TY - JOUR
T1 - Percutaneous thermal ablation for primary hepatocellular carcinoma: A systematic review and meta-analysis
AU - Chinnaratha, Mohamed
AU - Chuang, Anthony
AU - Fraser, Robert
AU - Woodman, Richard
AU - Wigg, Alan
PY - 2016/2/1
Y1 - 2016/2/1
N2 -
Background and Aim: Percutaneous thermal ablation using radiofrequency ablation (RFA) and microwave ablation (MWA) are both widely available curative treatments for hepatocellular carcinoma. Despite significant advances, it remains unclear which modality results in better outcomes. This meta-analysis of randomized controlled trials (RCT) and observational studies was undertaken to compare the techniques in terms of effectiveness and safety. Methods: Electronic reference databases (Medline, EMBASE and Cochrane Central) were searched between January 1980 and May 2014 for human studies comparing RFA and MWA. The primary outcome was the risk of local tumor progression (LTP). Secondary outcomes were complete ablation (CA), overall survival, and major adverse events (AE). The ORs were combined across studies using the random-effects model. Results: Ten studies (two prospective and eight retrospective) were included, and the overall LTP rate was 13.6% (176/1298). There was no difference in LTP rates between RFA and MWA [OR (95% CI): 1.01(0.67-1.50), P=0.9]. The CA rate, 1- and 3-year overall survival and major AE were similar between the two modalities (P>0.05 for all). In subgroup analysis, there was no difference in LTP rates according to study quality, but LTP rates were lower with MWA for treatment of larger tumors [1.88(1.10-3.23), P=0.02]. There was no significant publication bias or inter-study heterogeneity (I
2
<50% and P>0.1) observed in any of the measured outcomes. Conclusion: Overall, both RFA and MWA are equally effective and safe, but MWA may be more effective compared to RFA in preventing LTP when treating larger tumors. Well-designed, larger, multicentre RCTs are required to confirm these findings.
AB -
Background and Aim: Percutaneous thermal ablation using radiofrequency ablation (RFA) and microwave ablation (MWA) are both widely available curative treatments for hepatocellular carcinoma. Despite significant advances, it remains unclear which modality results in better outcomes. This meta-analysis of randomized controlled trials (RCT) and observational studies was undertaken to compare the techniques in terms of effectiveness and safety. Methods: Electronic reference databases (Medline, EMBASE and Cochrane Central) were searched between January 1980 and May 2014 for human studies comparing RFA and MWA. The primary outcome was the risk of local tumor progression (LTP). Secondary outcomes were complete ablation (CA), overall survival, and major adverse events (AE). The ORs were combined across studies using the random-effects model. Results: Ten studies (two prospective and eight retrospective) were included, and the overall LTP rate was 13.6% (176/1298). There was no difference in LTP rates between RFA and MWA [OR (95% CI): 1.01(0.67-1.50), P=0.9]. The CA rate, 1- and 3-year overall survival and major AE were similar between the two modalities (P>0.05 for all). In subgroup analysis, there was no difference in LTP rates according to study quality, but LTP rates were lower with MWA for treatment of larger tumors [1.88(1.10-3.23), P=0.02]. There was no significant publication bias or inter-study heterogeneity (I
2
<50% and P>0.1) observed in any of the measured outcomes. Conclusion: Overall, both RFA and MWA are equally effective and safe, but MWA may be more effective compared to RFA in preventing LTP when treating larger tumors. Well-designed, larger, multicentre RCTs are required to confirm these findings.
KW - Hepatocellular carcinoma
KW - Microwave ablation
KW - Radiofrequency ablation
UR - http://www.scopus.com/inward/record.url?scp=84955600701&partnerID=8YFLogxK
U2 - 10.1111/jgh.13028
DO - 10.1111/jgh.13028
M3 - Review article
SN - 0815-9319
VL - 31
SP - 294
EP - 301
JO - Journal of Gastroenterology and Hepatology
JF - Journal of Gastroenterology and Hepatology
IS - 2
ER -