| Eligibility |
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.
General Inclusion Criteria:
- 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.
Exclusion Criteria:
HCC specific criteria (Group A):
- Target Disease Exceptions
1. Known fibrolamellar HCC, sarcomatoid HCC, or mixed cholangiocarcinoma and HCC.
2. Any evidence of tumour metastasis or co-existing malignant disease.
3. Participants showing evidence of macrovascular invasion on imaging tests.
4. Participants who have undergone a liver transplant or those who are in the
waiting list for liver transplantation.
5. Participants previously receiving any prior systemic therapy, trans-arterial
embolization or chemoembolisation (TAE/TACE), selective internal radiation
therapy (SIRT) and stereotactic radiation therapy (SBRT) for HCC.
CRLM specific criteria (Group B)
- Target Disease Exceptions a) Patients with extra-hepatic colorectal metastases.
General Inclusion Criteria:
- 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
- Other Exclusion Criteria
1. Prisoners or participants who are involuntarily incarcerated.
2. Participants who are compulsorily detained for treatment of either a psychiatric
or physical (e.g., infectious disease) illness.
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