pBI-11 & TA-HPV (With Pembrolizumab as Treatment for Patients w/Advanced, PD-L1 CPS≥1, hrHPV+ Oropharyngeal Cancer

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorMichael K. Gibson

About this trial

This phase II trial tests how well pB1-11 and human papillomavirus tumor antigen (TA-HPV) vaccines in combination with pembrolizumab work in treating patients with oropharyngeal cancer that has come back (recurrent) or that has spread from where it first started (primary site) to other places in the body (metastatic) and that is PD-L1 and human papillomavirus (HPV) positive. Oropharyngeal cancer is a type of head and neck cancer involving structures in the back of the throat (the oropharynx), such as the non-bony back roof of the mouth (soft palate), sides and back wall of the throat, tonsils, and back third of the tongue. Scientists have found that some strains or types of a virus called HPV can cause oropharyngeal cancer. pBI-11 is a circular deoxyribonucleic acid (DNA) (plasmid) vaccine that promotes antibody, cytotoxic T cell, and protective immune responses. TA-HPV is an investigational recombinant vaccina virus derived from a strain of the vaccina virus which was widely used for smallpox vaccination. Vaccination with this TA-HPV vaccine may stimulate the immune system to mount a cytotoxic T cell response against tumor cells positive for HPV, resulting in decreased tumor growth. 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 by inhibiting the PD-1 receptor. These investigational vaccines could cause or enhance an immune response in the body against HPV, during which time the activity of pembrolizumab against oropharyngeal cancer associated with HPV may be strengthened. These drugs in combination may be more effective in increasing the ability of the immune system to fight oropharyngeal cancer than pembrolizumab alone.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Signed and dated written informed consent

Male or female >= 18 years of age on the day of signing informed consent

Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1

Having been diagnosed with R/M p16+ PD-L1 CPS >= 1 OPC not previously treated for R/M disease. They must be eligible for, and planning to start therapy with pembrolizumab, according to standard of care

Disqualifiers

Disease that can be treated with curative intent as assessed by patient's study physician. If patient in this situation wishes for treatment with palliative intent then they may enroll

Multiple primary oropharyngeal (OP) tumors

Primary cancer not originated from the oropharynx

Has received any therapy for R/M disease. Therapy in the setting of curative intent is allowed

Trial design

Design model

Single group

Treatments tested in this trial

  • DNA Vaccine

    Biological/Vaccine

    Given pBI-11 IM

  • Human Papillomavirus Tumor Antigen Vaccine

    Biological/Vaccine

    Given into a muscle

  • Pembrolizumab

    Biological/Vaccine

    Given into vein

  • Computed Tomography (CT)

    Procedure/Surgery

    Undergo a CT

  • Magnetic Resonance Imaging (MRI)

    Procedure/Surgery

    Undergo an MRI

  • Magnetic Resonance Imaging

    Procedure/Surgery

    Undergo blood sample collection

  • Biopsy

    Procedure/Surgery

    Undergo tumor biopsy

Treatment groups

54 Participants
are divided into 1 treatment group
Group A: Treatment (pBI-11, TA-HPV, pembrolizumab)Experimental treatment 7 interventions

Trial outcomes

Primary outcomes

1

Objective response rate (ORR)

The proportion of eligible, response evaluable patients with a best overall response (BOR). Objective response rate will be summarized as proportions of the total number of eligible, response evaluable patients with 95% confidence intervals. Logistic and Cox (proportional hazards) regression will be used to assess the association between important prognostic variables (e.g, gender, age) with objective response rate. Objective response rate will be monitored using Simon's minimax design.

Time frame
Up to approximately 1 year
2

Disease control rate (DCR)

The proportion of eligible, response evaluable patients with a best overall response of complete response, partial response or stable disease. Disease control rate will be summarized as proportions of the total number of eligible, response evaluable patients with 95% confidence intervals.

Time frame
Up to approximately 1 year
3

Progression-free survival (PFS)

Estimated using the method of Kaplan and Meier (product limit estimator). Logistic and Cox (proportional hazards) regression will be used to assess the association between important prognostic variables (e.g, gender, age) with progression-free survival. The odds ratio (OR) for response and hazard ratio (HR) for progression-free survival will be presented with 95% confidence intervals as measure of effect size.

Time frame
Up to approximately 1 year
4

Overall survival (OS)

Estimated using the method of Kaplan and Meier (product limit estimator). Logistic and Cox (proportional hazards) regression will be used to assess the association between important prognostic variables (e.g, gender, age) with overall survival. The odds ratio for response and hazard ratio for overall survival will be presented with 95% confidence intervals as measure of effect size.

Time frame
Up to approximately 1 year

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Michael K. Gibson

Lead sponsor

Vanderbilt-Ingram Cancer Center

Sponsor institution