Opening soonPhase 3Ages 18 Years and up
High Versus Lower Intensity Surveillance Following Resection of Retroperitoneal Sarcoma
Sponsor: Fondazione IRCCS Istituto Nazionale dei Tumori, Milano · NCT06480396 on ClinicalTrials.gov ↗
Conditions studied
Sarcoma,Soft TissueSarcoma Retroperitoneal
What it tests
- High-intensity radiological surveillancediagnostic_test
- Lower-intensity radiological surveillancediagnostic_test
Where it's running2 sites
2 international sites
Fondazione IRCCS Istituto Nazionale dei Tumori
Milan, Lombardy, Italy 20133
- Marco Fiore, MD(contact)022390 2910[email protected]
- Daniella Salvatore, PhD(contact)022390 2796[email protected]
- Marco Fiore, MD(contact)
University Hospitals Birmingham NHS Foundation Trust
Birmingham, West Midlands, United Kingdom B15 2GW
- Samuel Ford, PhD(contact)+44 121 3715880[email protected]
- James Glasbey, PhD(contact)+44 121 3715880[email protected]
- Samuel Ford, PhD(contact)
See the official eligibility language
Shown exactly as written on ClinicalTrials.gov. Your oncologist is the right person to judge whether it fits your situation.
Inclusion Criteria: * Adult patients (greater than 18 years) * Primary resection * Histologically confirmed retroperitoneal, abdominal or pelvic soft tissue sarcoma * R0/R1 resection * Eligible whether or not the participant undergoes neoadjuvant treatment Exclusion Criteria: * Metastatic disease at time of randomisation * Recurrent, metastatic or residual disease identified on baseline CT imaging (3-4 months post primary resection) * Reoperation for recurrent soft tissue sarcoma * Re-resection following previous inadequate surgery * R2 resection * Patients receiving adjuvant therapy that will delay, interrupt or render radiological surveillance unpredictable * Uterine sarcomas, gastrointestinal stromal tumour (GIST), fibromatosis, epithelial tumours, multifocal disease, sarcomas of bony origin * Patient declined to consent to data sharing with RESAR (unless in a centre contributing via pre-planned IPDMA)
Updated 2024-10-16 on ClinicalTrials.gov. Always confirm current details with the study team or your oncologist.