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Meta‐analysis: recurrence and survival following the use of sirolimus in liver transplantation for hepatocellular carcinoma
Summary Background The use of sirolimus (SRL)‐based immunosuppression protocols have been reported to reduce recurrence rates following liver transplantation (LT) for hepatocellular carcinoma (HCC), although this is still a matter for debate. Aim To undertake a systematic review and meta‐analysis of...
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Published in: | Alimentary pharmacology & therapeutics 2013-02, Vol.37 (4), p.411-419 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Background
The use of sirolimus (SRL)‐based immunosuppression protocols have been reported to reduce recurrence rates following liver transplantation (LT) for hepatocellular carcinoma (HCC), although this is still a matter for debate.
Aim
To undertake a systematic review and meta‐analysis of available literature on the usage of SRL as an immunosuppressive agent following LT for HCC, with a view to comparing cancer outcomes with the commonly used calcineurin inhibitors (CNIs).
Methods
Systematic review and meta‐analysis carried out in line with the Meta‐analysis Of Observational Studies in Epidemiology (MOOSE) guidelines. Primary outcomes of interest were tumour recurrence rate and recurrence‐free survival (RFS). Secondary outcomes were recurrence‐related mortality and overall survival (OS).
Results
In all, 5 studies met the inclusion criteria (n = 474). The recurrence rate was lower in SRL group (4.9–12.9%) in comparison with CNIs (17.3–38.7%). The 1‐, 3‐ and 5‐year RFS was 93–96%, 82–86% and 79–80% for SRL group, which was much better in comparison with the CNIs 70–78%, 64–65% and 54–60% respectively. Similarly, 1‐, 3‐ and 5‐year OS was much better for SRL group (94–95%, 85% and 80%) in comparison with CNIs (79–83%, 66% and 59–62%) respectively. Meta‐analysis demonstrated lower recurrence (OR = 0.30, 95% CI = 0.16–0.55, P |
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ISSN: | 0269-2813 1365-2036 |
DOI: | 10.1111/apt.12185 |