Long-Term Sirolimus for Primary Immunosuppression in Heart Transplant Recipients

被引:90
作者
Asleh, Rabea
Briasoulis, Alexandros
Kremers, Walter K.
Adigun, Rosalyn
Boilson, Barry A.
Pereira, Naveen L.
Edwards, Brooks S.
Clavell, Alfredo L.
Schirger, John A.
Rodeheffer, Richard J.
Frantz, Robert P.
Joyce, Lyle D.
Maltais, Simon
Stulak, John M.
Daly, Richard C.
Tilford, Jonella
Choi, Woong-Gil
Lerman, Amir
Kushwaha, Sudhir S.
机构
[1] Mayo Clin, Dept Cardiovasc Dis & Hlth Sci Res, Rochester, MN 55905 USA
[2] Mayo Clin, William J von Liebig Ctr Transplantat & Clin Rege, Rochester, MN 55905 USA
关键词
cardiac allograft vasculopathy; coronary intravascular ultrasound; heart transplantation; immunosuppression; CARDIAC ALLOGRAFT VASCULOPATHY; INTRAVASCULAR ULTRASOUND; LUNG TRANSPLANTATION; INTERNATIONAL SOCIETY; RANDOMIZED-TRIAL; ACUTE REJECTION; PROGRESSION; PROLIFERATION; EVEROLIMUS; INHIBITORS;
D O I
10.1016/j.jacc.2017.12.005
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Small studies have reported superiority of sirolimus (SRL) over calcineurin inhibitor (CNI) in mitigating cardiac allograft vascutopathy (CAV) after heart transplantation (HT). However, data on the tong-term effect on CAV progression and clinical outcomes are tacking. OBJECTIVES The aim of this study was to test the tong-term safety and efficacy of conversion from CNI to SRL as maintenance therapy on CAV progression and outcomes after HT. METHODS A cohort of 402 patients who underwent HT and were either treated with CNI alone (n = 134) or converted from CNI to SRL (n = 268) as primary immunosuppression was analyzed. CAV progression was assessed using serial coronary intravascutar ultrasound during treatment with CNI (n = 99) and after conversion to SRL (n = 235) in patients who underwent at least 2 intravascular ultrasound studies. RESULTS The progression in plaque volume (2.8 +/- 2.3 mm(3)/ mm vs. 0.46 +/- 1.8 mm(3)/mm; p < 0.0001) and plaque index (plaque volume-to-vessel volume ratio) (12.2 +/- 9.6% vs. 1.1 +/- 7.9%; p < 0.0001) were significantly attenuated when treated with SRL compared with CM. Over a mean follow-up period of 8.9 years from time of HT, all-cause mortality occurred in 25.6% of the patients and was tower during treatment with SRL compared with CNI (adjusted hazard ratio: 0.47; 95% confidence interval: 0.31 to 0.70; p < 0.0002), and CAV-related events were also less frequent during treatment with SRL (adjusted hazard ratio: 0.35; 95% confidence interval: 0.21 to 0.59; p < 0.0001). Further analyses suggested more attenuation of CAV and more favorable clinical outcomes with earlier conversion to SRL (<= 2 years) compared with tate conversion (>2 years) after HT. CONCLUSIONS Early conversion to SRL is associated with attenuated CAV progression and with tower long-term mortality and fewer CAV-related events compared with continued CNI use. (C) 2018 by the American College of Cardiology Foundation.
引用
收藏
页码:636 / 650
页数:15
相关论文
共 27 条
[1]   Everolimus Initiation and Early Calcineurin Inhibitor Withdrawal in Heart Transplant Recipients: A Randomized Trial [J].
Andreassen, A. K. ;
Andersson, B. ;
Gustafsson, F. ;
Eiskjaer, H. ;
Rdegran, G. ;
Gude, E. ;
Jansson, K. ;
Solbu, D. ;
Sigurdardottir, V. ;
Arora, S. ;
Dellgren, G. ;
Gullestad, L. .
AMERICAN JOURNAL OF TRANSPLANTATION, 2014, 14 (08) :1828-1838
[2]   Everolimus and mycophenolate mofetil are potent inhibitors of fibroblast proliferation after lung transplantation [J].
