ctHPVDNA in HPV Positive Squamous Cell Carcinoma of the Oropharynx

NARecruitingINTERVENTIONAL
Enrollment

120

Participants

Timeline

Start Date

June 11, 2025

Primary Completion Date

December 31, 2028

Study Completion Date

December 31, 2028

Conditions
Squamous Cell Carcinoma of OropharynxHPV Positive CancerThroat CancerTonsil Cancer
Interventions
DIAGNOSTIC_TEST

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.

RADIATION

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.

RADIATION

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.

Trial Locations (2)

46032

RECRUITING

IU Health Joe and Shelly Schwarz Cancer Center, Carmel

46202

RECRUITING

Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indianapolis

All Listed Sponsors
lead

Indiana University

OTHER