| Literature DB >> 28670746 |
Luc Cabel1, François-Clément Bidard1,2, Vincent Servois3, Wulfran Cacheux1, Pascale Mariani4, Emanuela Romano1,5, Mathieu Minsat6, Ivan Bieche7,8, Fereshteh Farkhondeh9, Emmanuelle Jeannot7, Bruno Buecher1.
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.Entities:
Keywords: anal canal; circulating tumor DNA; human papillomavirus; immunotherapy; nivolumab
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Year: 2017 PMID: 28670746 DOI: 10.1002/ijc.30863
Source DB: PubMed Journal: Int J Cancer ISSN: 0020-7136 Impact factor: 7.396