more advanced tumors than Whites May be a difference in health care access or a delay in seeking treatment AAIRs by race/ethnicity and odds ratios (ORs) of diagnosis with papillary carcinoma (vs. other histologies) or 20mm tumor thyroid cancer (vs. >20mm) differed significantly by gender, age, insurance coverage, tumor histology (papillary, follicular, medullary), tumor stage (I-IV), tumor size (0-40mm), and tumor sequence. Thyroid cancer AAIRs increased variably by race/ethnicity for tumors 20mm and >20mm and for histologies of papillary carcinoma and non-papillary carcinoma. Non-White (vs. White) were associated with larger tumors (ORs tumor 20mm= 0.67-0.77, 95% confidence interval (CI)= 0.56-0.82; all P<.0001). Medicaid/uninsured patients (vs. insured) were less associated with papillary carcinoma (OR=0.87, 95% CI=0.81-0.93) and tumors 20mm (OR=0.78, 95% CI=0.74-0.82). Multivariate Analysis of Thyroid Cancer Diagnosis with Papillary Histology or Thyroid Cancer Tumor 20mm for Tumor and Patient Characteristics, SEER 18, 2007-2014 6 8 10 12 14 16 2007 2008 2009 2010 2011 2012 2013 2014 AAIR for thyroid cancer Year AAIR of Thyorid Cancer by Race/Ethnicity from 2007-2014 White Hispanic African American Native American Asian 0 0.5 1 1.5 2 2.5 3 Uninsured Medicaid Private Insurance AAIR Ratio Relative to Whites Racial/ethnic AAIR ratios relative to Whites for thyroid cancer by type of insurance coverage Whites African American Hispanic Asian ABSTRACT Small tumor diagnostic tools, ultrasound-guided fine-needle aspiration (US-guided FNA) and computed tomography, could be causing rising and racially/ethnically different thyroid cancer incidence rates due to variable overdiagnosis of indolent tumors. Thyroid cancer tumors believed to be overdiagnosed with US-guided FNA have papillary histologies and sizes 20mm at diagnosis. Age-adjusted incidence rates (AAIRs) 2007-2014 were calculated for race/ethnicity (White, Hispanic, Asian, African American, Native American) by patient/tumor characteristics for microscopically confirmed malignant thyroid cancer cases in SEER 18 (N=93,224). Multivariate analysis determined odds ratios (OR) of diagnosis with papillary carcinoma or small (20mm) tumor thyroid cancer. OR of diagnosis with papillary carcinoma or 20mm tumor thyroid cancer differed significantly by race, gender, age, insurance coverage, tumor: histology, stage, size, sequence. Thyroid cancer AAIRs increased variably by race/ethnicity for tumors 20mm and >20mm and for histologies of papillary carcinoma and non-papillary carcinoma. Non-White (vs. White) were associated with larger tumors (OR tumor 20mm=0.67-0.77, 95% confidence interval (CI)= 0.56-0.82; all P<.0001). Medicaid/uninsured patients (vs. insured) were less associated with papillary carcinoma (OR=0.87, 95% CI=0.81-0.93) and tumors 20mm (OR=0.78, 95% CI=0.74-0.82). AAIRs increased variably by race/ethnicity for tumors that would be (papillary and 20mm) and would not be (>20mm and non-papillary) overdiagnosed by US-guided FNA suggesting overdiagnosis is not the sole reason for increasing incidence of thyroid cancer. Being non-White effects tumor characteristic at diagnosis leading non-Whites to have more advanced stage/histology/size thyroid tumors. Race/ethnicity AAIR trends depended on insurance coverage, where privately insured patients had the smallest tumors. OR* 95% CI OR* 95% CI Race White 1.00 Referent 1.00 Referent African American 0.69 (0.64, 0.75) 0.70 (0.66, 0.74) Hispanic 1.37 (1.28, 1.46) 0.67 (0.64, 0.70) Asian 1.42 (1.32, 1.54) 0.77 (0.73, 0.81) Native American 1.17 (0.89, 1.55) 0.67 (0.56, 0.82) Gender Male 1.00 Referent 1.00 Referent Female 1.07 (1.02, 1.12) 1.94 (1.88, 2.01) Age (years) 15-29 3.27 (2.79, 3.82) 1.58 (1.36, 1.83) 30-44 3.07 (2.65, 3.54) 2.68 (2.32, 3.10) 45-54 2.91 (2.54, 3.33) 3.36 (2.91, 3.88) 55-64 2.44 (2.13, 2.79) 3.47 (3.01, 4.01) 65-74 1.77 (1.55, 2.03) 2.95 (2.55, 3.41) 75-84 1.45 (1.26, 1.67) 1.83 (1.57, 2.13) 85+ 1.00 Referent 1.00 Referent Insurance Privately Insured 1.00 Referent 1.00 Referent Medicaid/Uninsured 0.87 (0.81, 0.93) 0.78 (0.74, 0.82) Unknown 0.88 (0.78, 0.99) 1.03 (0.92, 1.15) Histology at Papillary 1.00 Referent Diagnosis Follicular 0.14 (0.13, 0.14) Medullary 0.46 (0.42, 0.51) Anaplastic 0.02 (0.01, 0.03) Other 0.29 (0.26, 0.33) Tumor Sequence First 0.71 (0.67, 0.74) at Diagnosis Second or Greater 1.00 Referent Tumor Stage I 1.99 (1.83, 2.17) at Diagnosis II 0.83 (0.76, 0.90) III 2.42 (2.23, 2.62) IV 1.00 Referent Tumor Size at 0-4 15.93 (14.14, 17.94) Diagnosis (mm) 5-9 13.65 (12.24, 15.22) 10-20 6.27 (5.83, 6.75) 21-40 3.34 (3.11, 3.58) 41+ 1.00 Referent Poverty of County <20% 1.00 Referent 1.00 Referent 20% 1.13 (1.05, 1.23) 0.88 (0.84, 0.94) MODEL 1: PAPILLARY (vs. Other Histologies) (N=93,224) MODEL 2: TUMOR 20mm (vs. >20mm) (N=88,910)

