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Liver CancerPhase 2NCT01182272

Sorafenib Tosylate in Treating Patients With Liver Cancer That Can Be Removed by Surgery

A Phase 2 study testing sorafenib tosylate, laboratory biomarker analysis and neoadjuvant therapy in people with Liver Cancer, run by GERCOR - Multidisciplinary Oncology Cooperative Group at 1 site in France.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

RATIONALE: Sorafenib tosylate may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor. PURPOSE: This phase II trial is studying how well sorafenib tosylate works in treating patients with liver cancer that can be removed by surgery. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Liver Cancer
What is being tested?
sorafenib tosylate, laboratory biomarker analysis and neoadjuvant therapy
Type of treatment
Surgery or procedure
How many people
36 participants
Where
1 siteFrance
Study dates
May 2010to Jun 2012
Phase
Phase 2
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

DISEASE CHARACTERISTICS:

  • Histologically confirmed hepatocellular carcinoma (HCC)
  • Fibrolamellar or mixed histology allowed
  • No cholangiocarcinoma or other tubal disease
  • Must be eligible for conservative hepatic resection or liver resection with curative intent
  • No cirrhosis with Child-Pugh score > 7
  • Chronic liver disease without liver insufficiency and without portal liver hypertension allowed
  • No known history or presence of metastatic brain or meningeal tumors

PATIENT CHARACTERISTICS:

  • ECOG performance status 0-1
  • Life expectancy ≥ 3 months
  • WBC > 3,000/µL
  • ANC > 1,500/µL
  • Platelet count ≥ 100,000/µL
  • Hemoglobin ≥ 9 g/dL
  • Bilirubin < 1.5 times upper normal limit (ULN)
  • AST and ALT ≤ 5 times UNL
  • Alkaline phosphatase ≤ 5 times ULN
  • Serum creatinine < 2 times ULN
  • PT/INR/PTT < 1.5 times UNL
  • Amylase and lipase < 1.5 times ULN
  • Negative pregnancy test
  • Fertile patients must use effective contraception
  • Body mass index 18.5-30 kg/m^2 (WHO normal range: 18.5-25 kg/m^2)
  • Able to swallow oral compound
  • No criterion for unresectability or medical condition that contraindicates surgical resection
  • No serious concurrent systemic disorder incompatible with the study, including any of the following:
  • Uncontrolled hypertension (i.e., BP > 150/100 mm Hg despite optimal therapy)
  • Active uncontrolled infection
  • Active alcoholism
  • No prior medical disorder, including any of the following:
  • Cardiac arrhythmias requiring anti-arrhythmics (excluding beta-blockers or digoxin for chronic atrial fibrillation)
  • Active coronary artery disease or ischemia
  • Myocardial infarction within the past 6 months
  • NYHA class III-IV congestive heart failure
  • Pulmonary embolism within the past 6 months
  • Gastrointestinal bleeding within the past 6 months
  • No other prior malignancy within the past 5 years, except basal cell or squamous cell skin carcinoma or cured in situ cervical carcinoma
  • No history or concurrent seizure disorder requiring medications (e.g., antiepileptic drugs)
  • No history of HIV infection, or chronic hepatitis B or C
  • No active clinically serious bacterial or fungal infection (i.e., grade 2 CTCAE v. 3)
  • No condition that is unstable or could jeopardize the safety of the patient and his/her compliance with the study
  • No substance abuse or medical, psychological, or social condition that could interfere with adherence to the study
  • No known or suspected allergy to the investigational agent or to any agent given concurrently
  • No presence of asthenia or rash > CTC grade 1 at enrollment
  • Must be registered in a national health-care system

PRIOR CONCURRENT THERAPY:

  • No prior orthotopic liver transplantation
  • Not a candidate for orthotopic liver transplantation
  • No prior systemic or loco-regional treatment for HCC
  • No prior organ allograft
  • No treatment with any other investigational medicinal product within the past 28 days
  • No concurrent treatment with full-dose anticoagulants
  • Deep-vein or catheter-associated thrombosis prophylaxis allowed
  • Warfarin or heparin therapy allowed if the coagulation parameters were within the acceptable ranges prior to initiation of anticoagulant therapy
  • No concurrent or chronic co-administration of CYP3A4 inducers (e.g., rifampin, Hypericum perforatum, phenytoin, carbamazepine, phenobarbital, or dexamethasone)

Trial locations and contacts

1 site in 1 country.

