Molecular classification identifies a subset of human papillomavirus-associated oropharyngeal cancers with favorable prognosis

被引:599
作者
Weinberger, PM
Yu, ZW
Haffty, BG
Kowalski, D
Harigopal, M
Brandsma, J
Sasaki, C
Joe, J
Camp, RL
Rimm, DL
Psyrri, A
机构
[1] Yale Univ, Sch Med, Dept Med Oncol, New Haven, CT USA
[2] Yale Univ, Sch Med, Dept Otolaryngol Therapeut Radiol, New Haven, CT USA
[3] Yale Univ, Sch Med, Dept Pathol, New Haven, CT USA
[4] Yale Univ, Sch Med, Dept Comparat Anat, New Haven, CT USA
关键词
D O I
10.1200/JCO.2004.00.3335
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose We sought to determine the prevalence of biologically relevant human papillomavirus (HPV) in oropharyngeal squamous cell carcinoma (OSCC). Retinoblastoma (Rb) downregulation by HPV E7 results in p16 upregulation. We hypothesized that p16 overexpression in OSCC defines HPV-induced tumors with favorable prognosis. Methods Using real-time polymerase chain reaction for HPV16, we determined HPV16 viral load in a cohort of 79 OSCCs annotated with long-term patient follow-up. A tissue microarray including these cases was also analyzed for p53, p16, and Rb utilizing in situ quantitative protein expression analysis. Seventy-seven tumors were classified into a three-class model on the basis of p16 expression and HPV-DNA presence: class I, HPV-, p16 low; class II, HPV+, p16 low; and class III, HPV+, p16 high. Results Sixty-one percent of OSCCs were HPV16+; HPV status alone was of no prognostic value for local recurrence and was barely significant for survival times. Overall survival was improved in class III (79%) compared with the other two classes (20% and 18%; P =.0095). Disease-free survival for the same class was 75% versus 15% and 13% (P =.0025). The 5-year local recurrence was 14% in class III versus 45% and 74% (P =.03). Only patients in class III had significantly lower p53 and Rb expression (P =.017 and .001, respectively). Multivariable survival analysis confirmed the prognostic value of the three-class model. Conclusion Using this system for classification, we define the molecular profile of HPV+ OSCC with favorable prognosis, namely HPV+/p16 high (class 111). This study defines a novel classification scheme that may have value for patient stratification for clinical trials testing HPV-targeted therapies.
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页码:736 / 747
页数:12
相关论文
共 42 条
[1]   p16INK4a expression correlates with degree of cervical neoplasia:: A comparison detection of high-risk with Ki-67 expression and HPV types [J].
Agoff, SN ;
Lin, P ;
Morihara, J ;
Mao, C ;
Kiviat, NB ;
Koutsky, LA .
MODERN PATHOLOGY, 2003, 16 (07) :665-673
[2]   Human papillomaviruses and associated malignancies [J].
Alani, RM ;
Münger, K .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (01) :330-337
[3]   Involvement of the cyclin-dependent kinase inhibitor p16 (INK4a) in replicative senescence of normal human fibroblasts [J].
Alcorta, DA ;
Xiong, Y ;
Phelps, D ;
Hannon, G ;
Beach, D ;
Barrett, JC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (24) :13742-13747
[4]  
Andl T, 1998, CANCER RES, V58, P5
[5]  
Begum S, 2003, CLIN CANCER RES, V9, P6469
[6]   Genetic patterns in head and neck cancers that contain or lack transcriptionally active human papillomavirus [J].
Braakhuis, BJM ;
Snijders, PJF ;
Keune, WJH ;
Meijer, CJLM ;
Ruijter-Schippers, HJ ;
Leemans, CR ;
Brakenhoff, RH .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2004, 96 (13) :998-1006
[7]  
BRANDWEIN M, 1994, MODERN PATHOL, V7, P720
[8]   RATES OF P16(MTS1) MUTATIONS IN PRIMARY TUMORS WITH 9P LOSS [J].
CAIRNS, P ;
MAO, L ;
MERLO, A ;
LEE, DJ ;
SCHWAB, D ;
EBY, Y ;
TOKINO, K ;
VANDERRIET, P ;
BLAUGRUND, JE ;
SIDRANSKY, D .
SCIENCE, 1994, 265 (5170) :415-416
[9]   Automated subcellular localization and quantification of protein expression in tissue microarrays [J].
Camp, RL ;
Chung, GG ;
Rimm, DL .
NATURE MEDICINE, 2002, 8 (11) :1323-1327
[10]  
COOMS NJ, 1999, NUCLEIC ACIDS RES, V27, P15