A Vaccine (PDS0101) Alone or in Combination With Pembrolizumab for the Treatment of Locally Advanced Human Papillomavirus-Associated Oropharynx Cancer

Clinical Stage III HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8 Clinical Trial

Official title:

Stimulating Immune Response With Neoadjuvant Human Papilloma Virus (HPV)-16 Specific Vaccination in HPV-Oropharyngeal Squamous Cell Carcinoma (HPV-OPSCC)

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05232851
• Other study ID #: MC200710
• Secondary ID: NCI-2022-0049721
• Status: Recruiting
• Phase: Phase 1/Phase 2
• Start date: February 22, 2022
• Est. completion date: July 1, 2024

Study information

• Verified date: November 2023
• Source: Mayo Clinic
• Contact: Clinical Trials Referral Office
• Phone: 855-776-0015
• Email: mayocliniccancerstudies[@]mayo.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This phase I/II trial studies how well PDS0101 alone or in combination with pembrolizumab works to shrink tumor in patients with human papillomavirus-associated oropharynx cancer that has spread to nearby tissue or lymph nodes (locally advanced). PDS0101 is a vaccine made from specific peptides that may help the body build an effective immune response to kill tumor cells. 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. Giving PDS0101 with or without pembrolizumab may kill more tumor cells in patients with locally advanced human papillomavirus-associated oropharynx cancer before surgery so that it may make the tumor smaller and may reduce the amount of normal tissue that needs to be removed.

Description:

PRIMARY OBJECTIVE: I. To determine pathologic and human papillomavirus cell-free tumor deoxyribonucleic acid (ctHPVDNA) response to liposomal HPV-16 E6/E7 multipeptide vaccine PDS0101 (PDS0101) or PDS0101 plus pembrolizumab in patients with high risk human papillomavirus-associated oropharynx cancer (HPV-OPSCC). SECONDARY OBJECTIVES: I. To determine tumor response by Response Evaluation Criteria in Solid Tumors (RECIST) 1.1. II. To determine progression-free survival and overall survival. TERTIARY OBJECTIVES: I. To determine the safety of PDS0101 delivered alone or with pembrolizumab. CORRELATIVE RESEARCH OBJECTIVES: I. Determine the changes in tumor microenvironment (TME) with PDS0101 alone or with pembrolizumab. II. Determine circulating ctHPVDNA as a biomarker for tumor response. III. Determine HPV16-specific T-cell response utilizing multiplex flow cytometry and other parameters. OUTLINE: Patients are randomized to 1 of 2 arms. ARM A: Patients receive PDS0101 subcutaneously (SC) on day 1 of each cycle. Treatment repeats every 21 days for up to 2 cycles in the absence of disease progression or unacceptable toxicity. Patients also undergo computed tomography (CT) or fludeoxyglucose F-18 (FDG)-positron emission tomography (PET)/CT and blood sample collection throughout the trial. Patients may undergo a biopsy during screening and on the trial. ARM B: Patients receive PDS0101 SC on day 1 and pembrolizumab intravenously (IV) over 30 minutes on day 1 of each cycle. Treatment repeats every 21 days for up to 2 cycles in the absence of disease progression or unacceptable toxicity. Patients also undergo CT or FDG-PET/CT and blood sample collection throughout the trial. Patients may undergo a biopsy during screening and on the trial. After completion of study treatment, patients are followed every 3 months for up to 2 years.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 24
• Est. completion date: July 1, 2024
• Est. primary completion date: July 1, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Age >= 18 years
• Disease characteristics
• Locally advanced HPV-OPSCC and high-risk HPV-specific testing with at least one

of the following:

