I
patients
TACE and I
control group
6-month, 12-month stent cumulative patency rate, 6-month, 12-month, 24-month overall survival rate, objective response rate of PVTT, main portal venous pressure changes, treatment-related adverse events
Abstract
A meta-analysis aimed to systematically evaluate the safety and efficiency of I The Cochrane library, PubMed/Medline, EMBASE, CNKI, Wanfang Data and CQVIP were systematically screened out from the earliest to December 2019. The qualities of all included studies were assessed. The primary endpoints were the 6-month, 12-month stent cumulative patency rate and 6-month, 12-month, 24-month overall survival rate while the secondary endpoints were the objective response rate of PVTT, main portal venous pressure changes and treatment-related adverse events. Our meta-analysis was conducted using Stata 12.0 software. Totally seven studies with 1018 patients were included in the final analysis, in which 602 patients received TACE and I I
