A Randomized Trial of Alemtuzumab Versus Antithymocyte Globulin Induction in Renal and Pancreas Transplantation
BACKGROUND.: Alemtuzumab and rabbit antithymocyte globulin (rATG) are commonly used for induction of immunsuppression for kidney and pancreas transplantation, but the two agents have not been compared directly. METHODS.: We conducted a prospective randomized single-center trial comparing alemtuzumab...
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Veröffentlicht in: | Transplantation 2009-09, Vol.88 (6), p.810-819 |
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creator | FARNEY, Alan C DOARES, William MOORE, Phillip ADAMS, Patricia L STRATTA, Robert J ROGERS, Jeffrey SINGH, Rajinder HARTMANN, Erica HART, Lois ASHCRAFT, Elizabeth REEVES-DANIELS, Amber GAUTREAUX, Michael ISKANDAR, Samy S |
description | BACKGROUND.: Alemtuzumab and rabbit antithymocyte globulin (rATG) are commonly used for induction of immunsuppression for kidney and pancreas transplantation, but the two agents have not been compared directly. METHODS.: We conducted a prospective randomized single-center trial comparing alemtuzumab and rATG induction in adult kidney and pancreas transplantation in patients treated with similar maintenance immunosuppression. RESULTS.: Between February 1, 2005, and September 1, 2007, 222 patients randomly received either alemtuzumab (n=113) or rATG (n=109) induction; 180 (81%) underwent kidney alone, 38 (17%) simultaneous pancreas-kidney, and 4 (2%) pancreas after kidney transplants. Of 180 kidney-alone transplants, 152 (84%) were from deceased donors, including 61 (34%) from expanded criteria donors. Retransplantation, human leukocyte antigen match, antibody titer, expanded criteria donors, race, cytomegalovirus status, delayed graft function, and immunologic risks were similar between the two induction groups. With a median follow-up of 2 years (minimum 1 year), overall patient, kidney, and pancreas graft survival rates were 96%, 89%, and 90%, respectively. Survival, initial length of stay, and maintenance immunosuppression (including early steroid elimination) were similar between alemtuzumab and rATG groups, but biopsy-proven acute rejection (BPAR) episodes occurred in 16 (14%) alemtuzumab patients compared with 28 (26%) rATG patients (P=0.02). Late BPAR (>12 months after transplant) occurred in 1 (8%) alemtuzumab patient and 3 (11%) rATG patients (P=NS). Infections and malignancy were similar between the two induction arms. CONCLUSION.: Alemtuzumab and rATG induction therapies were equally safe, but alemtuzumab was associated with less BPAR. |
doi_str_mv | 10.1097/TP.0b013e3181b4acfb |
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METHODS.: We conducted a prospective randomized single-center trial comparing alemtuzumab and rATG induction in adult kidney and pancreas transplantation in patients treated with similar maintenance immunosuppression. RESULTS.: Between February 1, 2005, and September 1, 2007, 222 patients randomly received either alemtuzumab (n=113) or rATG (n=109) induction; 180 (81%) underwent kidney alone, 38 (17%) simultaneous pancreas-kidney, and 4 (2%) pancreas after kidney transplants. Of 180 kidney-alone transplants, 152 (84%) were from deceased donors, including 61 (34%) from expanded criteria donors. Retransplantation, human leukocyte antigen match, antibody titer, expanded criteria donors, race, cytomegalovirus status, delayed graft function, and immunologic risks were similar between the two induction groups. With a median follow-up of 2 years (minimum 1 year), overall patient, kidney, and pancreas graft survival rates were 96%, 89%, and 90%, respectively. Survival, initial length of stay, and maintenance immunosuppression (including early steroid elimination) were similar between alemtuzumab and rATG groups, but biopsy-proven acute rejection (BPAR) episodes occurred in 16 (14%) alemtuzumab patients compared with 28 (26%) rATG patients (P=0.02). Late BPAR (>12 months after transplant) occurred in 1 (8%) alemtuzumab patient and 3 (11%) rATG patients (P=NS). Infections and malignancy were similar between the two induction arms. CONCLUSION.: Alemtuzumab and rATG induction therapies were equally safe, but alemtuzumab was associated with less BPAR.