Comparison of Cyclosporine and Tacrolimus in Combination With Rabbit Antithymocyte Immunoglobulins as Induction Therapy in Cardiac Transplantation
Abstract Induction with rabbit antithymocyte immunoglobulins (RATG) for cardiac transplantation allows reduction of calcineurin inhibitor and reduces the incidence of acute rejection episodes (ARE). We compared induction with RATG combined with either cyclosporine (CsA) or tacrolimus (FK) in regard...
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description | Abstract Induction with rabbit antithymocyte immunoglobulins (RATG) for cardiac transplantation allows reduction of calcineurin inhibitor and reduces the incidence of acute rejection episodes (ARE). We compared induction with RATG combined with either cyclosporine (CsA) or tacrolimus (FK) in regard to the number of ARE in the first year after transplantation. We transplanted 111 patients from 2000 to 2008 including 61 who received CsA-RATG, and 19, FK-RATG. At 3 months and 1 year the CsA group displayed 3.29 ± 1.66 and 7.44 ± 2.45 ARE per patient of grade at least 1R respectively. The FK group showed 3.21 ± 1.71 and 8.13 ± 2.07 episodes per patient ( P = .86 at 3 months; P = .32 at 1 year). Among ARE 2R or greater, the CsA group displayed 0.51 ± 0.70 and 0.91 ± 0.95 episodes per patient at 3 months and 1 year, while the FK group showed 0.15 ± 0.38 and 0.31 ± 0.63 episodes, respectively ( P = .09 at 3 months; P = .016 at 1 year). Among type 3R ARE, the CsA group showed 0.11 ± 0.32 and 0.13 ± 0.34 episodes, whereas the FK group experienced 0.05 ± 0.23 and 0.05 ± 0.23 episodes at 3 months and 1 year, respectively ( P = .44 at 3 months, P = .35 at 1 year). The freedom rate from 1R, 2R, and 3R ARE was therefore similar between the two groups ( P = .76, P = .14, and P = .23, respectively). Induction with FK-RATG tended to reduce the number of type 2R and greater rejection episodes per patient at 1 year after transplantation compared to CsA-RATG. |
doi_str_mv | 10.1016/j.transproceed.2009.08.047 |
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We compared induction with RATG combined with either cyclosporine (CsA) or tacrolimus (FK) in regard to the number of ARE in the first year after transplantation. We transplanted 111 patients from 2000 to 2008 including 61 who received CsA-RATG, and 19, FK-RATG. At 3 months and 1 year the CsA group displayed 3.29 ± 1.66 and 7.44 ± 2.45 ARE per patient of grade at least 1R respectively. The FK group showed 3.21 ± 1.71 and 8.13 ± 2.07 episodes per patient ( P = .86 at 3 months; P = .32 at 1 year). Among ARE 2R or greater, the CsA group displayed 0.51 ± 0.70 and 0.91 ± 0.95 episodes per patient at 3 months and 1 year, while the FK group showed 0.15 ± 0.38 and 0.31 ± 0.63 episodes, respectively ( P = .09 at 3 months; P = .016 at 1 year). Among type 3R ARE, the CsA group showed 0.11 ± 0.32 and 0.13 ± 0.34 episodes, whereas the FK group experienced 0.05 ± 0.23 and 0.05 ± 0.23 episodes at 3 months and 1 year, respectively ( P = .44 at 3 months, P = .35 at 1 year). The freedom rate from 1R, 2R, and 3R ARE was therefore similar between the two groups ( P = .76, P = .14, and P = .23, respectively). Induction with FK-RATG tended to reduce the number of type 2R and greater rejection episodes per patient at 1 year after transplantation compared to CsA-RATG.