Does HPV type affect outcome in oropharyngeal cancer?

نویسندگان

  • Anthony C Nichols
  • Sandeep S Dhaliwal
  • David A Palma
  • John Basmaji
  • Corina Chapeskie
  • Samuel Dowthwaite
  • Jason H Franklin
  • Kevin Fung
  • Keith Kwan
  • Brett Wehrli
  • Chris Howlett
  • Iram Siddiqui
  • Marina I Salvadori
  • Eric Winquist
  • Scott Ernst
  • Sara Kuruvilla
  • Nancy Read
  • Varagur Venkatesan
  • Biljana Todorovic
  • J Alex Hammond
  • James Koropatnick
  • Joe S Mymryk
  • John Yoo
  • John W Barrett
چکیده

BACKGROUND An epidemic of human papillomavirus (HPV)-related oropharyngeal squamous cell cancer (OPSCC) has been reported worldwide largely due to oral infection with HPV type-16, which is responsible for approximately 90% of HPV-positive cases. The purpose of this study was to determine the rate of HPV-positive oropharyngeal cancer in Southwestern Ontario, Canada. METHODS A retrospective search identified ninety-five patients diagnosed with OPSCC. Pre-treatment biopsy specimens were tested for p16 expression using immunohistochemistry and for HPV-16, HPV-18 and other high-risk subtypes, including 31,33,35,39,45,51,52,56,58,59,67,68, by real-time qPCR. RESULTS Fifty-nine tumours (62%) were positive for p16 expression and fifty (53%) were positive for known high-risk HPV types. Of the latter, 45 tumors (90%) were identified as HPV-16 positive, and five tumors (10%) were positive for other high-risk HPV types (HPV-18 (2), HPV-67 (2), HPV-33 (1)). HPV status by qPCR and p16 expression were extremely tightly correlated (p < 0.001, Fishers exact test). Patients with HPV-positive tumors had improved 3-year overall (OS) and disease-free survival (DFS) compared to patients with HPV-negative tumors (90% vs 65%, p = 0.001; and 85% vs 49%, p = 0.005; respectively). HPV-16 related OPSCC presented with cervical metastases more frequently than other high-risk HPV types (p = 0.005) and poorer disease-free survival was observed, although this was not statistically significant. CONCLUSION HPV-16 infection is responsible for a significant proportion of OPSCC in Southwestern Ontario. Other high-risk subtypes are responsible for a smaller subset of OPSCC that present less frequently with cervical metastases and may have a different prognosis.

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عنوان ژورنال:

دوره 42  شماره 

صفحات  -

تاریخ انتشار 2013