Liver CancerPhase 1NCT00873002
Panobinostat and Sorafenib in Treating Patients With Liver Cancer That is Metastatic and/or Cannot Be Removed by Surgery
A Phase 1 study testing panobinostat and sorafenib tosylate in people with Liver Cancer, run by Case Comprehensive Cancer Center at 1 site in United States.
Trial summary
RATIONALE: Panobinostat and sorafenib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Sorafenib may also stop the growth of liver cancer by blocking blood flow to the tumor. 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?
- panobinostat and sorafenib tosylate
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 3 participants
- Where
- 1 siteUnited States
- Study dates
- Mar 2009to Jun 2010
- Phase
- Phase 1
- 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 or cytologically confirmed hepatocellular carcinoma
- Metastatic and/or unresectable disease
- Child-Pugh score A or B
PATIENT CHARACTERISTICS:
- ECOG performance status 0-2
- Neutrophil count > 1500/mm³
- Platelet count > 100,000/mm³
- Hemoglobin ≥ 9 g/dL
- AST and ALT ≤ 2.5 times upper limit of normal (ULN) (≤ 5.0 times ULN if elevation due to disease involvement)
- Serum bilirubin ≤ 1.5 times ULN
- Serum creatinine ≤ 1.5 times ULN or creatinine clearance ≥ 50 mL/min
- Total serum calcium (corrected for serum albumin) or ionized calcium ≥ lower limit of normal (LLN)
- Serum potassium ≥ LLN
- Serum sodium ≥ LLN
- Serum albumin ≥ LLN or 3 g/dL
- LVEF ≥ LLN as demonstrated by baseline MUGA or ECHO
- TSH and free T4 within normal limits (thyroid hormone replacement therapy allowed)
- Not pregnant or nursing
- Negative pregnancy test
- Fertile patients must use effective double-method contraception (one being a barrier method) during and for 3 months after completion of study treatment
- INR < 1.5 or PT/PTT within normal limits
- No impaired cardiac function including any 1 of the following:
- QTc > 450 msec on screening ECG
- Congenital long QT syndrome
- History of sustained ventricular tachycardia
- History of ventricular fibrillation or torsades de pointes
- Bradycardia, defined as heart rate < 50 beats per minute
- Patients with a pacemaker and heart rate ≥ 50 beats per minute are eligible
- Myocardial infarction or unstable angina within the past 6 months
- Congestive heart failure (NYHA class III-IV)
- Right bundle branch block and left anterior hemiblock (bifascicular block)
- No uncontrolled hypertension
- No thrombolic or embolic events (e.g., cerebrovascular accident and transient ischemic attacks) within the past 6 months
- No pulmonary hemorrhage/bleeding event > CTCAE Grade 2 within the past 4 weeks
- No other hemorrhage/bleeding event > CTCAE Grade 3 within the past 4 weeks
- No unresolved diarrhea > CTCAE grade 1
- No other concurrent severe and/or uncontrolled medical conditions
- No other primary malignancy within the past 5 years except curatively treated carcinoma in situ of the cervix or basal cell or squamous cell carcinoma of the skin
- No serious non-healing wound, ulcer, or bone fracture
- No evidence or history of bleeding diathesis or coagulopathy
- No significant traumatic injury within the past 4 weeks
- No known or suspected allergy to sorafenib tosylate or any other study drug
- No condition that would impair a patient's ability to swallow whole pills
- No malabsorption problem
- No known human immunodeficiency virus (HIV) or hepatitis C positivity (baseline testing for HIV and hepatitis C is not required)
- No significant history of non-compliance to medical regimens
PRIOR CONCURRENT THERAPY:
- No prior HDAC inhibitors, DAC inhibitors, HSP90 inhibitors, sorafenib tosylate, or valproic acid for the treatment of cancer
- More than 4 weeks since prior chemotherapy, investigational drugs, or major surgery and recovered
- More than 4 weeks since open biopsy
- More than 5 days since prior and no concurrent valproic acid for any medical condition
- No concurrent St. John's wort or rifampin
- No concurrent drugs with a risk of causing torsades de pointes
- No concurrent CYP3A4 inhibitors
- No concurrent radiotherapy
- No concurrent grapefruit, grapefruit juice, or Seville (sour) oranges
- No other concurrent investigational therapy
- No other concurrent anticancer agents
- Concurrent anticoagulation treatment with warfarin or heparin allowed
Trial locations and contacts
1 site in 1 country.
