Squamous Cell Carcinoma of the Head and Neck Clinical Trial
Official title:
The Role of the Central Memory Phenotype in Predicting Response to PD-1 Inhibition in Pre-clinical Models of Oral Cancer
NCT number | NCT03862066 |
Other study ID # | 102985 |
Secondary ID | |
Status | Terminated |
Phase | |
First received | |
Last updated | |
Start date | February 8, 2019 |
Est. completion date | November 22, 2021 |
Verified date | August 2022 |
Source | Medical University of South Carolina |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The purpose of this research study is collect tissue and blood samples from patients who are having surgery and use those samples in lab studies to see if there are any markers in blood and tissue that can help predict how cancer will react to different treatment. Participants in this study will have a blood sample and tissue samples collected for research. The blood and tissue collected will be tested in the laboratory. The tissue collected will be left over tissue from the standard of care surgery.
Status | Terminated |
Enrollment | 2 |
Est. completion date | November 22, 2021 |
Est. primary completion date | June 30, 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Newly diagnosed histologically proven locoregional oral squamous cell carcinoma (OSCC) without evidence of distant metastases. OSCC includes the subsites of oral tongue, floor of mouth, gingiva, retromolar trigone and buccal mucosa OR Recurrent or persistent histologically proven locoregional OSCC that was initially treated with surgery alone. - must be eligible for surgical resection - greater than 18 years of age Exclusion Criteria: - prior immunotherapy or treatment with another anti PD-1 agent besides nivolumab - prior chemotherapy including cetuximab or radiation therapy - concomitant malignancies except cutaneous squamous cell carcinoma or basal cell carcinoma - unresectable primary tumor or regional disease or distant metastases |
Country | Name | City | State |
---|---|---|---|
United States | Hollings Cancer Center at Medical University of South Carolina | Charleston | South Carolina |
Lead Sponsor | Collaborator |
---|---|
Medical University of South Carolina |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Count of PDX models that are developed from patient samples | It is anticipated that there will be 12 successful PDX models developed as part of this study. | 6 months | |
Secondary | Change in tumor growth in PDX models | Tumors will be measured with calipers bi-weekly and measurements will be plotted overtime. | 6 months | |
Secondary | Change in tumor volume in PDX models | Tumor volume with be calculated based on the two greatest dimensions of the tumor and will be plotted overtime. | 6 months |
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