Utility of TTMV-HPV DNA in resolving indeterminate findings during oropharyngeal cancer surveillance

Scott A. Roof, James Jabalee, Eleni M. Rettig, Susmita Chennareddy, Rocco M. Ferrandino, Sida Chen, Marshall R. Posner, Eric M. Genden, Raymond L. Chai, John Sims, Elaine Thrash, Scott J. Stern, Noah S. Kalman, Sreenija Yarlagadda, Adam Raben, Lydia Clements, Abie Mendelsohn, John M. Kaczmar, Yadav Pandey, Mihir BhayaniCatherine Del Vecchio Fitz, Glenn J. Hanna

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

Objectives: Clinical and imaging examinations frequently have indeterminate results during cancer surveillance, which can lead to overtreatment and cause psychological and financial harm to the patient. This study addresses the critical need to enhance diagnostic precision and decision-making in the management of HPV-associated oropharyngeal cancer. This study evaluated the utility of tumor tissue-modified viral (TTMV)-HPV DNA to resolve indeterminate disease status following definitive treatment for HPV-associated oropharyngeal cancer. Materials and Methods: In this retrospective cohort, patients treated for HPV-associated oropharyngeal cancer at eight U.S. institutions and who received one or more TTMV-HPV DNA tests during post-treatment surveillance between February 2020 and January 2022 were included. Results: Among 543 patients, 210 patients (38.7%; 210/543) experienced one or more clinically indeterminate findings (CIFs) during surveillance, with 503 CIFs recorded. Of those patients with an “indeterminate” disease status at a point during surveillance, 79 were associated with contemporaneous TTMV-HPV DNA testing. TTMV-HPV DNA testing demonstrated high accuracy (97.5%; 77/79) in correctly determining recurrence status. Patients whose disease status was “indeterminate” at the time of a positive TTMV-HPV DNA test were clinically confirmed to recur faster than those whose disease status was “no evidence of disease.” Only 3% of patients (17/543) experienced indeterminate TTMV-HPV DNA tests during surveillance. Discordance between TTMV-HPV DNA tests and clinical results was minimal, with only 0.6% (3/543) of patients showing positive tests without recurrence. Conclusion: Our findings support the utility of circulating TTMV-HPV DNA in resolving indeterminate disease status and informing the subsequent clinical course.

Original languageEnglish
Article number106874
JournalOral Oncology
Volume155
DOIs
StatePublished - Aug 2024

Keywords

  • Circulating tumor DNA
  • Head and neck cancer
  • Human papillomavirus
  • Oropharyngeal cancer
  • Tumor-tissue modified viral HPV DNA

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