Pembrolizumab in Combination With Anti-platelet Therapy for Patients With Recurrent or Metastatic Squamous Cell Carcinoma of the Head and Neck

• ClinicalTrials.gov Identifier: NCT03245489
• Recruitment Status: Recruiting
• First Posted: August 10, 2017
• Last Update Posted: April 30, 2024
• Sponsor: Medical University of South Carolina
• Information provided by (Responsible Party): Medical University of South Carolina

Study Description

Brief Summary:

The purpose of this study is to see if anti-platelet therapy combined with anti-PD-1 immunotherapy can cause a more favorable immunologic response thatn with immunotherapy alone in patients with recurrent or metastatic squamous cell carcinoma of the head and neck.

Condition or disease	Intervention/treatment	Phase
Head and Neck Cancer	Drug: Pembrolizumab; Drug: Clopidogrel; Drug: acetylsalicylic acid	Phase 1

Study Design

• Study Type: Interventional (Clinical Trial)
• Estimated Enrollment: 20 participants
• Allocation: Randomized
• Intervention Model: Crossover Assignment
• Masking: None (Open Label)
• Primary Purpose: Treatment
• Official Title: Pembrolizumab in Combination With Anti-platelet Therapy for Patients With Recurrent or Metastatic Squamous Cell Carcinoma of the Head and Neck
• Actual Study Start Date: March 6, 2018
• Estimated Primary Completion Date: June 30, 2024
• Estimated Study Completion Date: September 30, 2024

Arms and Interventions

Arm	Intervention/treatment
Experimental: Group 1; Group 1 will be treated with Regimen A, followed by Regimen B. Regimen A is pembrolizumab, ASA and clopidogrel daily for 6 weeks. Regimen B is pembrolizumab alone for 6 weeks.	Drug: Pembrolizumab; 200mg intravenous (IV) over 30 minutes; Other Name: Keytruda; Drug: Clopidogrel; 75mg/day oral; Other Name: Plavix; Drug: acetylsalicylic acid; 81mg/day oral; Other Names: ASA; aspirin
Experimental: Group 2; Group 2 will be treated with Regimen B, followed by Regimen A. Regimen B is pembrolizumab alone for 6 weeks. Regimen A is pembrolizumab, ASA and clopidogrel daily for 6 weeks.	Drug: Pembrolizumab; 200mg intravenous (IV) over 30 minutes; Other Name: Keytruda; Drug: Clopidogrel; 75mg/day oral; Other Name: Plavix; Drug: acetylsalicylic acid; 81mg/day oral; Other Names: ASA; aspirin

Outcome Measures

Primary Outcome Measures :

1. Effect of Pembro + antiplatelet on major cellular parameters [ Time Frame: 12 weeks ]
   Immunologic response profile will be measured by changes in major cellular parameters in peripheral blood mononuclear cells pheotyped by flow cytometry for MDSCs, T and B cell activation markers and polyclonal IFNy-production by CD4 and CD8 response after P/I stimulation) in pembrolizumab alone and pembrolizumab + antiplatelet therapy. Markers will be measured at baseline, end of the first regimen and end of the second regimen. Changes in cellular parameters from the previous timepoint will be evaluated using a repeated measures ANOVA model. Cellular parameters will be evaluated in aggregate to report the immunologic response.

Secondary Outcome Measures :

1. Effect of Pembro + antiplatelets on immunologic markers [ Time Frame: 12 weeks ]
   Immunologic markers will be measured in patients who have been treated with two cycles of pembrolizumab alone and who are pembrolizumab naive. Markers will be evaluated by looking at phyenotyping by flow cytometry and changes of 65-panel systemic cytokines and chemokine levels. Markers will be measured at baseline, end of the first regimen and end of the second regimen. Changes to markers will be reported in aggregate to show the overall immunologic effect of the combination of pembrolizumab + Anti-platelets in patients.
2. Frequency of adverse events reported [ Time Frame: 12 weeks ]
   Safety data will be tabulated by type and grade of adverse event and will use CTCAE v. 4.0
3. Tumor response rate [ Time Frame: 12 weeks ]
   Objective response will be evaluated with computed tomography (CT) of the neck, chest and abdomen at baseline and post-treatment using RECIST 1.1 criteria.

Eligibility Criteria

• Ages Eligible for Study: 18 Years and older (Adult, Older Adult)
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Criteria

Inclusion Criteria:

1. Subject has pathologic confirmation of recurrent or metastatic HNSCC, regardless of HPV status.
2. Subject has tumor that expresses PD-L1 (Combined Positive Score [CPS] > 1) as determined by an FDA-approved test or subject has experienced disease progression on or after platinum-containing chemotherapy.
3. Subject's scans have been reviewed at head and neck tumor board to assess tumor involvement.
4. Subject is 18 years of age or older.
5. Subject has measurable disease according to RECIST 1.1. Tumor lesions situated in previously irradiated areas are considered measurable if progression has been demonstrated in such lesions.
6. Subject has an ECOG performance status of 0 to 2
7. Subject has estimated life expectancy of at least 3 months.

8. Subject has adequate hematologic function, defined as:

   1. ANC >1000 K/CUMM
   2. Hemoglobin >8.0 Grams/dL
   3. Platelets >75,000 K/CUMM
   4. INR < 1.7
9. Subject has adequate renal function, defined as estimated creatinine clearance > 30 mL/min according to the Cockcroft-Gault formula.

