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.
尽管人乳头瘤病毒相关(HPV+)口咽鳞状细胞癌(OPSCC)的发病率不断上升,但转移性疾病的治疗仍然是姑息性的。即使采用免疫疗法等新疗法,缓解率也很低且可能延迟,而面对无效治疗时即使是轻微的肿瘤进展也可能导致迅速死亡。治疗反应的实时生物标志物可以通过在转移性情况下指导早期治疗改变来改善治疗结果。在此,我们开发并通过分析验证了一种基于液滴数字PCR(ddPCR)的新检测方法,用于检测HPV16循环肿瘤DNA(ctDNA),并评估血浆HPV16 ctDNA以预测转移性HPV+OPSCC的治疗反应。我们发现HPV16 ctDNA的纵向变化与治疗反应相关,并且ctDNA反应比传统成像更早观察到(平均70天,范围:35-166天)。通过在多中心研究中的进一步验证,该检测方法可能有助于早期识别治疗失败,使患者能够迅速转向临床试验或替代疗法。