Successful outcome following allogeneic hematopoietic stem cell transplantation in adults with primary immunodeficiency
The primary immunodeficiencies (PIDs), rare inherited diseases characterized by severe dysfunction of immunity, have been successfully treated by allogeneic hematopoietic stem cell transplantation (Allo-HSCT) in childhood. Controversy exists regarding optimal timing and use of Allo-HSCT in adults, d...
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Veröffentlicht in: | Blood 2018-02, Vol.131 (8), p.917-931 |
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creator | Fox, Thomas A. Chakraverty, Ronjon Burns, Siobhan Carpenter, Benjamin Thomson, Kirsty Lowe, David Fielding, Adele Peggs, Karl Kottaridis, Panagiotis Uttenthal, Benjamin Bigley, Venetia Buckland, Matthew Grandage, Victoria Denovan, Shari Grace, Sarah Dahlstrom, Julia Workman, Sarita Symes, Andrew Mackinnon, Stephen Hough, Rachael Morris, Emma |
description | The primary immunodeficiencies (PIDs), rare inherited diseases characterized by severe dysfunction of immunity, have been successfully treated by allogeneic hematopoietic stem cell transplantation (Allo-HSCT) in childhood. Controversy exists regarding optimal timing and use of Allo-HSCT in adults, due to lack of experience and previous poor outcomes. Twenty-nine consecutive adult patients, with a mean age at transplant of 24 years (range, 17-50 years), underwent Allo-HSCT. Reduced-intensity conditioning (RIC) included fludarabine (Flu)/melphalan/alemtuzumab (n = 20), Flu/busulfan (Bu)/alemtuzumab (n = 8), and Flu/Bu/antithymocyte globulin (n = 1). Stem cell donors were matched unrelated donors or mismatched unrelated donors (n = 18) and matched related donors (n = 11). Overall survival (OS), event-free survival, transplant-related mortality (TRM), acute and chronic graft-versus-host disease incidence and severity, time to engraftment, lineage-specific chimerism, immune reconstitution, and discontinuation of immunoglobulin replacement therapy were recorded. OS at 3 years for the whole cohort was 85.2%. The rarer PID patients without chronic granulomatous disease (CGD) achieved an OS at 3 years of 88.9% (n = 18), compared with 81.8% for CGD patients (n = 11). TRM was low with only 4 deaths observed at a median follow-up of 3.5 years. There were no cases of early or late rejection. In all surviving patients, either stable mixed chimerism or full donor chimerism were observed. At last follow-up, 87% of the surviving patients had no evidence of persistent or recurrent infections. Allo-HSCT is safe and effective in young adult patients with severe PID and should be considered the treatment of choice where an appropriate donor is available.
•Allo-HSCT with RIC is safe and effective in younger adults with severe PID.•Referral triggers should include severe infections, autoimmunity, malignancy, and disease progression despite conservative management. |
doi_str_mv | 10.1182/blood-2017-09-807487 |
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•Allo-HSCT with RIC is safe and effective in younger adults with severe PID.•Referral triggers should include severe infections, autoimmunity, malignancy, and disease progression despite conservative management.</description><identifier>ISSN: 0006-4971</identifier><identifier>EISSN: 1528-0020</identifier><identifier>DOI: 10.1182/blood-2017-09-807487</identifier><identifier>PMID: 29279357</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adolescent ; Adult ; Cohort Studies ; Female ; Hematopoietic Stem Cell Transplantation - mortality ; Humans ; Immunologic Deficiency Syndromes - mortality ; Immunologic Deficiency Syndromes - pathology ; Immunologic Deficiency Syndromes - therapy ; Middle Aged ; Prognosis ; Survival Rate ; Transplantation ; Transplantation Conditioning ; Transplantation, Homologous ; Young Adult</subject><ispartof>Blood, 2018-02, Vol.131 (8), p.917-931</ispartof><rights>2018 American Society of Hematology</rights><rights>2018 by The American Society of Hematology.