Efficacy of tacrolimus versus cyclosporine after lung transplantation: an updated systematic review, meta-analysis, and trial sequential analysis of randomized controlled trials

Background Little data supports using tacrolimus versus cyclosporin for immunosuppression concerning acute rejection and bronchiolitis obliterans syndrome/Chronic Lung Allograft Dysfunction CLAD complications following lung transplantation (LTx). Our goal was to evaluate the use of tacrolimus versus...

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Veröffentlicht in:European journal of clinical pharmacology 2024-12, Vol.80 (12), p.1923-1935
Hauptverfasser: Suilik, Husam Abu, Al-shammari, Ali Saad, Soliman, Youssef, Suilik, Mohamed Abu, Naeim, Kamal A., Nawlo, Ahmad, Abuelazm, Mohamed
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container_end_page 1935
container_issue 12
container_start_page 1923
container_title European journal of clinical pharmacology
container_volume 80
creator Suilik, Husam Abu
Al-shammari, Ali Saad
Soliman, Youssef
Suilik, Mohamed Abu
Naeim, Kamal A.
Nawlo, Ahmad
Abuelazm, Mohamed
description Background Little data supports using tacrolimus versus cyclosporin for immunosuppression concerning acute rejection and bronchiolitis obliterans syndrome/Chronic Lung Allograft Dysfunction CLAD complications following lung transplantation (LTx). Our goal was to evaluate the use of tacrolimus versus cyclosporine in preventing these complications after LTx. Methods We included randomized controlled trials (RCTs) by searching PubMed, Web of Science, SCOPUS, and Cochrane through January 10th, 2024. We pooled dichotomous data using the risk ratio (RR) and continuous data using the mean difference (MD) with a 95% confidence interval (CI). Results We included Four RCTs with a total of 677 patients. Tacrolimus was significantly associated with decreased risk of acute rejection (RR: 1.21, 95% CI [1.03, 1.42], I 2  = 25%, P = 0.02) compared with cyclosporine, bronchiolitis obliterans syndrome/CLAD (RR: 1.87, 95% CI [1.26, 2.77], I 2  = 52%, P = 0.002), and treatment withdrawal (RR: 3.11, 95% CI [2.06, 4.70], I 2  = 0%, P =  
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Our goal was to evaluate the use of tacrolimus versus cyclosporine in preventing these complications after LTx. Methods We included randomized controlled trials (RCTs) by searching PubMed, Web of Science, SCOPUS, and Cochrane through January 10th, 2024. We pooled dichotomous data using the risk ratio (RR) and continuous data using the mean difference (MD) with a 95% confidence interval (CI). Results We included Four RCTs with a total of 677 patients. Tacrolimus was significantly associated with decreased risk of acute rejection (RR: 1.21, 95% CI [1.03, 1.42], I 2  = 25%, P = 0.02) compared with cyclosporine, bronchiolitis obliterans syndrome/CLAD (RR: 1.87, 95% CI [1.26, 2.77], I 2  = 52%, P = 0.002), and treatment withdrawal (RR: 3.11, 95% CI [2.06, 4.70], I 2  = 0%, P =  &lt; 0.00001). However, tacrolimus significantly increased the risk of new-onset diabetes (RR: 0.33, 95% CI [0.12, 0.91], I 2  = 0%, P = 0.03), and kidney dysfunction (RR: 0.79, 95% CI [0.66, 0.93], I 2  = 0%, P = 0.006). In contrast, there was no difference in the incidence of all-cause mortality (RR: 91, 95% CI [0.68, 1.22], I 2  = 0%, P = 0.53), arterial hypertension (RR: 2.40, 95% CI [0.41, 14.21], I 2  = 92%, P = 0.33), and new cancer (RR: 1.57, 95% CI [0.79, 3.10], I 2  = 4%, P = 0.20). Conclusion Tacrolimus has decreased acute rejection episodes and CLAD rate than cyclosporine, but it increased the risk of new-onset diabetes and kidney dysfunction.</description><identifier>ISSN: 0031-6970</identifier><identifier>ISSN: 1432-1041</identifier><identifier>EISSN: 1432-1041</identifier><identifier>DOI: 10.1007/s00228-024-03750-1</identifier><identifier>PMID: 39261378</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Allografts ; Biomedical and Life Sciences ; Biomedicine ; Bronchiolitis Obliterans ; Bronchopneumonia ; Clinical trials ; Cyclosporine - adverse effects ; Cyclosporine - therapeutic use ; Cyclosporins ; Diabetes ; Diabetes mellitus ; Graft rejection ; Graft Rejection - prevention &amp; control ; Humans ; Immunosuppression ; Immunosuppressive Agents - adverse effects ; Immunosuppressive Agents - therapeutic use ; Kidney diseases ; Lung Transplantation ; Lung transplants ; Meta-analysis ; Pharmacology/Toxicology ; Randomized Controlled Trials as Topic ; Tacrolimus ; Tacrolimus - adverse effects ; Tacrolimus - therapeutic use</subject><ispartof>European journal of clinical pharmacology, 2024-12, Vol.80 (12), p.1923-1935</ispartof><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2024. