NCT05880797
Recruiting
Not Applicable
Multidimensional and Multimodal Profiling of Oropharyngeal Carcinoma
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Oropharyngeal Carcinoma
- Sponsor
- Stanford University
- Enrollment
- 1000
- Locations
- 1
- Primary Endpoint
- Sample collection
- Status
- Recruiting
- Last Updated
- 19 days ago
Overview
Brief Summary
The purpose of this study is to better understand the natural history of oropharyngeal carcinoma (OPC), with or without an association with the human papilloma virus (HPV). For this study, the investigators plan to collect blood from OPC patients prior to treatment and at six subsequent time points.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patients diagnosed with oropharyngeal carcinoma or patients with cancer of the unknown primary that is HPV associated, or possibly deemed to be originating from the oropharynx.
Exclusion Criteria
- •Not willing to sign consent
Outcomes
Primary Outcomes
Sample collection
Time Frame: up to 36 months post-op
30-50cc of blood
Sample collection
Time Frame: prior to start of treatment
30-50cc of blood
Secondary Outcomes
- tumor sample(Day 1)
Study Sites (1)
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