Phase 2
N=51
S0505 Sorafenib in Treating Patients With Advanced Soft Tissue Sarcomas
Sarcoma
Bottom Line
View on ClinicalTrials.gov: NCT00217620 ↗Enrolled (actual)
51
Serious AEs
27.0%
Results posted
Nov 2012
Primary outcome: Primary: Objective Response (Confirmed, Complete and Partial) — 1; 0; 1; 8 participants
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 2
- Interventions
- sorafenib (Drug)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- National Cancer Institute (NCI)
- Primary completion
- Apr 2008
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Objective Response (Confirmed, Complete and Partial) |
1; 0; 1; 8; 2; 5 | — |
| SECONDARY Four-month Progression-free Survival Rate |
42; 30; 63; 43 | — |
| SECONDARY Number of Patients With Grade 3 Through 5 Adverse Events That Are Related to Study Drug |
1; 1; 1; 1; 1; 1 | — |
Summary
RATIONALE: Sorafenib 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 works in treating patients with advanced soft tissue sarcomas.
Eligibility Criteria
DISEASE CHARACTERISTICS:
- Histologically confirmed soft tissue sarcoma of 1 of the following histologies:
- Angiosarcoma, cutaneous or visceral
- Malignant hemangiosarcoma
- Malignant hemangiopericytoma
- Grade 3-4 leiomyosarcoma
- Grade 3-4 liposarcoma
- Must have evidence of unresectable residual disease, metastatic disease, or recurrent disease by radiography
- Measurable disease by x-ray, scans, or physical examination
- Archived paraffin-embedded tumor sections available
- No known brain metastases
PATIENT CHARACTERISTICS:
Age
- 18 and over
Performance status
- Zubrod 0-1
Life expectancy
- Not specified
Hematopoietic
- WBC ≥ 3,000/mm^3
- Absolute neutrophil count ≥ 1,500/mm^3
- Platelet count ≥ 100,000/mm^3
Hepatic
- SGOT and SGPT ≤ 2.5 times upper limit of normal (ULN) (5 times ULN if due to liver metastases)
- Bilirubin normal (≤ 2.5 times ULN if due to liver metastases)
- PT, PTT, and INR normal
Renal
- Creatinine normal OR
- Creatinine clearance ≥ 60 mL/min
Cardiovascular
- No history of thromboembolic disease
- No uncontrolled hypertension
Other
- Not pregnant or nursing
- Fertile patients must use effective contraception
- Able to swallow oral medication
- No other malignancy within the past 5 years except adequately treated basal cell or squamous cell skin cancer, carcinoma in situ of the cervix, or adequately treated stage I or II cancer in complete remission
PRIOR CONCURRENT THERAPY:
Biologic therapy
- Not specified
Chemotherapy
- At least 28 days since prior chemotherapy (42 days for carmustine or mitomycin) and recovered
- Prior adjuvant chemotherapy allowed
- No more than 1 prior chemotherapy regimen for metastatic disease
Endocrine therapy
- Not specified
Radiotherapy
- At least 28 days since prior radiotherapy and recovered
- Must have evidence of disease progression within, or measurable disease outside of, the radiation field after completion of radiotherapy
Surgery
- At least 28 days since prior major surgery and recovered
Other
- No prior sorafenib
- No prior inhibitor of VEGFR or MAPK pathway
- No concurrent combination antiretroviral therapy for HIV-positive patients
- No other concurrent investigational agents
- No concurrent therapeutic anticoagulation
- No concurrent administration of any of the following medications:
- Rifampin
- Hypericum perforatum (St. John's wort)
- Cytochrome P450 enzyme-inducing antiepileptic drugs, including any of the following:
- Phenytoin
- Carbamazepine
- Phenobarbital
Data sourced from ClinicalTrials.gov (NCT00217620). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.