Siliphos in Advanced Hepatocellular Carcinoma

Advanced Hepatocellular Carcinoma Clinical Trial

Official title:

Phase I Trial of Siliphos in Patients With Advanced Hepatocellular Carcinoma

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01129570
• Other study ID #: AAAE7604
• Status: Completed
• Phase: Phase 1
• First received: April 12, 2010
• Last updated: November 21, 2013
• Start date: February 2010
• Est. completion date: June 2013

Study information

• Verified date: November 2013
• Source: Columbia University
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

Milk thistle is an herbal drug that may have some liver protection properties and may reduce inflammation in the liver. It may also have anticancer effects. However milk thistle is not approved by the Food and Drug Administration for any medical purpose in the United States.

It has not been used in patients with liver cancer previously, to our knowledge, but there have been many studies of its use in patients with hepatitis and cirrhosis. Some of these studies have shown that milk thistle may help reduce elevated liver function tests.

Siliphos is a derivative of milk thistle that can be absorbed better than some other types of milk thistle. The investigators would like to perform a study to identify doses of siliphos that are safe to take in advanced liver cancer and to identify positive or negative side effects this compound may have. The investigators will be using this information in future studies to see if siliphos can be used as a therapy in patients with advanced liver cancer to reduce elevated liver function tests.

Description:

Milk thistle (MT) has been historically used to treat patients with liver diseases, and has been shown to have antioxidant, anti inflammatory, and hepatoprotective properties. It may also have direct anticancer effects through inhibition of growth factors and promotion of cell cycle arrest. MT has been shown to improve LFTs in several studies of patients with cirrhosis. To our knowledge, there have been no published trials evaluating the clinical efficacy of MT in advanced HCC. We therefore propose a phase I study to identify the maximum tolerated dose (MTD) of silybinphosphatidylcholine (a commercially available preparation with increased bioavailability), in patients with advanced HCC. We will use a traditional dose escalation, open label design with a study intervention period of 3 months, followed by one year of observation, with a maximum total of 30 subjects, evaluating a dose range between 1 to 12 gm Siliphos. The data obtained from this study will be utilized in the future to evaluate MT efficacy in reducing liver function tests in advanced HCC, which will have significant implications in its use as a potential adjunctive agent in patients with currently limited treatment options.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 3
• Est. completion date: June 2013
• Est. primary completion date: June 2013
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Age =18 years

• ECOG performance score of 0-3

• Expected survival of >12 weeks

• Subjects with advanced HCC or locally advanced, unresectable HCC

• Elevated LFTs (including at least one of the following: TBili >1.5 times the upper limit of normal; serum AST >2.5 times the upper limit of normal

• HCC diagnosed/defined based on either biopsy, or by suggestive radiologic imaging according to the AASLD guidelines (arterial enhancement with venous washout) or an AFP >200 ng/ml

• Subjects must have measurable disease that can be accurately measured in at least one dimension (with at least >20mm diameter in the longest dimension by conventional imaging or >10 mm by helical CT)

• Elevated liver enzymes that are either due to underlying liver disease and/or tumor which is not amenable to stenting after discussion with interventional GI and/or IR

• Subjects must demonstrate an ability to understand the consent process and willingness to sign a written informed consent form

• Subjects must agree to use birth control pills or other active contraception during active study treatment

Exclusion Criteria:

• Pregnant women or women currently breastfeeding will be excluded from this study because the effects of silybin on pregnant women and/or nursing infants are not known

• Subjects must have < grade 4 hepatic toxicity

• Known brain metastases because of poor prognosis and as patients with brain metastases often develop neurological dysfunction that may confound evaluation of neurologic and other adverse side effects

• History of allergic reactions to the study medication

• Uncontrolled concurrent illness including, but not limited to: ongoing active infection (including SBP), symptomatic congestive heart failure, unstable angina, active cardiac arrhythmia, or psychiatric illness that would limit compliance with study requirements

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Advanced Hepatocellular Carcinoma
• Carcinoma
• Carcinoma, Hepatocellular

Intervention

Drug:
• Silybin
4 dose levels of siliphos: 2, 4, 8, and 12 grams daily in three divided doses. This study will follow a standard sequential Phase I dose escalation design.

Locations

Country	Name	City	State
United States	Columbia University Medical Center	New York	New York

Sponsors (2)

Lead Sponsor	Collaborator
Abby Siegel	Lotte & John Hecht Memorial Foundation

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The maximum tolerated dose of siliphos in patients with advanced hepatocellular carcinoma		Weeks 1, 3, 6, 9, and 12	Yes
Secondary	Mean intra-patient percent change in AST, ALT and total serum bilirubin levels	Fasting morning blood samples collected at baseline, weeks 1, 3, 6, 9, and 12	From baseline to 3 months	No
Secondary	Quality of life as measured by the FACT-hepatobiliary questionnaire	Questionnaire administered at baseline, weeks 1, 6, and 12	From baseline to 3 months	No
Secondary	Plasma concentrations of silybinin, silybinin B, silibinin glucoronide, and silibinin sulfate	Fasting morning blood samples collected at baseline, weeks 1, 3, 6, 9, and 12	From baseline to 3 months	No
Secondary	Mean intra-patient percent change in serum concentrations of CRP, IGF-1, and IGFBP-3	Fasting morning blood samples collected at baseline, weeks 1, 3, 6, and 12	From baseline to 3 months	No
Secondary	Tumor response as measured by RECIST criteria and AFP concentrations	Fasting blood samples collected at baseline, weeks 1, 3, 6, 9, and 12 for AFP concentrations.; MRI of abdomen/pelvis & CT of chest at baseline and week 12	From baseline to 3 months	No