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Basiliximab Treatment for Patients With Steroid-Refractory Acute Graft-Versus-Host Disease Following Matched Sibling Donor Hematopoietic Stem Cell Transplantation
Basiliximab is an important treatment for steroid-refractory acute graft-versus-host disease (SR-aGVHD). We performed this retrospective study to evaluate the efficacy and safety of basiliximab treatment in SR-aGVHD patients following matched sibling donor hematopoietic stem cell transplantation (MS...
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Published in: | Cell transplantation 2024-01, Vol.33, p.9636897241257568-9636897241257568 |
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creator | Jiang, Xin-Ya Zhang, Xiao-Hui Xu, Lan-Ping Wang, Yu Yan, Chen-Hua Chen, Huan Chen, Yu-Hong Han, Wei Wang, Feng-Rong Wang, Jing-Zhi Sun, Yu-Qian Mo, Xiao-Dong Huang, Xiao-Jun |
description | Basiliximab is an important treatment for steroid-refractory acute graft-versus-host disease (SR-aGVHD). We performed this retrospective study to evaluate the efficacy and safety of basiliximab treatment in SR-aGVHD patients following matched sibling donor hematopoietic stem cell transplantation (MSD-HSCT) (n = 63). Overall response rate (ORR) was 63.5% and 54% at any time and at day 28 after basiliximab treatment. Grade III–IV aGVHD before basiliximab treatment predicted a poor ORR after basiliximab treatment. The rates of virus, bacteria, and fungi infections were 54%, 23.8%, and 3.1%, respectively. With a median follow-up of 730 (range, 67–3,042) days, the 1-year probability of overall survival and disease-free survival after basiliximab treatment were 58.6% (95% confidence interval [CI] = 47.6%–72.2%) and 55.4% (95% CI = 44.3%–69.2%), respectively. The 3-year cumulative incidence of relapse and non-relapse mortality after basiliximab treatment were 18.9% (95% CI = 8.3%–29.5%) and 33.8% (95% CI = 21.8%–45.7%), respectively. Comorbidities burden before allo-HSCT, severity of aGVHD and liver aGVHD before basiliximab treatment showed negative influences on survival. Thus, basiliximab was safe and effective treatment for SR-aGVHD following MSD-HSCT. |
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We performed this retrospective study to evaluate the efficacy and safety of basiliximab treatment in SR-aGVHD patients following matched sibling donor hematopoietic stem cell transplantation (MSD-HSCT) (n = 63). Overall response rate (ORR) was 63.5% and 54% at any time and at day 28 after basiliximab treatment. Grade III–IV aGVHD before basiliximab treatment predicted a poor ORR after basiliximab treatment. The rates of virus, bacteria, and fungi infections were 54%, 23.8%, and 3.1%, respectively. With a median follow-up of 730 (range, 67–3,042) days, the 1-year probability of overall survival and disease-free survival after basiliximab treatment were 58.6% (95% confidence interval [CI] = 47.6%–72.2%) and 55.4% (95% CI = 44.3%–69.2%), respectively. The 3-year cumulative incidence of relapse and non-relapse mortality after basiliximab treatment were 18.9% (95% CI = 8.3%–29.5%) and 33.8% (95% CI = 21.8%–45.7%), respectively. Comorbidities burden before allo-HSCT, severity of aGVHD and liver aGVHD before basiliximab treatment showed negative influences on survival. Thus, basiliximab was safe and effective treatment for SR-aGVHD following MSD-HSCT.