Longitudinal measurement of HPV copy number in cell-free DNA is associated with patient outcomes in HPV-positive oropharyngeal cancer

• Published in: European journal of surgical oncology 2022-06, Vol.48 (6), p.1224-1234
• Main Authors: Warlow, Sophie J., Adamowicz, Martyna, Thomson, John P., Wescott, Robert A., Robert, Christelle, Carey, Lara M., Thain, Helen, Cuschieri, Kate, Li, Lucy Q., Conn, Brendan, Hay, Ashley, Nixon, Iain J., Aitman, Timothy J.
• Format: Article
• Language: English
• Subjects: Cell-free DNA; Cell-Free Nucleic Acids; DNA Copy Number Variations; Droplet digital PCR; Human papillomavirus; Humans; Liquid biopsy; Neoplasm Recurrence, Local; Oropharyngeal Neoplasms - diagnosis; Oropharyngeal Neoplasms - virology; Oropharyngeal squamous cell carcinoma; Papillomaviridae - genetics; Papillomavirus Infections - complications; Squamous Cell Carcinoma of Head and Neck - diagnosis; Squamous Cell Carcinoma of Head and Neck - virology
• ISSN: 0748-7983; 1532-2157
• DOI: 10.1016/j.ejso.2022.03.232

Oropharyngeal squamous cell carcinoma (OPSCC) is increasing in global prevalence and is divided into two types dependent on association with human papillomavirus (HPV). Assay of HPV copy number in plasma cell-free DNA (cfDNA) provides a minimally invasive method for detecting and monitoring tumour-derived HPV, with potential for enhancing clinical care. In a prospectively recruited cohort of 104 OPSCC patients, we evaluate the utility of cfDNA droplet digital PCR (ddPCR) as a method for characterisation and longitudinal monitoring of patients with OPSCC. ddPCR assay of pre-treatment plasma cfDNA for five HPV types showed overall 95% concordance with p16 immunohistochemistry and PCR analysis of tumour tissue. Longitudinal sampling in 48 HPV+ve patients, with median follow-up of 20 months, was strongly associated with patient outcomes. Persistently elevated cfDNA-HPV post-treatment was associated with treatment failure (2/2 patients) and an increase of cfDNA-HPV in patients whose HPV levels were initially undetectable post-treatment was associated with disease recurrence (5/6 patients). No recurrence was observed in patients in whom cfDNA-HPV was undetectable in all post-treatment samples. In two patients, sequential HPV measurement could have avoided surgical intervention which did not confirm recurrence. The high concordance of pre-treatment plasma cfDNA-HPV analysis with tissue-based assays, together with the clinical associations of sequentially measured post-treatment cfDNA-HPV copy number add to a growing body of evidence that suggest utility of cfDNA-HPV ddPCR in management of OPSCC. Standardised clinical trials based on these data are now needed to assess the impact of such testing on overall patient outcomes.