Clinical Stage III HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8Clinical Stage IV HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8Metastatic Oropharyngeal Squamous Cell CarcinomaOropharyngeal Squamous Cell CarcinomaRecurrent Oropharyngeal Squamous Cell CarcinomaStage III Oropharyngeal (p16-Negative) Carcinoma AJCC v8Stage IV Oropharyngeal (p16-Negative) Carcinoma AJCC v8Head and Neck CarcinomaHead and Neck NeoplasmSalivary Gland NeoplasmsThyroid Gland Neoplasm
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
560 (estimated)
Sponsor
Mayo Clinic · Other
Who this trial is looking for
This trial is looking for adults with oropharyngeal cancer or a related condition. Participation involves giving samples for research and attending follow-up visits at the enrolling institution.
Are You a Good Fit for This Trial?
You may be able to join if
I am at least 18 years old.
I am willing to provide written consent.
I have had a biopsy with p16 staining.
I am willing to return for follow-up visits.
I have a suspicion or diagnosis of head and neck cancer.
I can complete questionnaires by myself or with help.
My primary language is English, Spanish, or Arabic.
You may not be able to join if
I am currently receiving treatment for another cancer.
I had another active cancer within the last 5 years.
I have a history of head and neck cancer other than the current one.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
The purpose of this research is to identify a biomarker that is exists when human papillomavirus (HPV) mediated oropharyngeal squamous cell carcinoma is present and does not exist when HPV mediated oropharyngeal squamous cell carcinoma is absent.
Trial Locations
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City
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Status
Eligibility Criteria
Inclusion Criteria:
* Age ≥ 18 years
* Able to provide written consent
* Groups 1-3:
* Must undergo p16 staining on biopsy for enrollment
* Patients with \< 70% of tumor cells positive for p16 will be considered p16 negative
* Must undergo HPV16 family in situ hybridization (ISH) and/or RNA …
Inclusion Criteria:
* Age ≥ 18 years
* Able to provide written consent
* Groups 1-3:
* Must undergo p16 staining on biopsy for enrollment
* Patients with \< 70% of tumor cells positive for p16 will be considered p16 negative
* Must undergo HPV16 family in situ hybridization (ISH) and/or RNA on biopsy or surgical specimen, unless amount of tissue is too small to have conclusive HPV ISH testing done on it
* Willingness and intent to return in person to enrolling institution for follow-up (during the Active Monitoring Phase of the study) for at least 2 of the standard follow-up time points for a total of 3 time-points including pre-treatment. A participant who does not return in person to Mayo Clinic Rochester for every standard of care post-treatment follow up will not be considered deviating from the protocol
* Group 4:
* Clinical suspicion or histopathologic diagnosis of head and neck cancer or neoplasm
* Primary salivary neoplasm
* Primary thyroid neoplasm
* Primary head and neck neoplasm
* Multi-cancer early detection (MCED) testing concerning for cancer
* Patient has given permission to give his/her tumor/tissue/blood/saliva sample for research testing
* Ability to complete questionnaire(s) by themselves or with assistance
* Primary language: English, Spanish, Arabic
Exclusion Criteria:
* Receiving any other investigational agent which would be considered as a treatment for the primary neoplasm.
* Groups 1-3:
* Other active malignancy ≤ 5 years prior to registration
* EXCEPTIONS: Non-melanotic skin cancer, non-metastatic thyroid cancer, non-metastatic prostate cancer, carcinoma-in-situ of the cervix, HPV+ oropharyngeal squamous cell carcinoma (SCC) (which can be enrolled in group 3)
* NOTE: If there is a history of prior malignancy, they must not be receiving other specific treatment for their cancer
* History of any head and neck malignancy, other than the tumor for which they are being treated
* Group 4, Cohort A, B, C:
* Other active malignancy ≤ 5 years prior to registration
* EXCEPTIONS: Non-metastatic prostate cancer, carcinoma-in-situ of the cervix, non metastatic cutaneous basal cell carcinoma
* NOTE: If there is a history or prior malignancy, they must not be receiving other specific treatment for their cancer
* History of any head and neck malignancy, other than the present neoplasm
* Note these are clarifications of inclusion into Group 4, Cohorts D and E:
* Presence of other active malignancy or recurrent head and neck neoplasms are allowed in this arm
* Receipt of cancer specific therapy for other malignancy is allowed in this arm
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