Echevarria Michelle, Park Robin, Caudell Jimmy J, Kim Youngchul, Yang George Q, Kirtane Kedar, Chaudhary Ritu, Kumar Sunil, Amelio Antonio L, Giuliano Anna R, Chung Christine H
Department of Radiation Oncology, Moffitt Cancer Center, Tampa, Florida.
Department of Head and Neck-Endocrine Oncology, Moffitt Cancer Center, Tampa, Florida.
Cancer Res Commun. 2025 Jul 1;5(7):1194-1202. doi: 10.1158/2767-9764.CRC-25-0180.
Dynamic biomarkers that guide de-escalation strategies in human papillomavirus (HPV)-related oropharyngeal squamous cell carcinoma (OPSCC) remain an unmet need. In this study, we evaluated the kinetics of plasma cell-free HPV (cfHPV) DNA and oral gargle HPV DNA during radiotherapy in patients with low-risk HPV-related OPSCC. Data were obtained from a trial evaluating an adaptive model optimizing radiation fractionation in patients with low-risk (T0-2N0-1M0) HPV-related OPSCC undergoing radiotherapy. The primary objective was to determine whether week 4 plasma cfHPV DNA or oral gargle HPV DNA clearance is associated with reduction of target tumor volume (TTV) at week 4. A total of 325 plasma and 334 oral gargle samples from 50 patients with available baseline samples were analyzed. Higher baseline plasma cfHPV DNA was associated with higher nodal staging (P = 0.002), whereas oral gargle HPV DNA was detected more frequently in the tonsil or soft palate than occult or base of tongue primary tumors (P = 0.039). Week 4 plasma but not oral gargle HPV DNA clearance was associated with higher reduction of TTV at week 4 (P = 0.0063). Whereas week 4 plasma and oral gargle HPV DNA clearance was not associated with progression-free survival, a lower baseline plasma cfHPV DNA was associated with superior progression-free survival (P = 0.027). Week 4 plasma cfHPV DNA clearance aligns with reduction in TTV, and future studies are warranted to determine the role of early plasma cfHPV DNA clearance in biomarker-adapted de-escalation strategies.
Our findings may inform appropriate patient selection for low-risk HPV-related OPSCC based on cfHPV DNA in future deintensification studies, aimed at preventing or minimizing treatment-related toxicities in patients who may have lower risk of recurrence.
在人乳头瘤病毒(HPV)相关的口咽鳞状细胞癌(OPSCC)中,指导降阶梯治疗策略的动态生物标志物仍是未满足的需求。在本研究中,我们评估了低风险HPV相关OPSCC患者放疗期间血浆游离HPV(cfHPV)DNA和口腔含漱液HPV DNA的动力学。数据来自一项评估适应性模型优化低风险(T0-2N0-1M0)HPV相关OPSCC放疗患者分次放疗的试验。主要目的是确定第4周血浆cfHPV DNA或口腔含漱液HPV DNA清除是否与第4周靶肿瘤体积(TTV)的减小相关。对50例有可用基线样本患者的325份血浆和334份口腔含漱液样本进行了分析。较高的基线血浆cfHPV DNA与较高的淋巴结分期相关(P = 0.002),而口腔含漱液HPV DNA在扁桃体或软腭中比隐匿性或舌根原发性肿瘤中更频繁地检测到(P = 0.039)。第4周血浆而非口腔含漱液HPV DNA清除与第4周TTV的更大减小相关(P = 0.0063)。虽然第4周血浆和口腔含漱液HPV DNA清除与无进展生存期无关,但较低的基线血浆cfHPV DNA与较好的无进展生存期相关(P = 0.027)。第4周血浆cfHPV DNA清除与TTV的减小一致,未来研究有必要确定早期血浆cfHPV DNA清除在生物标志物适应性降阶梯治疗策略中的作用。
我们的发现可能为未来减强度研究中基于cfHPV DNA的低风险HPV相关OPSCC患者的适当选择提供信息,旨在预防或最小化可能复发风险较低患者的治疗相关毒性。