Department of Otolaryngology-Head and Neck Surgery, Regina Elena National Cancer Institute IRCCS, Rome, Italy.
Department of Sense Organs, Sapienza University of Rome, Rome, Italy.
Laryngoscope. 2022 Mar;132(3):560-568. doi: 10.1002/lary.29739. Epub 2021 Jul 8.
OBJECTIVES/HYPOTHESIS: The aim of this study was to assess the value of cell-free human papillomavirus-DNA (cfHPV-DNA) as a diagnostic test for the post-treatment surveillance of patients with HPV-positive head and neck squamous cell carcinoma (HNSCC) through a systematic review and meta-analysis.
Systematic review and meta-analysis.
A literature search was conducted in three databases (MEDLINE, Embase, and Scopus) in January 2021. The population included patients with HPV-positive HNSCC. The intervention was the use of the repeated liquid biopsy with circulating HPV-DNA detection during follow-up. The outcome was to establish the value of cfHPV-DNA as a diagnostic test for the post-treatment surveillance of patients with HPV-positive HNSCC.
Ten studies included in the meta-analysis provided a total of 457 patients with HPV-positive HNSCC. The meta-analytic study estimated the diagnostic performance of cfHPV-DNA as follows: pooled sensitivity and specificity of 0.65 (95% confidence interval [CI]: 0.40-0.84) and 0.99 (99% CI: 0.96-0.99), respectively; positive and negative likelihood ratios of 62.5 (99% CI: 22.9-170.2) and 0.05 (99% CI: 0.013-0.24), respectively; and pooled diagnostic odds ratio of 371.66 (99% CI: 60.4-2286.7).
Currently, the follow-up protocol for HNSCC patients includes routine clinical evaluation and radiological imaging. Biomarkers to monitor this disease are not established. Considering its high specificity, cfHPV-DNA represents a potential confirmatory test in the case of positive positron emission tomography and computed tomography. In the near future, cfHPV-DNA could be used as a biomarker for monitoring the treatment response during the clinical trials of de-escalation therapy or immunotherapy. Larger sample sizes and the homologation of study protocols and methodology are needed to better establish its utility in the clinical practice. Laryngoscope, 132:560-568, 2022.
目的/假设:本研究旨在通过系统评价和荟萃分析评估游离人乳头瘤病毒 -DNA(cfHPV-DNA)作为 HPV 阳性头颈部鳞状细胞癌(HNSCC)患者治疗后监测的诊断测试的价值。
系统评价和荟萃分析。
2021 年 1 月在三个数据库(MEDLINE、Embase 和 Scopus)中进行了文献检索。研究人群包括 HPV 阳性 HNSCC 患者。干预措施是在随访期间使用循环 HPV-DNA 检测进行重复液体活检。结局是确定 cfHPV-DNA 作为 HPV 阳性 HNSCC 患者治疗后监测的诊断测试的价值。
荟萃分析纳入的 10 项研究共纳入 457 例 HPV 阳性 HNSCC 患者。荟萃分析研究估计 cfHPV-DNA 的诊断性能如下: pooled sensitivity and specificity 分别为 0.65(95%CI:0.40-0.84)和 0.99(99%CI:0.96-0.99);positive and negative likelihood ratios 分别为 62.5(99%CI:22.9-170.2)和 0.05(99%CI:0.013-0.24);pooled diagnostic odds ratio 为 371.66(99%CI:60.4-2286.7)。
目前,HNSCC 患者的随访方案包括常规临床评估和影像学检查。尚未确定用于监测该疾病的生物标志物。考虑到其高特异性,cfHPV-DNA 代表正电子发射断层扫描和计算机断层扫描阳性时的潜在确认性测试。在不久的将来,cfHPV-DNA 可以用作减轻治疗或免疫治疗临床试验中监测治疗反应的生物标志物。需要更大的样本量以及研究方案和方法的标准化,以更好地确定其在临床实践中的应用。喉镜,132:560-568, 2022。