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Efficacy and safety of transhepatic arterial chemoembolization with drug-loaded microspheres in unresectable primary liver cancer. | LitMetric

AI Article Synopsis

Article Abstract

Background: Transhepatic arterial chemoembolization (TACE), as a local treatment, has been widely used in the treatment of unresectable liver cancer. The introduction of drug carrier microspheres has brought new hope for the therapeutic effect of TACE. Microspheres can realize the slow release and directional delivery of drugs, reduce systemic toxicity and improve local curative effect.

Aim: To compare the effectiveness of traditional transcatheter arterial chemoembolization against microsphere-assisted transcatheter arterial chemoembolization in the treatment of hepatocellular carcinoma that is incurable.

Methods: We searched the PubMed, Embase, Cochrane Library, and CNKI databases for clinical trials of drug-luting beads TACE (DEB-TACE) conventional TACE (cTACE) for the treatment of unresectable liver cancer. We screened references based on inclusion and exclusion criteria and then selected valid data for meta-analysis using RevMan 53 software. The complete response (CR) rate, partial response (PR) rate, postoperative stable disease (SD) rate, and 6-month and 12-month survival rates were compared.

Results: A total of 12 articles were included, including 1177 patients, 519 of whom received DEB-TACE and 658 of whom received cTACE. The CR rate in the DEB-TACE group was much greater than that in the cTACE group [relative risk (RR) = 1.42, 95%CI: 1.18-1.72, = 0.0002]. The 12-month survival rate significantly increased (RR = 1.09; 95%CI: 1.01- 1.17, = 0.03); the PR rate (RR = 1.13; 95%CI: 0.97-1.30, = 0.12); the SD rate (RR = 0.82; 95%CI: 0.64-1.05, = 0.12); and the 6-month survival rate (RR = 1.05; 95%CI: 1.00-1.10, = 0.07). There was no significant difference ( < 0.05).

Conclusion: Compared with those of iodized oil TACE, the drug-loaded microspheres tended to have therapeutic advantages.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11577372PMC
http://dx.doi.org/10.4251/wjgo.v16.i12.4728DOI Listing

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