</description><identifier>ISSN: 0963-6897</identifier><identifier>EISSN: 1555-3892</identifier><identifier>DOI: 10.1177/09636897241257568</identifier><identifier>PMID: 38832653</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>Acute Disease ; Adolescent ; Adult ; Antibodies, Monoclonal - therapeutic use ; Basiliximab - therapeutic use ; Child ; Comorbidity ; Female ; Graft versus host disease ; Graft vs Host Disease - drug therapy ; Graft-versus-host reaction ; Hematopoietic Stem Cell Transplantation - adverse effects ; Hematopoietic Stem Cell Transplantation - methods ; Hematopoietic stem cells ; Humans ; Immunosuppressive Agents - therapeutic use ; Male ; Middle Aged ; Original ; Recombinant Fusion Proteins - therapeutic use ; Retrospective Studies ; Siblings ; Stem cell transplantation ; Steroids ; Steroids - therapeutic use ; Tissue Donors ; Treatment Outcome ; Young Adult</subject><ispartof>Cell transplantation, 2024-01, Vol.33, p.9636897241257568-9636897241257568</ispartof><rights>The Author(s) 2024</rights><rights>The Author(s) 2024. This work is licensed under the Creative Commons Attribution – Non-Commercial License https://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2024 2024 SAGE Publications Inc, unless otherwise noted. Manuscript content on this site is licensed under Creative Commons Licenses</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0009-0007-5311-3024</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11151754/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/3149769190?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,21966,25753,27853,27924,27925,37012,37013,44590,44945,45333,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38832653$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jiang, Xin-Ya</creatorcontrib><creatorcontrib>Zhang, Xiao-Hui</creatorcontrib><creatorcontrib>Xu, Lan-Ping</creatorcontrib><creatorcontrib>Wang, Yu</creatorcontrib><creatorcontrib>Yan, Chen-Hua</creatorcontrib><creatorcontrib>Chen, Huan</creatorcontrib><creatorcontrib>Chen, Yu-Hong</creatorcontrib><creatorcontrib>Han, Wei</creatorcontrib><creatorcontrib>Wang, Feng-Rong</creatorcontrib><creatorcontrib>Wang, Jing-Zhi</creatorcontrib><creatorcontrib>Sun, Yu-Qian</creatorcontrib><creatorcontrib>Mo, Xiao-Dong</creatorcontrib><creatorcontrib>Huang, Xiao-Jun</creatorcontrib><title>Basiliximab Treatment for Patients With Steroid-Refractory Acute Graft-Versus-Host Disease Following Matched Sibling Donor Hematopoietic Stem Cell Transplantation</title><title>Cell transplantation</title><addtitle>Cell Transplant</addtitle><description>Basiliximab is an important treatment for steroid-refractory acute graft-versus-host disease (SR-aGVHD). We performed this retrospective study to evaluate the efficacy and safety of basiliximab treatment in SR-aGVHD patients following matched sibling donor hematopoietic stem cell transplantation (MSD-HSCT) (n = 63). Overall response rate (ORR) was 63.5% and 54% at any time and at day 28 after basiliximab treatment. Grade III–IV aGVHD before basiliximab treatment predicted a poor ORR after basiliximab treatment. The rates of virus, bacteria, and fungi infections were 54%, 23.8%, and 3.1%, respectively. With a median follow-up of 730 (range, 67–3,042) days, the 1-year probability of overall survival and disease-free survival after basiliximab treatment were 58.6% (95% confidence interval [CI] = 47.6%–72.2%) and 55.4% (95% CI = 44.3%–69.2%), respectively. The 3-year cumulative incidence of relapse and non-relapse mortality after basiliximab treatment were 18.9% (95% CI = 8.3%–29.5%) and 33.8% (95% CI = 21.8%–45.7%), respectively. Comorbidities burden before allo-HSCT, severity of aGVHD and liver aGVHD before basiliximab treatment showed negative influences on survival. Thus, basiliximab was safe and effective treatment for SR-aGVHD following MSD-HSCT.