</description><identifier>ISSN: 0041-1337</identifier><identifier>EISSN: 1534-6080</identifier><identifier>DOI: 10.1097/TP.0b013e3181b4acfb</identifier><identifier>PMID: 19920781</identifier><identifier>CODEN: TRPLAU</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams & Wilkins</publisher><subject>Adult ; Alemtuzumab ; Animals ; Antibodies, Monoclonal - therapeutic use ; Antibodies, Monoclonal, Humanized ; Antibodies, Neoplasm - therapeutic use ; Antilymphocyte Serum - therapeutic use ; Biological and medical sciences ; Female ; Fundamental and applied biological sciences. Psychology ; Fundamental immunology ; Graft Rejection - immunology ; Graft Rejection - prevention & control ; Graft Survival ; Human cytomegalovirus ; Humans ; Immunosuppression - methods ; Immunosuppressive Agents - therapeutic use ; Kidney Transplantation - adverse effects ; Kidney Transplantation - immunology ; Kidney Transplantation - mortality ; Kidney Transplantation - physiology ; Male ; Medical sciences ; Middle Aged ; Pancreas Transplantation - adverse effects ; Pancreas Transplantation - immunology ; Pancreas Transplantation - mortality ; Pancreas Transplantation - physiology ; Prospective Studies ; Rabbits ; Steroids - therapeutic use ; Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases ; Surgery of the urinary system ; Survival Rate ; T-Lymphocytes - immunology ; Tissue, organ and graft immunology</subject><ispartof>Transplantation, 2009-09, Vol.88 (6), p.810-819</ispartof><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c410t-1f8cb41789864c3b633edec762482d4286b2c24ab7f2c27c3b98dd155b09ad7d3</citedby><cites>FETCH-LOGICAL-c410t-1f8cb41789864c3b633edec762482d4286b2c24ab7f2c27c3b98dd155b09ad7d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22036986$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19920781$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>FARNEY, Alan C</creatorcontrib><creatorcontrib>DOARES, William</creatorcontrib><creatorcontrib>MOORE, Phillip</creatorcontrib><creatorcontrib>ADAMS, Patricia L</creatorcontrib><creatorcontrib>STRATTA, Robert J</creatorcontrib><creatorcontrib>ROGERS, Jeffrey</creatorcontrib><creatorcontrib>SINGH, Rajinder</creatorcontrib><creatorcontrib>HARTMANN, Erica</creatorcontrib><creatorcontrib>HART, Lois</creatorcontrib><creatorcontrib>ASHCRAFT, Elizabeth</creatorcontrib><creatorcontrib>REEVES-DANIELS, Amber</creatorcontrib><creatorcontrib>GAUTREAUX, Michael</creatorcontrib><creatorcontrib>ISKANDAR, Samy S</creatorcontrib><title>A Randomized Trial of Alemtuzumab Versus Antithymocyte Globulin Induction in Renal and Pancreas Transplantation</title><title>Transplantation</title><addtitle>Transplantation</addtitle><description>BACKGROUND.: Alemtuzumab and rabbit antithymocyte globulin (rATG) are commonly used for induction of immunsuppression for kidney and pancreas transplantation, but the two agents have not been compared directly. METHODS.: We conducted a prospective randomized single-center trial comparing alemtuzumab and rATG induction in adult kidney and pancreas transplantation in patients treated with similar maintenance immunosuppression. RESULTS.: Between February 1, 2005, and September 1, 2007, 222 patients randomly received either alemtuzumab (n=113) or rATG (n=109) induction; 180 (81%) underwent kidney alone, 38 (17%) simultaneous pancreas-kidney, and 4 (2%) pancreas after kidney transplants. Of 180 kidney-alone transplants, 152 (84%) were from deceased donors, including 61 (34%) from expanded criteria donors. Retransplantation, human leukocyte antigen match, antibody titer, expanded criteria donors, race, cytomegalovirus status, delayed graft function, and immunologic risks were similar between the two induction groups. With a median follow-up of 2 years (minimum 1 year), overall patient, kidney, and pancreas graft survival rates were 96%, 89%, and 90%, respectively. Survival, initial length of stay, and maintenance immunosuppression (including early steroid elimination) were similar between alemtuzumab and rATG groups, but biopsy-proven acute rejection (BPAR) episodes occurred in 16 (14%) alemtuzumab patients compared with 28 (26%) rATG patients (P=0.02). Late BPAR (>12 months after transplant) occurred in 1 (8%) alemtuzumab patient and 3 (11%) rATG patients (P=NS). Infections and malignancy were similar between the two induction arms. CONCLUSION.: Alemtuzumab and rATG induction therapies were equally safe, but alemtuzumab was associated with less BPAR.