Skip to main content
JAMA Network logoLink to JAMA Network
. 2023 Mar 2;9(5):712–714. doi: 10.1001/jamaoncol.2022.7944

Human Papillomavirus Vaccination Prevalence and Disproportionate Cancer Burden Among US Veterans

Smrithi Chidambaram 1,2,3, Su-Hsin Chang 3,4, Vlad C Sandulache 5,6,7, Angela L Mazul 1,4, Jose P Zevallos 8,9,10,
PMCID: PMC9982736  PMID: 36862390

Abstract

This cross-sectional study examines the rate of HPV vaccination and the number eligible for this vaccination among younger veterans and civilians.


In the US, over 45 000 cases of human papillomavirus (HPV)–associated malignant neoplasms are diagnosed annually.1 The Advisory Committee on Immunization Practices recommends HPV vaccination until age 26 years to prevent HPV-associated malignant neoplasms in males and females. Active-duty military service members and veterans are twice as likely as the general population to develop oncogenic HPV infections, resulting in a higher risk of HPV-associated cancers and mortality,2,3,4 and HPV-associated oropharyngeal cancer, which occurs predominantly in males, is rising more rapidly among veterans than civilians.3 There are no universal HPV vaccination requirements or campaigns targeted at service members or veterans.5 In this study, we provide, to our knowledge, the first national estimate of HPV vaccination prevalence among eligible veterans.

Methods

Using data from the Veterans Health Administration (VHA) Corporate Data Warehouse (CDW), we conducted a national cross-sectional study of veterans aged 18 to 26 years with at least 1 VHA primary care visit between January 1, 2018, and December 31, 2020. The St Louis VA Medical Center Review Board approved this study and deemed it exempt from the informed consent requirement because it involved only retrospective review. We followed the STROBE reporting guideline.

We constructed an age-matched representative sample of the US population using the 2017 to 2020 National Health and Nutrition Examination Survey to compare HPV vaccination prevalence between civilians and veterans. Logistic regression model was used to determine the association between sociodemographic and geographic factors and history of HPV vaccination. In the CDW, race and ethnicity are self-reported, and sex refers to birth sex, which can be changed by request to reflect gender identity. The SAS Enterprise Guide 9.2 (SAS Institute) and R 4.2.0 (R Core Team) were used to perform statistical analyses.

Results

Vaccination prevalence and multivariable regression analysis results are provided in the Table. A total of 128 279 veterans (mean [SD] age, 24.4 [1.6] years; 79.2% males and 20.8% females) were included in the analysis. Among veterans aged 18 to 26 years, 30.2% of females and 18.7% of males received HPV vaccination vs 62.4% of females and 37.0% of males in the general population. Vaccination odds decreased with 1-unit increase in age (adjusted odds ratio [aOR], 0.95; 95% CI, 0.94-0.96) and increase in percentage of households living at 125% of poverty level or under (aOR, 0.83; 95% CI, 0.72-0.96).

Table. HPV Vaccination Prevalence and aORs of HPV Vaccination of Veterans Aged 18 to 26 Years Receiving Primary Care Within the VHAa.

