Department of Otolaryngology/Head and Neck Surgery, VU University Medical Center, Amsterdam.
Ann Oncol. 2013 Nov;24(11):2740-5. doi: 10.1093/annonc/mdt319. Epub 2013 Aug 14.
The presence of human papillomavirus (HPV)-infection in oropharyngeal squamous cell carcinoma (OPSCC) is a major determinant in prognostic risk modeling. However, most risk models are based on clinical trials which only include a selected patient population. The clinical significance of HPV and other prognostic factors in patients with OPSCC remains to be evaluated in a large, unselected cohort, which also includes patients with stage I/II disease and patients with severe comorbidity.
All patients diagnosed with OPSCC in 2000-2006 in two Dutch university hospitals were included. The presence of an oncogenic HPV infection was determined by p16-immunostaining, followed by a high-risk HPV general primer 5+/6+ DNA PCR on the p16-positive cases. Cox regression analysis was carried out to compare survival rates between HPV-positive and HPV-negative patients and a prognostic model was generated by recursive partitioning.
In total, 163 of 841 (19.4%) tumors were HPV-positive. Patients with HPV-positive OPSCC had a more favorable overall survival [73.5% versus 40.9% after 5 years; P < 0.001; hazard ratio = 0.34, 95% confidence interval (CI) 0.25-0.48] compared with patients with HPV-negative OPSCC. Patients with p16-positive but HPV DNA-negative tumors showed a significantly less favorable survival than patients with p16-positive and HPV DNA-positive tumors (P < 0.001). A prognostic model was developed in which patients were classified into three risk groups according to HPV status, nodal stage and comorbidity. [Harrell's concordance index of 0.68 (95% CI 0.65-0.71)].
Tumor HPV status is a strong and independent prognostic factor for survival among patients with OPSCC. A prognostic risk model was proposed, based on our large, unselected cohort of patients with HPV status, comorbidity and nodal stage being the important prognostic factors. In addition, this study emphasizes the importance of performing an HPV DNA-specific test besides p16-immunostaining.
人乳头瘤病毒(HPV)感染在口咽鳞状细胞癌(OPSCC)中的存在是预后风险建模的主要决定因素。然而,大多数风险模型都是基于临床试验,这些试验仅包括选定的患者群体。HPV 以及其他预后因素在 OPSCC 患者中的临床意义仍需在一个大型、未选择的队列中进行评估,该队列还包括 I/II 期疾病患者和患有严重合并症的患者。
纳入了 2000-2006 年在荷兰两所大学医院诊断为 OPSCC 的所有患者。通过 p16 免疫染色确定致癌 HPV 感染的存在,然后对 p16 阳性病例进行高危 HPV 通用引物 5+/6+DNA PCR。进行 Cox 回归分析以比较 HPV 阳性和 HPV 阴性患者的生存率,并通过递归分区生成预后模型。
在总共 841 例肿瘤中,有 163 例(19.4%)为 HPV 阳性。HPV 阳性 OPSCC 患者的总生存率更高[5 年后分别为 73.5%和 40.9%;P<0.001;风险比=0.34,95%置信区间(CI)0.25-0.48],与 HPV 阴性 OPSCC 患者相比。p16 阳性但 HPV DNA 阴性肿瘤患者的生存明显不如 p16 阳性和 HPV DNA 阳性肿瘤患者(P<0.001)。根据 HPV 状态、淋巴结分期和合并症,开发了一种预后模型,将患者分为三个风险组。[Harrell 一致性指数为 0.68(95%CI 0.65-0.71)]。
肿瘤 HPV 状态是 OPSCC 患者生存的一个强有力且独立的预后因素。提出了一种预后风险模型,该模型基于我们的大型、未选择的 HPV 状态、合并症和淋巴结分期的患者队列,这些是重要的预后因素。此外,这项研究强调了除了 p16 免疫染色外,还进行 HPV DNA 特异性检测的重要性。