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Summary

for people ages 18 years and up (full criteria)
at San Francisco, California
study started
estimated completion:

Description

Summary

This study is designed to determine the best-tolerated dose and safety of sorafenib combined with the immune checkpoint inhibitor, nivolumab, in treating participants with hepatocellular carcinoma (primary liver cancer) that cannot be removed by surgery. Sorafenib may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Immune checkpoint inhibitors, such as nivolumab, may help the immune system inhibit the cancer.

Official Title

Multicenter Pilot Study of the Safety, Efficacy, and Immune Cell Profiling in Advanced Hepatocellular Carcinoma (HCC) Patients Treated With the Combination of Sorafenib Plus Nivolumab as First-Line of Systemic Therapy

Details

OUTLINE: This is a dose-escalation and expansion study of sorafenib in combination with nivolumab.

DOSE-ESCALATION (Part 1): Between 3-12 patients will be enrolled in Part 1. Participants receive sorafenib 400 mg orally (PO) once daily (QD) or twice daily (BID) on days 1-28, and nivolumab 240 mg intravenously (IV) over 30 minutes on days 1 and 15. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.

DOSE EXPANSION (Part 2): New participants are assigned to 1 of 2 arms.

LEAD-IN ARM I: Participants receive nivolumab IV over 30 minutes on days 1 and 15, and sorafenib PO beginning on day 15 of course 1, then on days 1-28 of subsequent courses. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.

LEAD-IN ARM II: Participants receive sorafenib PO on days 1-28, and nivolumab IV over 30 minutes beginning on day 15 of course 1, then on days 1 and 15 of subsequent courses. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, participants are followed up at 30 and 100 days, then every 3 months for up to 2 years.

Keywords

Stage III Hepatocellular Carcinoma AJCC v8 Stage IIIA Hepatocellular Carcinoma AJCC v8 Stage IIIB Hepatocellular Carcinoma AJCC v7 Stage IIIC Hepatocellular Carcinoma AJCC v7 Stage IV Hepatocellular Carcinoma AJCC v8 Stage IVA Hepatocellular Carcinoma AJCC v8 Stage IVB Hepatocellular Carcinoma AJCC v8 Carcinoma Carcinoma, Hepatocellular Nivolumab Sorafenib Antibodies, Monoclonal Niacinamide

Eligibility

You can join if…

Open to people ages 18 years and up

  • Histologic or cytologic diagnosis of unresectable, locally advanced and/or metastatic hepatocellular carcinoma (HCC) not amenable to curative surgery, transplantation, or ablative therapies based upon assessment of treating investigator
  • Radiographically measurable disease by RECIST version 1.1 in at least one site not previously treated with chemoembolization, radioembolization, radiation, or other local/liver-directed procedures (i.e. must have at least one measurable target lesion,either within the liver or in a measurable metastatic site); a new area of tumor progression within or adjacent to a previously-treated lesion, if clearly measurable by a radiologist, is acceptable
  • Untreated/pretreatment archival tumor tissue must be available for correlative analyses
  • Eastern Cooperative Oncology Group (ECOG) 0 or 1 at enrollment
  • At least 4 weeks after any prior chemoembolization, radioembolization, local ablative therapies, or hepatic radiation and recovery to =< grade 1 treatment-related toxicity
  • At least 6 weeks after any major surgery including prior hepatic resection and recovery to =< grade 1 treatment-related toxicity
  • At least 7 days after minor surgery (such as central venous access) or biopsy and recovery to =< grade 1 treatment-related toxicity
  • At least 2 weeks after any prior palliative radiation (e.g. to focal metastatic lesion such as bone metastases) and recovery to =< grade 1 treatment-related toxicity
  • Blood pressure less than 140/90 mm Hg with or without anti-hypertensive therapy
  • Patients may be rescreened after initial ineligibility if due to elevated blood pressure, if adequately medically managed within approximately 30 days
  • Absolute neutrophil count at least 1,200/mcL
  • Platelets at least 75,000/mcL
  • Hemoglobin at least 9 g/dL
  • Total bilirubin less than 2 mg/dL or 1.5 times upper limit of normal (ULN)
  • Aspartate aminotransferase (AST) (serum glutamic-oxaloacetic transaminase [SGOT]) and alanine aminotransferase (ALT) (serum glutamic-pyruvic transaminase [SGPT]) less than 5 X ULN
  • International normalized ratio (INR) less than 1. 5 X ULN
  • Albumin at least 2.8 g/dL
  • Creatinine less than 1. 5 X ULN and/or creatinine clearance >= 60 mL/min
  • Child Pugh A score 5 or 6 liver function
  • If HBV surface antigen (sAg) and/or core antibody (Ab) positive, must be treated with appropriate antiviral therapy according to institutional practice with HBV deoxyribonucleic acid (DNA) by polymerase chain reaction (PCR) less than 500 IU/mL
  • If clinical or histologic diagnosis of cirrhosis and/or clinical or radiographic evidence esophageal or gastric varices, must have had esophagogastroduodenoscopy (EGD)surveillance and adequate endoscopic therapy according to institutional standards
  • Able to swallow and retain oral medications
  • Women of child-bearing potential (WOCBP) must have a negative pregnancy test within 28 days before study enrollment
  • WOCBP and male partners of WOCBP must agree to use two methods of contraception until at least 5 months after last dose of each study drug for WOCBP subjects, and 7 months for male partners of WOCBP
  • Able to understand and willingness to provide informed consent, and the willingness to comply with the requirements of the protocol
  • Subjects must have signed and dated an Institutional Review Board(IRB)/Independent Ethics Committees (IEC) approved written informed consent form in accordance with regulatory and institutional guidelines and before the performance of any protocol related procedures that are not part of standard of care

You CAN'T join if...

