This phase II trial studies whether blood tests and clinical features (such as tumor stage and smoking status) can be used to determine the appropriate treatment following primary treatment (risk-adapted adjuvant treatment) for patients with human papillomavirus (HPV)-positive (+) oropharyngeal carcinoma (OPC). Treatment for patients with HPV+ OPC is similar to HPV-negative oropharyngeal cancers. There is insufficient data to alter therapy based on HPV status at present. Identification of less favorable subgroups, beyond tumor staging and smoking history, with HPV+ OPC is important in determining which patients may be candidates for de-intensified therapy to prevent short-term side effects and late complications without compromising overall survival or increasing the risk of the cancer coming back in the area around the tumor after a period of improvement. This trial will use a blood sample to test for HPV deoxyribonucleic acid (DNA) along with clinical features to determine which patients may have intermediate or high-risk disease. Identified patients then either receive adjuvant treatment with pembrolizumab or are closely watched using exams and tests to see if the cancer returns (active surveillance). Immunotherapy with monoclonal antibodies, such as pembrolizumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Researchers hope that they will be able to compare outcomes between the two groups and see if blood tests and clinical features can be used for the risk-adapted adjuvant treatment of HPV+ OPC.
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT07513324.
Locations matching your search criteria
United States
Massachusetts
Boston
Brigham and Women's HospitalStatus: Temporarily closed to accrual
Contact: Michael Dennis
Phone: 617-632-3090
Dana-Farber Cancer InstituteStatus: Temporarily closed to accrual
Contact: Michael Dennis
Phone: 617-632-3090
PRIMARY OBJECTIVES:
I. To estimate progression-free survival (PFS) at 2-years from the date of randomization among HPV+ OPC participants with PD-L1 combined positive score (CPS) ≥ 1 with higher risk clinical risk factors using HPV circulating tumor (ct)DNA profiling for treatment stratification. (Clinical)
II. To evaluate the ability of tumor-tissue modified virus (TTMV)-HPV DNA (NavDx®), an HPV ctDNA assay, to risk stratify participants with unfavorable or high-risk HPV+ OPC to appropriately intensified treatment with adjuvant immunotherapy to improve outcomes. (Translational)
III. To validate the CD8+PD-1+ T cell density and G-cross CD8+ T cell score as a prognostic biomarker across the entire cohort and among the adjuvant immunotherapy-treated subgroup. (Translational)
SECONDARY OBJECTIVES:
I. To evaluate safety and toxicity (reporting number of participants experiencing adverse events utilizing Common Terminology Criteria for Adverse Events [CTCAE] version [V] 5.0).
II. To estimate progression-free survival (PFS) from the date of randomization in the entire randomized study population.
III. To estimate overall survival (OS) from date of randomization in the PD-L1 subgroups and entire randomized population.
IV. To estimate distant metastatic-free survival (DMFS) from date of randomization in the PD-L1 subgroups and entire randomized population.
EXPLORATORY OBJECTIVES:
I. To estimate TTMV-HPV DNA clearance from the date of randomization in the entire randomized study population.
II. To explore the relationship between changes in HPV ctDNA and on-treatment imaging response (radiomics) in a subset of participants i.e. prior smoking history.
III. To bank peripheral blood mononuclear cells (PBMCs) for future circulating T cell phenotyping to identify predictive biomarkers of immunotherapy response in the higher risk subgroup treated with pembrolizumab.
OUTLINE: Patients are randomized to 1 of 2 arms.
ARM I: Patients receive pembrolizumab intravenously (IV) over 30 minutes on day 1 of each cycle. Cycles repeat every 42 days for up to 9 cycles in the absence of disease progression or unacceptable toxicity. Additionally, patients undergo biopsy during screening as well as blood sample collection and computed tomography (CT), positron emission tomography (PET)-CT, or magnetic resonance imaging (MRI) throughout the study. Patients may also optionally undergo MRI during screening.
ARM II: Patients undergo standard active surveillance for up to 2 years in the absence of disease progression. Additionally, patients undergo biopsy during screening as well as blood sample collection and CT, PET-CT, or MRI throughout the study. Patients may also optionally undergo MRI during screening.
After completion of study treatment, patients are followed up at 30 days and then every 12 weeks until death or 2 years from randomization.
Lead OrganizationDana-Farber Harvard Cancer Center
Principal InvestigatorMichael Dennis