Department of Otorhinolaryngology, Head and Neck Surgery, LMU Klinikum, Munich, Germany.
German Cancer Consortium (DKTK), Partner Site Munich, Munich, Germany.
Clin Otolaryngol. 2024 Jul;49(4):384-403. doi: 10.1111/coa.14161. Epub 2024 Apr 24.
About 17% of patients with human papillomavirus (HPV)-positive head and neck squamous cell carcinoma (HNSCC), which is mainly comprised of oropharyngeal SCC (OPSCC), will experience disease recurrence, which is often considered incurable when manifested at a metastatic and/or recurrent stage. We conducted a critical qualitative systematic review. Our objectives were to provide an overview of the molecular landscape of recurrent/metastatic HPV-positive HNSCC as well as novel molecular biomarkers.
A literature review was conducted to identify studies reporting on the molecular characteristics of recurrent/metastatic HPV-positive HNSCC, novel molecular biomarkers and treatment options. The reviews of abstracts, full articles, and revision of the included studies, followed by data extraction and quality assessment were performed by three independent assessors. All primary literature, such as retrospective, prospective, and clinical trials as well as basic research studies were considered, and the final search was conducted at the end of February 2023. The level of evidence was rated using the guidelines published by the Oxford Centre for Evidence-based Medicine and quality was assessed using the Newcastle-Ottawa Scale criteria.
The literature search resulted in the identification of 1991 articles. A total of 181 full articles were screened, and 66 articles were included in this analysis. Several studies reported that recurrent/metastatic HPV-positive HNSCC had higher rates of TP53 mutation and were genomically similar to HPV-negative HNSCC. The detection of circulating tumour tissue-modified HPV DNA (ctHPVDNA) as a specific biomarker has shown promising results for monitoring treatment response and recurrence in the subset of HPV-positive HNSCC. In addition, evidence for targeted therapy in recurrent/metastatic HPV-positive HNSCC has emerged, including agents that inhibit overexpressed EGFR. Studies of combination immunotherapy are also underway. Our review outlines the latest evidence on the distinct molecular profiles of recurrent/metastatic HPV-positive HNSCC as well as the clinical potential of ctHPVDNA testing in routine practice. More controlled and longitudinal studies are needed to identify additional molecular targets and to assess the performance and benefits of novel molecular biomarkers in clinical practice.
人乳头瘤病毒 (HPV) 阳性头颈部鳞状细胞癌 (HNSCC) 患者约有 17%会出现疾病复发,而 HPV 阳性口咽鳞状细胞癌 (OPSCC) 主要包含在其中,当疾病处于转移和/或复发阶段时,通常被认为是无法治愈的。我们进行了一项关键性的定性系统评价。我们的目的是提供 HPV 阳性复发性/转移性 HNSCC 的分子特征概述以及新型分子生物标志物。
进行文献综述以确定报告 HPV 阳性复发性/转移性 HNSCC 的分子特征、新型分子生物标志物和治疗选择的研究。三位独立评估员对摘要、全文的回顾以及纳入研究的修订、随后的数据提取和质量评估进行了评估。所有主要文献,如回顾性、前瞻性和临床试验以及基础研究都被考虑在内,最终的搜索是在 2023 年 2 月底进行的。证据水平使用牛津循证医学中心发布的指南进行评级,质量使用纽卡斯尔-渥太华量表标准进行评估。
文献检索共确定了 1991 篇文章。共筛选了 181 篇全文,其中 66 篇文章纳入本分析。几项研究报告称,HPV 阳性复发性/转移性 HNSCC 的 TP53 突变率更高,并且在基因组上与 HPV 阴性 HNSCC 相似。检测循环肿瘤组织修饰的 HPV DNA(ctHPVDNA)作为一种特定的生物标志物,已显示出在 HPV 阳性 HNSCC 亚组中监测治疗反应和复发的良好结果。此外,针对复发性/转移性 HPV 阳性 HNSCC 的靶向治疗证据已经出现,包括抑制过表达 EGFR 的药物。联合免疫疗法的研究也在进行中。本综述概述了 HPV 阳性复发性/转移性 HNSCC 独特分子谱的最新证据,以及在常规实践中使用 ctHPVDNA 检测的临床潜力。需要更多的对照和纵向研究来确定其他分子靶点,并评估新型分子生物标志物在临床实践中的性能和益处。