Neoantigen Dendritic Cell Vaccine and Nivolumab in HCC and Liver Metastases From CRC

Inclusion Criteria

• •HCC specific criteria (Group A):
• •Participants must have either newly diagnosed or recurrent HCC, confirmed by histology/cytology or clinically by AASLD criteria in cirrhotic subjects amenable for management with curative intent by resection (with or without the addition of local ablation), if they fulfil the following radiological criteria.
• •1. Up to three tumours, at least one with a diameter \> 3cm
• •2. More than three tumours, none with a diameter \> 5 cm
• •3. Recurrent HCCs are permitted if they were previously treated with curative intent (e.g. by surgery or ablative methods) and with liver-limited recurrence fulfilling criteria (a) and (b)
• •Child-Pugh Score 5 or 6
• •All participants are required to have imaging studies (CT chest, tri-phasic CT/MRI of the liver, contrast-enhanced CT/MRI of abdomen and pelvis and other suspected/known sites of disease, and bone scans if indicated) confirming no-extra-hepatic metastatic disease within 12 weeks prior to study enrolment.
• •CRLM specific criteria (Group B):
• •Patients with histologically- or cytologically-diagnosed colorectal cancer with liver-limited metastases are eligible to enrol if:
• •1. There are no other sites of metastases aside from the liver confirmed by imaging studies (contrast-enhanced CT chest, abdomen and pelvis or contrast-enhanced CT chest and MRI abdomen and pelvis and other suspected sites of disease, and bone scans if indicated) at least 12 weeks prior to study enrolment AND
• •2. The liver metastases are amenable and planned for curative surgical resection with or without the addition of local ablation AND
• •3. The primary colorectal tumour had previously been resected or is amendable and planned for surgical resection.
• •Participants must have received peri-operative chemotherapy or are being planned for adjuvant chemotherapy after curative surgical resection
• •Participants with rectal cancer who received neoadjuvant radiation or are planned for adjuvant radiation are allowed into the study.
• •Participants are eligible to enroll if they have non-viral related-HCC, or if they have HBV-HCC, or HCV-HCC defined as follows:
• •1. Non-HBV non-HCV related HCC
• •2. HBV-HCC:
• •1. Resolved HBV infection (as evidenced by detectable HBV surface antibody, detectable HBV core antibody, undetectable HBV DNA, and undetectable HBV surface antigen), OR
• •2. Chronic HBV infection as evidenced by detectable HBV surface antigen or HBV DNA. Participants with chronic HBV infection must be on antiviral therapy
• •3. HCV-HCC:
• •1. Resolved HCV infection as evidenced by detectable antibody, OR
• •2. Chronic HCV infection as evidenced by detectable HCV RNA.
• •Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0 or 1
• •Screening laboratory values must meet the following criteria, and should be obtained within 28 days prior to study enrolment:
• •1. Adequate hematologic function:
• •1. WBC ≥ 2,000/μL (stable, off any growth factor within 4 weeks of study treatment administration);
• •2. Neutrophils Absolute ≥ 1,500/μL (stable, off any growth factor within 4 weeks of study treatment administration);
• •3. Hemoglobin ≥ 8.5 g/dL (may be transfused to meet this requirement);
• •4. Platelet count ≥ 60 × 103/μL (transfusion to achieve this level is not permitted);
• •2. Adequate hepatic function:
• •1. Serum albumin \> 2.8 g/L (transfusion to meet this level is not permitted); and
• •2. Serum total bilirubin \< 3 mg/dL, and
• •3. Serum Aspartate Aminotransferase (AST) and Alanine Aminotransferase (ALT) ≤ 5 × ULN;
• •3. Prothrombin time (PT)-international normalized ratio (INR) \< 2.3 or Prothrombin time (PT) \< 6 seconds (transfusion to achieve this level is not permitted)
• •4. Adequate renal function with a serum creatinine of \< 1.5 × ULN or a creatinine clearance \> 40 mL/min (Cockcroft-Gault formula)
• •Age and Reproductive Status:
• •1. Males and females, ages 21 or older.
• •2. Women of childbearing potential (WOCBP) must have a negative serum or urine pregnancy test within 24 hours prior to the start of study treatment.
• •3. Women must not be breastfeeding.
• •4. WOCBP must agree to follow instructions for method(s) of contraception (i.e., a hormonal contraceptive, intra-uterine device, diaphragm with spermicide, or condom with spermicide, or abstinence) for the duration of study treatment with nivolumab and 7 months after the last dose of study treatment.
• •5. Males who are sexually active with WOCBP must agree to follow instructions for method(s) of contraception (i.e., a hormonal contraceptive, intra-uterine device, diaphragm with spermicide, or condom with spermicide, or abstinence) for the duration of study treatment with nivolumab and 7 months after the last dose of study treatment. In addition, male participants must be willing to refrain from sperm donation during this time.
• •6. Azoospermic males are exempt from contraceptive requirements. WOCBP who are continuously not heterosexually active are also exempt from contraceptive requirements, and still must undergo pregnancy testing as described in this section.
• •Medical Conditions
• •1. Active co-infection with:
• •1. Both hepatitis B and C as evidenced by detectable HBV surface antigen (HBs Ag) or HBV DNA and HCV RNA, OR
• •2. Hepatitis D infection in participants with hepatitis B
• •2. Known positive test for human immunodeficiency virus (HIV) or known acquired immunodeficiency syndrome (AIDS).
• •3. Any serious or uncontrolled medical disorder that, in the opinion of the investigator, may increase the risk associated with study participation or study drug administration, impair the ability of the participant to receive protocol therapy, or interfere with the interpretation of study results.
• •4. Participants with an active, known or suspected autoimmune disease. Participants with type I diabetes mellitus, hypothyroidism only requiring hormone replacement, skin disorders (such as vitiligo, psoriasis, or alopecia) not requiring systemic treatment, or conditions not expected to recur in the absence of an external trigger are permitted to enroll.
• •5. Participants with a condition requiring systemic treatment with either corticosteroids (\> 10 mg daily prednisone equivalent) or other immunosuppressive medications within 14 days of start of study treatment. Inhaled or topical steroids, and adrenal replacement steroid doses \> 10 mg daily prednisone equivalent, are permitted in the absence of active autoimmune disease.
• •6. Prior malignancy active within the previous 3 years except for locally curable cancers that have been apparently cured, such as basal or squamous cell skin cancer, superficial bladder cancer, or carcinoma in situ of the prostate, cervix, or breast.
• •Prior/Concomitant Therapy
• •1. Participants receiving or expected to receive IFN-based therapies during the study period.
• •2. Prior treatment with an anti-PD-1, anti-PD-L1, anti-PD-L2, or anti-CTLA-4 antibody, or any other antibody or drug specifically targeting T-cell co-stimulation or checkpoint pathways.
• •3. Treatment with botanical preparations (e.g., herbal supplements or traditional Chinese medicines) intended for general health support or to treat the disease under study within 2 weeks prior to start of therapy.
• •Physical and Laboratory Test Findings
• •a. Positive pregnancy test
• •Allergies and Adverse Drug Reaction
• •1. History of severe hypersensitivity to a monoclonal antibody.
• •2. History of allergy or hypersensitivity to study drug components