PRIMARY OBJECTIVE:
I. To evaluate the safety and tolerability of therapy and assess the pathologic response rate
including pathologic complete response (pCR) and degree of necrosis (> 50% in tumor volume)
with nivolumab + pegargiminase (ADI-PEG 20) in resectable hepatocellular carcinoma (HCC) in
the context of presurgical therapy.
SECONDARY OBJECTIVE:
I. To assess the efficacy of presurgical nivolumab + ADI-PEG 20 therapy in HCC by estimating
the time-to-progression (TTP), recurrence-free survival (RFS), and overall survival (OS).
EXPLORATORY OBJECTIVES:
I. To assess the immunological/biomarker changes (pre- versus [vs] post-treatment) in tumor
tissues and peripheral blood in response to nivolumab + ADI-PEG 20 in HCC therapy.
II. To explore any potential association between these biomarker measures and antitumor
response and immune-related response criteria (irRC) assessed by MD Anderson Department of
Diagnostic Imaging.
OUTLINE:
Patients receive nivolumab intravenously (IV) over 30 minutes on day 1 and pegargiminase
intramuscularly (IM) at 2 days before day 1 of cycle 1, day 8 of cycle 1, days 1 and 8 of
cycle 2, and day 1 of cycle 3. Treatments repeat every 2 weeks for up to 3 cycles in the
absence of disease progression or unacceptable toxicity. Patients then undergo standard of
care surgical resection at week 7.
After completion of study treatment, patients are followed up at 30 days, then every 12 weeks
for up to 2 years.
Inclusion Criteria:
- Must give written informed consent prior to initiation of therapy, in keeping with the
policies of the institution. Patients with a history of major psychiatric illness must
be judged able to fully understand the investigational nature of the study and the
risks associated with the therapy
- Must have histologically confirmed HCC (documentation of original biopsy for diagnosis
is acceptable if tumor tissue is unavailable) or clinical diagnosis by AASLD (American
Association for the Study for Liver Diseases) criteria in cirrhotic subjects (presence
of non-rim arterial phase hyperenhancement relative to the liver parenchyma with
venous washout for tumors >= 1 cm). For subjects without cirrhosis, histological
confirmation is mandatory. The determination of cirrhosis status will ultimately lie
in the clinical judgment of the surgical oncologist and medical oncologist involved in
the care of the patient
- Must be eligible for liver resection with curative intent; diagnosis must be confirmed
by pathologist review of screening biopsy and the determination of resectability
status will ultimately lie in the clinical judgment of the surgical oncologist and
medical oncologist involved in the care of the patient
- Must have measurable disease defined as a lesion that can be accurately measured in at
least one dimension (longest diameter to be recorded) and measures >= 15 mm with
conventional techniques or >= 10 mm with more sensitive techniques such as magnetic
resonance imaging (MRI) or spiral computed tomography (CT) scan
- Allowed are prior treatments for HCC including prior surgery, radiation therapy,
local-regional therapy (ablation or arterial directed therapies), or systemic therapy
including sorafenib or chemotherapy. (Prior anti-PD-1 or ADI-PEG 20 therapies are not
allowed)
- Must have Eastern Cooperative Oncology Group performance status (ECOG PS) score =< 1
- Absolute neutrophil count >= 1,500/uL (within 14 days of the first dose of study drug)
- Platelets >= 100,000/uL (within 14 days of the first dose of study drug)
- Hemoglobin > 9.0 g/dL (may be transfused or receive epoetin alfa [e.g., Epogen] to
maintain or exceed this level) (within 14 days of the first dose of study drug)
- Total bilirubin =< 1.5 mg/dL (within 14 days of the first dose of study drug)
- Serum creatinine =< 1.5 times the upper limit of normal (ULN) or estimated creatinine
clearance > 40mL/min (within 14 days of the first dose of study drug)
- Aspartate transaminase (AST) (serum glutamic-oxaloacetic transaminase [SGOT]) and/or
alanine transaminase (ALT) ) (serum glutamate pyruvate transaminase [SGPT]) =< 5 x
institutional ULN (within 14 days of the first dose of study drug)
- Serum uric acid =< 10 mg/dL (595 umol/L) (with or without medication control) (within
14 days of the first dose of study drug)
- Must be >= 18 years of age
- Must have a negative serum or urine pregnancy test (minimum sensitivity 25 IU/L or
equivalent units of human chorionic gonadotropin [HCG]) within 24 hours prior to the
start of study drug and every 4 weeks while taking nivolumab (for women of
childbearing potential [WOCBP])
- Must not be breastfeeding
- Must agree (WOCBP) to follow instructions for method(s) of contraception from the time
of enrollment for the duration of treatment with study drug (s) for a total of 12
months post treatment completion. Men who are sexually active with WOCBP must agree to
follow instructions for method(s) of contraception for the duration of treatment with
study drug(s) plus 5 half-lives of study drug (s) plus 90 days (duration of sperm
turnover) for a total of 7 months post-treatment completion
- NOTE: Azoospermic males and WOCBP who are continuously not heterosexually active
are exempt from contraceptive requirements. However, WOCBP must still undergo
pregnancy testing as described in these sections. Investigators shall counsel
WOCBP and male subjects who are sexually active with WOCBP on the importance of
pregnancy prevention and the implications of an unexpected pregnancy
Investigators shall advise WOCBP and male subjects who are sexually active with
WOCBP on the use of highly effective methods of contraception. Highly effective
methods of contraception have a failure rate of < 1% per year when used
consistently and correctly. At a minimum, subjects must agree to the use of two
methods of contraception, with one method being highly effective and the other
method being either highly effective or less effective as listed below:
HIGHLY EFFECTIVE METHODS OF CONTRACEPTION
- Male condoms with spermicide
- Hormonal methods of contraception including combined oral contraceptive pills, vaginal
ring, injectables, implants, and intrauterine devices (IUDs) such as Mirena by WOCBP
subject or male subject's WOCBP partner.
