Randomised Trial of Dose and Volume of Post-Operative Radiotherapy Given to Adult Patients with Extremity Soft Tissue Sarcoma.

Trial Objective

The objective of this trial is to increase limb function without compromising local control using a reduced treatment volume of post-operative radiotherapy.

QA procedure

1. Mandatory QA questionnaire to be completed before trial involvement.
2. Volume exercise involving abductor compartment:
1. Patient History
2. Pre-operative MRI data (zip file)
3. Planning CT data (zip file)
3. Routine plan review and follow up planning workshop after an agreed period.
4. Mandatory site visit from VorteX QA team to perform a dosimetric evaluation of the entire treatment process using an anthropomorphic tissue equivalent phantom.
5. Collection and review of in-vivo dosimetry results and verification images.

Contact:

Elaine Cowie

rttrialsqa.enh-tr@nhs.net

01923 844830