Haring Catherine T, Bhambhani Chandan, Brummel Collin, Jewell Brittany, Bellile Emily, Heft Neal Molly E, Sandford Erin, Spengler Ryan M, Bhangale Apurva, Spector Matthew E, McHugh Jonathan, Prince Mark E, Mierzwa Michelle, Worden Francis P, Tewari Muneesh, Swiecicki Paul L, Brenner J Chad
University of Michigan, Department of Otolaryngology-Head and Neck Surgery, Ann Arbor, MI 48109, USA.
Co-First Authors.
Oncotarget. 2021 Jun 22;12(13):1214-1229. doi: 10.18632/oncotarget.27992.
Despite the rising incidence of human papillomavirus related (HPV+) oropharyngeal squamous cell carcinoma (OPSCC), treatment of metastatic disease remains palliative. Even with new treatments such as immunotherapy, response rates are low and can be delayed, while even mild tumor progression in the face of an ineffective therapy can lead to rapid death. Real-time biomarkers of response to therapy could improve outcomes by guiding early change of therapy in the metastatic setting. Herein, we developed and analytically validated a new droplet digital PCR (ddPCR)-based assay for HPV16 circulating tumor DNA (ctDNA) and evaluated plasma HPV16 ctDNA for predicting treatment response in metastatic HPV+ OPSCC. We found that longitudinal changes HPV16 ctDNA correlate with treatment response and that ctDNA responses are observed earlier than conventional imaging (average 70 days, range: 35-166). With additional validation in multi-site studies, this assay may enable early identification of treatment failure, allowing patients to be directed promptly toward clinical trials or alternative therapies.
Microbiol Spectr. 2022-4-27
JCO Precis Oncol. 2019
Curr Treat Options Oncol. 2021-2-8