Characteristic Males Females All veterans, aOR (95% CI)
Total No. % Vaccinated (95% CI) Total No. % Vaccinated (95% CI)
Sex 101 646 18.7 (18.5-18.9) 26 633 30.2 (29.6-30.8) 0.52 (0.50-0.53) [Reference: female sex]
Race and ethnicityb
Asian American and Pacific Islander 3172 28.9 (28.6-29.2) 851 37.8 (34.5-41.1) 1.76 (1.63-1.60)
Black 14 644 18.2 (18-18.4) 6443 27.8 (26.7-28.9) 1.01 (0.97-1.05)
Hispanic 16 612 21.4 (21.1-21.6) 4406 32.5 (31.1-33.8) 1.09 (0.91-1.30)
Native American 566 20.1 (19.5-20.3) 198 25.2 (19.1-31.2) 1.28 (1.23-1.33)
White 53 798 17.5 (17.2-17.7) 10 728 31.5 (30.6-32.4) 1 [Reference]
Otherc 6695 19.8 (19.5-20) 2278 28.7 (26.8-30.6) 1.12 (1.06-1.19)
Missing data 6159 NA 1729 NA NA
Branch of service
Army 46 279 17.8 (17.6-18) 12 261 31.1 (30.2-31.9) 1 [Reference]
Air Force 8944 21.9 (21.6-22.1) 3187 33.2 (31.5-34.8) 1.25 (1.19-1.31)
Coast Guard 483 20.7 (20.4-20.9) 174 28.1 (21.4-34.8) 1.08 (0.89-1.31)
Marine Corps 32 665 18.9 (18.7-19.1) 4617 30 (28.7-31.3) 1.02 (0.99-1.06)
Navy 11 996 19.3 (19.1-19.5) 5724 27.6 (26.4-28.8) 0.97 (0.93-1.02)
Otherd 9 11.1 (10.9-11.3) 4 NA NA
Missing data 1270 NA 666 NA NA
Rural-urban status
Urban 87 188 18.9 (18.7-19.1) 23 402 30.2 (29.6-30.8) 1 [Reference]
Large rural 8315 16.9 (16.7-17.1) 1845 30.1 (28-32.2) 0.89 (0.84-0.94)
Small rural 3184 17.3 (17.1-17.5) 689 29.2 (25.8-32.6) 0.91 (0.83-0.99)
Isolated 1915 18.5 (18.3-18.7) 363 33.3 (28.4-38.1) 0.99 (0.89-1.10)
Missing data 1044 NA 334 NA NA
Regione
Pacific 22 238 21.7 (21.4-21.9) 5533 29.7 (28.5-30.9) 1 [Reference]
Continental 19 692 13.5 (13.2-13.7) 5920 23.7 (22.6-24.8) 0.64 (0.61-0.67)
Midwest 18 508 22.03 (21.8-22.3) 3590 38.4 (36.8-39.9) 1.24 (1.19-1.30)
North Atlantic 21 613 15.7 (15.4-15.9) 5655 26.7 (25.5-27.8) 0.77 (0.74-0.80)
Southeast 19 595 20.6 (20.3-20.8) 5935 35.4 (34.2-36.6) 1.12 (1.08-1.17)

Abbreviations: aOR, adjusted odds ratio; HPV, human papillomavirus; NA, not applicable; VHA, Veterans Health Administration.

a

Multivariable model was adjusted for variables shown in the table and the continuous variables of age and percentage living in households with income 125% of the poverty level or under.

b

Race and ethnicity were self-reported.

c

Other race and ethnicity included unknown or no response.

d

Other service branch included US Public Health Service Commissioned Corps and National Oceanic and Atmospheric Administration.

e

Regions included the following VA districts. Pacific: Washington, Oregon, Nevada, California, Arizona, New Mexico, Alaska, and Hawaii. Continental: Idaho, Montana, Utah, Texas, Oklahoma, Colorado, Mississippi, Louisiana, Arkansas, and Wyoming. Midwest: North Dakota, South Dakota, Nebraska, Kansas, Minnesota, Iowa, Missouri, Wisconsin, Michigan, Indiana, Illinois, and Ohio. North Atlantic: Maine, Vermont, New Hampshire, Massachusetts, Connecticut, New York, Rhode Island, Pennsylvania, New Jersey, West Virginia, Virginia, North Carolina, Delaware, Washington, DC, and Maryland. Southeast: Alabama, Georgia, South Carolina, Florida, Kentucky, and Tennessee.

