Radiofrequency ablation versus resection for resectable colorectal liver metastases: time for a randomized trial?
- PMID: 17906898
- DOI: 10.1245/s10434-007-9478-5
Radiofrequency ablation versus resection for resectable colorectal liver metastases: time for a randomized trial?
Abstract
Background: Surgical resection is the gold standard in the treatment of resectable colorectal liver metastases (CRLM). In several centers, resection is being replaced by radiofrequency ablation (RFA), even though there is no evidence yet from randomized trials to support this. The aim of this study was to critically review the oncological evidence for and against the use of RFA for resectable CRLM.
Methods: An exhaustive review of RFA of colorectal metastases was carried out.
Results: Five-year survival data after RFA for resectable CRLM are not available. Percutaneous RFA is associated with worse local control, worse staging, and a small risk of electrode track seeding when compared with resection (level V evidence). For tumors </=3 cm, local control after surgical RFA is equivalent to resection, especially if applied by experienced physicians to nonperivascular tumors (level V evidence). There is indirect evidence for profoundly different biological effects of RFA and resection.
Conclusions: A subgroup of patients has been identified for whom local control after RFA might be equivalent to resection. Whether this is true, and whether this translates into equivalent survival, remains to be proven. The time has come for a randomized trial.
Comment in
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Radiofrequency ablation versus resection for resectable colorectal liver metastases: time for a randomized trial?Ann Surg Oncol. 2008 Jan;15(1):11-3. doi: 10.1245/s10434-007-9668-1. Epub 2007 Oct 23. Ann Surg Oncol. 2008. PMID: 17955298 Free PMC article. No abstract available.
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A place for radiofrequency ablation in the treatment of resectable colorectal liver metastases?Ann Surg Oncol. 2008 Jul;15(7):2063; author reply 2064-5. doi: 10.1245/s10434-008-9843-z. Epub 2008 Mar 8. Ann Surg Oncol. 2008. PMID: 18327529 Free PMC article. No abstract available.
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