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Phase 2 N=51 Treatment

S0505 Sorafenib in Treating Patients With Advanced Soft Tissue Sarcomas

Sarcoma

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

OutcomeResultp-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
View full record on ClinicalTrials.gov →

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.

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