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Imaging, Diagnosis, Prognosis

Improved Survival with HPV among African Americans with Oropharyngeal Cancer

Maria J. Worsham, Josena K. Stephen, Kang Mei Chen, Meredith Mahan, Vanessa Schweitzer, Shaleta Havard and George Divine
Maria J. Worsham
Departments of 1Otolaryngology/Head and Neck Surgery and 2Public Health Sciences, Henry Ford Hospital, Detroit, Michigan
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Josena K. Stephen
Departments of 1Otolaryngology/Head and Neck Surgery and 2Public Health Sciences, Henry Ford Hospital, Detroit, Michigan
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Kang Mei Chen
Departments of 1Otolaryngology/Head and Neck Surgery and 2Public Health Sciences, Henry Ford Hospital, Detroit, Michigan
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Meredith Mahan
Departments of 1Otolaryngology/Head and Neck Surgery and 2Public Health Sciences, Henry Ford Hospital, Detroit, Michigan
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Vanessa Schweitzer
Departments of 1Otolaryngology/Head and Neck Surgery and 2Public Health Sciences, Henry Ford Hospital, Detroit, Michigan
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Shaleta Havard
Departments of 1Otolaryngology/Head and Neck Surgery and 2Public Health Sciences, Henry Ford Hospital, Detroit, Michigan
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George Divine
Departments of 1Otolaryngology/Head and Neck Surgery and 2Public Health Sciences, Henry Ford Hospital, Detroit, Michigan
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DOI: 10.1158/1078-0432.CCR-12-3003 Published May 2013
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Abstract

Purpose: A major limitation of studies reporting a lower prevalence rate of human papilloma virus (HPV) in African American patients with oropharyngeal squamous cell cancer (OPSCC) than Caucasian Americans, with corresponding worse outcomes, was adequate representation of HPV-positive African American patients. This study examined survival outcomes in HPV-positive and HPV-negative African Americans with OPSCC.

Experimental Design: The study cohort of 121 patients with primary OPSCC had 42% African Americans. Variables of interest included age, race, gender, HPV status, stage, marital status, smoking, treatment, and date of diagnosis.

Results: Caucasian Americans are more likely to be HPV positive (OR = 3.28; P = 0.035), as are younger age (age < 50 OR = 7.14; P = 0.023 compared with age > 65) or being married (OR = 3.44; P = 0.016). HPV positivity and being unmarried were associated with being late stage (OR = 3.10; P = 0.047 and OR = 3.23; P = 0.038, respectively). HPV-negative patients had 2.7 times the risk of death as HPV-positive patients (P = 0.004). Overall, the HPV-race groups differed (log-rank P < 0.001), with significantly worse survival for HPV-negative African Americans versus (i) HPV-positive African Americans (HR = 3.44; P = 0.0012); (ii) HPV-positive Caucasian Americans (HR = 3.11; P = < 0.049); and (iii) HPV-negative Caucasian Americans (HR = 2.21; P = 0.049).

Conclusions: HPV has a substantial impact on overall survival in African American patients with OPSCC. Among African American patients with OPSCC, HPV-positive patients had better survival than HPV negative. HPV-negative African Americans also did worse than both HPV-positive Caucasian Americans and HPV-negative Caucasian Americans. This study adds to the mounting evidence of HPV as a racially linked sexual behavior life style risk factor impacting survival outcomes for both African American and Caucasian American patients with OPSCC. Clin Cancer Res; 19(9); 2486–92. ©2013 AACR.

Footnotes

  • Note: Supplementary data for this article are available at Clinical Cancer Research Online (http://clincancerres.aacrjournals.org/).

  • Received September 19, 2012.
  • Revision received February 14, 2013.
  • Accepted March 11, 2013.
  • ©2013 American Association for Cancer Research.
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Clinical Cancer Research: 19 (9)
May 2013
Volume 19, Issue 9
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Improved Survival with HPV among African Americans with Oropharyngeal Cancer
Maria J. Worsham, Josena K. Stephen, Kang Mei Chen, Meredith Mahan, Vanessa Schweitzer, Shaleta Havard and George Divine
Clin Cancer Res May 1 2013 (19) (9) 2486-2492; DOI: 10.1158/1078-0432.CCR-12-3003

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Improved Survival with HPV among African Americans with Oropharyngeal Cancer
Maria J. Worsham, Josena K. Stephen, Kang Mei Chen, Meredith Mahan, Vanessa Schweitzer, Shaleta Havard and George Divine
Clin Cancer Res May 1 2013 (19) (9) 2486-2492; DOI: 10.1158/1078-0432.CCR-12-3003
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