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c256t-b680642e3cce6c2cca30229492f8429c0a79979015f6302de0d00b33d2a5b63a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00228-024-03750-1$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00228-024-03750-1$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39261378$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Suilik, Husam Abu</creatorcontrib><creatorcontrib>Al-shammari, Ali Saad</creatorcontrib><creatorcontrib>Soliman, Youssef</creatorcontrib><creatorcontrib>Suilik, Mohamed Abu</creatorcontrib><creatorcontrib>Naeim, Kamal A.</creatorcontrib><creatorcontrib>Nawlo, Ahmad</creatorcontrib><creatorcontrib>Abuelazm, Mohamed</creatorcontrib><title>Efficacy of tacrolimus versus cyclosporine after lung transplantation: an updated systematic review, meta-analysis, and trial sequential analysis of randomized controlled trials</title><title>European journal of clinical pharmacology</title><addtitle>Eur J Clin Pharmacol</addtitle><addtitle>Eur J Clin Pharmacol</addtitle><description>Background Little data supports using tacrolimus versus cyclosporin for immunosuppression concerning acute rejection and bronchiolitis obliterans syndrome/Chronic Lung Allograft Dysfunction CLAD complications following lung transplantation (LTx). Our goal was to evaluate the use of tacrolimus versus cyclosporine in preventing these complications after LTx. Methods We included randomized controlled trials (RCTs) by searching PubMed, Web of Science, SCOPUS, and Cochrane through January 10th, 2024. We pooled dichotomous data using the risk ratio (RR) and continuous data using the mean difference (MD) with a 95% confidence interval (CI). Results We included Four RCTs with a total of 677 patients. Tacrolimus was significantly associated with decreased risk of acute rejection (RR: 1.21, 95% CI [1.03, 1.42], I 2  = 25%, P = 0.02) compared with cyclosporine, bronchiolitis obliterans syndrome/CLAD (RR: 1.87, 95% CI [1.26, 2.77], I 2  = 52%, P = 0.002), and treatment withdrawal (RR: 3.11, 95% CI [2.06, 4.70], I 2  = 0%, P =  &lt; 0.00001). However, tacrolimus significantly increased the risk of new-onset diabetes (RR: 0.33, 95% CI [0.12, 0.91], I 2  = 0%, P = 0.03), and kidney dysfunction (RR: 0.79, 95% CI [0.66, 0.93], I 2  = 0%, P = 0.006). In contrast, there was no difference in the incidence of all-cause mortality (RR: 91, 95% CI [0.68, 1.22], I 2  = 0%, P = 0.53), arterial hypertension (RR: 2.40, 95% CI [0.41, 14.21], I 2  = 92%, P = 0.33), and new cancer (RR: 1.57, 95% CI [0.79, 3.10], I 2  = 4%, P = 0.20). Conclusion Tacrolimus has decreased acute rejection episodes and CLAD rate than cyclosporine, but it increased the risk of new-onset diabetes and kidney dysfunction.</description><subject>Allografts</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Bronchiolitis Obliterans</subject><subject>Bronchopneumonia</subject><subject>Clinical trials</subject><subject>Cyclosporine - adverse effects</subject><subject>Cyclosporine - therapeutic use</subject><subject>Cyclosporins</subject><subject>Diabetes</subject><subject>Diabetes mellitus</subject><subject>Graft rejection</subject><subject>Graft Rejection - prevention &amp; control</subject><subject>Humans</subject><subject>Immunosuppression</subject><subject>Immunosuppressive Agents - adverse effects</subject><subject>Immunosuppressive Agents - therapeutic use</subject><subject>Kidney diseases</subject><subject>Lung Transplantation</subject><subject>Lung transplants</subject><subject>Meta-analysis</subject><subject>Pharmacology/Toxicology</subject><subject>Randomized Controlled Trials as Topic</subject><subject>Tacrolimus</subject><subject>Tacrolimus - adverse effects</subject><subject>Tacrolimus - therapeutic use</subject><issn>0031-6970</issn><issn>1432-1041</issn><issn>1432-1041</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kctu1TAQhi0EoofCC7BAltiwaGB8iZOwQ1W5SJXYwDrycSaVq8QOtlMU3oo3ZA7nFCQWrMbyfPPP5WfsuYDXAqB5kwGkbCuQugLV1FCJB2wntJKVAC0esh2AEpXpGjhjT3K-BRB1B-oxO1OdNEI17Y79vBpH76zbeBx5sS7Fyc9r5neYMgW3uSnmJSYfkNuxYOLTGm54STbkZbKh2OJjeMtt4Osy2IIDz1suONO_4wnvPH6_4DMWW9lgpy37fEHwQAreTjzjtxVDOTzv04dBSH2Is_9Bai6GQkNNeCrJT9mjkQI-O8Vz9vX91ZfLj9X15w-fLt9dV07WplR704LREpVzaJx0ziq6Vqc7ObZadg5s03VNRycZDWUGhAFgr9Qgbb03yqpz9uqou6RIQ-bSzz47nGhpjGvulQCltTGyJvTlP-htXBPtc6Bko6VpdUOUPFJ05JwTjv2S_GzT1gvoD4b2R0N7MrT_bWgvqOjFSXrdzzj8Kbl3kAB1BDKlwg2mv73_I_sLvjOvYg</recordid><startdate>20241201</startdate><enddate>20241201</enddate><creator>Suilik, Husam Abu</creator><creator>Al-shammari, Ali Saad</creator><creator>Soliman, Youssef</creator><creator>Suilik, Mohamed Abu</creator><creator>Naeim, Kamal A.