United States1 site
Cleveland Clinic Taussig Cancer Institute, Case Comprehensive Cancer Center
Cleveland, Ohio, 44195
About this study
Official title: Phase I Study of Combination of Sorafenib and LBH589 in Hepatocellular Carcinoma
RATIONALE: Panobinostat and sorafenib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Sorafenib may also stop the growth of liver cancer by blocking blood flow to the tumor.
PURPOSE: This phase I trial is studying the side effects and best dose of panobinostat when given together with sorafenib in treating patients with liver cancer that is metastatic and/or cannot be removed by surgery.
Read the detailed description
OBJECTIVES:
Primary
- Assess the safety and tolerability of panobinostat when combined with standard doses of sorafenib tosylate in patients with metastatic and/or unresectable hepatocellular carcinoma.
- Determine the maximum tolerated dose of panobinostat when combined with standard doses of sorafenib tosylate in these patients.
Secondary
- Determine the response rate.
- Determine the progression-free survival.
- Determine the overall survival rate.
OUTLINE: This is a dose escalation study of panobinostat.
Patients receive panobinostat IV on days 1 and 8 and oral sorafenib tosylate twice daily on days 1-21. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity.
After completion of study therapy, patients are followed for 30 days.
- Conditions
- Liver Cancer
- Being tested
- panobinostat, sorafenib tosylate
- Keywords
- adult primary hepatocellular carcinoma, advanced adult primary liver cancer, recurrent adult primary liver cancer, localized unresectable 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.
panobinostatDrug
Dose escalation: 7.5 mg/m2 day 1 and day 8 of 21 days cycle 10 mg/m2 day 1 and day 8 of 21 days cycle 15 mg/m2 day 1 and day 8 of 21 days cycle 20 mg/m2 day 1 and day 8 of 21 days cycle 30 mg/m2 day 1 and day 8 of 21 days cycle
sorafenib tosylateDrug
400 mg PO BID
| Study group | Role | What they receive |
|---|---|---|
| LBH589 | Active comparator | This study utilizes a sequential dose-escalation design to define the MTD of LBH589 when combined with standard doses of sorafenib. Receives: Drug: panobinostat; Drug: sorafenib tosylate |
What is being measured
The primary outcome is the main question the study is designed to answer.
Assessment of Safety and Tolerability
•Primary objective of the phase I trial will be to assess the safety and tolerability and to determine the maximum tolerated dose (MTD) of LBH 589 when combined with standard doses of sorafenib in the treatment of hepatocellular carcinoma.
Measured: 6months to 1 year
Secondary outcomes (4)
Progression-free survival
Evaluate time to progression vs progression free survival
Measured: 6mo 1 year
Overall survival
Overall survival (OS) will be measured from study entry until death from any cause.
Measured: until death
Response as assessed by RECIST
To ensure comparability, baseline methods and on-study methods for response assessment must be performed using identical techniques. In addition, all subjects with evidence of objective tumor response (CR, PR or SD) should have the response confirmed with repeat assessments at least 21 days after the first documentation of response, resuming bimonthly (every 42 days) assessments thereafter. Objective tumor response will be assessed using the RECIST method.
Measured: every 42 days
Adverse events and abnormal laboratory value severity as assessed by NCI CTCAE version 3.0
Events should be documented and recorded at each visit. Subjects should be followed for adverse events for 30 days after the last protocol related assessment, or until drug-related toxicities have resolved, whichever is later.
Measured: weekly during treatment to 30 days after treatment
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted1 Apr 2009 (estimated)
- Study startMar 2009
- Primary completionMay 2010
- Study completionJun 2010
Why it stopped: Dose Limiting Toxicity
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Liver CancerStudies of the same condition, open and under way.
