Surveillance AFter Extremity Tumor surgerY (SAFETY)
Soft Tissue Sarcoma, Lung Metastases
About this trial
This is an interventional prevention trial for Soft Tissue Sarcoma focused on measuring Soft Tissue Sarcoma, Lung Metastases, Overall Survival, Surveillance, Randomized Controlled Trial
Eligibility Criteria
Inclusion Criteria:
- The patient is 18 years of age or older;
- The patient has been diagnosed with a primary extremity grade II or III soft-tissue sarcoma (STS);
- The patient has undergone surgical excision of the tumor with curative intent and with no evidence of gross residual disease based on the pathology report;
- The patient has completed all planned neoadjuvant or adjuvant radiation and / or chemotherapy, if applicable;
- The tumor size is greater than or equal to (≥) five centimeters according to the pathology report or based on the pre-treatment MRI if neoadjuvant radiation and / or chemotherapy are given; and
- The patient provides informed consent.
Exclusion Criteria:
- The patient has metastases at initial presentation based on the radiology report of the initial thoracic imaging†;
- The patient has recently undergone surgical excision of a local recurrence;
- The patient has been diagnosed with one of the special sub-types, myxoid / round cell liposarcoma or extra-skeletal Ewing's sarcoma*;
- The patient has been previously diagnosed with a genetic syndrome with an elevated risk of malignancy, such as Li-Freumeni Syndrome‡;
- The patient has been previously diagnosed with a co-morbid condition that has a life expectancy of less than (<) one year;
- The site-specific surveillance protocol for the patient's disease is not compatible with the study protocol (i.e., regular planned whole-body imaging with positron emission tomography [PET] scans);
- Likely problems, in the judgment of the investigator, with the patient maintaining follow-up (with the specific reasoning requiring approval of the Methods Center);
- The patient is currently enrolled in a study that does not permit co-enrolment; and
The patient has already been enrolled in the SAFETY trial.
A second CT scan may be required to confirm that indeterminate nodules are false positives before the patient can be enrolled (provided that the second CT scan shows no evidence of metastatic disease);
Myxoid liposarcoma and extra-skeletal Ewing's sarcoma have different metastatic patterns, which necessitate different surveillance protocols;
- Individuals with Li-Freumeni Syndrome, or other genetic syndromes with an elevated risk of malignancy, appear to be at an elevated risk for radiation-induced cancers, so the use of CT scans should be limited.
Sites / Locations
- University of California Davis Medical CenterRecruiting
- Hartford HealthCareRecruiting
- University of Florida Health Shands HospitalRecruiting
- Parkview Cancer InstituteRecruiting
- Holden Comprehensive Cancer CenterRecruiting
- Albany Medical CenterRecruiting
- Montefiore Medical CenterRecruiting
- NYU Langone Orthopaedic Hospital/Perlmutter Cancer CenterRecruiting
- Cleveland ClinicRecruiting
- Oregon Health and Science University HospitalRecruiting
- Texas Tech Health Sciences CenterRecruiting
- Huntsman Cancer InstituteRecruiting
- Virginia Cancer Specialists
- Hospital Universitario AustralRecruiting
- St. Vincent's Hospital MelbourneRecruiting
- LKH - Universitätsklinikum GrazRecruiting
- Hospital de Clínicas de Porto AlegreRecruiting
- Nova Scotia HealthRecruiting
- Juravinski Hospital and Cancer CentreRecruiting
- The Ottawa HospitalRecruiting
- Mount Sinai HospitalRecruiting
- Hôpital Maisonneuve-RosemontRecruiting
- McGill University Health CentreRecruiting
- Hôtel Dieu du QuebecRecruiting
- Centro Traumatologico Ortopedico HospitalRecruiting
- Leiden University Medical CenterRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Active Comparator
Experimental
Experimental
Experimental
Surveillance Arm I
Surveillance Arm II
Surveillance Arm III
Surveillance Arm IV
Clinical assessment and chest radiograph (CXR) every six months for two years
Clinical assessment and CXR every three months for two years
Clinical assessment and chest computed tomography (CT) every six months for two years
Clinical assessment and chest CT every three months for two years