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Clinical Trials/NCT01357486
NCT01357486
Completed
Phase 2

Phase II Randomized Trial Evaluating the Administration of Sorafenib or Pravastatin or Association Sorafenib-pravastatin or Best Supportive Care for the Palliative Treatment of Hepatocellular Carcinoma in Patient With CHILD B Cirrhosis

University Hospital, Bordeaux35 sites in 1 country160 target enrollmentNovember 14, 2011

Overview

Phase
Phase 2
Intervention
sorafenib
Conditions
Hepatocellular Carcinoma
Sponsor
University Hospital, Bordeaux
Enrollment
160
Locations
35
Primary Endpoint
Time to radiologic progression
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The incidence of Hepatocellular Carcinoma (HCC) is currently increasing in Europe and in France and about 2 / 3 of patients, are not eligible for curative treatment at the time of diagnosis. The palliative management of patients with advanced and symptomatic disease is complex and requires treatment combining anti-tumor activity and safety in patients with impaired liver functions. Sorafenib is the standard of care in a palliative setting, but the benefit of sorafenib in patient with altered liver function is uncertain. The aim of this trial is to study the interest of sorafenib in patients with HCC and impaired liver function compared to pravastatin (a drug with anti-tumoral activity in HCC) or to the combination sorafenib/pravastatin or to best supportive care (usually used in these patients).

Detailed Description

The incidence of Hepatocellular Carcinoma (HCC) is currently increasing in Europe and in France. It almost always occurs on liver disease and in 80 to 90% of cases, at least in France, on liver with cirrhosis. If curative treatment may be proposed for some "small" HCC (transplantation, resection, percutaneous destruction), about 2 / 3 of patients, which represents nearly 4,000 new cases per year in France, are not eligible for such treatment. The palliative management of patients with advanced and symptomatic disease is complex and requires treatment combining anti-tumor activity and safety in patients with impaired liver functions. Indeed, in most cases the palliative treatment of HCC is applied to patients with altered liver function (stage B of the Child-Pugh classification). To date, the proposed treatment in France for such patients is based on best supportive care. The objective of this study is to assess the interest in this situation of 2 molecules - taken alone or in combination: * Sorafenib, the reference in the palliative treatment of advanced hepatocellular carcinoma (Stage C of the BCLC classification). Yet the safety and efficacy of sorafenib in patients with altered liver function (CHILD B) are not clearly defined and its use remains discouraged by French recommendations in these patients. * Pravastatin whose interest in the palliative treatment of HCC was suggested by several phase II studies with a good safety profile in cirrhotic patients. In this French multicenter open randomized study, 160 patients will be included in 4 arms (40/arms): sorafenib, pravastatin, pravastatin + sorafenib, and supportive care. The aim of this phase II multicenter study is to select the two best arms for further Phase III study in order to identify a reference treatment in this palliative situation.

Registry
clinicaltrials.gov
Start Date
November 14, 2011
End Date
April 12, 2017
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
University Hospital, Bordeaux
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Male and female subjects \> 18 years age
  • Hepatocellular carcinoma histologically diagnosed or in case of inability to perform a histology by non invasive radiological criteria in presence of known cirrhosis: (i) Hepatic lesion measuring between 1 and 2 cm in diameter : CT-scan + MRI (eventually an Ultrasound contrast) : HCC diagnosed with contrast uptake in the arterial phase and rapid wash out in the venous /late phase on two imaging techniques.
  • (ii)Hepatic lesion with a diameter \> 2 cm : CT-scan or MRI +alpha fetoprotein : HCC diagnosed with contrast uptake in the arterial phase and a rapid wash out in the venous /late phase or a alpha fetoprotein \> 200µg/L
  • Patient not eligible for curative treatment (transplantation, resection, destruction or percutaneous chemo-embolization) or HCC still evolving after failure of a specific treatment
  • Score CHILD B
  • ECOG performance status 0/1/2
  • Score BCLC B or C
  • Adequate haematologic function with haemoglobin \> 8 g/dl, platelet count \> 50000x 109/L, absolute neutrophil count \> 1000 / mm3
  • Creatinine \< 2 times the upper limit of normal
  • Written informed consent

Exclusion Criteria

  • Any condition that is unstable or could jeopardize the safety of the subject and their compliance in the study
  • Pregnancy
  • Myocardial infarction less than 6 months, uncontrolled hypertension, congestive heart failure(NYHA class \> 2) , anti- arrhythmic treatment other than beta-blockers or digoxin
  • Digestive bleeding within 30 days before inclusion
  • Hepatic transplantation
  • Patients receiving or having received a statine for less than 6 months before HCC diagnostic
  • Prior use of sorafenib
  • Psychiatric illness/social situations that would limit compliance with study requirements.
  • Previous or concurrent cancer, except cervical carcinoma in situ, treated basal cell carcinoma, superficial bladder tumor. Any cancer curatively treated \> 5 years prior to entry is permitted
  • Known or suspected history of allergy to sorafenib or pravastatin.

Arms & Interventions

A

patients receiving sorafenib 400 mg - twice a day

Intervention: sorafenib

B

patients receiving pravastatin 40 mg - once a day

Intervention: Pravastatin

C

patients receiving sorafenib 400 mg (twice a day) and pravastatin 40 mg (once a day)

Intervention: Sorafenib + Pravastatin

D

patients receiving best supportive care

Intervention: patients receiving best supportive care

Outcomes

Primary Outcomes

Time to radiologic progression

Time Frame: Every 4 weeks (CT-scan or MRI) until progression of HCC or date of last news (for patients alive or dead without progression)

Secondary Outcomes

  • Overall survival(End of the study (estimated date August 2012))
  • Survival without progression(Every 4 weeks (CT-scan or MRI) until progression of HCC or date of last news (for patients alive or dead without progression))
  • Time to treatment failure(every 4 weeks (CT-scan or MRI) until clinical or radiological progression of HCC or date of last news (for patients alive or dead without progression))
  • Objective response rate at four months(Radiological evaluation at 4 months)
  • Number and description of AE for toxicity and SAE(Clinical evaluation every month)
  • Quality of life(Clinical evaluation every month)

Study Sites (35)

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