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循环肿瘤人乳头瘤病毒DNA动力学对人乳头瘤病毒相关口咽癌疾病转归的影响

Impact of circulating tumor human papillomavirus DNA kinetics on disease outcomes in HPV-associated oropharyngeal cancer.

作者信息

Jhawar Sachin R, Haring Catherine, Pan Xueliang, Ma Jianing, Bhateja Priyanka, Kubi Emmanuel Appiah, Limbach Abberly Lott, Gogineni Emile, Mitchell Darrion, Konieczkowski David, Grecula John, Ma Sung Jun, Zhu Simeng, Old Matthew, Bonomi Marcelo, Rocco James W, Blakaj Dukagjin M, Baliga Sujith

机构信息

Department of Radiation Oncology, The Ohio State University Wexner Medical Center, Columbus, Ohio, USA.

Department of Otolaryngology-Head and Neck Surgery, The Ohio State University Wexner Medical Center, Columbus, Ohio, USA.

出版信息

Int J Cancer. 2025 Apr 15;156(8):1656-1663. doi: 10.1002/ijc.35291. Epub 2024 Dec 16.

Abstract

Circulating tumor tissue modified (TTMV)-HPV DNA has emerged as a promising biomarker in human papillomavirus associated oropharyngeal squamous cell carcinoma (HPV-OPSCC). The objective of this study was to assess ctHPVDNA TTMV clearance kinetics during RT and its relationship with progression in HPV-OPSCC. We identified 80 non-metastatic HPV-OPSCC patients with 366 TTMV samples who underwent prospective plasma TTMV testing before, during and after curative intent RT or CRT between June 2021 and February 2023. Patients with rapid favorable clearance (>95% decline from pre-treatment value) of TTMV were compared to those with suboptimal clearance (<95%). The primary objective was to evaluate the relationship between TTMV clearance during CRT and its impact on progression free survival (PFS). The median follow-up was 14.7 months. Clinical nodal stage was associated with higher TTMV-HPV DNA scores at baseline, with a median score of 128, 778, and 1219 for N0/N1, N2a/b, and N2c/3 patients, respectively. Patients who had persistent TTMV at the end of RT had an inferior PFS compared to those who cleared their TTMV at 2 years (91.7% vs. 71.7%) (log rank, p = .042). Among patients who had complete clearance of their TTMV at 3 months, those who had a negative, equivocal, and incomplete PET response had a 2-year PFS of 94.3%, 77.8%, and 59.3%, respectively (log-rank, p = .029). Our study indicates that persistent TTMV-HPV DNA is associated with worse PFS and may portend unfavorable outcomes. Thus, monitoring TTMV clearance kinetics could be a valuable biomarker for guiding treatment decisions in patients with HPV-OPSCC.

摘要

循环肿瘤组织修饰(TTMV)-人乳头瘤病毒(HPV)DNA已成为人乳头瘤病毒相关口咽鳞状细胞癌(HPV-OPSCC)中有前景的生物标志物。本研究的目的是评估HPV-OPSCC患者在放疗期间ctHPVDNA TTMV的清除动力学及其与疾病进展的关系。我们纳入了80例非转移性HPV-OPSCC患者,共366份TTMV样本,这些患者在2021年6月至2023年2月期间接受了根治性放疗或同步放化疗,放疗前、放疗期间及放疗后均进行了前瞻性血浆TTMV检测。将TTMV快速良好清除(较治疗前值下降>95%)的患者与清除欠佳(<95%)的患者进行比较。主要目的是评估同步放化疗期间TTMV清除与其对无进展生存期(PFS)影响之间的关系。中位随访时间为14.7个月。临床淋巴结分期与基线时较高的TTMV-HPV DNA评分相关,N0/N1、N2a/b和N2c/3患者的中位评分分别为128、778和1219。放疗结束时TTMV持续存在的患者的PFS低于2年时TTMV清除的患者(91.7%对71.7%)(对数秩检验,p = 0.042)。在3个月时TTMV完全清除的患者中,PET反应为阴性、不确定和不完全的患者2年PFS分别为94.3%、77.8%和59.3%(对数秩检验,p = 0.029)。我们的研究表明,TTMV-HPV DNA持续存在与较差的PFS相关,可能预示不良预后。因此,监测TTMV清除动力学可能是指导HPV-OPSCC患者治疗决策的有价值的生物标志物。

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