Overview

The investigators propose a phase II single-arm study on using stereotactic body radiation therapy in combination with durvalumab for inoperable/unresectable hepatocellular carcinoma. In addition, the investigators will also measure the change in number and intensity of PD-L1-positive circulating tumor cells before and after stereotactic body radiation therapy and durvalumab and evaluate their correlation with treatment response.

Eligibility

Inclusion Criteria:

1. Patients must have histologically or radiologically confirmed HCC. For radiological diagnosis of HCC, a contrast-enhanced computed tomography or magnetic resonance imaging is mandatory to demonstrate the early arterial enhancement in arterial phase and contrast washout in the porto-venous phase on the imaging.
2. Inoperable or unresectable non-metastatic HCC (in the form of tumor resection or liver transplantation) amenable to stereotactic body radiation therapy given in 5 fractions. Prior locoregional therapy including radiofrequency ablation, transarterial chemoembolisation, radioembolisation is allowed provided that radiologically progressive disease is demonstrated following these locoregional therapies.
3. Capable of giving signed informed consent which includes compliance with the requirements and restrictions listed in the informed consent form (ICF) and in this protocol. Written informed consent and any locally required authorisation (e.g. Health Insurance Portability and Accountability Act in the US, European Union [EU] Data Privacy Directive in the EU) obtained from the patient/legal representative prior to performing any protocol-related procedures, including screening evaluations.
4. Be >/= 18 years of age on day of signing informed consent.
5. Have a performance status of 0 or 1 on the Eastern Cooperative Oncology Group (ECOG) Performance Scale.
6. A stage C or earlier HCC based on Barcelona Clinic Liver Cancer (BCLC) staging system.
7. A Child-Pugh of 7 or less.
8. Demonstrate adequate organ function as defined in Inclusion Criteria 7, all screening labs should be performed 28 days prior to study registration up to the first dose of study drug.
9. Adequate serum hematological functions defined as:
   • Absolute neutrophil count (ANC) ≥1.0 x 10^9/l
   • Platelet ≥50 x 10^9/l
   • Hemoglobin ≥9 g/dL

Adequate serum biochemistry functions defined as:

• Serum bilirubin ≤1.5 x institutional upper limit of normal (ULN). <<This will not apply to patients with confirmed Gilbert's syndrome (persistent or recurrent hyperbilirubinemia that is predominantly unconjugated in the absence of hemolysis or hepatic pathology), who will be allowed only in consultation with their physician.>>
• Serum aspartate aminotransferase (AST) / alanine aminotransferase (ALT) ≤2.5 times of institutional upper limit of normal unless liver metastases are present, in which case it must be ≤5 times of ULN
• Measured creatinine clearance (CL) >40 mL/min or Calculated creatinine CL>40 mL/min by the Cockcroft-Gault formula (Cockcroft and Gault 1976) or by 24-hour urine collection for determination of creatinine clearance:

  Males

Creatinine CL (mL/min) = Weight (kg) x (140 - Age) 72 x serum creatinine (mg/dL)

