Institute for Clinical and Experimental Pathology, ARUP Laboratories, Salt Lake City, UT, USA.
Department of Pathology, University of Utah, Salt Lake City, UT, USA.
Head Neck Pathol. 2021 Jun;15(2):532-536. doi: 10.1007/s12105-020-01240-1. Epub 2020 Oct 31.
Testing for high risk human papillomavirus (HR-HPV) status is standard of care in squamous cell carcinomas of the oropharynx as well as cervical lymph node squamous cell carcinomas of unknown primary origin. DNA or RNA in-situ hybridization (ISH) and p16 immunohistochemistry, widely used currently for HPV detection are operator-dependent. In addition, DNA ISH has a relatively low sensitivity, and p16 is not entirely specific for HR-HPV infection. In this study, we examined the performance of the cobas® HPV genotyping assay in formalin-fixed, paraffin-embedded (FFPE) samples of head and neck squamous cell carcinoma. FFPE samples from head neck and other anatomic sites tested by ISH and p16 for HR-HPV at ARUP Laboratories were selected for this study. Samples were deparaffinized, stained and micro-dissected for tumor contents followed by tissue lysis, then tested with cobas® for HR-HPV. All the samples were also tested by HPV Linear Array for confirmation. All (N = 18) high risk HPV positive specimens tested by cobas® were confirmed as positive by the Linear Array test. All the specimens tested as negative by cobas® were tested as negative (N = 5) or positive only for low risk HPV (N = 3) by Linear Array, as cobas® only detects HR HPV. Limits of detection for HPV16 and 18 were established at 160-320 and 320-1600 copies, respectively. Our data suggest that cobas® HR-HPV genotyping is a viable option for detection of HR-HPV in formalin-fixed, paraffin-embedded samples from head and neck and other anatomic sites and has been validated for clinical use.
检测高危型人乳头瘤病毒(HR-HPV)状态是口咽鳞癌以及原发灶不明的颈部淋巴结鳞状细胞癌的标准治疗方法。目前广泛用于 HPV 检测的 DNA 或 RNA 原位杂交(ISH)和 p16 免疫组化是依赖于操作者的。此外,DNA ISH 的敏感性相对较低,并且 p16 不完全特异于 HR-HPV 感染。在这项研究中,我们研究了 cobas® HPV 基因分型检测在头颈部鳞状细胞癌福尔马林固定、石蜡包埋(FFPE)样本中的性能。ISH 和 p16 检测 HR-HPV 的 ARUP 实验室的头颈部和其他解剖部位的 FFPE 样本被选择用于这项研究。对样本进行脱蜡、染色和肿瘤内容物的微切割,然后进行组织裂解,然后用 cobas® 进行 HR-HPV 检测。所有样本均通过 HPV 线性阵列进行验证。所有(N=18)通过 cobas® 检测为高危 HPV 阳性的标本均通过线性阵列检测确认为阳性。所有通过 cobas® 检测为阴性的标本均通过线性阵列检测为阴性(N=5)或仅为低危 HPV 阳性(N=3),因为 cobas® 仅检测 HR HPV。HPV16 和 18 的检测下限分别设定为 160-320 和 320-1600 拷贝。我们的数据表明,cobas® HR-HPV 基因分型是检测头颈部和其他解剖部位福尔马林固定、石蜡包埋样本中 HR-HPV 的可行选择,并且已经验证可用于临床。