10. Subject has adequate hepatic function, defined as:

    1. Total bilirubin ≤ 1.5 x ULN
    2. AST and ALT ≤ 2.5 x ULN
11. Female and male subjects of childbearing potential must be willing to use an adequate method of contraception for the course of the study through 120 days after the last dose of study medication. Effective forms of contraception include abstinence, hormonal contraceptive in conjunction with a barrier method, or a double barrier method. Women of non-child-bearing potential may be included if they are either surgically sterile or have been post-menopausal for > 1 year.

Note: Female subjects of childbearing potential must have a negative urine or serum pregnancy test within 14 days of registration. If the urine test is positive or cannot be confirmed as negative, a serum pregnancy test will be required.

Exclusion Criteria:

1. Subject is receiving concomitant immunosuppressive therapy, defined as:

   1. Immunosuppressants, including: tacrolimus, sirolimus, everolimus, cyclosporine, azathioprine, mycophenolate mofetil, antithymocyte globulin, basiliximab, belatacept
   2. Systemic corticosteroids (except for short term treatment of allergic reactions or for treatment of irAE). Steroids with no or minimal systemic effect (topical, inhalation) are allowed.
   3. Chemotherapy
   4. Immunotherapy
   5. Monoclonal antibodies
2. Concurrent anticancer treatment within 14 days before the start of trial treatment.
3. Subject has had major surgery within the last 28 days.
4. Subject has an underlying bleeding disorder.
5. Subjects requiring re-irradiation to head and neck.
6. Subject is receiving anticoagulation (see section 7.2 for medication examples). Subjects must have a washout period of 7 days from registration.
7. Subject has HNSCC with abutment or encasement of the internal carotid artery, external carotid artery or common carotid artery or any of the arterial branches.
8. Subject has a draining fistula or wound in the head/neck.
9. Subject with known aneurysm or pseudoaneurysm of the head/neck related to surgery.
10. Subject has uncontrolled CNS metastases. Subjects with previously treated brain metastases will be allowed if the brain metastases have been stable without CNS-directed therapy (such as radiation or surgery) or steroid treatment for for at least 4 weeks prior to registration.
11. Receipt of any organ transplantation.
12. Active or history of any autoimmune disease (except type I DM, vitiligo, psoriasis, hypo- or hyperthyroid disease not requiring immunosuppressive treatment, which are allowed) or immunodeficiencies.
13. Known severe hypersensitivity reactions to monoclonal antibodies (grade ≥ 3NCI-CTCAE v4.0), any history of anaphylaxis or uncontrolled asthma.
14. Subjects who have a hypersensitivity to aspirin or NSAIDs.
15. Concurrent NSAID therapy (see section 7 for examples). Subjects must have a washout period of 7 days from registration.
16. Subjects with an acute gastrointestinal ulcer.
17. Subjects with active hemorrhagic diathesis.
18. Clinically significant (i.e., active) cardiovascular disease: cerebral vascular accident/stroke (< 6 months prior to enrollment), myocardial infarction (< 6 months prior to enrollment), unstable angina, congestive heart failure (NYHA class ≥ II), or serious uncontrolled cardiac arrhythmia.
19. All other significant diseases, which in the opinion of the investigator, may impair the subject's tolerance of trial treatment.
20. Vaccination within 4 weeks of the 1st dose of pembrolizumab and while on study is prohibited EXCEPT for administration of inactivated vaccines (e.g. inactivated influenza vaccine).
21. Women who are pregnant or nursing.

Contacts and Locations

Contacts

Contact: Christina Godwin; 843-792-8876; hcc-clinical-trials@musc.edu

Locations

United States, South Carolina

Medical University of South Carolina; Recruiting

Charleston, South Carolina, United States, 29425

Contact: Christina Godwin 843-792-8876 hcc-clinical-trials@musc.edu

Sponsors and Collaborators

Medical University of South Carolina

Investigators

• Principal Investigator: John Kaczmar, MD; Medical University of South Carolina

More Information

• Responsible Party: Medical University of South Carolina
• ClinicalTrials.gov Identifier: NCT03245489
• Other Study ID Numbers: 102727
• First Posted: August 10, 2017
• Last Update Posted: April 30, 2024
• Last Verified: April 2024

Individual Participant Data (IPD) Sharing Statement:

• Plan to Share IPD: No

• Studies a U.S. FDA-regulated Drug Product: Yes
• Studies a U.S. FDA-regulated Device Product: No
• Product Manufactured in and Exported from the U.S.: No

Additional relevant MeSH terms:

Carcinoma, Squamous Cell; Squamous Cell Carcinoma of Head and Neck; Carcinoma; Neoplasms, Glandular and Epithelial; Neoplasms by Histologic Type; Neoplasms; Neoplasms, Squamous Cell; Head and Neck Neoplasms; Neoplasms by Site; Aspirin; Pembrolizumab; Clopidogrel; Antineoplastic Agents, Immunological; Antineoplastic Agents; Immune Checkpoint Inhibitors; Molecular Mechanisms of Pharmacological Action; Anti-Inflammatory Agents, Non-Steroidal; Analgesics, Non-Narcotic; Analgesics; Sensory System Agents; Peripheral Nervous System Agents; Physiological Effects of Drugs; Anti-Inflammatory Agents; Antirheumatic Agents; Fibrinolytic Agents; Fibrin Modulating Agents; Platelet Aggregation Inhibitors; Cyclooxygenase Inhibitors; Enzyme Inhibitors; Antipyretics