</description><identifier>ISSN: 0041-1345</identifier><identifier>EISSN: 1873-2623</identifier><identifier>DOI: 10.1016/j.transproceed.2009.08.047</identifier><identifier>PMID: 19857745</identifier><identifier>CODEN: TRPPA8</identifier><language>eng</language><publisher>Amsterdam: Elsevier Inc</publisher><subject>Adult ; Animals ; Antibacterial agents ; Antibiotics. Antiinfectious agents. Antiparasitic agents ; Antilymphocyte Serum - therapeutic use ; Biological and medical sciences ; Calcineurin Inhibitors ; Cardiomyopathies - surgery ; Cyclosporine - therapeutic use ; Drug Therapy, Combination ; Female ; Follow-Up Studies ; Fundamental and applied biological sciences. Psychology ; Fundamental immunology ; Graft Rejection - prevention & control ; Heart Transplantation - immunology ; Humans ; Immunosuppressive Agents - therapeutic use ; Male ; Medical sciences ; Middle Aged ; Pharmacology. Drug treatments ; Rabbits ; Retrospective Studies ; Surgery ; Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases ; Tacrolimus - therapeutic use ; Time Factors ; Tissue, organ and graft immunology</subject><ispartof>Transplantation proceedings, 2009-10, Vol.41 (8), p.3337-3341</ispartof><rights>Elsevier Inc.</rights><rights>2009 Elsevier Inc.</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c464t-316a30a657d278d5b000a8fb494cf0eb502a6b74f9edaab3f0e24055fcbf21a83</citedby><cites>FETCH-LOGICAL-c464t-316a30a657d278d5b000a8fb494cf0eb502a6b74f9edaab3f0e24055fcbf21a83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.transproceed.2009.08.047$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>309,310,314,780,784,789,790,3550,23930,23931,25140,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22076068$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19857745$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jacques, F</creatorcontrib><creatorcontrib>Carrier, M</creatorcontrib><creatorcontrib>Pelletier, G.B</creatorcontrib><creatorcontrib>Racine, N</creatorcontrib><creatorcontrib>White, M</creatorcontrib><creatorcontrib>Perrault, L.P</creatorcontrib><creatorcontrib>Pellerin, M</creatorcontrib><title>Comparison of Cyclosporine and Tacrolimus in Combination With Rabbit Antithymocyte Immunoglobulins as Induction Therapy in Cardiac Transplantation</title><title>Transplantation proceedings</title><addtitle>Transplant Proc</addtitle><description>Abstract Induction with rabbit antithymocyte immunoglobulins (RATG) for cardiac transplantation allows reduction of calcineurin inhibitor and reduces the incidence of acute rejection episodes (ARE). We compared induction with RATG combined with either cyclosporine (CsA) or tacrolimus (FK) in regard to the number of ARE in the first year after transplantation. We transplanted 111 patients from 2000 to 2008 including 61 who received CsA-RATG, and 19, FK-RATG. At 3 months and 1 year the CsA group displayed 3.29 ± 1.66 and 7.44 ± 2.45 ARE per patient of grade at least 1R respectively. The FK group showed 3.21 ± 1.71 and 8.13 ± 2.07 episodes per patient ( P = .86 at 3 months; P = .32 at 1 year). Among ARE 2R or greater, the CsA group displayed 0.51 ± 0.70 and 0.91 ± 0.95 episodes per patient at 3 months and 1 year, while the FK group showed 0.15 ± 0.38 and 0.31 ± 0.63 episodes, respectively ( P = .09 at 3 months; P = .016 at 1 year). Among type 3R ARE, the CsA group showed 0.11 ± 0.32 and 0.13 ± 0.34 episodes, whereas the FK group experienced 0.05 ± 0.23 and 0.05 ± 0.23 episodes at 3 months and 1 year, respectively ( P = .44 at 3 months, P = .35 at 1 year). The freedom rate from 1R, 2R, and 3R ARE was therefore similar between the two groups ( P = .76, P = .14, and P = .23, respectively). Induction with FK-RATG tended to reduce the number of type 2R and greater rejection episodes per patient at 1 year after transplantation compared to CsA-RATG.