France1 site, 1 recruiting
  • Hopital Beaujon

    Clichy, 92110

    Contact Person, 33-1-4087-5614, sandrine.faivre@bjn.aphp.fr

    Recruiting

Other trials in France

About this study

Official title: Proof-of-Concept Phase II Study to Evaluate the Anti-Tumor Activity of Sorafenib Along With Pathological and Molecular Changes in Tumor Samples From Patients With Resectable Hepatocellular Carcinoma

RATIONALE: Sorafenib tosylate may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor.

PURPOSE: This phase II trial is studying how well sorafenib tosylate works in treating patients with liver cancer that can be removed by surgery.

Read the detailed description

OBJECTIVES:

Primary

  • To assess anti-tumor activity of neoadjuvant sorafenib tosylate in tumor samples from patients with resectable hepatocellular carcinoma (HCC).

Secondary

  • To characterize pathologic findings in sorafenib tosylate pre-treated patients undergoing surgical resection for HCC: 1-2 core tumor biopsies will be performed prior to treatment and at day 35.
  • To evaluate the number of R0 resections in these patients.
  • To correlate pathological biomarker changes in resected tumors after 4-week treatment with sorafenib tosylate in comparison with biopsies obtained prior to treatment in these patients.
  • To evaluate plasma biomarkers, including PIGF, VEGF-A, VEGF-C, sVEGFR2, sVEGFR3, sKIT, IL-6, Ang2, IL-8, bFGF, AFP, collagen 4, endostatin, thrombospondin, TSP-1 and angiostatin, and CXCL12 at baseline, day 28, and the day before surgery.
  • To identify potential biomarkers of sensitivity and/or resistance on biological and pathological samples of these patients (exploratory).
  • To characterize the safety profile of sorafenib tosylate in these patients.
  • To assess the tolerance of liver resection after sorafenib tosylate treatment of these patients.

OUTLINE: This is a multicenter study.

Patients receive oral sorafenib tosylate twice daily on days 1-28 in the absence of unacceptable toxicity. Approximately 7 days after completion of sorafenib tosylate therapy, patients undergo liver resection.

Blood and tissue specimens are collected periodically for laboratory and biomarker assessments. Biomarkers include both molecular markers investigating the direct antitumor effects of sorafenib tosylate against cancer cells vs the effects of the drug on angiogenesis.

After completion of study treatment, patients are followed up on day 50 and at 3 months after surgery.

Conditions
Liver Cancer
Being tested
sorafenib tosylate, laboratory biomarker analysis, neoadjuvant therapy, therapeutic conventional surgery
Keywords
adult primary hepatocellular carcinoma, localized resectable adult primary liver cancer
Medical subject headings
Liver Neoplasms, Carcinoma, Hepatocellular

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Antiangiogenic effects of sorafenib tosylate

  2. Significant pathological changes

Secondary outcomes (6)
  1. Pathologic findings in sorafenib tosylate pre-treated patients undergoing surgical resection for hepatocellular carcinoma

  2. Number of R0 resections

  3. Correlations between baseline patient characteristics, cancer biomarkers, and outcome variables and resected tumors

  4. Plasma biomarkers at baseline, day 28, and the day before surgery

  5. Safety profile of sorafenib tosylate

  6. Tolerance of liver resection after sorafenib tosylate treatment

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted16 Aug 2010 (estimated)
  2. Study startMay 2010
  3. Primary completionJun 2012 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2
Primary purpose
Treatment
Masking
None (open label)
Enrolment
36 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01182272
Sponsor's protocol ID
CDR0000682840
Other IDs
FRE-GERCOR-D09-1-BIOSHARE, EUDRACT-2009-018058-44, EU-21058
Status last verified
Aug 2010
First submitted
13 Aug 2010
Last updated
16 Aug 2010
Results posted
No

Questions about this trial

What is this clinical trial studying?

A Phase 2 study testing sorafenib tosylate, laboratory biomarker analysis and neoadjuvant therapy in people with Liver Cancer, run by GERCOR - Multidisciplinary Oncology Cooperative Group at 1 site in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 16 Aug 2010. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Antiangiogenic effects of sorafenib tosylate. The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 Aug 2010.

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