Sirolimus-based immunosuppression is associated with increased survival after liver transplantation for hepatocellular carcinoma
- PMID: 20187107
- DOI: 10.1002/hep.23437
Sirolimus-based immunosuppression is associated with increased survival after liver transplantation for hepatocellular carcinoma
Abstract
Liver transplantation is an important treatment option for selected patients with nonresectable hepatocellular carcinoma (HCC). Several reports have suggested a lower risk of posttransplant tumor recurrence with the use of sirolimus and a higher one with calcineurin inhibitors, but the selection of an ideal immunosuppression protocol is still a matter of debate. The aim of this study was to define the immunosuppression associated with the best survival after liver transplantation for HCC. It was based on the Scientific Registry of Transplant Recipients and included 2,491 adult recipients of isolated liver transplantation for HCC and 12,167 for non-HCC diagnoses between March 2002 and March 2009. All patients remained on stable maintenance immunosuppression protocols for at least 6 months posttransplant. In a multivariate analysis, only anti-CD25 antibody induction and sirolimus-based maintenance therapy were associated with improved survivals after transplantation for HCC (hazard ratio [HR] 0.64, 95% confidence interval [CI]: 0.45-0.9, P < or = 0.01; HR 0.53, 95% CI: 0.31-0.92, P < or = 0.05, respectively). The other studied drugs, including calcineurin inhibitors, did not demonstrate a significant impact. In an effort to understand whether the observed effects were due to a direct impact of the drug on tumor or more on liver transplant in general, we conducted a similar analysis on non-HCC patients. Although anti-CD25 induction was again associated with a trend toward improved survival, sirolimus showed a trend toward lower rates of survival in non-HCC recipients, confirming the specificity of its beneficial impact to cancer patients.
Conclusion: According to these data, sirolimus-based immunosuppression has unique posttransplant effects on HCC patients that lead to improved survival.
Comment in
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Inhibition of mammalian target of rapamycin: the janus face of immunosuppression?Hepatology. 2010 Apr;51(4):1113-5. doi: 10.1002/hep.23582. Hepatology. 2010. PMID: 20373365 No abstract available.
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Activation of the mammalian target of rapamycin signaling pathway in hepatocellular carcinoma.Hepatology. 2010 Oct;52(4):1524. doi: 10.1002/hep.23763. Hepatology. 2010. PMID: 20680964 No abstract available.
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Inhibition of mammalian target of rapamycin: two goals with one shot?J Hepatol. 2011 Jan;54(1):182-3. doi: 10.1016/j.jhep.2010.07.049. Epub 2010 Sep 25. J Hepatol. 2011. PMID: 20952085 No abstract available.
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