- Nonhormonal IUDs, such as ParaGard
- Tubal ligation
- Vasectomy
- Complete Abstinence*
- Complete abstinence is defined as complete avoidance of heterosexual intercourse and
is an acceptable form of contraception for all study drugs. Abstinence is only
acceptable when this is in line with the preferred and usual lifestyle of the subject.
Periodic abstinence (eg, calendar, ovulation, symptothermal, profession of abstinence
for entry into a clinical trial, post-ovulation methods) and withdrawal are not
acceptable methods of contraception. Subjects who choose complete abstinence are not
required to use a second method of contraception, but female subjects must continue to
have pregnancy tests. Acceptable alternate methods of highly effective contraception
must be discussed in the event that the subject chooses to forego complete abstinence.
LESS EFFECTIVE METHODS OF CONTRACEPTION
- Diaphragm with spermicide
- Cervical cap with spermicide
- Vaginal sponge
- Male condom without spermicide*
- Progestin only pills by WOCBP subject or male subject's WOCBP partner
- Female condom*
- A male and female condom must not be used together
- Must not have received prior anticancer therapy with ADI-PEG 20 or anti-PD1 for
HCC. Must not be receiving any concomitant systemic therapy for HCC
Exclusion Criteria:
- Has any other malignancy from which the patient has been disease-free for less than 2
years (exceptions: non-melanoma skin cancer or in situ carcinoma of any site are
allowed)
- Has an organ allograft(s)
- Has had a major surgical procedure, open biopsy, or significant traumatic injury with
poorly healed wound within 6 weeks prior to first dose of study drug; or anticipates
needing for a major surgical procedure during the course of the study (other than
defined by protocol such as the pre-treatment fine needle aspirations or core
biopsies) within 7 days prior to first dose of study drug
- Has a history of inflammatory bowel disease (including Crohn's disease and ulcerative
colitis) or a history of autoimmune disease (e.g., rheumatoid arthritis, systemic
progressive sclerosis [scleroderma], systemic lupus erythematosus, autoimmune
vasculitis [e.g., Wegener's granulomatosis])
- Has a history of testing positive for human immunodeficiency virus or has acquired
immunodeficiency syndrome (AIDS)
- Has any underlying medical condition, which in the opinion of the investigator, will
make the administration of study drug hazardous or will obscure the interpretation of
adverse events, such as a condition associated with frequent diarrhea
- Has a known risk factor for bowel perforation including a history of acute
diverticulitis, abdominal fistula, gastrointestinal perforation, intra-abdominal
abscess, or gastrointestinal obstruction
- Has a primary brain tumor (excluding meningiomas and other benign lesions), any brain
metastases, leptomeningeal disease, seizure disorders not controlled with standard
medical therapy, or (within the past year) a history of stroke
- Has a history of serious systemic disease, including myocardial infarction or unstable
angina within the last 12 months; a history of hypertensive crisis or hypertensive
encephalopathy, uncontrolled hypertension (blood pressure of > 140/90 mmHg) at the
time of enrollment; New York Heart Association (NYHA) grade II or greater congestive
heart failure, unstable symptomatic arrhythmia requiring medication (patients with
chronic atrial arrhythmia, i.e., atrial fibrillation or paroxysmal supraventricular
tachycardia are eligible); significant vascular disease or symptomatic peripheral
vascular disease
- Has a history of other diseases, metabolic dysfunction, physical examination finding,
or clinical laboratory finding giving reasonable suspicion of a disease or condition
that contraindicates the use of an investigational drug or that might affect the
interpretation of the results of the study or render the subject at high risk from
treatment complications
- Is receiving a high dose steroid (e.g., > 10 mg prednisone daily or equivalent) or
other more potent immune suppression medications (e.g., infliximab)
- Has had influenza-, hepatitis-, or other vaccines within a month prior to initiation
of study drugs
- Has had a clinical history of coagulopathy, bleeding diathesis or thrombosis within
the past year
- Has a serious, non-healing wound, ulcer, or bone fracture
- Is pregnant (positive pregnancy test) or lactating
- Had a prior orthotropic liver transplantation
- Has cirrhosis and severe synthetic liver dysfunction (Child Pugh B-C)
- Has received any complementary medications (e.g., herbal supplements or traditional
Chinese medicines) intended to treat the disease under study unless patients agree to
stop the complementary medicines at least 14 days before the first study dose. Such
medications are permitted if they are used as supportive care
- Has received any live / attenuated vaccine (e.g., varicella; zoster; yellow fever;
rotavirus; oral polio; or and measles, mumps, rubella) within a month prior to
initiation of study drug or during treatment are excluded
- Must not be scheduled to receive another experimental drug while on this study
- Must not require ongoing anticoagulation therapy (although aspirin and pre- and
postsurgical prophylactic anti coagulation treatment are permitted
- Must not require total parenteral nutrition
- Not able to be compliant with the appointments required in this protocol
- Has a history of seizure disorder not related to underlying cancer
- Has a known allergy to pegylated compounds
- Has a known allergy to E. coli drug products (such as granulocyte-macrophage colony
stimulating factor)