</creator><creator>Nawlo, Ahmad</creator><creator>Abuelazm, Mohamed</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><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>7TK</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope></search><sort><creationdate>20241201</creationdate><title>Efficacy of tacrolimus versus cyclosporine after lung transplantation: an updated systematic review, meta-analysis, and trial sequential analysis of randomized controlled trials</title><author>Suilik, Husam Abu ; 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Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of clinical pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Suilik, Husam Abu</au><au>Al-shammari, Ali Saad</au><au>Soliman, Youssef</au><au>Suilik, Mohamed Abu</au><au>Naeim, Kamal A.</au><au>Nawlo, Ahmad</au><au>Abuelazm, Mohamed</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Efficacy of tacrolimus versus cyclosporine after lung transplantation: an updated systematic review, meta-analysis, and trial sequential analysis of randomized controlled trials</atitle><jtitle>European journal of clinical pharmacology</jtitle><stitle>Eur J Clin Pharmacol</stitle><addtitle>Eur J Clin Pharmacol</addtitle><date>2024-12-01</date><risdate>2024</risdate><volume>80</volume><issue>12</issue><spage>1923</spage><epage>1935</epage><pages>1923-1935</pages><issn>0031-6970</issn><issn>1432-1041</issn><eissn>1432-1041</eissn><abstract>Background Little data supports using tacrolimus versus cyclosporin for immunosuppression concerning acute rejection and bronchiolitis obliterans syndrome/Chronic Lung Allograft Dysfunction CLAD complications following lung transplantation (LTx). Our goal was to evaluate the use of tacrolimus versus cyclosporine in preventing these complications after LTx. Methods We included randomized controlled trials (RCTs) by searching PubMed, Web of Science, SCOPUS, and Cochrane through January 10th, 2024. We pooled dichotomous data using the risk ratio (RR) and continuous data using the mean difference (MD) with a 95% confidence interval (CI). Results We included Four RCTs with a total of 677 patients. Tacrolimus was significantly associated with decreased risk of acute rejection (RR: 1.21, 95% CI [1.03, 1.42], I 2  = 25%, P = 0.02) compared with cyclosporine, bronchiolitis obliterans syndrome/CLAD (RR: 1.87, 95% CI [1.26, 2.77], I 2  = 52%, P = 0.002), and treatment withdrawal (RR: 3.11, 95% CI [2.06, 4.70], I 2  = 0%, P =  &lt; 0.00001). However, tacrolimus significantly increased the risk of new-onset diabetes (RR: 0.33, 95% CI [0.12, 0.91], I 2  = 0%, P = 0.03), and kidney dysfunction (RR: 0.79, 95% CI [0.66, 0.93], I 2  = 0%, P = 0.006). In contrast, there was no difference in the incidence of all-cause mortality (RR: 91, 95% CI [0.68, 1.22], I 2  = 0%, P = 0.53), arterial hypertension (RR: 2.40, 95% CI [0.41, 14.21], I 2  = 92%, P = 0.33), and new cancer (RR: 1.57, 95% CI [0.79, 3.10], I 2  = 4%, P = 0.20). Conclusion Tacrolimus has decreased acute rejection episodes and CLAD rate than cyclosporine, but it increased the risk of new-onset diabetes and kidney dysfunction.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>39261378</pmid><doi>10.1007/s00228-024-03750-1</doi><tpages>13</tpages></addata></record>
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subjects Allografts
Biomedical and Life Sciences
Biomedicine
Bronchiolitis Obliterans
Bronchopneumonia
Clinical trials
Cyclosporine - adverse effects
Cyclosporine - therapeutic use
Cyclosporins
Diabetes
Diabetes mellitus
Graft rejection
Graft Rejection - prevention & control
Humans
Immunosuppression
Immunosuppressive Agents - adverse effects
Immunosuppressive Agents - therapeutic use
Kidney diseases
Lung Transplantation
Lung transplants
Meta-analysis
Pharmacology/Toxicology
Randomized Controlled Trials as Topic
Tacrolimus
Tacrolimus - adverse effects
Tacrolimus - therapeutic use
title Efficacy of tacrolimus versus cyclosporine after lung transplantation: an updated systematic review, meta-analysis, and trial sequential analysis of randomized controlled trials
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