- More trials run by Case Comprehensive Cancer CenterThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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 1
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 3 participants (actual)
Sponsor and investigators
- Lead sponsor
- Case Comprehensive Cancer Center
- Sponsor type
- University, hospital or other
- Collaborators
- National Cancer Institute (NCI)
- Responsible party
- Sponsor
- Investigators
- Richard Kim, MD, Principal investigator, Cleveland Clinic Taussig Cancer Institute, Case Comprehensive Cancer Center
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00873002
- Sponsor's protocol ID
- CASE6208
- Other IDs
- P30CA043703, CASE6208, CLBH589BUS23T
- Status last verified
- Mar 2012
- First submitted
- 31 Mar 2009
- Last updated
- 20 Mar 2012
- Results posted
- No
- Data monitoring committee
- Yes
Study at a glance
From the registry record, last updated by the sponsor on 20 Mar 2012. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Phase I Study of Combination of Sorafenib and LBH589 in Hepatocellular Carcinoma
- ClinicalTrials.gov ID
- NCT00873002
- Acronym / sponsor ID
- CASE6208
- Conditions
- Liver Cancer
- Keywords
- adult primary hepatocellular carcinoma, advanced adult primary liver cancer, recurrent adult primary liver cancer, localized unresectable adult primary liver cancer
- Phase
- Phase 1
- Study type
- Interventional
- Recruitment status
- TerminatedReason stopped: Dose Limiting Toxicity
- Enrolment
- 3 participants (actual)
- Lead sponsor
- Case Comprehensive Cancer CenterUniversity, hospital or other
- Collaborators
- National Cancer Institute (NCI)
- Study start
- Mar 2009
- Primary completion
- May 2010 (actual)
- Study completion
- Jun 2010 (actual)
- First posted
- 1 Apr 2009 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
RATIONALE: Panobinostat and sorafenib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Sorafenib may also stop the growth of liver cancer by blocking blood flow to the tumor.
PURPOSE: This phase I trial is studying the side effects and best dose of panobinostat when given together with sorafenib in treating patients with liver cancer that is metastatic and/or cannot be removed by surgery.
Detailed description
OBJECTIVES:
Primary
- Assess the safety and tolerability of panobinostat when combined with standard doses of sorafenib tosylate in patients with metastatic and/or unresectable hepatocellular carcinoma.
- Determine the maximum tolerated dose of panobinostat when combined with standard doses of sorafenib tosylate in these patients.
Secondary
- Determine the response rate.
- Determine the progression-free survival.
- Determine the overall survival rate.
OUTLINE: This is a dose escalation study of panobinostat.
Patients receive panobinostat IV on days 1 and 8 and oral sorafenib tosylate twice daily on days 1-21. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity.
After completion of study therapy, patients are followed for 30 days.
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| LBH589 | Active comparator | Drug: panobinostat, Drug: sorafenib tosylateThis study utilizes a sequential dose-escalation design to define the MTD of LBH589 when combined with standard doses of sorafenib. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| panobinostatDose escalation: 7.5 mg/m2 day 1 and day 8 of 21 days cycle 10 mg/m2 day 1 and day 8 of 21 days cycle 15 mg/m2 day 1 and day 8 of 21 days cycle 20 mg/m2 day 1 and day 8 of 21 days cycle 30 mg/m2 day 1 and day 8 of 21 days cycle | Drug | LBH589 |
| sorafenib tosylate400 mg PO BID | Drug | LBH589 |
Primary outcome
Assessment of Safety and Tolerability
Time frame: 6months to 1 year
•Primary objective of the phase I trial will be to assess the safety and tolerability and to determine the maximum tolerated dose (MTD) of LBH 589 when combined with standard doses of sorafenib in the treatment of hepatocellular carcinoma.
4 secondary outcomes
Progression-free survival
Time frame: 6mo 1 year
Overall survival
Time frame: until death
Response as assessed by RECIST
Time frame: every 42 days
Adverse events and abnormal laboratory value severity as assessed by NCI CTCAE version 3.0
Time frame: weekly during treatment to 30 days after treatment
Results and safety
The study was stopped early (reason given: Dose Limiting Toxicity). Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 20 Mar 2012.
- Clinical trial summary from the National Cancer Institute's PDQ® databaseLink provided by the sponsor.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Richard Kim, MD principal investigator
Cleveland Clinic Taussig Cancer Institute, Case Comprehensive Cancer Center
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 1 study testing panobinostat and sorafenib tosylate in people with Liver Cancer, run by Case Comprehensive Cancer Center at 1 site in United States.
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: stopped early, as of the sponsor's last update on 20 Mar 2012. 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 United States. 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 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study was stopped early (reason given: Dose Limiting Toxicity). Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Assessment of Safety and Tolerability (time frame: 6months to 1 year). 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 20 Mar 2012.