About this trial
This prospective observational study aims to investigate the effectiveness and safety of SBRT in the management of oligometastases from rare tumors. In addition, the study aims to identify potential differences in treatment efficacy and toxicity between different types of cancer and to provide valuable information on the use of SBRT in these contexts, potentially leading to better treatment options and outcomes for these patients.
Eligibility criteria
Qualifiers
ECOG PS 0 - 2
histologically confirmed diagnosis of rare solid tumors including melanoma, soft tissue sarcoma, head-neck tumors, gynaecological tumors, Merkel cell carcinoma, thymic carcinoma, gastrointestinal stromal tumors (GIST) and urothelial tumors
No limit to the number of metastases treated with SBRT but all active lesions must be treated with radical intent (primary tumor and metastases)
Synchronous and metachronous oligometastases, as well as oligorecurrent and oligoprogressive disease are allowed
Disqualifiers
prior treatment with radiation to the same metastatic site
inability to provide informed consent
contraindications to SBRT
Trial design
Treatments tested in this trial
- SBRT