</description><subject>Adult</subject><subject>Alemtuzumab</subject><subject>Animals</subject><subject>Antibodies, Monoclonal - therapeutic use</subject><subject>Antibodies, Monoclonal, Humanized</subject><subject>Antibodies, Neoplasm - therapeutic use</subject><subject>Antilymphocyte Serum - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fundamental immunology</subject><subject>Graft Rejection - immunology</subject><subject>Graft Rejection - prevention & control</subject><subject>Graft Survival</subject><subject>Human cytomegalovirus</subject><subject>Humans</subject><subject>Immunosuppression - methods</subject><subject>Immunosuppressive Agents - therapeutic use</subject><subject>Kidney Transplantation - adverse effects</subject><subject>Kidney Transplantation - immunology</subject><subject>Kidney Transplantation - mortality</subject><subject>Kidney Transplantation - physiology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Pancreas Transplantation - adverse effects</subject><subject>Pancreas Transplantation - immunology</subject><subject>Pancreas Transplantation - mortality</subject><subject>Pancreas Transplantation - physiology</subject><subject>Prospective Studies</subject><subject>Rabbits</subject><subject>Steroids - therapeutic use</subject><subject>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</subject><subject>Surgery of the urinary system</subject><subject>Survival Rate</subject><subject>T-Lymphocytes - immunology</subject><subject>Tissue, organ and graft immunology</subject><issn>0041-1337</issn><issn>1534-6080</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kUtLAzEUhYMoWqu_QJBs1NXU3CSdZJal-ALBUqrbIa_BkZmkTmYW7a83xaLgwtXhwncOl3MQugAyAVKI29ViQjQB5hhI0FyZSh-gEUwZz3IiySEaEcIhA8bECTqN8YMQMmVCHKMTKApKhIQRCjO8VN6Gtt46i1ddrRocKjxrXNsP26FVGr-5Lg4Rz3xf9--bNphN7_BDE_TQ1B4_eTuYvg4ep2PpfPKnPLxQ3nROxRSpfFw3yvdqR52ho0o10Z3vdYxe7-9W88fs-eXhaT57zgwH0mdQSaM5CFnInBumc8acdUbklEtqOZW5poZypUWVVCSikNbCdKpJoaywbIxuvnPXXfgcXOzLto7GNekRF4ZYCsaBC1oUibz-l6QANLW1A9k3aLoQY-eqct3Vreo2JZByt0i5WpR_F0muy338oFtnfz37CRJwtQdUNKqpUl-mjj8cpYTlqQX2BQ19lto</recordid><startdate>20090927</startdate><enddate>20090927</enddate><creator>FARNEY, Alan C</creator><creator>DOARES, William</creator><creator>MOORE, Phillip</creator><creator>ADAMS, Patricia L</creator><creator>STRATTA, Robert J</creator><creator>ROGERS, Jeffrey</creator><creator>SINGH, Rajinder</creator><creator>HARTMANN, Erica</creator><creator>HART, Lois</creator><creator>ASHCRAFT, Elizabeth</creator><creator>REEVES-DANIELS, Amber</creator><creator>GAUTREAUX, Michael</creator><creator>ISKANDAR, Samy S</creator><general>Lippincott Williams & Wilkins</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>7T5</scope><scope>7U9</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20090927</creationdate><title>A Randomized Trial of Alemtuzumab Versus Antithymocyte Globulin Induction in Renal and Pancreas Transplantation</title><author>FARNEY, Alan C ; DOARES, William ; MOORE, Phillip ; ADAMS, Patricia L ; STRATTA, Robert J ; ROGERS, Jeffrey ; SINGH, Rajinder ; HARTMANN, Erica ; HART, Lois ; ASHCRAFT, Elizabeth ; REEVES-DANIELS, Amber ; GAUTREAUX, Michael ; ISKANDAR, Samy S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c410t-1f8cb41789864c3b633edec762482d4286b2c24ab7f2c27c3b98dd155b09ad7d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adult</topic><topic>Alemtuzumab</topic><topic>Animals</topic><topic>Antibodies, Monoclonal - therapeutic use</topic><topic>Antibodies, Monoclonal, Humanized</topic><topic>Antibodies, Neoplasm - therapeutic use</topic><topic>Antilymphocyte Serum - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fundamental immunology</topic><topic>Graft Rejection - immunology</topic><topic>Graft Rejection - prevention & control</topic><topic>Graft Survival</topic><topic>Human cytomegalovirus</topic><topic>Humans</topic><topic>Immunosuppression - methods</topic><topic>Immunosuppressive Agents - therapeutic use</topic><topic>Kidney Transplantation - adverse effects</topic><topic>Kidney Transplantation - immunology</topic><topic>Kidney Transplantation - mortality</topic><topic>Kidney Transplantation - physiology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Pancreas Transplantation - adverse effects</topic><topic>Pancreas Transplantation - immunology</topic><topic>Pancreas Transplantation - mortality</topic><topic>Pancreas Transplantation - physiology</topic><topic>Prospective Studies</topic><topic>Rabbits</topic><topic>Steroids - therapeutic use</topic><topic>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</topic><topic>Surgery of the urinary system</topic><topic>Survival Rate</topic><topic>T-Lymphocytes - immunology</topic><topic>Tissue, organ and graft immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>FARNEY, Alan C</creatorcontrib><creatorcontrib>DOARES, William</creatorcontrib><creatorcontrib>MOORE, Phillip</creatorcontrib><creatorcontrib>ADAMS, Patricia