Neoantigen Vaccines Prior to Surgery for the Treatment of Patients with Pancreatic Cancer

Inclusion Criteria

• STEP 0 INCLUSION CRITERIA
• Histologically or cytologically confirmed, newly diagnosed, treatment-naïve patients with localized or borderline resectable adenocarcinoma of the pancreas for whom neoadjuvant chemotherapy is considered appropriate; mixed histology will be included as long as the predominant histology is adenocarcinoma. Patients with clinical suspicion of pancreatic adenocarcinoma can be enrolled for pre-treatment biopsy, and must be histologically confirmed to have adenocarcinoma before being treated on study. Patients with squamous carcinoma or neuroendocrine tumor will be excluded
• Evaluable disease, in the opinion of the treating investigator or principal investigator (PI)
• Tissue cores available in sufficient quantity to allow for sequencing. Fine needle aspirate (FNA) specimens are not permitted
• At least 18 years of age
• Life expectancy of > 12 months
• Easter Cooperative Oncology Group (ECOG) performance status =< 1
• White blood count (WBC) ≥ 1.5 K/cumm * Labs can be repeated prior to chemo if needed
• Absolute neutrophil count ≥ 1.0 K/cumm * Labs can be repeated prior to chemo if needed
• Platelets ≥ 50 K/cumm * Labs can be repeated prior to chemo if needed
• Hemoglobin ≥ 8.0 g/dL * Labs can be repeated prior to chemo if needed
• Total bilirubin ≤ 5.0 X institutional upper limit of normal * Patients who have had a stent placed for biliary obstruction and whose liver function is expected to improve may enroll provided serum bilirubin at time of enrollment is within the limits above
• Aspartate aminotransferase (AST)/alanine aminotransferase (ALT) ≤ 5.0 X institutional upper limit of normal * Labs can be repeated prior to chemo if needed
• Creatinine ≤ 2.5 X institutional upper limit of normal OR creatinine clearance ≥ 30 mL/min by Cockcroft-Gault for patients with creatinine levels above institutional normal * Labs can be repeated prior to chemo if needed
• International Normalized Ratio (INR) and activated partial thromboplastin time (PTT) < 2.0 X upper limit of normal (ULN) provided the patient is not on anticoagulation therapy
• Women of childbearing potential and men must agree to use two forms of adequate contraception (hormonal or barrier method of birth control, abstinence) prior to study entry, for the duration of study participation, and for 3 months after completion of the study. Should a woman become pregnant or suspect she is pregnant while participating in this study, she must inform her treating physician immediately
• Able to understand and willing to sign an Institutional Review Board (IRB) approved written informed consent document
• STEP 1 ELIGIBILITY
• Completed at least 4 months of neoadjuvant chemotherapy such as fluorouracil, irinotecan, leucovorin and oxaliplatin (FOLFIRINOX), modified FOLFIRINOX, or gemcitabine + nab-paclitaxel. Dose modifications and/or delays in neoadjuvant chemotherapy may be made at the discretion of the treating physician
• Reimaging within 4 weeks of last dose of chemotherapy demonstrates no evidence of progressive disease. Patients who progress on mFOLFIRINOX and transition to gemcitabine + nab-paclitaxel may still be eligible for vaccine administration at discretion of PI and treating MD provided they do not show progression following completion of chemotherapy and the patient continues to be eligible for surgical resection. Patients who, in the opinion of the treating physician, require SBRT prior to surgery will receive vaccine after surgery regardless of randomization * Patients who progress or recur following neoadjuvant chemotherapy or who are otherwise unable to complete a surgical resection, but who still meet other Step 1 criteria, may still be eligible for vaccine administration with documented treating physician and PI approval
• There is a 1 week washout prior to day 1 of vaccine for patients on daily systemic steroids at doses exceeding 10 mg prednisone
• Must not be receiving or have received any other investigational agents within the last 30 days. Note that patients who are receiving or will be receiving adjuvant chemotherapy are permitted to continue on study and are considered eligible
• Patients may not have received a live vaccine within 30 days prior to the first day of treatment. 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 (e.g. FluMist) are live attenuated vaccines and are not allowed
• Sufficient wound healing per the evaluation of the treating physician

Exclusion Criteria

• STEP 0 EXCLUSION CRITERIA
• Evidence of predominantly neuroendocrine (defined by > 50% histology) tumor, pure neuroendocrine tumor, duodenal adenocarcinoma, or ampullary adenocarcinoma
• History of other malignancy =< 3 years previous with the exception of basal cell or squamous cell carcinoma of the skin which were treated with local resection only, carcinoma in situ of the cervix, or lobular carcinoma in situ (LCIS)/ductal carcinoma in situ (DCIS) of the breast
• Receiving any other investigational agents, or planning to receive other investigational agents as part of neoadjuvant therapy
• Known allergy, or history of serious adverse reaction to vaccines such as anaphylaxis, hives, or respiratory difficulty
• Acute or chronic, clinically significant hematologic, pulmonary, cardiovascular, hepatic renal, and/or other functional abnormality that might jeopardize the health and safety of the participant as determined by the investigator based on medical history, physical examination, laboratory values, and/or diagnostic studies. If needed and appropriate. The final determination related to study eligibility prior to the administration of the first vaccine will be documented by both the PI and sub-investigators in consultation with a specialist
• A psychiatric illness/social situations that would limit compliance with study requirements as determined by the investigator from the medical history, physical exam, and/or medical record
• Prior or currently active autoimmune disease requiring management with immunosuppression. This includes inflammatory bowel disease, ulcerative colitis, Crohn’s disease, systemic vasculitis, scleroderma, psoriasis, multiple sclerosis, hemolytic anemia, immune-mediated thrombocytopenia, rheumatoid arthritis, systemic lupus erythematosus, Sjogren’s syndrome, sarcoidosis, or other rheumatologic disease or any other medical condition or use of medication (e.g., corticosteroids) which might make it difficult for the patient to complete the full course of treatments or to generate an immune response to vaccines. In the case of asthma or chronic obstructive pulmonary disease taking inhaled corticosteroids that does not require daily systemic corticosteroids is acceptable. Additionally, local acting steroids (topical, inhaled, or intraarticular) will be allowed. Patients on intermittent or short course steroids will be allow if the dose does not exceed 4 mg of dexamethasone (or equivalent) per day for > 7 consecutive days. Premedication for chemotherapy does not apply to this criteria and may be administered as per standard of care (SOC) practice. Any patients receiving steroids should be discussed with the PI to determine if eligible
• Pregnant and/or breastfeeding
• Known human immunodeficiency virus (HIV)-positive status
• History of positive test for hepatitis B virus surface antigen (HBsAg) and/or positive hepatitis C antibody result with detectable hepatitis C virus (HCV) ribonucleic acid (RNA) indicating acute or chronic infection