</description><subject>Adult</subject><subject>Animals</subject><subject>Antibacterial agents</subject><subject>Antibiotics. Antiinfectious agents. Antiparasitic agents</subject><subject>Antilymphocyte Serum - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Calcineurin Inhibitors</subject><subject>Cardiomyopathies - surgery</subject><subject>Cyclosporine - therapeutic use</subject><subject>Drug Therapy, Combination</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fundamental immunology</subject><subject>Graft Rejection - prevention & control</subject><subject>Heart Transplantation - immunology</subject><subject>Humans</subject><subject>Immunosuppressive Agents - therapeutic use</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Pharmacology. Drug treatments</subject><subject>Rabbits</subject><subject>Retrospective Studies</subject><subject>Surgery</subject><subject>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</subject><subject>Tacrolimus - therapeutic use</subject><subject>Time Factors</subject><subject>Tissue, organ and graft immunology</subject><issn>0041-1345</issn><issn>1873-2623</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkt-K1DAUxoso7uzqK0gQxKvWkzT954WwjK4OLAg64mU4SVM3Y5t0k1boa_jEpjPDIl55FZL8zndOvi9J8pJCRoGWbw7Z5NGG0TuldZsxgCaDOgNePUo2tK7ylJUsf5xsADhNac6Li-QyhAPEPeP50-SCNnVRVbzYJL-3bhjRm-AscR3ZLqp3YXTeWE3QtmSPyrveDHMgxpIIS2NxMpH-bqY78gWlNBO5tlPcLYNTy6TJbhhm6370Ts69sYFgIDvbzupYtr_THsflqIa-NajI_viaHu10VH6WPOmwD_r5eb1Kvt182G8_pbefP-6217ep4iWf0pyWmAOWRdWyqm4LGZ-HdSd5w1UHWhbAsJQV7xrdIso8njEORdEp2TGKdX6VvD7pRiPvZx0mMZigdB8H0W4Ooso5BVbXTSTfnsjoRQhed2L0ZkC_CApijUQcxN-RiDUSAbWIkcTiF-c2sxzi3UPpOYMIvDoDGBT2XRRSJjxwjEFVQrnO-_7E6WjKL6O9CMpoq3RrvFaTaJ35v3ne_SOjYkomdv6pFx0ObvY22i6oCEyA-Lp-ovUPQQM0GljnfwDbiMo0</recordid><startdate>20091001</startdate><enddate>20091001</enddate><creator>Jacques, F</creator><creator>Carrier, M</creator><creator>Pelletier, G.B</creator><creator>Racine, N</creator><creator>White, M</creator><creator>Perrault, L.P</creator><creator>Pellerin, M</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20091001</creationdate><title>Comparison of Cyclosporine and Tacrolimus in Combination With Rabbit Antithymocyte Immunoglobulins as Induction Therapy in Cardiac Transplantation</title><author>Jacques, F ; Carrier, M ; Pelletier, G.B ; Racine, N ; White, M ; Perrault, L.P ; Pellerin, M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c464t-316a30a657d278d5b000a8fb494cf0eb502a6b74f9edaab3f0e24055fcbf21a83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adult</topic><topic>Animals</topic><topic>Antibacterial agents</topic><topic>Antibiotics. Antiinfectious agents. Antiparasitic agents</topic><topic>Antilymphocyte Serum - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Calcineurin Inhibitors</topic><topic>Cardiomyopathies - surgery</topic><topic>Cyclosporine - therapeutic use</topic><topic>Drug Therapy, Combination</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fundamental immunology</topic><topic>Graft Rejection - prevention & control</topic><topic>Heart Transplantation - immunology</topic><topic>Humans</topic><topic>Immunosuppressive Agents - therapeutic use</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Pharmacology. Drug treatments</topic><topic>Rabbits</topic><topic>Retrospective Studies</topic><topic>Surgery</topic><topic>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</topic><topic>Tacrolimus - therapeutic use</topic><topic>Time Factors</topic><topic>Tissue, organ and graft immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jacques, F</creatorcontrib><creatorcontrib>Carrier, M</creatorcontrib><creatorcontrib>Pelletier, G.B</creatorcontrib><creatorcontrib>Racine, N</creatorcontrib><creatorcontrib>White, M</creatorcontrib><creatorcontrib>Perrault, L.P</creatorcontrib><creatorcontrib>Pellerin, M</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Transplantation proceedings</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jacques, F</au><au>Carrier, M</au><au>Pelletier, G.B</au><au>Racine, N</au><au>White, M</au><au>Perrault, L.P</au><au>Pellerin, M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparison of Cyclosporine and Tacrolimus in Combination With Rabbit Antithymocyte Immunoglobulins as Induction Therapy in Cardiac Transplantation</atitle><jtitle>Transplantation proceedings</jtitle><addtitle>Transplant Proc</addtitle><date>2009-10-01</date><risdate>2009</risdate><volume>41</volume><issue>8</issue><spage>3337</spage><epage>3341</epage><pages>3337-3341</pages><issn>0041-1345</issn><eissn>1873-2623</eissn><coden>TRPPA8</coden><abstract>Abstract Induction with rabbit antithymocyte immunoglobulins (RATG) for cardiac transplantation allows reduction of calcineurin inhibitor and reduces the incidence of acute rejection episodes (ARE). We compared induction with RATG combined with either cyclosporine (CsA) or tacrolimus (FK) in regard to the number of ARE in the first year after transplantation. We transplanted 111 patients from 2000 to 2008 including 61 who received CsA-RATG, and 19, FK-RATG. At 3 months and 1 year the CsA group displayed 3.29 ± 1.66 and 7.44 ± 2.45 ARE per patient of grade at least 1R respectively. The FK group showed 3.21 ± 1.71 and 8.13 ± 2.07 episodes per patient ( P = .86 at 3 months; P = .32 at 1 year). Among ARE 2R or greater, the CsA group displayed 0.51 ± 0.70 and 0.91 ± 0.95 episodes per patient at 3 months and 1 year, while the FK group showed 0.15 ± 0.38 and 0.31 ± 0.63 episodes, respectively ( P = .09 at 3 months; P = .016 at 1 year). Among type 3R ARE, the CsA group showed 0.11 ± 0.32 and 0.13 ± 0.34 episodes, whereas the FK group experienced 0.05 ± 0.23 and 0.05 ± 0.23 episodes at 3 months and 1 year, respectively ( P = .44 at 3 months, P = .35 at 1 year). The freedom rate from 1R, 2R, and 3R ARE was therefore similar between the two groups ( P = .76, P = .14, and P = .23, respectively). Induction with FK-RATG tended to reduce the number of type 2R and greater rejection episodes per patient at 1 year after transplantation compared to CsA-RATG.</abstract><cop>Amsterdam</cop><pub>Elsevier Inc</pub><pmid>19857745</pmid><doi>10.1016/j.transproceed.2009.08.047</doi><tpages>5</tpages></addata></record> |
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subjects | Adult Animals Antibacterial agents Antibiotics. Antiinfectious agents. Antiparasitic agents Antilymphocyte Serum - therapeutic use Biological and medical sciences Calcineurin Inhibitors Cardiomyopathies - surgery Cyclosporine - therapeutic use Drug Therapy, Combination Female Follow-Up Studies Fundamental and applied biological sciences. Psychology Fundamental immunology Graft Rejection - prevention & control Heart Transplantation - immunology Humans Immunosuppressive Agents - therapeutic use Male Medical sciences Middle Aged Pharmacology. Drug treatments Rabbits Retrospective Studies Surgery Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases Tacrolimus - therapeutic use Time Factors Tissue, organ and graft immunology |
title | Comparison of Cyclosporine and Tacrolimus in Combination With Rabbit Antithymocyte Immunoglobulins as Induction Therapy in Cardiac Transplantation |
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