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Racial/EthnicDifferencesinThyroidCancerIncidenceintheUS:2007-2014Kristin Weeks, BS1,2; Amanda Kahl, MPH2 ; Charles Lynch, MD, PhD2; Mary Charlton, PhD2

1 Medical Scientist Training Program, Carver College of Medicine, University of Iowa, Grant: 5 T32 GM0073372 Department of Epidemiology, College of Public Health, University of Iowa

BACKGROUND

OBJECTIVE

METHODS

Thyroid cancer incidence rates are projected to increase by 2030 from the 8th

most common cancer currently to the 4th most common cancer.

TC incidence varies by race in an order opposite to all other head and neck, colorectal, prostate, and lung cancer.

Past studies have argued that small tumor diagnostic tools, ultrasound-guided fine-needle aspiration (US-guided FNA) and computed tomography, could be causing rising and racially/ethnically different thyroid cancer incidence rates due to variable overdiagnosis of indolent tumors. Thyroid cancer tumors believed to be overdiagnosed with US-guided FNA have papillary histologies and sizes ≤20mm at diagnosis.

RESULTS

CONCLUSION

To investigate recent age-adjusted incidence rates (AAIRs) by race/ethnicity across tumor and patient characteristics to determine their likely relationship to diagnostic technology.

SEER 18 (Surveillance Epidemiology End Result of the National Cancer Institute Registry) was used to calculate AAIRs from 2007-2014 for five races/ethnicties.

SAS (Statistical Analysis System) was used to develop logistic regression model to examine association between race/ethnicity and tumor size/histology at diagnosis.

Inclusion: microscopically confirmed malignant thyroid cancer with known ages were included (N= 93,224).

Exposure Interest: White, African American, Asian, Native American, Hispanic.

Covariates: gender, age, insurance coverage, histology (ICD-O-3), tumor size at diagnosis (AJCC), tumor stage at diagnosis (AJCC), tumor sequence, county level poverty and education.

