Sorafenib and Vorinostat in Treating Patients With Advanced Liver Cancer

Liver Cancer Clinical Trial

Official title:

A Phase I Study of Sorafenib and Vorinostat in Advanced Hepatocellular Carcinoma

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01075113
• Other study ID #: MCC-12122
• Secondary ID: NCI-2010-00185
• Status: Completed
• Phase: Phase 1
• Start date: August 10, 2010
• Est. completion date: July 18, 2019

Study information

• Verified date: August 2019
• Source: Virginia Commonwealth University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This phase I trial is studying the side effects and best dose of vorinostat when given together with sorafenib tosylate in treating patients with advanced liver cancer. Sorafenib tosylate and vorinostat may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth or by blocking blood flow to the tumor.

Description:

Outline: This is a dose-escalation study of vorinostat. The purpose of this research study is to test the safety and effectiveness of a combination of two cancer drugs, sorafenib (Nexavar) and vorinostat (Zolinza), in advanced liver cancer (hepatocellular carcinoma). Advanced means that the cancer has spread too far to consider surgery. Approximately 19 people will take part in this study.

After enrollment of 6 patients at sorafenib 400 mg orally twice a day and vorinostat 300 mg orally, only 2 of the 6 patients were evaluable for DLT (no DLTs). The other 4 patients were not evaluable for DLT because of required dose modifications. Because of this dose modification need, Cohort A has been modified to include 2 dose levels: Dose level A-1a (sorafenib 400 mg orally twice a day and vorinostat 200 mg orally once a day) and dose level A1 (sorafenib 400 mg orally twice a day with vorinostat 100 mg orally once a day). The starting dose upon reopening after approval of this version will be dose level A-1a. Dose level A1 will only be used if dose level A-1a is not tolerable.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 16
• Est. completion date: July 18, 2019
• Est. primary completion date: February 2, 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Diagnosis of HCC by biopsy-proven pathologic diagnosis or by clinical criteria as defined below:

• Clinical criteria to be met if patient has a history of cirrhosis or chronic hepatitis B infection:

• Imaging abnormalities > 1 cm in size with classic enhancement by magnetic resonance imaging (MRI) or triple-phase computed tomography (CT) scan

• Alpha-fetoprotein (AFP) of any value

• Performance status Eastern Cooperative Oncology Group (ECOG) =< 1

• If cirrhosis, Child-Pugh classification A or B

• Total bilirubin =< 3.0 mg/dL

• Creatinine =< 1.5 x upper limit of normal for the laboratory

• International normalized ratio (INR) =< 1.7 (if not due to anticoagulants)

• Absolute neutrophil count (ANC) >= 1,500/mm^3

• Platelets >= 80,000/mm^3

• Hemoglobin (Hgb) >= 8.5 g/dL (transfusion or erythropoietin-like substances not permitted prior to baseline evaluation)

• Any prior therapies such as surgery, chemoembolization, radiofrequency ablation, and alcohol injection are allowed as long as toxicity from such prior therapy is =< grade 1

• Prior sorafenib is allowed as long as toxicity from ongoing is = grade 2 and prior intolerance of 400 mg sorafenib PO daily is felt amenable, by the principal investigator, to supportive care measures or dose modifications.

• Measurable or evaluable disease by Response Evaluation Criteria in Solid Tumors (RECIST) criteria version (v) 1.1 mRECIST or elevated AFP

• Ability to understand and willingness to sign a written informed consent; a signed informed consent must be obtained prior to any study specific procedures

• Women of childbearing potential must have a negative pregnancy test performed within 2 weeks prior to the start of treatment

• Women of childbearing potential and men must agree to use a medically accepted form of birth control for the duration of study participation and for 4 months following completion of study treatment

Exclusion Criteria:

• Candidate for curative therapy including surgical resection or orthotopic liver transplantation

• Known central nervous system metastasis

• Any investigational agent within 4 weeks of first dose of study treatment

• Known intolerance of vorinostat

• Unable to swallow medication

• Unable to swallow medication; suspected malabsorption

• Active alcohol abuse

• Contraindication to antiangiogenic agents, including:

• Pulmonary hemorrhage/bleeding event >= grade 2 within 4 weeks of first dose of study drug

• Any other hemorrhage/bleeding event >= grade 3 within 4 weeks of first dose of study treatment

• Serious non-healing wound, ulcer, or bone fracture

• Thrombolic or embolic events such as a cerebrovascular accident including transient ischemic attacks within the past 6 months; hepatic portal vein thrombus is not considered an exclusion criterion

• Major cardiac dysfunction, such as uncontrolled angina, congestive heart failure with New York Heart Association (NYHA) class III or higher, known left ventricular ejection fraction less than 40%

• Systolic blood pressure > 160 mmHg or diastolic pressure > 90 mmHg despite optimal medical management

• Significant lung disease (oxygen [O2] saturation less than 88% in room air)

• Serious uncontrolled infection; known human immunodeficiency virus (HIV)-seropositivity requiring retroviral therapy, or diagnosis of acquired immune deficiency syndrome (AIDS); diagnosis of chronic hepatitis B or C allowed

• Medical, psychological, or social conditions that, in the opinion of the investigator, may increase the patient's risk or interfere with the patient's participation in the study or hinder evaluation of the study results

Related Conditions & MeSH terms

• Liver Cancer
• Liver Neoplasms

Intervention

Drug:
• sorafenib tosylate
Given orally
• vorinostat
Given orally

Locations

Country	Name	City	State
United States	Hunter Holmes McGuire VA Medical Center	Richmond	Virginia
United States	Virginia Commonwealth University/Massey Cancer Center	Richmond	Virginia

Sponsors (2)

Lead Sponsor	Collaborator
Virginia Commonwealth University	Massey Cancer Center

Country where clinical trial is conducted

United States, 

References & Publications (1)

Gordon SW, McGuire WP 3rd, Shafer DA, Sterling RK, Lee HM, Matherly SC, Roberts JD, Bose P, Tombes MB, Shrader EE, Ryan AA, Kmieciak M, Nguyen T, Deng X, Bandyopadhyay D, Dent P, Poklepovic AS. Phase I Study of Sorafenib and Vorinostat in Advanced Hepatoc — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Determine the appropriate Doses for the combination of sorafenib tosylate and vorinostat appropriate for phase II study in hepatocellular carcinoma (HCC).	Identify the maximum tolerated dose of the combination regimen of vorinostat and sorafenib to study further for efficacy of treatment for hepatocellular carcinoma	4 weeks
Secondary	Adverse events will be characterized in terms of nature, severity, attribution, onset and resolution according to the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) v4.0.	Safety, tolerance, and toxicity of the combination of sorafenib tosylate and vorinostat in patients with HCC. Observe toxicities experienced by patients treated in cohorts of escalating doses of the drug combination.	Up to 30 days post-treatment
Secondary	Anti-tumor effects of the combination of sorafenib tosylate and vorinostat	Tumor masses will be evaluated for response according to the RECIST Criteria. Summarized using descriptive statistics for each cohort, along with their corresponding 95% confidence intervals.	Up to 6 years