Sirolimus Use in Liver Transplant Recipients With Hepatocellular Carcinoma: A Randomized, Multicenter, Open-Label Phase 3 Trial. Issue 1 (January 2016)
- Record Type:
- Journal Article
- Title:
- Sirolimus Use in Liver Transplant Recipients With Hepatocellular Carcinoma: A Randomized, Multicenter, Open-Label Phase 3 Trial. Issue 1 (January 2016)
- Main Title:
- Sirolimus Use in Liver Transplant Recipients With Hepatocellular Carcinoma
- Authors:
- Geissler, Edward K.
Schnitzbauer, Andreas A.
Zülke, Carl
Lamby, Philipp E.
Proneth, Andrea
Duvoux, Christophe
Burra, Patrizia
Jauch, Karl-Walter
Rentsch, Markus
Ganten, Tom M.
Schmidt, Jan
Settmacher, Utz
Heise, Michael
Rossi, Giorgio
Cillo, Umberto
Kneteman, Norman
Adam, René
van Hoek, Bart
Bachellier, Philippe
Wolf, Philippe
Rostaing, Lionel
Bechstein, Wolf O.
Rizell, Magnus
Powell, James
Hidalgo, Ernest
Gugenheim, Jean
Wolters, Heiner
Brockmann, Jens
Roy, André
Mutzbauer, Ingrid
Schlitt, Angela
Beckebaum, Susanne
Graeb, Christian
Nadalin, Silvio
Valente, Umberto
Turrión, Victor Sánchez
Jamieson, Neville
Scholz, Tim
Colledan, Michele
Fändrich, Fred
Becker, Thomas
Söderdahl, Gunnar
Chazouillères, Olivier
Mäkisalo, Heikki
Pageaux, Georges-Philippe
Steininger, Rudolf
Soliman, Thomas
de Jong, Koert P.
Pirenne, Jacques
Margreiter, Raimund
Pratschke, Johann
Pinna, Antonio D.
Hauss, Johann
Schreiber, Stefan
Strasser, Simone
Klempnauer, Jürgen
Troisi, Roberto I.
Bhoori, Sherrie
Lerut, Jan
Bilbao, Itxarone
Klein, Christian G.
Königsrainer, Alfred
Mirza, Darius F.
Otto, Gerd
Mazzaferro, Vincenzo
Neuhaus, Peter
Schlitt, Hans J.
… (more) - Abstract:
- Abstract : Background: We investigated whether sirolimus-based immunosuppression improves outcomes in liver transplantation (LTx) candidates with hepatocellular carcinoma (HCC). Methods: In a prospective-randomized open-label international trial, 525 LTx recipients with HCC initially receiving mammalian target of rapamycin inhibitor–free immunosuppression were randomized 4 to 6 weeks after transplantation into a group on mammalian target of rapamycin inhibitor–free immunosuppression (group A: 264 patients) or a group incorporating sirolimus (group B: 261). The primary endpoint was recurrence-free survival (RFS); intention-to-treat (ITT) analysis was conducted after 8 years. Overall survival (OS) was a secondary endpoint. Results: Recurrence-free survival was 64.5% in group A and 70.2% in group B at study end, this difference was not significant ( P = 0.28; hazard ratio [HR], 0.84; 95% confidence interval [95% CI], 0.62; 1.15). In a planned analysis of RFS rates at yearly intervals, group B showed better outcomes 3 years after transplantation (HR, 0.7; 95% CI, 0.48-1.00). Similarly, OS ( P = 0.21; HR, 0.81; 95% CI, 0.58-1.13) was not statistically better in group B at study end, but yearly analyses showed improvement out to 5 years (HR, 0.7; 95% CI, 0.49-1.00). Interestingly, subgroup (Milan Criteria-based) analyses revealed that low-risk, rather than high-risk, patients benefited most from sirolimus; furthermore, younger recipients (age ⩽60) also benefited, as well sirolimusAbstract : Background: We investigated whether sirolimus-based immunosuppression improves outcomes in liver transplantation (LTx) candidates with hepatocellular carcinoma (HCC). Methods: In a prospective-randomized open-label international trial, 525 LTx recipients with HCC initially receiving mammalian target of rapamycin inhibitor–free immunosuppression were randomized 4 to 6 weeks after transplantation into a group on mammalian target of rapamycin inhibitor–free immunosuppression (group A: 264 patients) or a group incorporating sirolimus (group B: 261). The primary endpoint was recurrence-free survival (RFS); intention-to-treat (ITT) analysis was conducted after 8 years. Overall survival (OS) was a secondary endpoint. Results: Recurrence-free survival was 64.5% in group A and 70.2% in group B at study end, this difference was not significant ( P = 0.28; hazard ratio [HR], 0.84; 95% confidence interval [95% CI], 0.62; 1.15). In a planned analysis of RFS rates at yearly intervals, group B showed better outcomes 3 years after transplantation (HR, 0.7; 95% CI, 0.48-1.00). Similarly, OS ( P = 0.21; HR, 0.81; 95% CI, 0.58-1.13) was not statistically better in group B at study end, but yearly analyses showed improvement out to 5 years (HR, 0.7; 95% CI, 0.49-1.00). Interestingly, subgroup (Milan Criteria-based) analyses revealed that low-risk, rather than high-risk, patients benefited most from sirolimus; furthermore, younger recipients (age ⩽60) also benefited, as well sirolimus monotherapy patients. Serious adverse event numbers were alike in groups A (860) and B (874). Conclusions: Sirolimus in LTx recipients with HCC does not improve long-term RFS beyond 5 years. However, a RFS and OS benefit is evident in the first 3 to 5 years, especially in low-risk patients. This trial provides the first high-level evidence base for selecting immunosuppression in LTx recipients with HCC. Abstract : In a large prospective randomized open-label international trial, liver transplant recipients for HCC were randomized to receive non-mTOR-inhibitor-based-treatment or mTOR-inhibitor-based-treatment. Results indicate overall sirolimus does not improve long-term recurrence-free survival beyond 5 years while a benefit was seen in low-risk patients. Supplemental digital content is available in the text. … (more)
- Is Part Of:
- Transplantation. Volume 100:Issue 1(2016)
- Journal:
- Transplantation
- Issue:
- Volume 100:Issue 1(2016)
- Issue Display:
- Volume 100, Issue 1 (2016)
- Year:
- 2016
- Volume:
- 100
- Issue:
- 1
- Issue Sort Value:
- 2016-0100-0001-0000
- Page Start:
- Page End:
- Publication Date:
- 2016-01
- Subjects:
- Transplantation of organs, tissues, etc -- Periodicals
Transplantation immunology -- Periodicals
617.95 - Journal URLs:
- http://journals.lww.com/pages/default.aspx ↗
- DOI:
- 10.1097/TP.0000000000000965 ↗
- Languages:
- English
- ISSNs:
- 0041-1337
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 9024.990000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 5074.xml