Rabbit antithymocyte globulin for the treatment of chronic lung allograft dysfunction

Background Chronic lung allograft dysfunction (CLAD) is the leading cause of death beyond the first year after lung transplantation. Several treatments have been used to prevent the progression or reverse the effects of CLAD. Cytolytic therapy with rabbit antithymocyte globulin (rATG) has previously...

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Veröffentlicht in:Clinical transplantation 2019-10, Vol.33 (10), p.e13708-n/a
Hauptverfasser: January, Spenser E., Fester, Keith A., Bain, Karen Bennett, Kulkarni, Hrishikesh S., Witt, Chad A., Byers, Derek E., Alexander‐Brett, Jennifer, Trulock, Elbert P., Hachem, Ramsey R.
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container_issue 10
container_start_page e13708
container_title Clinical transplantation
container_volume 33
creator January, Spenser E.
Fester, Keith A.
Bain, Karen Bennett
Kulkarni, Hrishikesh S.
Witt, Chad A.
Byers, Derek E.
Alexander‐Brett, Jennifer
Trulock, Elbert P.
Hachem, Ramsey R.
description Background Chronic lung allograft dysfunction (CLAD) is the leading cause of death beyond the first year after lung transplantation. Several treatments have been used to prevent the progression or reverse the effects of CLAD. Cytolytic therapy with rabbit antithymocyte globulin (rATG) has previously shown to be a potential option. However, the effect on patients with restrictive allograft syndrome (RAS) versus bronchiolitis obliterans syndrome (BOS) and the effect of cumulative dosing are unknown. Methods The charts of lung transplant patients treated with rATG at Barnes‐Jewish Hospital from 2009 to 2016 were retrospectively reviewed. The primary outcome was response to rATG; patients were deemed responders if their FEV1 improved in the 6 months after rATG treatment. Safety endpoints included incidence of serum sickness, cytokine release syndrome, malignancy, and infectious complications. Results 108 patients were included in this study; 43 (40%) patients were responders who experienced an increase in FEV1 after rATG therapy. No predictors of response to rATG therapy were identified. Serum sickness occurred in 22% of patients, 15% experienced cytokine release syndrome, and 19% developed an infection after therapy. Conclusion 40% of patients with CLAD have an improvement in lung function after treatment with rATG although the improvement was typically minimal.
doi_str_mv 10.1111/ctr.13708
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Several treatments have been used to prevent the progression or reverse the effects of CLAD. Cytolytic therapy with rabbit antithymocyte globulin (rATG) has previously shown to be a potential option. However, the effect on patients with restrictive allograft syndrome (RAS) versus bronchiolitis obliterans syndrome (BOS) and the effect of cumulative dosing are unknown. Methods The charts of lung transplant patients treated with rATG at Barnes‐Jewish Hospital from 2009 to 2016 were retrospectively reviewed. The primary outcome was response to rATG; patients were deemed responders if their FEV1 improved in the 6 months after rATG treatment. Safety endpoints included incidence of serum sickness, cytokine release syndrome, malignancy, and infectious complications. Results 108 patients were included in this study; 43 (40%) patients were responders who experienced an increase in FEV1 after rATG therapy. No predictors of response to rATG therapy were identified. Serum sickness occurred in 22% of patients, 15% experienced cytokine release syndrome, and 19% developed an infection after therapy. Conclusion 40% of patients with CLAD have an improvement in lung function after treatment with rATG although the improvement was typically minimal.</description><identifier>ISSN: 0902-0063</identifier><identifier>EISSN: 1399-0012</identifier><identifier>DOI: 10.1111/ctr.13708</identifier><identifier>PMID: 31494969</identifier><language>eng</language><publisher>Denmark</publisher><subject>chronic lung allograft dysfunction ; lung transplantation ; rabbit antithymocyte globulin</subject><ispartof>Clinical transplantation, 2019-10, Vol.33 (10), p.e13708-n/a</ispartof><rights>2019 John Wiley &amp; Sons A/S. Published by John Wiley &amp; Sons Ltd</rights><rights>2019 John Wiley &amp; Sons A/S. 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Several treatments have been used to prevent the progression or reverse the effects of CLAD. Cytolytic therapy with rabbit antithymocyte globulin (rATG) has previously shown to be a potential option. However, the effect on patients with restrictive allograft syndrome (RAS) versus bronchiolitis obliterans syndrome (BOS) and the effect of cumulative dosing are unknown. Methods The charts of lung transplant patients treated with rATG at Barnes‐Jewish Hospital from 2009 to 2016 were retrospectively reviewed. The primary outcome was response to rATG; patients were deemed responders if their FEV1 improved in the 6 months after rATG treatment. Safety endpoints included incidence of serum sickness, cytokine release syndrome, malignancy, and infectious complications. Results 108 patients were included in this study; 43 (40%) patients were responders who experienced an increase in FEV1 after rATG therapy. No predictors of response to rATG therapy were identified. Serum sickness occurred in 22% of patients, 15% experienced cytokine release syndrome, and 19% developed an infection after therapy. Conclusion 40% of patients with CLAD have an improvement in lung function after treatment with rATG although the improvement was typically minimal.