</description><subject>Acute Disease</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Antibodies, Monoclonal - therapeutic use</subject><subject>Basiliximab - therapeutic use</subject><subject>Child</subject><subject>Comorbidity</subject><subject>Female</subject><subject>Graft versus host disease</subject><subject>Graft vs Host Disease - drug therapy</subject><subject>Graft-versus-host reaction</subject><subject>Hematopoietic Stem Cell Transplantation - adverse effects</subject><subject>Hematopoietic Stem Cell Transplantation - methods</subject><subject>Hematopoietic stem cells</subject><subject>Humans</subject><subject>Immunosuppressive Agents - therapeutic use</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Original</subject><subject>Recombinant Fusion Proteins - therapeutic use</subject><subject>Retrospective Studies</subject><subject>Siblings</subject><subject>Stem cell transplantation</subject><subject>Steroids</subject><subject>Steroids - therapeutic use</subject><subject>Tissue Donors</subject><subject>Treatment Outcome</subject><subject>Young Adult</subject><issn>0963-6897</issn><issn>1555-3892</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>AFRWT</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNplks9u1DAQxiMEokvhAbggS1y4pHhiO7ZPqGxpt1IRiK7gaE0SZ9erbLzYDtDX4UnxsuVPQT7Y4_n0m0-fpiieAj0BkPIl1TWrlZYVh0pIUat7xQyEECVTurpfzPb9ci84Kh7FuKGUSlaJh8URU4pVtWCz4vtrjG5w39wWG7IMFtPWjon0PpD3mFx-R_LJpTW5TjZ415UfbB-wTT7ckNN2SpZcBOxT-dGGOMVy4WMiZy5ajJac-2HwX924Im8xtWvbkWvXDPv6zI95wMJuMfmddza5dj9gS-Z2GLINHONuwDFlB358XDzocYj2ye19XCzP3yzni_Lq3cXl_PSq7JhkqbRCcmiwblpg2PJWU67rRlcIrOay5RXvKDaWC6Rd3yhUUkEFDeegWpCKHReXB2zncWN2IScSboxHZ35--LAyGLLRwZq6toD59AoUB9boTkrsaS943whgLLNeHVi7qdnars0xBhzuQO92Rrc2K__FAIAAKXgmvLglBP95sjGZrYttTgdH66doGK25UJXWkKXP_5Fu_BTGHJVhwLWsNWiaVc_-tvTby69VyIKTgyDiyv5BADX7XTP_7Rr7Ab5yxiQ</recordid><startdate>20240101</startdate><enddate>20240101</enddate><creator>Jiang, Xin-Ya</creator><creator>Zhang, Xiao-Hui</creator><creator>Xu, Lan-Ping</creator><creator>Wang, Yu</creator><creator>Yan, Chen-Hua</creator><creator>Chen, Huan</creator><creator>Chen, Yu-Hong</creator><creator>Han, Wei</creator><creator>Wang, Feng-Rong</creator><creator>Wang, Jing-Zhi</creator><creator>Sun, Yu-Qian</creator><creator>Mo, Xiao-Dong</creator><creator>Huang, Xiao-Jun</creator><general>SAGE Publications</general><general>Sage Publications Ltd</general><general>SAGE Publishing</general><scope>AFRWT</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>3V.</scope><scope>7T5</scope><scope>7X7</scope><scope>7XB</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0009-0007-5311-3024</orcidid></search><sort><creationdate>20240101</creationdate><title>Basiliximab Treatment for Patients With Steroid-Refractory Acute Graft-Versus-Host Disease Following Matched Sibling Donor Hematopoietic Stem Cell Transplantation</title><author>Jiang, Xin-Ya ; Zhang, Xiao-Hui ; Xu, Lan-Ping ; Wang, Yu ; Yan, Chen-Hua ; Chen, Huan ; Chen, Yu-Hong ; Han, Wei ; Wang, Feng-Rong ; Wang, Jing-Zhi ; Sun, Yu-Qian ; Mo, Xiao-Dong ; Huang, Xiao-Jun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-d373t-e5741ba6bc13ac4c90496b92a13647c424d0abe45a0dfb8a878121b4418c1783</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Acute Disease</topic><topic>Adolescent</topic><topic>Adult</topic><topic>Antibodies, Monoclonal - therapeutic use</topic><topic>Basiliximab - therapeutic use</topic><topic>Child</topic><topic>Comorbidity</topic><topic>Female</topic><topic>Graft versus host disease</topic><topic>Graft vs Host Disease - drug therapy</topic><topic>Graft-versus-host reaction</topic><topic>Hematopoietic Stem Cell Transplantation - adverse effects</topic><topic>Hematopoietic Stem Cell Transplantation - methods</topic><topic>Hematopoietic stem cells</topic><topic>Humans</topic><topic>Immunosuppressive Agents - therapeutic use</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Original</topic><topic>Recombinant Fusion Proteins - therapeutic use</topic><topic>Retrospective Studies</topic><topic>Siblings</topic><topic>Stem cell transplantation</topic><topic>Steroids</topic><topic>Steroids - therapeutic use</topic><topic>Tissue Donors</topic><topic>Treatment