Stereotactic Radiosurgery for Soft Tissue Sarcoma

Withdrawn before enrolling · Not applicable

Conditions studied: Soft Tissue Sarcoma

In brief

This study is evaluating treatment with CyberKnife for soft tissue sarcomas.

Key facts

Study ID

NCT02706171

Run by

The Cooper Health System

People needed

0

Starts

2015-06-01

Expected to finish

2018-12-01

Last updated by the study team

2024-03-15

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• All cohorts:
• Age > 18
• Patients of child-bearing age must agree to contraception until radiosurgery has been completed.
• Note that patients with metastatic disease are eligible for protocol
• Cohort 1: Soft tissue sarcoma (of any histology subtype) in patients that are -planned to have pre-operative radiation followed by surgical resection
• Anatomical site to include upper extremity (including shoulder) and lower extremity (including hip)
• Patient performance status and co-morbid conditions to allow for surgical resection
• Cohort 2: soft tissue sarcoma (of any histologic subtype) post-resection with no further plans for additional surgery.
• Patients must have high risk feature requiring post-operative radiation which can include Large tumor (> 5 cm), High grade, Previous unplanned, non, oncologic surgery, Close margins
• Anatomical site to include upper extremity (including shoulder) and lower extremity (including hip)
• Cohort 3: soft tissue sarcoma (of any histologic subtype) that is not amenable to surgical resection for any reason
• Anatomical site to include upper extremity (including shoulder) and lower extremity (including hip and pelvis)
• Patients cannot have planned surgical resection
• Note that retroperitoneal sarcomas are not eligible

You may not qualify if…

• Tumors that do not fit criteria for any of the above cohorts

Where it is running

• MD Anderson Cancer Center at Cooper — Camden, New Jersey, United States

Full record on ClinicalTrials.gov

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