</description><subject>chronic lung allograft dysfunction</subject><subject>lung transplantation</subject><subject>rabbit antithymocyte globulin</subject><issn>0902-0063</issn><issn>1399-0012</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp1kE1LwzAYgIMobk4P_gHJUQ9z-WjT9ijDLxgIYzuHNE22SJrMJEX67612evO9vC8vD8_hAeAao3s8zEKmcI9pgcoTMMW0quYIYXIKpqhCZLgZnYCLGN-HL8MsPwcTirMqq1g1Bdu1qGuToHDJpH3fetknBXfW1501DmofYNormIISqVUuQa-h3AfvjIS2czsorPW7IHSCTR9152Qy3l2CMy1sVFfHPQPbp8fN8mW-ent-XT6s5pKSvJwTQjPKNCtFgYUkRBaYMiYRYYiUTaVrmTVFJhWhitaE1qxsVMOIpkLkmUINnYHb0XsI_qNTMfHWRKmsFU75LnJCyiInOc2KAb0bURl8jEFpfgimFaHnGPHvinyoyH8qDuzNUdvVrWr-yN9sA7AYgU9jVf-_iS8361H5BTuIfMc</recordid><startdate>201910</startdate><enddate>201910</enddate><creator>January, Spenser E.</creator><creator>Fester, Keith A.</creator><creator>Bain, Karen Bennett</creator><creator>Kulkarni, Hrishikesh S.</creator><creator>Witt, Chad A.</creator><creator>Byers, Derek E.</creator><creator>Alexander‐Brett, Jennifer</creator><creator>Trulock, Elbert P.</creator><creator>Hachem, Ramsey R.</creator><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-5783-5581</orcidid></search><sort><creationdate>201910</creationdate><title>Rabbit antithymocyte globulin for the treatment of chronic lung allograft dysfunction</title><author>January, Spenser E. ; Fester, Keith A. ; Bain, Karen Bennett ; Kulkarni, Hrishikesh S. ; Witt, Chad A. ; Byers, Derek E. ; Alexander‐Brett, Jennifer ; Trulock, Elbert P. ; Hachem, Ramsey R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3258-223436f68a71ac22c71366c026028d9fbc4d74ce23e3b23b68ded62f3aa54e0d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>chronic lung allograft dysfunction</topic><topic>lung transplantation</topic><topic>rabbit antithymocyte globulin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>January, Spenser E.</creatorcontrib><creatorcontrib>Fester, Keith A.</creatorcontrib><creatorcontrib>Bain, Karen Bennett</creatorcontrib><creatorcontrib>Kulkarni, Hrishikesh S.</creatorcontrib><creatorcontrib>Witt, Chad A.</creatorcontrib><creatorcontrib>Byers, Derek E.</creatorcontrib><creatorcontrib>Alexander‐Brett, Jennifer</creatorcontrib><creatorcontrib>Trulock, Elbert P.</creatorcontrib><creatorcontrib>Hachem, Ramsey R.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>January, Spenser E.</au><au>Fester, Keith A.</au><au>Bain, Karen Bennett</au><au>Kulkarni, Hrishikesh S.</au><au>Witt, Chad A.</au><au>Byers, Derek E.</au><au>Alexander‐Brett, Jennifer</au><au>Trulock, Elbert P.</au><au>Hachem, Ramsey R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rabbit antithymocyte globulin for the treatment of chronic lung allograft dysfunction</atitle><jtitle>Clinical transplantation</jtitle><addtitle>Clin Transplant</addtitle><date>2019-10</date><risdate>2019</risdate><volume>33</volume><issue>10</issue><spage>e13708</spage><epage>n/a</epage><pages>e13708-n/a</pages><issn>0902-0063</issn><eissn>1399-0012</eissn><abstract>Background Chronic lung allograft dysfunction (CLAD) is the leading cause of death beyond the first year after lung transplantation. Several treatments have been used to prevent the progression or reverse the effects of CLAD. Cytolytic therapy with rabbit antithymocyte globulin (rATG) has previously shown to be a potential option. However, the effect on patients with restrictive allograft syndrome (RAS) versus bronchiolitis obliterans syndrome (BOS) and the effect of cumulative dosing are unknown. Methods The charts of lung transplant patients treated with rATG at Barnes‐Jewish Hospital from 2009 to 2016 were retrospectively reviewed. The primary outcome was response to rATG; patients were deemed responders if their FEV1 improved in the 6 months after rATG treatment. Safety endpoints included incidence of serum sickness, cytokine release syndrome, malignancy, and infectious complications. Results 108 patients were included in this study; 43 (40%) patients were responders who experienced an increase in FEV1 after rATG therapy. No predictors of response to rATG therapy were identified. Serum sickness occurred in 22% of patients, 15% experienced cytokine release syndrome, and 19% developed an infection after therapy. Conclusion 40% of patients with CLAD have an improvement in lung function after treatment with rATG although the improvement was typically minimal.</abstract><cop>Denmark</cop><pmid>31494969</pmid><doi>10.1111/ctr.13708</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-5783-5581</orcidid></addata></record>
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subjects chronic lung allograft dysfunction
lung transplantation
rabbit antithymocyte globulin
title Rabbit antithymocyte globulin for the treatment of chronic lung allograft dysfunction
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