L</creatorcontrib><creatorcontrib>STRATTA, Robert J</creatorcontrib><creatorcontrib>ROGERS, Jeffrey</creatorcontrib><creatorcontrib>SINGH, Rajinder</creatorcontrib><creatorcontrib>HARTMANN, Erica</creatorcontrib><creatorcontrib>HART, Lois</creatorcontrib><creatorcontrib>ASHCRAFT, Elizabeth</creatorcontrib><creatorcontrib>REEVES-DANIELS, Amber</creatorcontrib><creatorcontrib>GAUTREAUX, Michael</creatorcontrib><creatorcontrib>ISKANDAR, Samy S</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>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>FARNEY, Alan C</au><au>DOARES, William</au><au>MOORE, Phillip</au><au>ADAMS, Patricia L</au><au>STRATTA, Robert J</au><au>ROGERS, Jeffrey</au><au>SINGH, Rajinder</au><au>HARTMANN, Erica</au><au>HART, Lois</au><au>ASHCRAFT, Elizabeth</au><au>REEVES-DANIELS, Amber</au><au>GAUTREAUX, Michael</au><au>ISKANDAR, Samy S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Randomized Trial of Alemtuzumab Versus Antithymocyte Globulin Induction in Renal and Pancreas Transplantation</atitle><jtitle>Transplantation</jtitle><addtitle>Transplantation</addtitle><date>2009-09-27</date><risdate>2009</risdate><volume>88</volume><issue>6</issue><spage>810</spage><epage>819</epage><pages>810-819</pages><issn>0041-1337</issn><eissn>1534-6080</eissn><coden>TRPLAU</coden><abstract>BACKGROUND.: Alemtuzumab and rabbit antithymocyte globulin (rATG) are commonly used for induction of immunsuppression for kidney and pancreas transplantation, but the two agents have not been compared directly. METHODS.: We conducted a prospective randomized single-center trial comparing alemtuzumab and rATG induction in adult kidney and pancreas transplantation in patients treated with similar maintenance immunosuppression. RESULTS.: Between February 1, 2005, and September 1, 2007, 222 patients randomly received either alemtuzumab (n=113) or rATG (n=109) induction; 180 (81%) underwent kidney alone, 38 (17%) simultaneous pancreas-kidney, and 4 (2%) pancreas after kidney transplants. Of 180 kidney-alone transplants, 152 (84%) were from deceased donors, including 61 (34%) from expanded criteria donors. Retransplantation, human leukocyte antigen match, antibody titer, expanded criteria donors, race, cytomegalovirus status, delayed graft function, and immunologic risks were similar between the two induction groups. With a median follow-up of 2 years (minimum 1 year), overall patient, kidney, and pancreas graft survival rates were 96%, 89%, and 90%, respectively. Survival, initial length of stay, and maintenance immunosuppression (including early steroid elimination) were similar between alemtuzumab and rATG groups, but biopsy-proven acute rejection (BPAR) episodes occurred in 16 (14%) alemtuzumab patients compared with 28 (26%) rATG patients (P=0.02). Late BPAR (>12 months after transplant) occurred in 1 (8%) alemtuzumab patient and 3 (11%) rATG patients (P=NS). Infections and malignancy were similar between the two induction arms. CONCLUSION.: Alemtuzumab and rATG induction therapies were equally safe, but alemtuzumab was associated with less BPAR.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams & Wilkins</pub><pmid>19920781</pmid><doi>10.1097/TP.0b013e3181b4acfb</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Alemtuzumab Animals Antibodies, Monoclonal - therapeutic use Antibodies, Monoclonal, Humanized Antibodies, Neoplasm - therapeutic use Antilymphocyte Serum - therapeutic use Biological and medical sciences Female Fundamental and applied biological sciences. Psychology Fundamental immunology Graft Rejection - immunology Graft Rejection - prevention & control Graft Survival Human cytomegalovirus Humans Immunosuppression - methods Immunosuppressive Agents - therapeutic use Kidney Transplantation - adverse effects Kidney Transplantation - immunology Kidney Transplantation - mortality Kidney Transplantation - physiology Male Medical sciences Middle Aged Pancreas Transplantation - adverse effects Pancreas Transplantation - immunology Pancreas Transplantation - mortality Pancreas Transplantation - physiology Prospective Studies Rabbits Steroids - therapeutic use Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases Surgery of the urinary system Survival Rate T-Lymphocytes - immunology Tissue, organ and graft immunology |
title | A Randomized Trial of Alemtuzumab Versus Antithymocyte Globulin Induction in Renal and Pancreas Transplantation |
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