Early Initiation of Everolimus After Liver Transplantation: A Single-Center Experience

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Early Initiation of Everolimus After Liver Transplantation: A Single-Center Experience. / Herden, Uta; Galante, Antonio; Fischer, Lutz; Pischke, Sven; Li, Jun; Achilles, Eike; Koch, Martina; Nashan, Bjoern; Sterneck, Martina.

in: ANN TRANSPL, Jahrgang 21, 04.02.2016, S. 77-85.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

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@article{620a3e4b4c464fd6b6bf314727469696,
title = "Early Initiation of Everolimus After Liver Transplantation: A Single-Center Experience",
abstract = "BACKGROUND: Evidence relating to early everolimus use after liver transplantation remains limited.MATERIAL AND METHODS: Ninety-one adult patients undergoing liver transplantation at our center during 2007-2012 in whom everolimus therapy was initiated <3 months post-transplant were analyzed retrospectively. Everolimus was started on days 1-5 in 50 patients (group 1) and after day 5 in 41 patients (group 2). Most patients continued to receive low-dose cyclosporine (59.3%, target 50-80 ng/ml) or low-dose tacrolimus (25.3%; target 3-5 ng/ml). Mean follow-up was 4.6 years.RESULTS: One-, three- and five-year patient survival rates were 80.5%, 74.2%, and 70.5%, respectively, and did not differ between groups 1 and 2. Six patients (6.6%) developed biopsy-proven acute rejection after a median of 47 days (range 27-356 days). Everolimus was discontinued due to adverse events in 21 patients (23.1%). Incisional hernia repair occurred in 14.0% and 9.4% of patients in group 1 and 2, respectively. Renal function remained stable during follow-up, despite poor baseline function.CONCLUSIONS: Everolimus with very low-dose calcineurin inhibitor given immediately after liver transplantation appears safe and effective, achieving a low rejection rate with well-preserved renal function.",
keywords = "Adolescent, Adult, Aged, Aged, 80 and over, Cyclosporine, Drug Administration Schedule, Drug Therapy, Combination, Everolimus, Female, Follow-Up Studies, Graft Rejection, Humans, Immunosuppressive Agents, Liver Transplantation, Male, Middle Aged, Retrospective Studies, Tacrolimus, Treatment Outcome, Young Adult, Journal Article, Research Support, Non-U.S. Gov't",
author = "Uta Herden and Antonio Galante and Lutz Fischer and Sven Pischke and Jun Li and Eike Achilles and Martina Koch and Bjoern Nashan and Martina Sterneck",
year = "2016",
month = feb,
day = "4",
doi = "10.12659/AOT.895800",
language = "English",
volume = "21",
pages = "77--85",
journal = "ANN TRANSPL",
issn = "1425-9524",
publisher = "International Scientific Information, Inc.",

}

RIS

TY - JOUR

T1 - Early Initiation of Everolimus After Liver Transplantation: A Single-Center Experience

AU - Herden, Uta

AU - Galante, Antonio

AU - Fischer, Lutz

AU - Pischke, Sven

AU - Li, Jun

AU - Achilles, Eike

AU - Koch, Martina

AU - Nashan, Bjoern

AU - Sterneck, Martina

PY - 2016/2/4

Y1 - 2016/2/4

N2 - BACKGROUND: Evidence relating to early everolimus use after liver transplantation remains limited.MATERIAL AND METHODS: Ninety-one adult patients undergoing liver transplantation at our center during 2007-2012 in whom everolimus therapy was initiated <3 months post-transplant were analyzed retrospectively. Everolimus was started on days 1-5 in 50 patients (group 1) and after day 5 in 41 patients (group 2). Most patients continued to receive low-dose cyclosporine (59.3%, target 50-80 ng/ml) or low-dose tacrolimus (25.3%; target 3-5 ng/ml). Mean follow-up was 4.6 years.RESULTS: One-, three- and five-year patient survival rates were 80.5%, 74.2%, and 70.5%, respectively, and did not differ between groups 1 and 2. Six patients (6.6%) developed biopsy-proven acute rejection after a median of 47 days (range 27-356 days). Everolimus was discontinued due to adverse events in 21 patients (23.1%). Incisional hernia repair occurred in 14.0% and 9.4% of patients in group 1 and 2, respectively. Renal function remained stable during follow-up, despite poor baseline function.CONCLUSIONS: Everolimus with very low-dose calcineurin inhibitor given immediately after liver transplantation appears safe and effective, achieving a low rejection rate with well-preserved renal function.

AB - BACKGROUND: Evidence relating to early everolimus use after liver transplantation remains limited.MATERIAL AND METHODS: Ninety-one adult patients undergoing liver transplantation at our center during 2007-2012 in whom everolimus therapy was initiated <3 months post-transplant were analyzed retrospectively. Everolimus was started on days 1-5 in 50 patients (group 1) and after day 5 in 41 patients (group 2). Most patients continued to receive low-dose cyclosporine (59.3%, target 50-80 ng/ml) or low-dose tacrolimus (25.3%; target 3-5 ng/ml). Mean follow-up was 4.6 years.RESULTS: One-, three- and five-year patient survival rates were 80.5%, 74.2%, and 70.5%, respectively, and did not differ between groups 1 and 2. Six patients (6.6%) developed biopsy-proven acute rejection after a median of 47 days (range 27-356 days). Everolimus was discontinued due to adverse events in 21 patients (23.1%). Incisional hernia repair occurred in 14.0% and 9.4% of patients in group 1 and 2, respectively. Renal function remained stable during follow-up, despite poor baseline function.CONCLUSIONS: Everolimus with very low-dose calcineurin inhibitor given immediately after liver transplantation appears safe and effective, achieving a low rejection rate with well-preserved renal function.

KW - Adolescent

KW - Adult

KW - Aged

KW - Aged, 80 and over

KW - Cyclosporine

KW - Drug Administration Schedule

KW - Drug Therapy, Combination

KW - Everolimus

KW - Female

KW - Follow-Up Studies

KW - Graft Rejection

KW - Humans

KW - Immunosuppressive Agents

KW - Liver Transplantation

KW - Male

KW - Middle Aged

KW - Retrospective Studies

KW - Tacrolimus

KW - Treatment Outcome

KW - Young Adult

KW - Journal Article

KW - Research Support, Non-U.S. Gov't

U2 - 10.12659/AOT.895800

DO - 10.12659/AOT.895800

M3 - SCORING: Journal article

C2 - 26842532

VL - 21

SP - 77

EP - 85

JO - ANN TRANSPL

JF - ANN TRANSPL

SN - 1425-9524

ER -