About this trial
This study will see whether collecting and analyzing needle biopsy samples from cancer liver metastases after a tumor ablation procedure will be able to identify cancer cells that are still alive. The results of these biopsies could help determine the next treatment for your cancer, but the biopsies could cause side effects.
Eligibility criteria
Qualifiers
Diagnosis of liver metastases from various primary tumors
Confined liver disease or limited extrahepatic disease stable/controlled for at least 4 months (extrahepatic disease amenable to treatment is allowed)
Lesions of ≤3 cm in maximum diameter
At least one FDG-avid lesion to be treated***
Disqualifiers
Age < 18
Less than 5 mm distance to a structure (GI or biliary tract), that cannot be protected from ablation injury with technical modifications such as hydro or air dissection
INR > 1.5 that cannot be corrected with fresh frozen plasma **
Platelet count of <50,000 that cannot be corrected with transfusion
Trial design
Treatments tested in this trial
- [18-F]- FDG - PET
- Tumor ablation (TA)
- PET/CT Scan
Treatment groups
Locations
1Sponsors and collaborators
Memorial Sloan Kettering Cancer Center
Lead sponsor