Iowa

Seattle/Puget Sound

San Francisco/

San Jose/Monterey

LosAngeles

NewMexico

Utah

Georgia excluding AT/RG

Detroit Connecticut

Surveillance, Epidemiology, and End Results (SEER) Program: SEER 9, 13, & 18 Geographic Areas

National Cancer Institute, USA

http://seer.cancer.gov

Figure 1.1

Alaska Hawaii

Atlanta

Oakland

Louisiana

Kentucky

New Jersey

SF/SJM/LACalifornia excluding

Rural Georgia

San Francisco/Oakland, Connecticut, Detroit, Hawaii, Iowa, New Mexico, Seattle/Puget Sound, Utah, Atlanta. SEER 9 is this group.San Jose-Monterey, Los Angeles, Alaska Native Registry, Rural Georgia. SEER 13 is this group plus SEER 9.California excluding SF/SJM/LA, Georgia excluding AT/RG, Kentucky,Louisiana, New Jersey. SEER 18 is this group plus SEER 13.

AAIRs increased variably by race/ethnicity for tumors that would be (papillary and ≤20mm) and should not be (>20mm and non-papillary) overdiagnosed by US-guided FNA. • This suggests overdiagnosis is not the sole reason for increasing incidence

of thyroid cancer.

Insurance coverage affected stage/histology at diagnosis and AAIR trends. • Within each race, those privately insured have a 5 to 13-fold greater AAIR

than Medicaid, and a 15 to 40-fold greater AAIR then uninsured.• Privately insured, Whites had the highest AAIR and African Americans had

the lowest. Conversely, Medicaid/uninsured, Whites had the lowest AAIR.

Non-White race is associated with more advanced tumors than Whites• May be a difference in health care access or a delay in seeking treatment

AAIRs by race/ethnicity and odds ratios (ORs) of diagnosis with papillary carcinoma (vs. other histologies) or ≤20mm tumor thyroid cancer (vs. >20mm) differed significantly by gender, age, insurance coverage, tumor histology (papillary, follicular, medullary), tumor stage (I-IV), tumor size (0-40mm), and tumor sequence.

Thyroid cancer AAIRs increased variably by race/ethnicity for tumors ≤20mm and >20mm and for histologies of papillary carcinoma and non-papillary carcinoma.

Non-White (vs. White) were associated with larger tumors (ORs tumor ≤20mm= 0.67-0.77, 95% confidence interval (CI)= 0.56-0.82; all P<.0001).

Medicaid/uninsured patients (vs. insured) were less associated with papillary carcinoma (OR=0.87, 95% CI=0.81-0.93) and tumors ≤20mm (OR=0.78, 95% CI=0.74-0.82).

Multivariate Analysis of Thyroid Cancer Diagnosis with Papillary Histology or Thyroid Cancer Tumor ≤20mm for Tumor and Patient Characteristics, SEER 18, 2007-2014

6

8

10

12

14

16

2007 2008 2009 2010 2011 2012 2013 2014

AAIRforth

yroidcance

r

Year

AAIRofThyoridCancerbyRace/Ethnicityfrom2007-2014

White Hispanic AfricanAmerican NativeAmerican Asian

0

0.5

1

1.5

2

2.5

3

Uninsured Medicaid Private Insurance

AAIRRatioRelativetoW

hites

Racial/ethnic AAIR ratios relative to Whites for thyroid cancer by type of insurance coverage

