| Eligibility |
Inclusion Criteria:
1. Fully-informed written consent.
2. Males and females = 18 years of age
*There are no data that indicate special gender distribution. Therefore patients will
be enrolled in the study gender-independently.
3. Unresectable, multinodular tumour, not eligible for resection or local ablation
4. Histologically confirmed diagnosis of hepatocellular carcinoma
5. Has a Child-Pugh Classification score = 6 for assessed liver function within 7 days
before allocation (Appendix 4: Child-Pugh Score)
6. At least one measurable site of disease as defined by RECIST 1.1 criteria with spiral
CT scan or MRI.
7. Eastern Cooperative Oncology Group (ECOG) performance status = 1.
8. Life expectancy of at least 12 weeks.
9. Adequate bone marrow, hepatic and renal function including the following:
- Haemoglobin = 10.0 g/dL, absolute neutrophil count = 1,500 /µL, platelets =70,000
/µL;
- Total bilirubin = 3.0 mg/dL upper normal limit;
- AST (SGOT), ALT (SGPT) = 5 x upper normal limit;
- International normalized ratio (INR) =1.25;
- Albumin = 30 g/dL;
- Creatinine = 1.5 x upper normal limit OR measured or calculated creatinine
clearance (according to Cockcroft-Gault) =30 mL/min for participant with
creatinine levels >1.5 × institutional ULN (GFR can also be used in place of
creatinine or CrCl)
10. Female patients with reproductive potential must have a negative urine or serum
pregnancy test within 7 days prior to start of trial. Women must not be breastfeeding.
11. If patient has concurrent Hepatitis B virus (HBV) or Hepatitis C virus (HCV)
infection, meets the following criteria:
- Patients with HBV or HCV infection should be monitored for viral levels during
study participation.
- Patients with detectable hepatitis B surface antigen (HBsAg) or detectable HBV
DNA should have HBV DNA < 100 IU/ml and should be managed per local treatment
guidelines.
Controlled (treated) hepatitis B subjects will be allowed if they started treatment at
the time point of enrollment into the study by the latest and treatment is continued
during study participation and for = 6 months after end of study treatment.
- HCV patients with with advanced HCC are mostly not treated for their HCV infection.
However, patients treated for HCV are considered suitable for inclusion if antiviral
therapy has been completed = 30 days prior to first administration of study drug.
12. The patient is willing and able to comply with the protocol for the duration of the
study, including hospital visits for treatment and scheduled follow-up visits and
examinations.
13. WOCBP must agree to follow instructions for method(s) of contraception for a period of
30 days (duration of ovulatory cycle) plus the time required for the investigational
drug to undergo 5 half-lives. The terminal half-lives of nivolumab is approximately 25
days. WOCBP should use an adequate method to avoid pregnancy for approximately 5
months (30 days plus the time required for nivolumab to undergo 5 half-lives) after
the last dose of investigational drug.
14. Males who are sexually active with WOCBP must agree to follow instructions for
method(s) of contraception for a period of 90 days (duration of sperm turnover) plus
the time required for the investigational drug to undergo 5 half-lives. The terminal
half-lives of nivolumab is approximately 25 days. Males who are sexually active with
WOCBP must continue contraception for approximately 7 months (90 days plus the time
required for nivolumab to undergo 5 half-lives) after the last dose of investigational
drug. In addition, male subjects must be willing to refrain from sperm donation during
this time.
Exclusion Criteria:
1. Previous systemic therapy in the first-line setting.
2. Patients on a liver transplantation list or with advanced liver disease as defined
below:
- Encephalopathy
- Untreatable Ascites.
3. Known fibrolamellar HCC, sarcomatoid HCC, or mixed cholangiocarcinoma and HCC.
4. Prior organ allograft or allogeneic bone marrow transplantation.
5. Local therapies ongoing or completed <4 weeks prior to the baseline scan.
6. Thrombotic or embolic events such as cerebrovascular accident (including transient
ischemic attacks), deep vein thrombosis or pulmonary embolism within the 6 months
prior to the first dose of study drug with the exception of thrombosis of a segmental
portal vein.
7. Prior, systemic anti-cancer chemotherapy, radiotherapy administered <4 weeks prior to
study entry, endocrine- or immunotherapy or use of other investigational agents.
8. History of (non-infectious) pneumonitis that required steroids or current pneumonitis.
9. Major surgery within 4 weeks of starting the study. Patients must have recovered from
effects of major surgery.
10. Malignancies other than disease under study within 5 years prior to inclusion, with
the exception of those with a negligible risk of metastasis or death (e.g., expected
5-year OS > 90%) treated with expected curative outcome (such as adequately treated
carcinoma in situ of the cervix, basal or squamous cell skin cancer, localized
prostate cancer treated surgically with curative intent, ductal carcinoma in situ
treated surgically with curative intent)
11. Uncontrolled hypertension.
12. Clinically significant cardiovascular disease.
13. Any serious or uncontrolled medical disorder or active infection that, in the opinion
of the investigator, may increase the risk associated with study participation, study
drug administration, or would impair the ability of the subject to receive study drug.
14. Proteinuria (=2g/24h)
15. Psychiatric disorders or altered mental status precluding understanding of the
informed consent process and/or compliance with the study protocol.
16. Subjects with a history of or current CNS metastases. A scan to confirm the absence of
brain metastases is not required. Patients with unknown CNS metastatic status and any
clinical signs indicative of CNS metastases are eligible if CNS metastases are
excluded using CT and/or MRI scans.
17. Pregnant or breast-feeding women.
18. Immunocompromised patients, e.g. patients who are known to be serologically positive
for human immunodeficiency virus (HIV).
19. Subjects with active, known, or suspected autoimmune disease. Subjects with Type I
diabetes mellitus, residual hypothyroidism due to autoimmune thyroiditis only
requiring hormone replacement, or skin disorders (such as vitiligo, psoriasis, or
alopecia) not requiring systemic treatment are permitted to enroll. For any cases of
uncertainty, it is recommended that the medical monitor be consulted prior to signing
informed consent.
20. Subjects with a condition requiring systemic treatment with either corticosteroids (>
10 mg daily prednisone equivalents) or other immunosuppressive medications within 14
days of study drug administration. Inhaled or topical steroids, and adrenal
replacement doses > 10 mg daily prednisone equivalents are permitted in the absence of
active autoimmune disease.
21. Prior treatment with an anti-PD-1, anti-PD-L1, anti-PD-L2, anti-CD137, or anti-CTLA-4
antibody, or any other antibody or drug specifically targeting T-cell co-stimulation
or checkpoint pathways.
22. All toxicities attributed to prior anti-cancer therapy other than hearing loss,
alopecia and fatigue must have resolved to Grade 1 (NCI CTCAE version 4.03) or
baseline before administration of study drug.
23. > Grade 1 peripheral neuropathy according to CTCAE version 4.03
24. Patients who have received a live vaccine within 30 days prior to enrolment.
25. History of allergy or hypersensitivity to study drugs or any constituent of the
products
26. Is currently participating in or has participated in a study of an investigational
agent or has used an investigational device within 4 weeks prior to the first dose of
study treatment.
27. Patient who has been incarcerated or involuntarily institutionalized by court order or
by the authorities § 40 Abs. 1 S. 3 Nr. 4 AMG.
28. Patients who are unable to consent because they do not understand the nature,
significance and implications of the clinical trial and therefore cannot form a
rational intention in the light of the facts [§ 40 Abs. 1 S. 3 Nr. 3a AMG].
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