• Radiology extranodal extension (ENE) OR
• cN2 (AJCC 8th Edition) disease (contralateral/bilateral nodes) OR
• cN3(AJCC 8th Edition) disease (lymph node [LN] > 6 cm) OR
• Radiographic evidence of 2 or more involved lymph nodes
• Candidate for curative intent surgery or chemo-radiation
• Measurable or unmeasurable disease as defined by RECIST 1.1 criteria
• Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
• White blood cell (WBC) count >= 3,000/mm^3 (=< 15 days prior to registration)
• Platelet count >= 75,000/mm^3 (=< 15 days prior to registration)
• Hemoglobin >= 9.0 g/dL (5.6 mmol/L) (=< 15 days prior to registration)
• NOTE: Transfusions are not allowed =< 7 days prior to registration
• Total bilirubin =< 1.5 X upper limit of normal (ULN) (or total bilirubin =< 3.0 X ULN with direct bilirubin =<1.5 X ULN in patients with well-documented Gilbert's Syndrome) (=< 15 days prior to registration)
• Aspartate aminotransferase/serum glutamic-oxaloacetic transaminase (AST/SGOT) =< 2.5 X ULN (=< 15 days prior to registration)
• Creatinine =< 1.5 mg/dL (133 umol/L) OR calculated creatinine clearance >= 30 mL/min/1.73m^2 for patients with creatinine levels above ULN (=< 15 days prior to registration)
• Prothrombin time (PT)/international normalized ratio (INR)/partial thromboplastin time (PTT) =< 1.5 X ULN OR if patient is receiving anticoagulant therapy and PT or PTT is within therapeutic range of intended use of anticoagulants (=< 15 days prior to registration)
• Negative pregnancy test done =< 3 days prior to registration for persons of childbearing potential only
• Persons of childbearing potential or able to father a child must be willing to use an effective method of contraception for the course of the study starting with the first dose of study therapy through 120 days after the last dose of study medication
• NOTE: Abstinence is acceptable if this is the usual lifestyle and preferred method of contraception for the patient
• Provide written informed consent
• Willing to return to enrolling institution for follow-up (during the Active Monitoring Phase of the study)
• Willingness to provide mandatory blood specimens for correlative research
• Willingness to provide mandatory tissue specimens for correlative research

Exclusion Criteria:

• Active autoimmune disease requiring systemic treatment, documented history of severe autoimmune disease, or a syndrome that requires systemic steroids or immunosuppressive agents
• NOTE: Exceptions are allowed for:
• Vitiligo
• Resolved childhood asthma/atopy
• Intermittent use of bronchodilators or inhaled steroids
• Daily steroids at dose of =< 10mg of prednisone (or equivalent)
• Local steroid injections
• Stable hypothyroidism on replacement therapy
• Stable diabetes mellitus
• Sjogren's syndrome
• Any prior head or neck chemotherapy, radiotherapy, and/or immunotherapy
• Any of the following prior therapies:
• Live vaccine < 30 days prior to registration, including intranasal flu vaccine (e.g. Flu-Mist®) (Note: Seasonal influenza vaccines for injection are generally killed virus vaccines and are allowed). Examples of live vaccines include, but are not limited to, the following: measles, mumps, rubella, varicella/zoster (chicken pox), yellow fever, rabies, Bacillus Calmette-Guerin (BCG), and typhoid vaccine. Seasonal influenza vaccines for injection are generally killed virus vaccines and are allowed; however, intranasal influenza vaccines (eg, FluMist) are live attenuated vaccines and are not allowed
• Chemotherapy or targeted small molecule therapy < 21 days prior to registration
• Investigational therapy or investigational device < 30 days prior to registration
• Any prior investigational HPV-specific therapeutic vaccine
• Current or prior use of immunosuppressive medication < 14 days prior to registration
• The following are exceptions to this criterion:
• Intranasal, inhaled, topical steroids, or local steroid injections (e.g., intraarticular injection)
• Systemic corticosteroids at physiologic doses not to exceed 10 mg/day of prednisone or its equivalent
• Steroids as premedication for hypersensitivity reactions (e.g., premedication for computed tomography [CT] scans)
• Uncontrolled intercurrent illness including, but not limited to:
• Ongoing or active infection requiring systemic therapy
• Interstitial lung disease
• Serious, chronic gastrointestinal conditions associated with diarrhea (e.g., Crohn's disease or others)
• Known active hepatitis B (i.e., known positive HBV surface antigen (HBsAg) reactive)
• Known active hepatitis C (i.e., positive for HCV ribonucleic acid [RNA] detected by polymerase chain reaction [PCR])
• Known human immunodeficiency virus (HIV) (Note: Patients on stable highly active antiretroviral therapy (HAART) for >= 6 weeks with CD4 counts >= 200 cells/mm^3 undetectable HIV viral load by quantitative PCR and no opportunistic infections Castlemaan's Disease =< 12 months prior to enrollment are allowed)
• Known active tuberculosis (TB)
• Symptomatic congestive heart failure
• Unstable angina pectoris
• Unstable cardiac arrhythmia or
• Psychiatric illness/social situations that would limit compliance with study requirements (e.g., substance abuse)
• History of allogeneic hematopoietic transplant or any solid organ transplant
• Receiving any other investigational agent which would be considered as a treatment for the primary neoplasm
• Other active malignancy < 2 years prior to registration
• EXCEPTIONS: Non-melanotic skin cancer (SCC/BCC), micropapillary thyroid cancer, Gleason 6 prostate cancer, carcinoma-in-situ of the breast or cervix
• Any of the following conditions =< 6 weeks prior to registration:
• Cerebrovascular accident (CVA)
• Admission for unstable angina
• Cardiac angioplasty or stenting or coronary artery bypass graft surgery
• Untreated pulmonary embolism or untreated deep venous thrombosis (DVT)
• Arterial thrombosis
• Receipt of immunotherapy/immunomodulatory or immunosuppressive agents (e.g., IFNs, tumor necrosis factor, interleukins, immunoglobulins or other biologic response modifiers [GM-CSF, GCSF] =< 6 weeks prior to registration

