p16 Protein Expression and Human Papillomavirus Status As Prognostic Biomarkers of Nonoropharyngeal Head and Neck Squamous Cell Carcinoma

被引:288
作者
Chung, Christine H. [1 ]
Zhang, Qiang [2 ]
Kong, Christina S.
Harris, Jonathan [2 ]
Fertig, Elana J. [1 ]
Harari, Paul M. [5 ]
Wang, Dian [6 ]
Redmond, Kevin P. [7 ]
Shenouda, George [9 ]
Trotti, Andy [10 ]
Raben, David [11 ]
Gillison, Maura L. [8 ]
Jordan, Richard C. [4 ]
Quynh-Thu Le [3 ]
机构
[1] Johns Hopkins Univ, Baltimore, MD 21287 USA
[2] Radiat Therapy Oncol Grp Stat Ctr, Philadelphia, PA USA
[3] Stanford Univ, Stanford, CA 94305 USA
[4] Univ Calif San Francisco, San Francisco, CA 94143 USA
[5] Univ Wisconsin, Carbone Canc Ctr, Madison, WI 53706 USA
[6] Med Coll Wisconsin, Milwaukee, WI 53226 USA
[7] Univ Cincinnati, Cincinnati, OH USA
[8] Ohio State Univ, Columbus, OH 43210 USA
[9] McGill Univ, Ctr Hlth, Montreal, PQ, Canada
[10] H Lee Moffitt Canc Ctr & Res Inst, Tampa, FL USA
[11] Univ Colorado, Denver, CO 80202 USA
关键词
SUPPRESSOR GENE-PRODUCT; PHASE-III TRIAL; OROPHARYNGEAL CANCER; CYCLE CONTROL; ORAL TONGUE; HPV STATUS; RISK; TUMOR; P16(INK4A); SURVIVAL;
D O I
10.1200/JCO.2013.54.5228
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Although p16 protein expression, a surrogate marker of oncogenic human papillomavirus (HPV) infection, is recognized as a prognostic marker in oropharyngeal squamous cell carcinoma (OPSCC), its prevalence and significance have not been well established in cancer of the oral cavity, hypopharynx, or larynx, collectively referred as non-OPSCC, where HPV infection is less common than in the oropharynx. Patients and Methods p16 expression and high-risk HPV status in non-OPSCCs from RTOG 0129, 0234, and 0522 studies were determined by immunohistochemistry (IHC) and in situ hybridization (ISH). Hazard ratios from Cox models were expressed as positive or negative, stratified by trial, and adjusted for clinical characteristics. Results p16 expression was positive in 14.1% (12 of 85), 24.2% (23 of 95), and 19.0% (27 of 142) and HPV ISH was positive in 6.5% (six of 93), 14.6% (15 of 103), and 6.9% (seven of 101) of non-OPSCCs from RTOG 0129, 0234, and 0522 studies, respectively. Hazard ratios for p16 expression were 0.63 (95% CI, 0.42 to 0.95; P = .03) and 0.56 (95% CI, 0.35 to 0.89; P = .01) for progression-free (PFS) and overall survival (OS), respectively. Comparing OPSCC and non-OPSCC, patients with p16-positive OPSCC have better PFS and OS than patients with p16-positive non-OPSCC, but patients with p16-negative OPSCC and non-OPSCC have similar outcomes. Conclusion Similar to results in patients with OPSCC, patients with p16-negative non-OPSCC have worse outcomes than patients with p16-positive non-OPSCC, and HPV may also have a role in outcome in a subset of non-OPSCC. However, further development of a p16 IHC scoring system in non-OPSCC and improvement of HPV detection methods are warranted before broad application in the clinical setting. (C) 2014 by American Society of Clinical Oncology
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收藏
页码:3930 / U212
页数:15
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