Krasniqi Eriseld, Barba Maddalena, Venuti Aldo, Pizzuti Laura, Cappuzzo Federico, Landi Lorenza, Carpano Silvia, Marchetti Paolo, Villa Alice, Vizza Enrico, Giuliano Greta, Mazzotta Marco, Marinelli Daniele, Gnignera Sandra, Vincenzoni Cristina, Stranges Vincenzo, Sergi Domenico, Giordano Antonio, Tomao Federica, Maugeri-Saccà Marcello, Sanguineti Giuseppe, Di Lisa Francesca Sofia, Tomao Silverio, Ciliberto Gennaro, Vici Patrizia
Division of Medical Oncology 2, IRCCS Regina Elena National Cancer Institute, 00144 Rome, Italy.
HPV-UNIT-UOSD Tumor Immunology and Immunotherapy, IRCCS Regina Elena National Cancer Institute, 00144 Rome, Italy.
J Clin Med. 2021 Apr 6;10(7):1525. doi: 10.3390/jcm10071525.
Human papillomaviruses (HPVs) are associated with invasive malignancies, including almost 100% of cervical cancers (CECs), and 35-70% of oropharyngeal cancers (OPCs). HPV infection leads to clinical implications in related tumors by determining better prognosis and predicting treatment response, especially in OPC. Currently, specific and minimally invasive tests allow for detecting HPV-related cancer at an early phase, informing more appropriately therapeutical decisions, and allowing for timely disease monitoring. A blood-based biomarker detectable in liquid biopsy represents an ideal candidate, and the use of circulating HPV DNA (ct-DNA) itself could offer the highest specificity for such a scope. Circulating HPV DNA is detectable in the greatest part of patients affected by HPV-related cancers, and studies have demonstrated its potential usefulness for CEC and OPC clinical management. Unfortunately, when using conventional polymerase chain reaction (PCR), the detection rate of serum HPV DNA is low. Innovative techniques such as droplet-based digital PCR and next generation sequencing are becoming increasingly available for the purpose of boosting HPV ct-DNA detection rate. We herein review and critically discuss the most recent and representative literature, concerning the role of HPV ctDNA in OPC and CEC in the light of new technologies that could improve the potential of this biomarker in fulfilling many of the unmet needs in the clinical management of OPC and CEC patients.
人乳头瘤病毒(HPV)与侵袭性恶性肿瘤相关,包括几乎100%的宫颈癌(CEC)以及35%-70%的口咽癌(OPC)。HPV感染通过确定更好的预后和预测治疗反应,对相关肿瘤产生临床影响,尤其是在口咽癌中。目前,特异性和微创检测能够在早期检测出HPV相关癌症,为治疗决策提供更合适的信息,并实现对疾病的及时监测。在液体活检中可检测到的基于血液的生物标志物是一个理想的候选者,而循环HPV DNA(ct-DNA)本身在此方面可能具有最高的特异性。在受HPV相关癌症影响的大部分患者中都可检测到循环HPV DNA,并且研究已证明其在宫颈癌和口咽癌临床管理中的潜在用途。不幸的是,使用传统聚合酶链反应(PCR)时,血清HPV DNA的检测率较低。诸如基于微滴的数字PCR和下一代测序等创新技术正越来越多地用于提高HPV ct-DNA的检测率。我们在此回顾并批判性地讨论最新的代表性文献,鉴于新技术可以提高这种生物标志物在满足口咽癌和宫颈癌患者临床管理中许多未满足需求方面的潜力,探讨HPV ctDNA在口咽癌和宫颈癌中的作用。