Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 2:36 AM
Ignite Modification Date:
2025-12-25 @ 2:36 AM
NCT ID:
NCT01347034
Eligibility Criteria:
Inclusion Criteria:
* Intermediate or High grade (AJCC 7th edition Grade 3 and 4 or Grade 2 and 3 of a 3 tier system) STS as determined by local pathology diagnostic biopsy specimen review
* Musculoskeletal tumor in extremities, trunk or chest wall
* Primary tumor or isolated locally recurrent tumor greater than 5 cm in diameter as measured by Response Evaluation Criteria In Solid Tumors (RECIST) criteria v1.1
* Clinical Stage T2N0M0 (AJCC 7th edition)
* Age ≥18 years at time of consent
* Eastern Cooperative Oncology Group (ECOG)/Zubrod performance status of 0 or 1
* Patient's written study specific, Institutional Review Board (IRB) stamped informed consent.
* Adequate organ function (measured within a week prior to beginning treatment for Arm B and within 2 weeks of beginning treatment for Arm A): white blood count (WBC) \> 3,000/mm³ and absolute neutrophil count (ANC) \>1500/mm³; Platelets \> 100,000/mm³; Hematocrit \> 25%; Bilirubin \< 2.0 mg/dL; Creatinine \< 2.0 mg/dL, or creatinine clearance \> 60 mL/min
* Radiation Oncologist must confirm that a 2-3 cm strip of skin can be spared from RT.
Exclusion Criteria:
* Retroperitoneal or Head and Neck primary locations
* Gastrointestinal stromal tumor (GIST)
* Demonstrated metastatic disease
* Contraindication to resection
* Prior RT if the current tumor is locally recurrent after prior resection
* Concurrent treatment with any anticancer agent other than RT as dictated by the protocol
* Prior chemotherapy for the pre-surgical treatment of the primary tumor (neoadjuvant chemotherapy)Bleeding/coagulation disorder
* Human Immunodeficiency Virus (HIV) infection or other primary immunodeficiency disorder
* Ongoing systemic therapy with immunosuppressant drugs (e.g. corticosteroids, azathioprine, cyclosporin, methotrexate)
* Steroid therapy within 4 weeks of first DC administration
* Any serious ongoing infection
* Pregnant or lactating women. Patients in reproductive age must agree to use contraceptive methods for the duration of the study (\*A pregnancy test will be obtained before treatment).
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT01347034
Study Brief:
Protocol Section:
NCT01347034