Whites AfricanAmerican Hispanic Asian

ABSTRACTSmall tumor diagnostic tools, ultrasound-guided fine-needle aspiration (US-guided FNA) and computed tomography, could be causing rising and racially/ethnically different thyroid cancer incidence rates due to variable overdiagnosis of indolent tumors. Thyroid cancer tumors believed to be overdiagnosed with US-guided FNA have papillary histologies and sizes ≤20mm at diagnosis.Age-adjusted incidence rates (AAIRs) 2007-2014 were calculated for race/ethnicity (White, Hispanic, Asian, African American, Native American) by patient/tumor characteristics for microscopically confirmed malignant thyroid cancer cases in SEER 18 (N=93,224). Multivariate analysis determined odds ratios (OR) of diagnosis with papillary carcinoma or small (≤20mm) tumor thyroid cancer.OR of diagnosis with papillary carcinoma or ≤20mm tumor thyroid cancer differed significantly by race, gender, age, insurance coverage, tumor: histology, stage, size, sequence. Thyroid cancer AAIRs increased variably by race/ethnicity for tumors ≤20mm and >20mm and for histologies of papillary carcinoma and non-papillary carcinoma. Non-White (vs. White) were associated with larger tumors (OR tumor ≤20mm=0.67-0.77, 95% confidence interval (CI)= 0.56-0.82; all P<.0001). Medicaid/uninsured patients (vs. insured) were less associated with papillary carcinoma (OR=0.87, 95% CI=0.81-0.93) and tumors ≤20mm (OR=0.78, 95% CI=0.74-0.82).AAIRs increased variably by race/ethnicity for tumors that would be (papillary and ≤20mm) and would not be (>20mm and non-papillary) overdiagnosed by US-guided FNA suggesting overdiagnosis is not the sole reason for increasing incidence of thyroid cancer. Being non-White effects tumor characteristic at diagnosis leading non-Whites to have more advanced stage/histology/size thyroid tumors. Race/ethnicity AAIR trends depended on insurance coverage, where privately insured patients had the smallest tumors.

OR* 95% CI OR* 95% CIRace White 1.00 Referent 1.00 Referent

African American 0.69 (0.64, 0.75) 0.70 (0.66, 0.74)Hispanic 1.37 (1.28, 1.46) 0.67 (0.64, 0.70)Asian 1.42 (1.32, 1.54) 0.77 (0.73, 0.81)Native American 1.17 (0.89, 1.55) 0.67 (0.56, 0.82)

Gender Male 1.00 Referent 1.00 ReferentFemale 1.07 (1.02, 1.12) 1.94 (1.88, 2.01)

Age (years) 15-29 3.27 (2.79, 3.82) 1.58 (1.36, 1.83)30-44 3.07 (2.65, 3.54) 2.68 (2.32, 3.10)45-54 2.91 (2.54, 3.33) 3.36 (2.91, 3.88)55-64 2.44 (2.13, 2.79) 3.47 (3.01, 4.01)65-74 1.77 (1.55, 2.03) 2.95 (2.55, 3.41)75-84 1.45 (1.26, 1.67) 1.83 (1.57, 2.13)85+ 1.00 Referent 1.00 Referent

Insurance Privately Insured 1.00 Referent 1.00 ReferentMedicaid/Uninsured 0.87 (0.81, 0.93) 0.78 (0.74, 0.82)Unknown 0.88 (0.78, 0.99) 1.03 (0.92, 1.15)

Histology at Papillary 1.00 ReferentDiagnosis Follicular 0.14 (0.13, 0.14)

Medullary 0.46 (0.42, 0.51)Anaplastic 0.02 (0.01, 0.03)Other 0.29 (0.26, 0.33)

Tumor Sequence First 0.71 (0.67, 0.74)at Diagnosis Second or Greater 1.00 ReferentTumor Stage I 1.99 (1.83, 2.17)at Diagnosis II 0.83 (0.76, 0.90)

III 2.42 (2.23, 2.62)IV 1.00 Referent

Tumor Size at 0-4 15.93 (14.14, 17.94) Diagnosis (mm) 5-9 13.65 (12.24, 15.22)

10-20 6.27 (5.83, 6.75)21-40 3.34 (3.11, 3.58)41+ 1.00 Referent

Poverty of County <20% 1.00 Referent 1.00 Referent≥20% 1.13 (1.05, 1.23) 0.88 (0.84, 0.94)

MODEL 1: PAPILLARY (vs. Other Histologies)

(N=93,224)

MODEL 2: TUMOR ≤20mm (vs. >20mm)

(N=88,910)