4.6 Article

Tobacco exposure as a major modifier of oncologic outcomes in human papillomavirus (HPV) associated oropharyngeal squamous cell carcinoma

期刊

BMC CANCER
卷 20, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12885-020-07427-7

关键词

Oropharyngeal carcinoma; Radiotherapy; Tobacco; Human papillomavirus

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资金

  1. National Institutes of Health (NIH)/National Cancer Institute (NCI) Head and Neck Specialized Programs of Research Excellence (SPORE) Developmental Research Program Award [P50 CA097007-10]
  2. National Institute for Dental and Craniofacial Research Award [1R01DE025248-01/R56DE025248-01]
  3. NCI Early Phase Clinical Trials in Imaging and Image-Guided Interventions Program [1R01CA218148-01]
  4. NCI Big Data to Knowledge (BD2K) Early Stage Development of Technologies in Biomedical Computing, Informatics, and Big Data Science Award [1R01CA214825-01]
  5. NCI Cancer Center Support Grant (CCSG) Radiation Oncology and Cancer Imaging Program Pilot Research Program Award [P30CA016672]
  6. NCI/National Science Foundation Joint NSF/NIH Initiative on Quantitative Approaches to Biomedical Big Data (QuBBD) award [5R01CA225190-0]
  7. National Institute of Biomedical Imaging and Bioengineering (NIBIB) Research Education Program [R25EB025787]
  8. Andrew Sabin Family Foundation
  9. Elekta AB via a Elekta AB/MD Anderson Department of Radiation Oncology Seed Grant
  10. Egyptian Ministry of Cultural and Higher Education
  11. FDA [1R01FD005109-01]
  12. NCI
  13. NIDCR [U01DE028233]
  14. Veterans Administration [1 I01 BX004183]
  15. Caroline Weiss Law Foundation for Academic Excellence
  16. Department of Veterans Affairs Million Veteran Program [BX004183-01A1]
  17. National Institute of Dental and Craniofacial Research (NIDCR) [R03DE028858]
  18. American Head and Neck Society
  19. American Academy of Otolaryngology -Head and Neck Surgery Foundation
  20. United States (U.S.) Department of Veterans Affairs Clinical Sciences R&D (CSRD) Service [IK2 CX001953]

向作者/读者索取更多资源

BackgroundThe incidence of oropharyngeal squamous cell carcinoma (OPSCC) in the US is rapidly increasing, driven largely by the epidemic of human papillomavirus (HPV)-mediated OPSCC. Although survival for patients with HPV mediated OPSCC (HPV+ OPSCC) is generally better than that of patients with non-virally mediated OPSCC, this effect is not uniform. We hypothesized that tobacco exposure remains a critical modifier of survival for HPV+ OPSCC patients.MethodsWe conducted a retrospective analysis of 611 OPSCC patients with concordant p16 and HPV testing treated at a single institute (2002-2013). Survival analysis was performed using Kaplan-Meier analysis and Cox regression. Recursive partitioning analysis (RPA) was used to define tobacco exposure associated with survival (p<0.05).ResultsTobacco exposure impacted overall survival (OS) for HPV+ patients on univariate and multivariate analysis (p=0.002, p=0.003 respectively). RPA identified 30 pack-years (PY) as a threshold at which survival became significantly worse in HPV+ patients. OS and disease-free survival (DFS) for HPV+ >30 PY patients didn't differ significantly from HPV- patients (p=0.72, p=0.27, respectively). HPV+ >30 PY patients had substantially lower 5-year OS when compared to their <= 30 PYs counterparts: 78.4% vs 91.6%; p=0.03, 76% vs 88.3%; p=0.07, and 52.3% vs 74%; p=0.05, for stages I, II, and III (AJCC 8th Edition Manual), respectively.ConclusionsTobacco exposure can eliminate the survival benefit associated with HPV+ status in OPSCC patients. Until this effect can be clearly quantified using prospective datasets, de-escalation of treatment for HPV+OPSCC smokers should be avoided.

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