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Journal of Clinical Oncology· 2014Q1

Human Papillomavirus and Overall Survival After Progression of Oropharyngeal Squamous Cell Carcinoma

Carole Fakhry, Qiang Zhang, Phuc Félix Nguyen‐Tan, David I. Rosenthal et al.

Short summary

Patients with HPV-positive oropharyngeal squamous cell carcinoma (OPSCC) have significantly better overall survival (OS) after disease progression compared to those with HPV-negative OPSCC (2-year OS: 54.6% vs. 27.6%).

AI-generated from the title and abstract; the full text is not read.

Key points

  • HPV-positive OPC patients had a 2-year overall survival rate of 54.6% after progression, versus 27.6% for HPV-negative patients.
  • Median survival after progression was 2.6 years for HPV-positive OPC and 0.8 years for HPV-negative OPC (P < .001).
  • HPV (p16-positive) status was an independent predictor of reduced risk of death after progression (HR, 0.48).
  • Receipt of salvage surgery also reduced the risk of death after progression (HR, 0.48).

AI-generated from the title and abstract; the full text is not read.

Abstract

PURPOSE: Risk of cancer progression is reduced for patients with human papillomavirus (HPV) -positive oropharynx cancer (OPC) relative to HPV-negative OPC, but it is unknown whether risk of death after progression is similarly reduced. PATIENTS AND METHODS: Patients with stage III-IV OPC enrolled onto Radiation Therapy Oncology Group trials 0129 or RTOG 0522 who had known tumor p16 status plus local, regional, and/or distant progression after receiving platinum-based chemoradiotherapy were eligible for a retrospective analysis of the association between tumor p16 status and overall survival (OS) after disease progression. Rates were estimated by Kaplan-Meier method and compared by log-rank; hazard ratios (HRs) were estimated by Cox models. Tests and models were stratified by treatment protocol. RESULTS: A total of 181 patients with p16-positive (n = 105) or p16-negative (n = 76) OPC were included in the analysis. Patterns of failure and median time to progression (8.2 v 7.3 months; P = .67) were similar for patients with p16-positive and p16-negative tumors. After a median follow-up period of 4.0 years after disease progression, patients with p16-positive OPC had significantly improved survival rates compared with p16-negative patients (2-year OS, 54.6% v 27.6%; median, 2.6 v 0.8 years; P < .001). p16-positive tumor status (HR, 0.48; 95% CI, 0.31 to 0.74) and receipt of salvage surgery (HR, 0.48; 95% CI; 0.27 to 0.84) reduced risk of death after disease progression whereas distant versus locoregional progression (HR, 1.99; 95% CI, 1.28 to 3.09) increased risk, after adjustment for tumor stage and cigarette pack-years at enrollment. CONCLUSION: Tumor HPV status is a strong and independent predictor of OS after disease progression and should be a stratification factor for clinical trials for patients with recurrent or metastatic OPC.

The authors' abstract, as published at the source. Journal of Clinical Oncology, 2014 · DOI ↗

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Field: Otorhinolaryngology

OtorhinolaryngologyMedicine