  • Any prior systemic therapy for HCC
  • Known fibrolamellar or mixed HCC-cholangiocarcinoma histology
  • Requirement for diuretics, paracentesis, or other medications or procedures to control ascites or hepatic encephalopathy within 6 months before enrollment
  • Diuretics or medications such as lactulose used for other indications (e.g.edema, constipation) are allowed
  • History of upper gastrointestinal (GI) bleeding from esophageal and/or gastric varices within 12 months before enrollment
  • Requirement for systemic corticosteroids unless used for adrenal replacement, acute therapy for asthma or bronchitis exacerbation (=< 2 weeks), or premedication for contrast allergy
  • Topical, intranasal, or inhaled steroids are not excluded
  • Active autoimmune condition requiring systemic immunosuppressive medication
  • Known human immunodeficiency virus (HIV) infection
  • Active coinfection with HBV plus hepatitis delta (D) virus (HDV) or HCV:
  • Both hepatitis B and C as evidenced by detectable HBV surface antigen or HBV DNA and detectable HCV ribonucleic acid (RNA)
  • Hepatitis D infection (HDV antibody positive) in subjects with detectable hepatitis B surface antigen or HBV DNA
  • Prior allogeneic transplant of any solid organ or bone marrow/stem cells
  • Symptomatic hypothyroidism without replacement
  • Patients may be rescreened after initiating adequate replacement therapy
  • History of seizure disorder requiring antiepileptic medication or brain metastases with seizures
  • Non-healing wound, ulcer, non-healing traumatic bone fracture, or abscess within 30 days of enrollment
  • Nondisplaced, uncomplicated pathologic fracture due to tumor may be eligible provided adequately treated with radiation, surgery or other treatments with full recovery based upon investigator assessment
  • Central or necrotic lung metastases
  • Known brain or leptomeningeal metastases
  • Uncontrolled hypertension (systolic pressure >140 mm Hg and/or diastolic pressure > 90 mm Hg [National Cancer Institute (NCI)-Common Terminology Criteria for Adverse Events(CTCAE) v4.0] on repeated measurement) despite optimal medical management
  • Active or clinically significant cardiac disease including:
  • Congestive heart failure ? New York Heart Association (NYHA) > class II
  • Active coronary artery disease including unstable or newly diagnosed angina or myocardial infarction within 6 months prior to study entry
  • Cardiac arrhythmias requiring anti-arrhythmic therapy other than beta blockers or digoxin
  • Corrected QT interval (QTc) (Fridericia) > 450 msec on two consecutive electrocardiograms (ECGs) (baseline ECG should be repeated if QTc is found to be> 450 msec)
  • Subject with any pulmonary hemorrhage/bleeding event of NCI-CTCAE v4.0 Grade 2 or higher within 6 months before first dose of study treatment any other hemorrhage/bleeding event of NCI-CTCAE v4.0 Grade 3 or higher within 6 months before first dose of study treatment
  • Subjects with thrombotic, embolic, venous, or arterial events, such as cerebrovascular accident (including transient ischemic attacks) or deep venous thrombosis (DVT) within 6 months of informed consent
  • Tumor or bland thrombus in hepatic vasculature is not a contraindication provided hepatic function criteria are met
  • Subjects who have used strong CYP3A4 inducers (eg, phenytoin, carbamazepine,phenobarbital, St. John?s wort [hypericum perforatum], dexamethasone at a dose of greater than 16 mg daily, or rifampin [rifampicin], and/or rifabutin) within 28 days before first dose of study treatment
  • Subjects who require therapeutic anticoagulation or anti-platelet therapy
  • Low dose aspirin (=< 100 mg/day) is allowed
  • Prophylactic doses of low molecular weight heparin (LMWH) are allowed if approved by study chair or designee
  • Subjects with any previously untreated and concurrent cancer that is distinct in primary site or histology from HCC except cervical cancer in-situ, treated nonmelanoma skin cancers, localized prostate cancer not requiring systemic therapy undergoing surveillance, or superficial bladder tumor; subjects surviving a cancer that was curatively treated and without evidence of disease for more than 2 years before enrollment are allowed provided that cancer therapy was completed at least 2 years prior to study entry (date of the informed consent form)
  • Any uncontrolled intercurrent illness including, but not limited to: ongoing or active infection requiring antibiotic therapy, pulmonary disease impairing functional status or requiring oxygen, impairment in gastrointestinal function that may affect or alter absorption of oral medications (such as malabsorption or history of gastrectomy or bowel resection), or uncontrolled diarrhea
  • Known or suspected allergy or hypersensitivity to any of the study drugs, study drug classes, or excipients of the formulations given during the course of this trial
  • Women who are pregnant or breast-feeding at enrollment
  • Inability to comply with the protocol and/or not willing or not available for followup assessments
  • Any condition which, in the investigator's opinion, makes the subject unsuitable for trial participation

Location

  • University of California, San Francisco accepting new patients
    San Francisco, California, 94158, United States

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
University of California, San Francisco
ID
NCT03439891
Phase
Phase 2
Lead Scientist
Robin Kelley
Study Type
Interventional
Last Updated
March 6, 2018
I’m interested in this study!