Females

             Creatinine CL (mL/min) = Weight (kg) x (140 - Age) x 0.85 72 x serum creatinine
             (mg/dL)
         10. International Normalized Ratio (INR) or Prothrombin Time (PT) ≤1.5 times of ULN unless
             subject is receiving anticoagulant therapy as long as PT or activated partitional
             thromboplastin time (APTT) is within therapeutic range of intended use of
             anticoagulants. APTT ≤1.5 times of ULN unless subject is receiving anticoagulant
             therapy as long as PT or APTT is within therapeutic range of intended use of
             anticoagulants.
         11. Female subject of childbearing potential should have a negative urine or serum
             pregnancy within 24 hours of study enrollment up to administration of the dose of
             study drug. If the urine test is positive or cannot be confirmed as negative, a serum
             pregnancy test will be required.
         12. Female subjects of childbearing potential should be willing to use 2 methods of birth
             control or be surgically sterile, or abstain from heterosexual activity for the course
             of the study through 31 weeks after the last dose of study medication. Subjects of
             childbearing potential are those who have not been surgically sterilized or have not
             been free from menses for >1 year. The following age-specific requirements apply:
               -  Women <50 years of age would be considered post-menopausal if they have been
                  amenorrheic for 12 months or more following cessation of exogenous hormonal
                  treatments and if they have luteinizing hormone and follicle-stimulating hormone
                  levels in the post-menopausal range for the institution or underwent surgical
                  sterilization (bilateral oophorectomy or hysterectomy).
               -  Women ≥ 50 years of age would be considered post-menopausal if they have been
                  amenorrheic for 12 months or more following cessation of all exogenous hormonal
                  treatments, had radiation-induced menopause with last menses >1 year ago, had
                  chemotherapy-induced menopause with last menses >1 year ago, or underwent
                  surgical sterilization (bilateral oophorectomy, bilateral salpingectomy or
                  hysterectomy).
         13. Male subjects should agree to use an adequate method of contraception starting with
             the first dose of study therapy through 31 weeks after the last dose of study therapy.
         14. We will allow prior radiation to other sites, with no washout period, prior to study
             entry as long as the high dose regions of the prior and proposed radiation fields do
             not overlap. In patients where the prior high dose area would overlap with the high
             dose area of the intended radiation, a 4 month washout period will be required. The
             safety of such treatment will be at discretion of the treating radiation oncologist.
         15. Prior central nervous system (CNS) radiation is allowed as long as cumulative
             radiation doses do not exceed tolerance of critical structures as judged by the
             treating radiation oncologist.
         16. Patient is willing and able to comply with the protocol for the duration of the study
             including undergoing treatment and scheduled visits and examinations including follow
             up.
         17. Must have a life expectancy of at least 12 weeks.
        Exclusion Criteria:
          1. Is currently participating in or has participated in a study of an investigational
             agent or using an investigational device within 4 weeks of the first dose of treatment
             or 5 half-lives, whichever is shorter.
          2. Has a diagnosis of severe active scleroderma, lupus, other rheumatologic or autoimmune
             disease within the past 3 months before study recruitment. Patients with a documented
             history of clinically severe autoimmune disease or a syndrome requiring systemic
             steroids or immunosuppressive agents will not be allowed on this study. Subjects with
             vitiligo or resolved childhood asthma/atopy are an exception to this rule. Subjects
             that require intermittent use of bronchodilators or local steroid injections are not
             excluded from the study. Subjects with hypothyroidism stable on hormone replacement
             are not excluded from this study.
          3. Has had a prior monoclonal antibody, immunotherapy or immune checkpoint inhibitors
             before recruitment into this study .
          4. Has had prior chemotherapy or targeted small molecule therapy (including sorafenib or
             other anti-vascular endothelial growth factor inhibitor) within 3 weeks prior to
             administration of the study drug or who has not recovered (i.e., ≤Grade 1 or at
             baseline) from adverse events due to a previously administered agent. *Note: Subjects
             with permanent ≤ Grade 2 toxicities (e.g. neuropathy) or toxicities corrected through
             routine medical management (e.g. thyroid replacement for hypothyroidism), are an
             exception to this criterion and may qualify for the study. *Note: If subject received
             major surgery, they must have recovered adequately from the toxicity and/or
             complications from the intervention prior to starting therapy. *Note: Subjects with ≤
             Grade 2 amylase or lipase elevations abnormalities that have no corresponding clinical
             manifestations (e.g. manifestation of pancreatitis), are an exception to this
             criterion and may qualify for the study.
          5. Has a known additional malignancy that is progressing or requires active treatment.
             Exceptions include basal cell carcinoma of the skin, squamous cell carcinoma of the
             skin, indolent lymphomas, or in situ cervical cancer that has undergone potentially
             curative therapy
          6. Has a history of prior solid organ transplants with or without any episodes of
             graft-versus-host disease.
          7. Has a history of allogeneic bone marrow transplantation and peripheral stem cell
             rescue, with or without any episodes of graft-versus-host disease.
          8. Has clinically significant or symptomatic ascites requiring either diuretic therapy or
             paracentesis.
          9. Has known active extra-hepatic metastases. Patients with treated extra-hepatic
             metastases which are stable and not requiring any systemic treatment for ≥ 4 weeks are
             eligible.
         10. Has known carcinomatous meningitis (also known as leptomeningeal carcinomatosis).
         11. Has an active infection requiring intravenous systemic therapy or hospital admission.
         12. Has a history or current evidence of any condition, therapy, or laboratory
             abnormality, including psychiatric or substance abuse disorder, that might confound
             the results of the trial, interfere with the subject's participation for the full
             duration of the trial, or is not in the best interest of the subject to participate,
             in the opinion of the treating investigator.
         13. Is pregnant or breastfeeding, or expecting to conceive or father children within the
             projected duration of the trial, starting with the screening visit through 31 weeks
             after the last dose of trial treatment.
         14. Has a known history of Human Immunodeficiency Virus (HIV) (HIV 1/2 antibodies).
             Routine checking for Anti-HIV1 or Anti-HIV2 is not mandatory.
         15. Untreated hepatitis B infection. Patients with chronic hepatitis B infection (defined
             as HBsAg positive) are eligible if they have started anti-viral therapy for at least 1
             month and is continuing anti-viral treatment throughout the whole duration of this
             study.
         16. Has received a live vaccine 30 days prior to the first dose of trial treatment.
         17. Has experienced Grade 4 toxicity on treatment with prior radiation.
         18. Has experienced Grade 3-4 intracranial toxicity (hypophysitis or CNS toxicity) with
             either prior intracranial radiation, anti programmed cell death-1 (PD-1), or cytotoxic
             T-lymphocyte-associated protein 4 (CTLA-4) inhibitor therapy.
         19. Is taking >4mg/day of dexamethasone or its equivalent at the start of immunotherapy or
             has required >4mg/day of dexamethasone or its equivalent for 3 consecutive days within
             1 week of starting treatment.
         20. Allergies and adverse drug reaction to the following: History of allergy to study drug
             components; History of severe hypersensitivity reaction to any monoclonal antibody.
         21. Prior systemic therapy utilizing an anti CTLA-4 or PD-1/PD-L1 agent or other forms of
             immunotherapy.
         22. Has had prior radiation therapy (defined as >1Gy) to the area planning to be treated
             with SBRT.
         23. Major surgical procedure (as defined by the Investigator) within 28 days prior to the
             first dose of IP. Note: Local surgery of isolated lesions for palliative intent is
             acceptable.
         24. Mean QT interval corrected for heart rate using Fridericia's formula (QTcF) ≥470 ms
             calculated from 3 ECGs (within 15 minutes at 5 minutes apart)
         25. Current or prior use of immunosuppressive medication within 14 days before the first
             dose of durvalumab. The following are exceptions to this criterion:
        (A) Intranasal, inhaled, topical steroids, or local steroid injections (e.g., intra
        articular injection) (B) Systemic corticosteroids at physiologic doses not to exceed <<10
        mg/day>> of prednisone or its equivalent (C) Steroids as premedication for hypersensitivity
        reactions (e.g., CT scan premedication)