Outcome</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jiang, Xin-Ya</creatorcontrib><creatorcontrib>Zhang, Xiao-Hui</creatorcontrib><creatorcontrib>Xu, Lan-Ping</creatorcontrib><creatorcontrib>Wang, Yu</creatorcontrib><creatorcontrib>Yan, Chen-Hua</creatorcontrib><creatorcontrib>Chen, Huan</creatorcontrib><creatorcontrib>Chen, Yu-Hong</creatorcontrib><creatorcontrib>Han, Wei</creatorcontrib><creatorcontrib>Wang, Feng-Rong</creatorcontrib><creatorcontrib>Wang, Jing-Zhi</creatorcontrib><creatorcontrib>Sun, Yu-Qian</creatorcontrib><creatorcontrib>Mo, Xiao-Dong</creatorcontrib><creatorcontrib>Huang, Xiao-Jun</creatorcontrib><collection>Sage Journals GOLD Open Access 2024</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Technology Research Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Databases</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Cell transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jiang, Xin-Ya</au><au>Zhang, Xiao-Hui</au><au>Xu, Lan-Ping</au><au>Wang, Yu</au><au>Yan, Chen-Hua</au><au>Chen, Huan</au><au>Chen, Yu-Hong</au><au>Han, Wei</au><au>Wang, Feng-Rong</au><au>Wang, Jing-Zhi</au><au>Sun, Yu-Qian</au><au>Mo, Xiao-Dong</au><au>Huang, Xiao-Jun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Basiliximab Treatment for Patients With Steroid-Refractory Acute Graft-Versus-Host Disease Following Matched Sibling Donor Hematopoietic Stem Cell Transplantation</atitle><jtitle>Cell transplantation</jtitle><addtitle>Cell Transplant</addtitle><date>2024-01-01</date><risdate>2024</risdate><volume>33</volume><spage>9636897241257568</spage><epage>9636897241257568</epage><pages>9636897241257568-9636897241257568</pages><issn>0963-6897</issn><eissn>1555-3892</eissn><abstract>Basiliximab is an important treatment for steroid-refractory acute graft-versus-host disease (SR-aGVHD). We performed this retrospective study to evaluate the efficacy and safety of basiliximab treatment in SR-aGVHD patients following matched sibling donor hematopoietic stem cell transplantation (MSD-HSCT) (n = 63). Overall response rate (ORR) was 63.5% and 54% at any time and at day 28 after basiliximab treatment. Grade III–IV aGVHD before basiliximab treatment predicted a poor ORR after basiliximab treatment. The rates of virus, bacteria, and fungi infections were 54%, 23.8%, and 3.1%, respectively. With a median follow-up of 730 (range, 67–3,042) days, the 1-year probability of overall survival and disease-free survival after basiliximab treatment were 58.6% (95% confidence interval [CI] = 47.6%–72.2%) and 55.4% (95% CI = 44.3%–69.2%), respectively. The 3-year cumulative incidence of relapse and non-relapse mortality after basiliximab treatment were 18.9% (95% CI = 8.3%–29.5%) and 33.8% (95% CI = 21.8%–45.7%), respectively. Comorbidities burden before allo-HSCT, severity of aGVHD and liver aGVHD before basiliximab treatment showed negative influences on survival. Thus, basiliximab was safe and effective treatment for SR-aGVHD following MSD-HSCT.</abstract><cop>Los Angeles, CA</cop><pub>SAGE Publications</pub><pmid>38832653</pmid><doi>10.1177/09636897241257568</doi><orcidid>https://orcid.org/0009-0007-5311-3024</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acute Disease Adolescent Adult Antibodies, Monoclonal - therapeutic use Basiliximab - therapeutic use Child Comorbidity Female Graft versus host disease Graft vs Host Disease - drug therapy Graft-versus-host reaction Hematopoietic Stem Cell Transplantation - adverse effects Hematopoietic Stem Cell Transplantation - methods Hematopoietic stem cells Humans Immunosuppressive Agents - therapeutic use Male Middle Aged Original Recombinant Fusion Proteins - therapeutic use Retrospective Studies Siblings Stem cell transplantation Steroids Steroids - therapeutic use Tissue Donors Treatment Outcome Young Adult |
title | Basiliximab Treatment for Patients With Steroid-Refractory Acute Graft-Versus-Host Disease Following Matched Sibling Donor Hematopoietic Stem Cell Transplantation |
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