Biomarkers of HPV in Head and Neck Squamous Cell Carcinoma

被引:94
作者
Liang, Caihua [1 ]
Marsit, Carmen J. [3 ,4 ]
McClean, Michael D. [5 ]
Nelson, Heather H. [11 ]
Christensen, Brock C. [3 ,4 ]
Haddad, Robert I. [6 ]
Clark, John R. [7 ]
Wein, Richard O. [8 ]
Grillone, Gregory A. [9 ]
Houseman, E. Andres [12 ]
Halec, Gordana [13 ]
Waterboer, Tim [13 ]
Pawlita, Michael [13 ]
Krane, Jeffrey F. [10 ]
Kelsey, Karl T. [1 ,2 ]
机构
[1] Brown Univ, Dept Epidemiol, Providence, RI 02912 USA
[2] Brown Univ, Dept Pathol & Lab Med, Div Biol & Med, Providence, RI 02912 USA
[3] Dartmouth Coll, Hitchcock Med Ctr, Dartmouth Med Sch, Dept Pharmacol & Toxicol, Hanover, NH 03756 USA
[4] Dartmouth Coll, Hitchcock Med Ctr, Dartmouth Med Sch, Dept Community & Family Med, Hanover, NH 03756 USA
[5] Boston Univ, Dept Environm Hlth, Sch Publ Hlth, Boston, MA 02215 USA
[6] Dana Farber Canc Inst, Dept Med Oncol Solid Tumor Oncol, Boston, MA USA
[7] Massachusetts Gen Hosp, Dept Med Hematol Oncol, Boston, MA 02114 USA
[8] Tufts Med Ctr, Dept Otolaryngol Head & Neck Surg, Boston, MA USA
[9] Boston Univ, Dept Otolaryngol Head & Neck Surg, Med Ctr, Boston, MA USA
[10] Brigham & Womens Hosp, Dept Pathol, Boston, MA 02115 USA
[11] Univ Minnesota, Masonic Canc Ctr, Div Epidemiol & Community Hlth, Minneapolis, MN USA
[12] Oregon State Univ, Coll Publ Hlth & Human Sci, Corvallis, OR 97331 USA
[13] Deutsch Krebsforschungszentrum, Infect & Canc Program, German Canc Res Ctr, D-6900 Heidelberg, Germany
关键词
HUMAN-PAPILLOMAVIRUS INFECTION; GLUTATHIONE-S-TRANSFERASE; PROGNOSTIC-SIGNIFICANCE; NATURAL-HISTORY; SEXUAL-BEHAVIOR; ORAL-CANCER; P16; PROTEIN; SURVIVAL; ANTIBODIES; EXPRESSION;
D O I
10.1158/0008-5472.CAN-11-3277
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Human papillomavirus (HPV) is an accepted cause of head and neck squamous cell carcinoma (HNSCC), and patients with HPV-associated HNSCC have a favorable prognosis. Currently, there is no general guidance on the most appropriate biomarkers for clinical assessment of HPV in these malignancies. We compared PCR-based and serologic HPV assays, as well as p16 immunohistochemistry, individually and in combination in a single population-based study to assess their associations with overall survival among patients with HNSCC, and thus their potential value as biomarkers. HPV16 serology was determined for 488 patients; immunohistochemical detection of p16 expression in tumors was conducted in a subset of 233 cases, and PCR-based methods to assess the presence of HPV16 DNA in a subset of 179 cases of tumors. Considering each biomarker individually in the subset of patients studied for all endpoints, seropositivity for the E6 and E7 proteins was significantly associated with enhanced all-cause survival in oropharyngeal disease [HRE6/E7+ = 0.1, 95% confidence interval (CI) = 0.02-0.3]. Neither the presence of HPV16 DNA nor p16 immunostaining was associated with significant enhanced overall survival in oropharyngeal disease (HRDNA = 0.9, 95% CI = 0.3-2.9; HRp16 = 0.3, 95% CI = 0.1-1.1). However, the combination of HPV-positive DNA and E6 or E7 serology was associated with enhanced overall survival in oropharyngeal disease (HRDNA+/E6/E7+ = 0.1, 95% CI = 0.02-1.0), whereas E6/E7 seronegative patients with evidence of HPV in tumor DNA did not show any evidence of favorable survival (HRDNA+/E6-/E7- = 3.4, 95% CI = 0.6-18.1). Furthermore, patients with p16 staining and E6 or E7 seropositivity had favorable survival from oropharyngeal disease (HRp16+/E6/E7+ = 0.1, 95% CI = 0.02-0.4), whereas patients who were p16 positive and E6/E7 seronegative had significantly increased hazard of all causes of death (HRp16+/E6-/E7- = 3.1, 95% CI = 1.2-7.7). A stronger association of HPV presence with prognosis (assessed by all-cause survival) is observed when "HPV-associated" HNSCC is defined using tumor status (HPV DNA status or P16) and HPV E6/E7 serology in combination rather using tumor HPV status alone. Cancer Res; 72(19); 5004-13. (C)2012 AACR.
引用
收藏
页码:5004 / 5013
页数:10
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