Monitoring of Cell-free Human Papillomavirus DNA in Metastatic or Recurrent Cervical Cancer: Clinical Significance and Treatment Implications

Zhuomin Yin, Tao Feng, Qing Xu, Wumin Dai, Maowei Ni, Juan Ni, Hanmei Lou
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Abstract

Purpose: Monitoring of circulating human papillomavirus (HPV) cell-free DNA (cfDNA) is a minimally invasive approach for surveillance in HPV-associated cancers, particularly cervical cancer. The aim of this study was to monitor circulating HPV cfDNA levels in patients with recurrent or metastatic cervical cancer during treatment and follow-up to assess the utility of HPV cfDNA as a tumor marker for disease surveillance and in guiding clinical treatment decisions. Experimental Design: In this prospective pilot observational study, levels of HPV cfDNA in serum samples from 28 patients with recurrent or metastatic HPV+ cervical cancer were measured via digital droplet polymerase chain reaction. Results for HPV cfDNA levels were matched to clinical outcomes and to serum levels of squamous cell carcinoma antigen (SCC-Ag) to assess the clinical potential of HPV cfDNA as a tumor marker. Results: HPV cfDNA was detected in all 28 patients (100%). Notably, median baseline HPV cfDNA levels varied according to the metastatic pattern in individual patients (P=0.019). Specifically, patients with a combined multiple-metastasis pattern had higher median baseline HPV cfDNA levels than patients with a single metastasis (P=0.003). All participants exhibited changes in HPV cfDNA levels over a median monitoring period of 2 months (range 0.3–16.9) before evaluations for treatment response or disease progression. Among 26 patients initially diagnosed with squamous cell cervical cancer, the positivity rate was 100% for HPV cfDNA and 69.2% for SCC-Ag (P=0.004, 95% confidence interval, 0–0.391). Among 20 patients longitudinally monitored for squamous cell cervical cancer, the concordance with changes in disease status was 90% for HPV cfDNA and 50% for SCC-Ag (P=0.014, 95% confidence interval, 0.022–0.621). Conclusions: HPV cfDNA is a promising tumor marker for HPV+ cervical cancer that offers advantages over SCC-Ag. In the context of precision medicine, HPV cfDNA is poised to play an increasingly pivotal role in monitoring treatment efficacy, providing valuable insights into disease progression, and guiding clinical decisions.
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监测转移性或复发性宫颈癌患者的无细胞人乳头状瘤病毒 DNA:临床意义和治疗影响
目的:监测循环人乳头瘤病毒(HPV)无细胞DNA(cfDNA)是监测HPV相关癌症(尤其是宫颈癌)的一种微创方法。本研究旨在监测复发性或转移性宫颈癌患者在治疗和随访期间的循环 HPV cfDNA 水平,以评估 HPV cfDNA 作为肿瘤标志物在疾病监测和指导临床治疗决策方面的效用。实验设计:在这项前瞻性试点观察研究中,通过数字液滴聚合酶链反应测量了28例复发性或转移性HPV+宫颈癌患者血清样本中的HPV cfDNA水平。HPV cfDNA 含量结果与临床结果和血清中鳞状细胞癌抗原 (SCC-Ag) 含量相匹配,以评估 HPV cfDNA 作为肿瘤标志物的临床潜力。研究结果所有28名患者(100%)都检测到了HPV cfDNA。值得注意的是,HPV cfDNA 的中位基线水平因患者的转移模式而异(P=0.019)。具体来说,合并多处转移模式的患者的 HPV cfDNA 中位基线水平高于单处转移的患者(P=0.003)。在评估治疗反应或疾病进展之前,所有参与者的 HPV cfDNA 水平在 2 个月的中位监测期内(范围 0.3-16.9)都出现了变化。在 26 名初步诊断为鳞状细胞宫颈癌的患者中,HPV cfDNA 阳性率为 100%,SCC-Ag 阳性率为 69.2%(P=0.004,95% 置信区间为 0-0.391)。在纵向监测的 20 名鳞状细胞宫颈癌患者中,HPV cfDNA 与疾病状态变化的一致性为 90%,SCC-Ag 为 50%(P=0.014,95% 置信区间为 0.022-0.621)。结论:HPV cfDNA与 SCC-Ag 相比,HPV cfDNA 是一种很有前景的 HPV+ 宫颈癌肿瘤标记物。在精准医疗的背景下,HPV cfDNA 将在监测治疗效果、深入了解疾病进展情况以及指导临床决策方面发挥越来越重要的作用。
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