Azzola, A ;
Havryk, A ;
Chhajed, P ;
Hostettler, K ;
Black, J ;
Johnson, P ;
Roth, M ;
Glanville, A ;
Tamm, M .
TRANSPLANTATION, 2004, 77 (02) :275-280
[3]   Volumetric analysis of in-stent intimal hyperplasia in diabetic patients treated with or without abciximab - Results of the Diabetes Abciximab SteNT Evaluation (DANTE) randomized trial [J].
Chaves, AJ ;
Sousa, AGMR ;
Mattos, LA ;
Abizaid, A ;
Staico, R ;
Feres, F ;
Centemero, M ;
Tanajura, LF ;
Abizaid, A ;
Pinto, I ;
Maldonado, G ;
Seixas, A ;
Costa, MA ;
Paes, A ;
Mintz, GS ;
Sousa, JE .
CIRCULATION, 2004, 109 (07) :861-866
[4]   Rapamycin modulates the eNOS vs. shear stress relationship [J].
Cheng, Caroline ;
Tempel, Dennie ;
Oostlander, Angela ;
Helderman, Frank ;
Gijsen, Frank ;
Wentzel, Jolanda ;
van Haperen, Rien ;
Haitsma, David B. ;
Serruys, Patrick W. ;
van der Steen, Anton F. W. ;
de Crom, Rini ;
Krams, Rob .
CARDIOVASCULAR RESEARCH, 2008, 78 (01) :123-129
[5]  
COSTANZONORDIN MR, 1992, J HEART LUNG TRANSPL, V11, pS90
[6]   Everolimus for the prevention of allograft rejection and vasculopathy in cardiac-transplant recipients [J].
Eisen, HJ ;
Tuzcu, EM ;
Dorent, R ;
Kobashigawa, J ;
Mancini, D ;
Valantine-von Kaeppler, HA ;
Starling, RC ;
Sorensen, K ;
Hummel, M ;
Lind, JM ;
Abeywickrama, KH ;
Bernhardt, P .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 349 (09) :847-858
[7]   Avoidance of calcineurin inhibitors with use of proliferation signal inhibitors in de novo heart transplantation with renal failure [J].
Gonzalez-Vilchez, Francisco ;
Antonio Vazquez de Prada, Jose ;
Exposito, Victor ;
Garcia-Camarero, Tamara ;
Fernandez-Friera, Leticia ;
Llano, Miguel ;
Ruano, Javier ;
Martin-Duran, Rafael .
JOURNAL OF HEART AND LUNG TRANSPLANTATION, 2008, 27 (10) :1135-1141
[8]   Benefit of early conversion from CNI-based to everolimus-based immunosuppression in heart transplantation [J].
Gude, Einar ;
Gullestad, Lars ;
Arora, Satish ;
Simonsen, Svein ;
Hoel, Ina ;
Hartmann, Anders ;
Holdaas, Hallvard ;
Fiane, Arnt E. ;
Geiran, Odd R. ;
Andreassen, Arne K. .
JOURNAL OF HEART AND LUNG TRANSPLANTATION, 2010, 29 (06) :641-647
[9]   Tacrolimus with mycophenotate mofetil or sirolimus compared with calcineurin inhibitor-free immunosuppression (sirolimus/mycophenolate mofetil) after heart transplantation: 5-year results [J].
Kaczmarek, Ingo ;
Zaruba, Marc-Michael ;
Beiras-Fernandez, Andres ;
Reimann, Ricarda ;
Nickel, Thomas ;
Grinninger, Carola ;
Sadoni, Sebastian ;
Hagl, Christian ;
Meiser, Bruno .
JOURNAL OF HEART AND LUNG TRANSPLANTATION, 2013, 32 (03) :277-284
[10]   Sirolimus in de novo heart transplant recipients reduces acute rejection and prevents coronary artery disease at 2 years - A randomized clinical trial [J].
Keogh, A ;
Richardson, M ;
Ruygrok, P ;
Spratt, P ;
Galbraith, A ;
O'Driscoll, G ;
Macdonald, P ;
Esmore, D ;
Muller, D ;
Faddy, S .
CIRCULATION, 2004, 110 (17) :2694-2700