Status:
COMPLETED
Vorinostat and Bortezomib in Treating Patients With Advanced Soft Tissue Sarcoma
Lead Sponsor:
National Cancer Institute (NCI)
Conditions:
Recurrent Adult Soft Tissue Sarcoma
Stage III Adult Soft Tissue Sarcoma
Eligibility:
All Genders
18+ years
Phase:
PHASE2
Brief Summary
This phase II trial is studying how well giving vorinostat together with bortezomib works in treating patients with advanced soft tissue sarcoma. Vorinostat and bortezomib may stop the growth of tumor...
Detailed Description
PRIMARY OBJECTIVES: I. To determine the objective response rate in patients with advanced soft tissue sarcoma treated with vorinostat and bortezomib. SECONDARY OBJECTIVES: I. Characterize the toxic...
Eligibility Criteria
Inclusion
- Inclusion Criteria:
- Histologically or cytologically confirmed advanced, unresectable, or metastatic soft tissue sarcoma (STS)
- Measurable disease, defined as \>= 1 lesion that can be accurately measured in \>= 1 dimension as \>= 2 cm by conventional techniques OR \>= 1 cm by spiral computed tomography (CT) scan
- No small round cell tumors, including the following:
- Primitive neuroectodermal tumor
- Rhabdomyosarcoma
- Ewing sarcoma
- Osteosarcoma
- No known active and/or untreated brain metastases and/or brain metastases requiring ongoing therapy (e.g., corticosteroids)
- Treated, inactive brain metastases not requiring ongoing therapy allowed provided the brain metastases have been stable for \>= 1 month as assessed by intracranial imaging AND there is no indication of increased vascularity of the treated metastases within 14 days before study entry as assessed by magnetic resonance imaging (MRI)
- Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0-1 OR Karnofsky PS 70-100%
- Life expectancy \>= 12 weeks
- Absolute neutrophil count (ANC) \>= 1,500/mm\^3
- Platelet count \>= 100,000/mm\^3
- Total bilirubin normal
- Aspartate aminotransferase (AST) and/or alanine aminotransferase (ALT) =\< 2.5 times upper limit of normal
- Creatinine normal OR creatinine clearance \>= 60 mL/min
- Not pregnant or nursing
- Negative pregnancy test
- Fertile patients must use effective contraception
- Able to take oral medication
- No peripheral neuropathy \>= grade 2
- No concurrent uncontrolled illness including, but not limited to, any of the following:
- Ongoing or active infection
- Symptomatic congestive heart failure
- Unstable angina pectoris
- Cardiac arrhythmia or myocardial infarction within the past 6 months
- Psychiatric illness and/or social situation that would limit compliance with study requirements
- No history of Torsades de Pointes
- No history of allergic reactions attributed to compounds of similar chemical or biological composition to vorinostat or bortezomib
- No more than 1 prior systemic treatment for advanced STS, including investigational agents
- Adjuvant therapy is not considered a systemic regimen
- More than 2 weeks since prior valproic acid
- More than 4 weeks since prior and no concurrent chemotherapy (\> 6 weeks for nitrosoureas or mitomycin C) or radiotherapy and recovered
- Radiotherapy to bone metastasis within the past 2 weeks allowed provided there is active non-bone disease outside the radiation port
- No prior radiotherapy to \>= 33% of the bone marrow
- No prior vorinostat or bortezomib
- No concurrent category I medications that are generally accepted to have a risk of causing Torsades de Pointes, including any of the following:
- Quinidine, procainamide, disopyramide
- Amiodarone, sotalol, ibutilide, dofetilide
- Erythromycin, clarithromycin
- Chlorpromazine, haloperidol, mesoridazine, thioridazine, pimozide, cisapride, bepridil, droperidol, methadone, arsenic, chloroquine, domperidone, halofantrine, levomethadyl, pentamidine, sparfloxacin, lidoflazine
- No concurrent combination antiretroviral therapy for human immunodeficiency virus (HIV)-positive patients
- No other concurrent investigational agents for the primary malignancy
- No other concurrent anticancer therapy
Exclusion
Key Trial Info
Start Date :
June 1 2009
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
June 1 2011
Estimated Enrollment :
16 Patients enrolled
Trial Details
Trial ID
NCT00937495
Start Date
June 1 2009
End Date
June 1 2011
Last Update
May 14 2014
Active Locations (6)
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1
Mayo Clinic in Florida
Jacksonville, Florida, United States, 32224-9980
2
Johns Hopkins University
Baltimore, Maryland, United States, 21287-8936
3
Mayo Clinic
Rochester, Minnesota, United States, 55905
4
Metro-Minnesota CCOP
Saint Louis Park, Minnesota, United States, 55416