Copyright
©The Author(s) 2016.
World J Gastroenterol. Nov 28, 2016; 22(44): 9661-9673
Published online Nov 28, 2016. doi: 10.3748/wjg.v22.i44.9661
Published online Nov 28, 2016. doi: 10.3748/wjg.v22.i44.9661
Table 1 Summary of studies concerning radiofrequency ablation
Authors | Number of patients | Lesion type | Location | Treatment type | Approach | Needle | Mean treatment duration | Conclusion |
D’Onofrio et al[8] | 18 | Pancreatic ductal adenocarcinoma | Head | Radiofrequency ablation | Percutaneous with US | 17 G | 3 min and 13 s | High success rate, with 40% of cases showing CA 19.9 reduction |
Carrafiello et al[26] | 1 | Pancreatic metastases from renal cell | Body-tail | Radiofrequency ablation | Percutaneous with CT | 19 G | 8 min and 35 s | RFA is feasible for |
metastatic lesions at body-tail | ||||||||
Limmer et al[27] | 1 | Insulinoma | Body-tail | Radiofrequency ablation | Percutaneous with CT | 16 G | 18 min | RFA proved to be a clinically successful |
procedure | ||||||||
Wu et al[28] | 1 | Gastrinoma | Tail | Radiofrequency ablation | Percutaneous transplenic with CT | - | - | Percutaneous transplenic RFA is feasible |
Singh et al[29] | 11 | Pancreatic ductal adenocarcinoma | - | Radiofrequency ablation | 1 percutaneous with CT + 10 laparoscopic | - | - | RFA is a safe and feasible technique of tumor cytoreduction |
Rossi et al[30] | 8 | Pancreatic neuroendocrine tumors | Head and body-tail | Radiofrequency ablation | Percutaneous with CT | 17 and 19 G | 9 min | RFA is a feasible, safe, and effective option |
Table 2 Summary of study concerning microwave ablation
Authors | Number of patients | Lesion | Location | Treatment type | Approach | Needle | Mean treatment duration | Conclusion |
Carrafiello et al[47] | 5 | Pancreatic ductal adenocarcinoma | Head | Microwave ablation | Percutaneous with US | - | - | Microwave ablation appears to be feasible in palliative treatment |
Table 3 Summary of studies concerning cryosurgery
Authors | Number of patients | Lesion | Location | Treatment type | Approach | Needle | Mean treatment duration | Conclusion |
Xu et al[9] | 49 | Pancreatic ductal adenocarcinoma | - | Cryosurgery | 36 percutaneous with US or CT + 13 intraoperative | 2 or 3 mm | - | Cryosurgery is associated with a low rate of adverse effects |
Li et al[54] | 2 | Neuroendocrine tumors | Head and tail | Cryosurgery | Percutaneous with US and CT | 1.7 mm and 2 mm | 10 and 15 min | Percutaneous cryosurgery is minimally invasive and |
has advantages compared with conventional surgery | ||||||||
Niu et al[55] | 67 | Pancreatic ductal adenocarcinoma | - | Cryosurgery | Percutaneous with US and CT | 1.7 mm | - | Cryoimmunotherapy significantly increased overall survival in metastatic |
pancreatic cancer |
Table 4 Summary of studies concerning irreversible ablation
Authors | Number of patients | Lesion | Location | Treatment type | Approach | Needle | Mean treatment duration | Conclusion |
Bagla et al[72] | 1 | Pancreatic ductal adenocarcinoma | Body-tail | Irreversible electroporation | Percutaneous with US and CT | 22 G | - | Percutaneous IRE showed promise as a feasible and potentially safe method for unresectable tumor |
Martin et al[73] | 27 | Pancreatic ductal adenocarcinoma | 15 head + 12 body-tail | Irreversible electroporation | 1 percutaneous + 26 surgical | - | - | IRE ablation is safe and feasible as a primary local treatment in unresectable locally advanced disease |
Narayanan et al[10] | 14 | Pancreatic ductal adenocarcinoma | 6 head + 1 uncinated process + 7 body-tail | Irreversible electroporation | Percutaneous with CT | - | - | Percutaneous IRE in pancreatic adenocarcinoma is feasible and safe |
Månsson et al[11] | 24 | Pancreatic ductal adenocarcinoma | 19 head + 5 body-tail | Irreversible electroporation | Percutaneous with US | - | - | Percutaneous IRE is reasonably safe and shows promising results for efficacy |
- Citation: D’Onofrio M, Ciaravino V, De Robertis R, Barbi E, Salvia R, Girelli R, Paiella S, Gasparini C, Cardobi N, Bassi C. Percutaneous ablation of pancreatic cancer. World J Gastroenterol 2016; 22(44): 9661-9673
- URL: https://www.wjgnet.com/1007-9327/full/v22/i44/9661.htm
- DOI: https://dx.doi.org/10.3748/wjg.v22.i44.9661