Related Conditions & MeSH terms

• Carcinoma
• Clinical Stage III HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8
• Human Papillomavirus-Related Carcinoma
• Oropharyngeal Neoplasms
• Stage IVA Oropharyngeal (p16-Negative) Carcinoma AJCC v8
• Stage IVB Oropharyngeal (p16-Negative) Carcinoma AJCC v8

Intervention

Biological:
• Liposomal HPV-16 E6/E7 Multipeptide Vaccine PDS0101
Given SC
• Pembrolizumab
Given IV

Procedure:
• Computed Tomography
Undergo CT, FDG-PET/CT
• FDG-Positron Emission Tomography
Undergo FDG-PET/CT
• Biospecimen Collection
Undergo blood sample collection
• Biopsy
Undergo biopsy

Locations

Country	Name	City	State
United States	Mayo Clinic in Rochester	Rochester	Minnesota

Sponsors (1)

Lead Sponsor	Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Proportion of pathologic and human papillomavirus cell-free tumor deoxyribonucleic acid (ctHPVDNA) response	Will be estimated by the number of successes divided by the total number of evaluable patients. Ninety-five percent confidence intervals for the true success proportion will be calculated according to the exact binomial method for each arm separately.	Up to 2 years
Secondary	Progression-free survival (PFS)	Patients who receive the study drug, but then never return for an evaluation will be censored on their last follow-up date. PFS will be estimated using the method of Kaplan-Meier. PFS rates at 12 and 24 months will also be reported.	From registration to the first of either disease progression or death from any cause, assessed up to 2 years
Secondary	Overall survival (OS)	OS will be estimated using the method of Kaplan Meier.	From registration to death from any cause, assessed up to 2 years
Secondary	Response rate	Will be estimated using Response Evaluation Criteria in Solid Tumors 1.1 criteria. A tumor response is defined to be either a complete response or partial response noted up until surgery. All patients meeting the eligibility criteria who have signed a consent form and have begun treatment will be evaluable for response. Patients who go off study early before having a tumor assessment performed will be considered a failure.	Up to 2 years
Secondary	Incidence of adverse events (AEs)	All patients that have initiated treatment will be considered evaluable for AE analyses. The maximum grade for each type of AE will be recorded for each patient, and frequency tables will be reviewed to determine AE patterns. AEs will be analyzed separately by arm.	Up to 30 days after treatment discontinuation

External Links

•   Mayo Clinic Clinical Trials