120
Participants
Start Date
June 11, 2025
Primary Completion Date
December 31, 2028
Study Completion Date
December 31, 2028
NavDx
NavDx is a clinically validated blood test to detect circulating tumor HPV DNA (ctHPVDNA). In this study, ctHPVDNA results, in conjuction with specimen analysis, will be used to assign post-surgical adjuvant treatment.
Adjuvant Radiation 30 Gray
If undetectable postoperative ctHPVDNA levels and five or more positive nodes, or confirmed extranodal extension (ENE) (greater than 2 mm) deintensified radiation treatment of 30 gray.
Adjuvant Radiation 40 Gray
If detectable postoperative ctHPVDNA, then reimage to evaluate for potentially operable disease, followed by appropriate surgery as indicated. If surgery is performed, repeat ctHPVDNA levels will be checked, and if then negative, subject will be placed in observation if N0 or N1 disease, and 30 Gy of radiation if N2 disease on final pathologic staging. If repeat ctHPVDNA level is positive, or shows no obvious operable disease, then subject will undergo 40 Gy of radiation.
RECRUITING
IU Health Joe and Shelly Schwarz Cancer Center, Carmel
RECRUITING
Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indianapolis
Indiana University
OTHER