High-risk human papillomavirus affects prognosis in patients with surgically treated oropharyngeal squamous cell carcinoma

被引:501
|
作者
Licitra, Lisa
Perrone, Federica
Bossi, Paolo
Suardi, Simona
Mariani, Luigi
Artusi, Raffaella
Oggionni, Maria
Rossini, Chiara
Cantu, Giulio
Squadrelli, Massimo
Quattrone, Pasquale
Locati, Laura D.
Bergamini, Cristiana
Olmi, Patrizia
Pierotti, Marco A.
Pilotti, Silvana
机构
[1] Ist Nazl Studio & Cura Tumori, Dept Canc Med, Head & Neck Canc Med Oncol Unit, I-20133 Milan, Italy
[2] Ist Nazl Studio & Cura Tumori, Unit Expt Mol Pathol Med Stat & Biometry, I-20133 Milan, Italy
[3] Ist Nazl Studio & Cura Tumori, Dept Head & Neck Surg, I-20133 Milan, Italy
[4] Ist Nazl Studio & Cura Tumori, Dept Pathol, I-20133 Milan, Italy
[5] Ist Nazl Studio & Cura Tumori, Dept Expt Oncol, I-20133 Milan, Italy
[6] FIRC, Inst Mol Oncol, Milan, Italy
关键词
D O I
10.1200/JCO.2005.04.6136
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Human papillomavirus (HPV) DNA tumors actively integrating the E6 and E7 oncogenes have a distinct biologic behavior resulting in a more favorable prognosis. To which extent the viral integration by itself, and/or the associated wild-type (wt) TP53 status, and/or a functional p16 contribute to prognosis is unclear. Patients and Methods To clarify how the presence of high-risk (HR)-HPV, TP53, and p16(INK4a) status interact with clinical outcome, we considered a retrospective series of 90 consecutive oropharyngeal cancer patients treated primarily with surgery. Results Seventeen (19%) patients showed integrated HPV 16 DNA (HPV positive), wt TP53 in all but two patients, normal p16(INK4a) in 15 assessable patients, and p16 expression in all 17 patients. Thirty-five patients (39%), two of whom were HPV positive, harbored TP53 mutations. p16(INK4a) deletion and p16 null immunophenotype occurred in 28 and 58 patients, respectively, and was similarly distributed in both patients with mutated TP53 (48% and 82%, respectively) and in patients with wt TP53 (46% and 77%, respectively). Statistical analysis showed that HPV-positive status significantly affects all investigated end points: overall survival (P = .0018), incidence of tumor relapse (P = .0371), and second tumor (P = .0152), whereas TP53 and p16(INK4a) status and p16 expression were not prognostic by themselves. Conclusion Our molecular and clinical results are in agreement with previous findings but provide additional information into the biologic mechanisms involved in HR-HPV oropharyngeal cancer in comparison to HPV-negative tumors. According to the reduced risk of relapse and second tumors associated with HR-HPV positivity of oropharyngeal cancer, the therapeutic strategy and follow-up procedures should be reviewed.
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收藏
页码:5630 / 5636
页数:7
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