Status:
COMPLETED
Trial of Neoadjuvant Conformal Radiotherapy Plus Sorafenib for Patients With Soft Tissue Sarcoma of the Extremity and Body Wall
Lead Sponsor:
University of California, Davis
Collaborating Sponsors:
Bayer
Conditions:
Soft Tissue Sarcoma
Eligibility:
All Genders
18+ years
Phase:
PHASE1
PHASE2
Brief Summary
Patients will receive neoadjuvant sorafenib (investigational agent) in combination with preoperative external beam conformal radiotherapy (50 Gy in 25 fractions) for localized, large soft tissue sarco...
Detailed Description
Patients will receive neoadjuvant sorafenib (investigational agent) in combination with preoperative external beam conformal radiotherapy (50 Gy in 25 fractions) for localized, large soft tissue sarco...
Eligibility Criteria
Inclusion
- Histologically confirmed soft-tissue sarcoma located on the extremity or body wall.
- Intermediate or High grade (NCI grade 2 or 3/3-tier system), \> 5 cm in maximal dimension.
- Low grade (NCI grade 1/3-tier system), \> 8 cm in maximal dimension.
- No evidence of regional or distant metastatic disease.
- Patient must be 18 years of age or older.
- Patient must have an ECOG performance status of ≤ 2.
- Patient must have a histologic diagnosis of soft tissue sarcoma.
- Patient must have adequate bone marrow, liver, and renal function as assessed by the following:
- Hemoglobin ≥ 9.0 g/dl
- Absolute neutrophil count (ANC) ≥ 1,500/mm3
- Platelets ≥ 100,000/mm3.
- Total bilirubin ≤ 1.5 mg/dL. NOTE: Patients with elevated bilirubin secondary to Gilbert's syndrome are eligible to participate in the study.
- AST and ALT ≤ 2.5 times the institution upper limit of normal (ULN).
- Creatinine ≤ 1.5 times ULN.
- Females of childbearing potential must have a negative serum pregnancy test within 7 days prior to the start of treatment . NOTE: Postmenopausal women must be amenorrheic for at least 12 months to be deemed not of reproductive potential.
- Women of childbearing potential and men must agree to use adequate contraception (barrier method of birth control) prior to study entry and for the duration of study participation. Men should use adequate birth control for at least three months after the last administration of sorafenib.
- Ability to understand and the willingness to sign a written informed consent. A signed informed consent must be obtained prior to any study specific procedures.
- INR \< 1.5 or a PT/PTT within normal limits. Patients receiving anti-coagulation treatment with an agent such as warfarin or heparin may be allowed to participate. For patients on warfarin, the INR should be measured prior to initiation of sorafenib and monitored at least weekly, or as defined by the local standard of care, until INR is stable.
Exclusion
- Patient is receiving additional cancer-directed therapy at time of entry into trial.
- Patient has received or is receiving preoperative investigational treatment.
- Patient has congestive heart failure \> class II NYHA. Patients must not have unstable angina (anginal symptoms at rest) or new onset angina (began within the last 3 months) or myocardial infarction within the past 6 months.
- Patient has history of cardiac ventricular arrhythmia requiring ongoing anti-arrhythmic therapy.
- Patient has uncontrolled hypertension, defined as systolic blood pressure \> 150 mmHg or diastolic pressure \> 90 mmHg, despite optimal medical management.
- Patient has known human immunodeficiency virus (HIV) infection or chronic Hepatitis B or C.
- Patient has active clinically serious infection \> CTCAE Grade 2.
- Patient has thrombotic or embolic events such as a cerebrovascular accident including transient ischemic attacks within the past 6 months.
- Patient has history of pulmonary hemorrhage/bleeding event \> CTCAE Grade 2 within 4 weeks of first dose of study drug.
- Patient has history of any other hemorrhage/bleeding event \> CTCAE Grade 3 within 4 weeks of first dose of study drug.
- Patient has history of clinical or laboratory evidence of bleeding diathesis or coagulopathy.
- Patient has history of major surgery or significant traumatic injury within 4 weeks of first study drug.
- Patient has concomitant use of St. John's Wort or rifampin (rifampicin).
- Patient has known or suspected allergy to sorafenib or any agent given in the course of this trial.
- Patient has any condition that impairs his or her ability to swallow whole pills.
Key Trial Info
Start Date :
March 1 2009
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
August 1 2011
Estimated Enrollment :
8 Patients enrolled
Trial Details
Trial ID
NCT00864032
Start Date
March 1 2009
End Date
August 1 2011
Last Update
April 10 2013
Active Locations (1)
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1
University of california, Davis Medical Center
Sacramento, California, United States, 95817