Anti-platelet + Pembro for H&N Tumors

Prior treatment

• Subject is receiving concomitant immunosuppressive therapy, defined as:
  • Immunosuppressants, including: tacrolimus, sirolimus, everolimus, cyclosporine, azathioprine, mycophenolate mofetil, antithymocyte globulin, basiliximab, belatacept
  • 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.
  • Chemotherapy
  • Immunotherapy
  • Monoclonal antibodies
• Concurrent anticancer treatment within 14 days before the start of trial treatment.
• Subject has had major surgery within the last 28 days.
• Subjects requiring re-irradiation to head and neck.
• Subject is receiving anticoagulation (see section 7.2 for medication examples). Subjects must have a washout period of 7 days from registration.
• Subject with known aneurysm or pseudoaneurysm of the head/neck related to surgery.
• 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.
• Receipt of any organ transplantation.
• Concurrent NSAID therapy (see section 7 for examples). Subjects must have a washout period of 7 days from registration.
• 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.
• 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).

Other illness

• Subject has an underlying bleeding disorder.
• Subject has a draining fistula or wound in the head/neck.
• 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.
• Known severe hypersensitivity reactions to monoclonal antibodies (grade ≥ 3NCI-CTCAE v4.0), any history of anaphylaxis or uncontrolled asthma.
• Subjects who have a hypersensitivity to aspirin or NSAIDs.
• Subjects with an acute gastrointestinal ulcer.
• All other significant diseases, which in the opinion of the investigator, may impair the subject's tolerance of trial treatment.

Other

• 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.
• Subjects with active hemorrhagic diathesis.
• Women who are pregnant or nursing.

• Subject has pathologic confirmation of recurrent or metastatic HNSCC, regardless of HPV status.
• 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.
• Subject's scans have been reviewed at head and neck tumor board to assess tumor involvement.
• Subject is 18 years of age or older.
• 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.
• Subject has an ECOG performance status of 0 to 2
• Subject has estimated life expectancy of at least 3 months.
• Subject has adequate hematologic function, defined as:
  • ANC \>1000 K/CUMM
  • Hemoglobin \>8.0 Grams/dL
  • Platelets \>75,000 K/CUMM
  • INR \< 1.7
• Subject has adequate renal function, defined as estimated creatinine clearance \> 30 mL/min according to the Cockcroft-Gault formula.
• Subject has adequate hepatic function, defined as:
  • Total bilirubin ≤ 1.5 x ULN
  • AST and ALT ≤ 2.5 x ULN
• 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.