PO.CL01.09 · 临床研究
基于液体活检监测HPV阳性口咽癌(OPSCC)患者的疾病状态
Liquid biopsy-based monitoring of disease status in patients with HPV-positive oropharyngeal carcinoma (OPSCC)
作者与单位 Authors & Affiliations
摘要 Abstract
中文摘要
引言:HPV相关口咽癌(HPV+ OPSCC)的发病率在全球范围内不断上升。在肿瘤复发病例中,远处转移往往已经存在,这使得根治性肿瘤治疗变得复杂。因此,收集分子参数以监测患者对治疗的反应至关重要。
材料/方法:本研究旨在建立一种HPV特异性的血液分析(液体活检),以实现早期诊断和疾病进展监测。为此,我们的临床生物库纳入了来自>300名HPV相关OPSCC患者的>1800份循环肿瘤DNA(ct-DNA)样本,采集时点涵盖初诊时、肿瘤治疗期间、作为临床随访诊疗的一部分以及肿瘤复发时。
结果:在来自53名HPV+ OPSCC患者的434份纵向采集的ctDNA样本队列中,进行了定量PCR(qPCR)和数字微滴PCR(ddPCR),探测E6 HPV-16 DNA序列。在所有病例中,HPV状态均通过p16-IHC、针对E6和L1的HPV16 DNA PCR以及肿瘤中病毒载量的测定得到确认。基于qPCR和ddPCR的HPV E6检测之间具有高度一致性(P<0.001),其中ddPCR产生更高的灵敏度和特异性(>80%)。HPV-16 ctDNA水平与肿瘤分期和肿瘤体积显著相关(P<0.05)。在个别病例中,阳性HPV ctDNA信号可在肿瘤复发诊断前数月被检测到。
讨论:基于ddPCR对血液中ct-HPV16-E6 DNA的定量是一种有前景的诊断方法,可监测HPV+ OPSCC患者的治疗反应和肿瘤进展。有必要开展前瞻性临床研究,以临床验证ct-HPV16-E6 DNA作为治疗疗效和纵向疾病监测的定量生物标志物。
查看英文原文 English abstract
Introduction: The incidence of HPV-associated oropharyngeal carcinoma (HPV+ OPSCC) is increasing worldwide. In cases of tumor recurrence, distant metastases are often already present, which complicates curative tumor treatment. It is therefore of highly critical to collect molecular parameters to monitor the response of patients to therapy.
Material/Method: The aim of this study is to establish an HPV-specific blood-based analysis (liquid biopsy) to enable both early diagnosis and monitoring of disease progression. To this end, our clinical biobank includes >1800 circulating tumor DNA (ct-DNA) samples from> 300 patients with HPV-associated OPSCC at the time of initial diagnosis, during tumor treatment, as part of clinical follow-up care, and in the event of tumor recurrence.
Results: In a cohort of 434 longitudinally collected ctDNA samples from 53 patients with HPV+ OPSCC quantitative PCR (qPCR) and digital droplet PCR (ddPCR) was performed probing for E6 HPV-16 DNA sequences. In all cases, the HPV status was confirmed by p16-IHC, HPV16 DNA PCR for E6 and L1, and determination of the viral load in the tumor. There was a high concordance between qPCR- and ddPCR-based detection of HPV E6 (P<0.001), with ddPCR yielding higher sensitivity and specificity (>80%). HPV-16 ctDNA levels significantly correlated with tumor stage and tumor volume (P<0.05). In individual cases, a positive HPV ctDNA signal could be determined months before the diagnosis of tumor recurrence.
Discussion: ddPCR-based quantification of ct-HPV16-E6 DNA in blood is a promising diagnostic method to monitor therapy response and tumor progression in patients with HPV+ OPSCC. Prospective clinical studies are warranted to clinically validate ct-HPV16-E6 DNA as a quantitative biomarker for therapeutic efficacy and longitudinal disease monitoring.
利益披露 Disclosure
J. P. Klussmann, None..
O. Siefer, None..
Z. M. Uzun, None..
J. Johannsen, None..
D. Firmenich, None..
N. Wuerdemann, None..
E. J. Speel, None.