“…Molecular and proliferation markers (Ki67, thymidylate synthase, p53, KRAS, and BRAF) may contribute to the prediction of outcomes post-ablation, offering a valuable stratification tool for tumor-tailored therapeutic approach [ 11 ]. The identification of tumor Ki67 at the end of ablation is a strong independent predictor of local tumor progression and overall patient survival, with high Ki67 ratios, suggesting that these tumors may possess an ablation resistance mechanism [ 11 , 41 ]. Margins over 10 mm were associated with no local progression, especially in patients with KRAS wild-type disease, whereas in RAS mutant tumors, ablation margins larger than 10 mm are mandatory to achieve local cure and sustained local tumor control [ 42 , 43 , 44 , 45 , 46 , 47 ].…”