The Figure shows vaccination prevalence and number of veterans under age 30 years. Wyoming (6.1%; 95% CI, 3.1%-9.1%), Oklahoma (10.9%; 95% CI, 9.39%-12.41%), and Texas (11.9%; 95% CI, 11.35-12.45) had the lowest vaccination rates. Hawaii (53.9%; 95% CI, 50.1-57.6%) and North Dakota (49.2%; 95% CI, 43.8%-54.6%) had the highest rates. Texas and Virginia were among states with the lowest rates and the largest populations of veterans younger than 30 years.

Figure. Human Papillomavirus Vaccination Prevalence Among US Veterans Aged 18 to 26 Years and Number of Veterans Younger Than 30 Years by State .

Figure.

aData are from the Veterans Health Administration Corporate Data Warehouse (https://www.data.va.gov/dataset/Corporate-Data-Warehouse-CDW-/ftpi-epf7).

bData are from the US Department of Veterans Affairs Veteran Population Projection Model (https://www.va.gov/vetdata/veteran_population.asp).

Discussion

Prevalence of HPV vaccination among eligible veterans was one-half that among civilians. High HPV-infection prevalence, rising HPV-associated oropharyngeal cancer incidence,3 and low vaccination rates may be associated with increases in HPV-associated cancer morbidity and mortality among veterans.

Findings suggest catch-up HPV vaccination campaigns are needed for younger service members and veterans. We identified regions with low veteran vaccination prevalence and large eligible veteran populations wherein these interventions may be most impactful. Only 37.8% female and 3.9% male active-duty service members have reported initiating the HPV vaccine series.6 The VHA has spent approximately $136 million to treat HPV-associated cancers that are preventable with vaccination.4 Without effective HPV vaccination strategies, the VHA will bear the financial burden of HPV-associated malignant neoplasms for decades to come.

Study limitations were inclusion of only veterans interacting with the VHA and imperfect transfer of historical medical records to new settings such as the VHA that could result in underestimation of vaccination prevalence. The findings provide the VHA and Department of Defense an opportunity to design and implement HPV prevention campaigns, which could be extrapolated to civilians, among whom vaccination rates remain suboptimal. In doing so, the VHA can prioritize cancer prevention and impart lessons to other health care delivery systems.

Supplement.

Data Sharing Statement

References

  • 1.Division of Cancer Prevention and Control, Centers for Disease Control and Prevention . How many cancers are linked with HPV each year? Accessed July 18, 2022. https://www.cdc.gov/cancer/hpv/statistics/cases.htm
  • 2.Nsouli-Maktabi H, Ludwig SL, Yerubandi UD, Gaydos JC. Incidence of genital warts among U.S. service members before and after the introduction of the quadrivalent human papillomavirus vaccine. MSMR. 2013;20(2):17-20. [PubMed] [Google Scholar]
  • 3.Zevallos JP, Kramer JR, Sandulache VC, et al. National trends in oropharyngeal cancer incidence and survival within the Veterans Affairs Health Care System. Head Neck. 2021;43(1):108-115. doi: 10.1002/hed.26465 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Saxena K, Dawson RS, Cyhaniuk A, Bello T, Janjan N. Clinical and economic burden of HPV-related cancers in the US veteran population. J Med Econ. 2022;25(1):299-308. doi: 10.1080/13696998.2022.2041855 [DOI] [PubMed] [Google Scholar]
  • 5.Nobel T, Rajupet S, Sigel K, Oliver K. Using Veterans Affairs Medical Center (VAMC) data to identify missed opportunities for HPV vaccination. Hum Vaccin Immunother. 2019;15(7-8):1878-1883. doi: 10.1080/21645515.2018.1559684 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Matsuno RK, Seay J, Porter B, Tannenbaum K, Warner S, Wells N. Factors associated with human papillomavirus vaccine initiation and compliance among U.S. military service members. Mil Med. 2022;usab562. doi: 10.1093/milmed/usab562 [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Supplement.

Data Sharing Statement


Articles from JAMA Oncology are provided here courtesy of American Medical Association

RESOURCES