Institute of Otolaryngology, Università Cattolica del Sacro Cuore, Policlinico A. Gemelli, Roma, Italy.
Institute of Microbiology, Università Cattolica del Sacro Cuore, Policlinico A. Gemelli, Roma, Italy.
Int J Radiat Oncol Biol Phys. 2014 Aug 1;89(5):1115-1120. doi: 10.1016/j.ijrobp.2014.04.044. Epub 2014 Jul 8.
Human papillomavirus (HPV) 16 infection is associated with oropharyngeal carcinogenesis and is likely the cause of the reported increase in disease incidence. We evaluated the prevalence of HPV infection and the reliability of different diagnostic tools using primary tumor samples from a cohort of 50 patients.
Formalin-fixed paraffin-embedded (FFPE) tumor samples were collected from all 50 consecutive primary oropharyngeal SCC patients who were enrolled in the study; fresh tumor samples were available in 22 cases. NucliSENS EasyQ HPVv1 was used for RNA, and Digene Hybrid Capture-2(HC2) was used for DNA detection. p16 Expression was evaluated by immunohistochemistry in FPPE specimens.
Based on the DNA detection assay on FFPE samples, the frequency of high-risk HPV infection was 32%. The agreement rate between HPV RNA and HPV DNA detection in fresh samples was 100%. The agreement rate between p16 immunohistochemistry (IHC) and the detection of HPV DNA in the FFPE samples was fair but not excellent (κ = 0.618). HPV DNA detection was highly significant, as measured by disease-specific survival and determined using a Wilcoxon test (P=.001). p16 IHC also exhibited a prognostic value but with a lower statistical significance (P=.0475). The detection of HPV DNA, but not p16 IHC, was also significantly correlated with locoregional control (P=.0461).
Diagnostic methods based on the detection of HPV nucleic acids appear to be more reliable and objective because they do not require reading by a trained histopathologist. Furthermore, the detection of HPV DNA exhibits an improved correlation with survival, and therefore appears definitely more reliable than p16 IHC for routine use in clinical practice.
人乳头瘤病毒(HPV)16 感染与口咽癌的发生有关,可能是导致该病发病率上升的原因。我们评估了 50 例患者队列中原发性肿瘤样本中 HPV 感染的流行率和不同诊断工具的可靠性。
从所有 50 例连续的原发性口咽鳞癌患者中收集福尔马林固定石蜡包埋(FFPE)肿瘤样本;22 例患者有新鲜肿瘤样本。使用 NucliSENS EasyQ HPVv1 进行 RNA 检测,使用 Digene Hybrid Capture-2(HC2)进行 DNA 检测。在 FFPE 标本中通过免疫组化评估 p16 表达。
基于 FFPE 样本的 DNA 检测,高危 HPV 感染的频率为 32%。新鲜样本中 HPV RNA 和 HPV DNA 检测的一致性率为 100%。p16 免疫组化(IHC)与 FFPE 样本中 HPV DNA 检测的一致性率为中度但非极佳(κ=0.618)。HPV DNA 检测具有高度显著性,通过疾病特异性生存进行衡量,并通过 Wilcoxon 检验确定(P=.001)。p16 IHC 也具有预后价值,但统计学意义较低(P=.0475)。HPV DNA 检测而非 p16 IHC 也与局部区域控制显著相关(P=.0461)。
基于 HPV 核酸检测的诊断方法似乎更可靠和客观,因为它们不需要经过训练有素的组织病理学家进行解读。此外,HPV DNA 的检测与生存的相关性得到改善,因此与 p16 IHC 相比,在临床实践中用于常规使用时肯定更可靠。