Prognostic Role of p16 in Nonoropharyngeal Head and Neck Cancer

被引:44
作者
Bryant, Alex K. [1 ]
Sojourner, Elena J. [1 ]
Vitzthum, Lucas K. [1 ]
Zakeri, Kaveh [1 ]
Shen, Hanjie [2 ]
Nguyen, Cammie [3 ]
Murphy, James D. [1 ]
Califano, Joseph A. [4 ]
Cohen, Ezra E. W. [5 ]
Mell, Loren K. [1 ]
机构
[1] Univ Calif San Diego, Dept Radiat Med & Appl Sci, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Family Med & Publ Hlth, Div Biostat & Bioinformat, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Moores Canc Ctr, La Jolla, CA 92093 USA
[4] Univ Calif San Diego, Dept Surg, Div Otolaryngol, La Jolla, CA 92093 USA
[5] Univ Calif San Diego, Dept Med, Div Hematol & Oncol, La Jolla, CA 92093 USA
来源
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE | 2018年 / 110卷 / 12期
基金
美国国家卫生研究院;
关键词
SQUAMOUS-CELL CARCINOMA; HUMAN-PAPILLOMAVIRUS INFECTION; POSITIVE HEAD; OROPHARYNGEAL; SURVIVAL; EXPRESSION; MORTALITY; LARYNX; DEATH; STAGE;
D O I
10.1093/jnci/djy072
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Previous studies have reported conflicting information regarding the prognostic role of p16 in nonoropharyngeal head and neck squamous cell carcinoma (HNSCC). Methods: Using the US Veterans Affairs database, we analyzed 1448 patients with locoregionally advanced HNSCC and known p16 status diagnosed between 2005 and 2015 and treated with surgery, radiotherapy, or chemoradiotherapy. Tumor p16 status was determined through manual review of pathology reports of primary tumor specimens. Oropharyngeal (n = 1061) or nonoropharyngeal (n = 387; hypopharyngeal, laryngeal, or oral cavity) tumor site was determined from tumor registry data and manually reviewed for accuracy. We used multivariable Cox regression to analyze the effect of p16 status on overall survival (OS), cancer-specific survival (CSS), and competing mortality (CM) for oropharyngeal or nonoropharyngeal tumor sites. All statistical tests were two-sided. Results: In multivariable models adjusting for treatment, stage, age, comorbidity, and body mass index, patients with p16-positive tumors had improved OS, CSS, and CM compared with patients with p16-negative tumors in both oropharyngeal (OS: hazard ratio [HR] = 0.53, 95% confidence interval [CI] = 0.40 to 0.71, P < .001; CSS: HR = 0.50, 95% CI = 0.35 to 0.73, P < .001; CM: HR = 0.59, 95% CI = 0.38 to 0.93, P = .02) and nonoropharyngeal primary sites (OS: HR = 0.41, 95% CI = 0.25 to 0.69, P < .001; CSS: HR = 0.37, 95% CI = 0.18 to 0.77, P = .008; CM: HR = 0.46, 95% CI = 0.23 to 0.95, P = .04). The prognostic impact of p16 status did not statistically significantly differ by primary tumor site for OS, CSS, or CM (P-interaction > .05). Conclusions: Our findings support the hypothesis that p16 has a similar prognostic role in both nonoropharyngeal and oropharyngeal cancer. Consideration should be given to increased testing for p16 in laryngeal, hypopharyngeal, and oral cavity primaries.
引用
收藏
页码:1393 / 1399
页数:7
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