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HPV 循环肿瘤 DNA 监测抗 PD-1 治疗转移性肛门鳞癌的疗效:一例报告。

HPV circulating tumor DNA to monitor the efficacy of anti-PD-1 therapy in metastatic squamous cell carcinoma of the anal canal: A case report.

机构信息

Department of Medical Oncology, Institut Curie, PSL Research University, Paris and Saint Cloud, France.

Versailles Saint-Quentin-en-Yvelines & Paris-Saclay University, Saint Cloud, France.

出版信息

Int J Cancer. 2017 Oct 15;141(8):1667-1670. doi: 10.1002/ijc.30863. Epub 2017 Jul 12.

Abstract

Squamous cell carcinoma of the anal canal (SCCA) is a rare HPV-associated cancer with limited sensitivity to standard chemotherapy. In a phase 2 study, nivolumab, an anti PD-1 immune checkpoint inhibitor, demonstrated significant efficacy as single-agent therapy in metastatic SCCA patients. Nevertheless, imaging assessment by standard RECIST criteria of the efficacy of immune therapy can be difficult in some patients due to tumor immune cell infiltration, and biomarkers of treatment efficacy are needed. We have previously developed a quantitative droplet digital PCR (ddPCR) technique to detect HPV circulating tumor DNA (HPV ctDNA), with excellent sensitivity and specificity. Here, we report, for the first time, the kinetics of HPV ctDNA during therapy in a patient with metastatic SCCA, who obtained sustained partial response to single-agent nivolumab. We observed an early and very significant decrease of HPV ctDNA during therapy from the baseline level of 3713 copies/ml plasma to 564 copies/ml plasma at 4 weeks, and 156 copies/ml at 6 weeks, followed by a plateau. This observation provides proof-of-concept that HPV ctDNA can be used as a noninvasive early dynamic biomarker to monitor the efficacy of new immunotherapy agents.

摘要

肛门鳞状细胞癌 (SCCA) 是一种罕见的 HPV 相关癌症,对标准化疗的敏感性有限。在一项 2 期研究中,抗 PD-1 免疫检查点抑制剂纳武利尤单抗作为单一药物在转移性 SCCA 患者中显示出显著疗效。然而,由于肿瘤免疫细胞浸润,一些患者的标准 RECIST 标准影像学评估可能很困难,需要治疗效果的生物标志物。我们之前开发了一种定量液滴数字 PCR(ddPCR)技术来检测 HPV 循环肿瘤 DNA(HPV ctDNA),具有出色的灵敏度和特异性。在这里,我们首次报告了一名转移性 SCCA 患者在接受单一药物纳武利尤单抗治疗期间 HPV ctDNA 的动力学,该患者对单药纳武利尤单抗获得持续的部分缓解。我们观察到治疗期间 HPV ctDNA 从基线水平 3713 拷贝/ml 血浆早期且非常显著地下降至 4 周时的 564 拷贝/ml 血浆和 6 周时的 156 拷贝/ml 血浆,随后达到平台期。这一观察结果提供了证据,证明 HPV ctDNA 可作为一种非侵入性的早期动态生物标志物,用于监测新型免疫治疗药物的疗效。

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