</rights><rights>2018 by The American Society of Hematology 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c463t-5e1bf77af84d96a587df1d624fa22cc0eca61f7e4e38685b830866673d1973383</citedby><cites>FETCH-LOGICAL-c463t-5e1bf77af84d96a587df1d624fa22cc0eca61f7e4e38685b830866673d1973383</cites><orcidid>0000-0003-4834-1130</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29279357$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fox, Thomas A.</creatorcontrib><creatorcontrib>Chakraverty, Ronjon</creatorcontrib><creatorcontrib>Burns, Siobhan</creatorcontrib><creatorcontrib>Carpenter, Benjamin</creatorcontrib><creatorcontrib>Thomson, Kirsty</creatorcontrib><creatorcontrib>Lowe, David</creatorcontrib><creatorcontrib>Fielding, Adele</creatorcontrib><creatorcontrib>Peggs, Karl</creatorcontrib><creatorcontrib>Kottaridis, Panagiotis</creatorcontrib><creatorcontrib>Uttenthal, Benjamin</creatorcontrib><creatorcontrib>Bigley, Venetia</creatorcontrib><creatorcontrib>Buckland, Matthew</creatorcontrib><creatorcontrib>Grandage, Victoria</creatorcontrib><creatorcontrib>Denovan, Shari</creatorcontrib><creatorcontrib>Grace, Sarah</creatorcontrib><creatorcontrib>Dahlstrom, Julia</creatorcontrib><creatorcontrib>Workman, Sarita</creatorcontrib><creatorcontrib>Symes, Andrew</creatorcontrib><creatorcontrib>Mackinnon, Stephen</creatorcontrib><creatorcontrib>Hough, Rachael</creatorcontrib><creatorcontrib>Morris, Emma</creatorcontrib><title>Successful outcome following allogeneic hematopoietic stem cell transplantation in adults with primary immunodeficiency</title><title>Blood</title><addtitle>Blood</addtitle><description>The primary immunodeficiencies (PIDs), rare inherited diseases characterized by severe dysfunction of immunity, have been successfully treated by allogeneic hematopoietic stem cell transplantation (Allo-HSCT) in childhood. Controversy exists regarding optimal timing and use of Allo-HSCT in adults, due to lack of experience and previous poor outcomes. Twenty-nine consecutive adult patients, with a mean age at transplant of 24 years (range, 17-50 years), underwent Allo-HSCT. Reduced-intensity conditioning (RIC) included fludarabine (Flu)/melphalan/alemtuzumab (n = 20), Flu/busulfan (Bu)/alemtuzumab (n = 8), and Flu/Bu/antithymocyte globulin (n = 1). Stem cell donors were matched unrelated donors or mismatched unrelated donors (n = 18) and matched related donors (n = 11). Overall survival (OS), event-free survival, transplant-related mortality (TRM), acute and chronic graft-versus-host disease incidence and severity, time to engraftment, lineage-specific chimerism, immune reconstitution, and discontinuation of immunoglobulin replacement therapy were recorded. OS at 3 years for the whole cohort was 85.2%. The rarer PID patients without chronic granulomatous disease (CGD) achieved an OS at 3 years of 88.9% (n = 18), compared with 81.8% for CGD patients (n = 11). TRM was low with only 4 deaths observed at a median follow-up of 3.5 years. There were no cases of early or late rejection. In all surviving patients, either stable mixed chimerism or full donor chimerism were observed. At last follow-up, 87% of the surviving patients had no evidence of persistent or recurrent infections. Allo-HSCT is safe and effective in young adult patients with severe PID and should be considered the treatment of choice where an appropriate donor is available.
•Allo-HSCT with RIC is safe and effective in younger adults with severe PID.•Referral triggers should include severe infections, autoimmunity, malignancy, and disease progression despite conservative management.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Cohort Studies</subject><subject>Female</subject><subject>Hematopoietic Stem Cell Transplantation - mortality</subject><subject>Humans</subject><subject>Immunologic Deficiency Syndromes - mortality</subject><subject>Immunologic Deficiency Syndromes - pathology</subject><subject>Immunologic Deficiency Syndromes - therapy</subject><subject>Middle Aged</subject><subject>Prognosis</subject><subject>Survival Rate</subject><subject>Transplantation</subject><subject>Transplantation Conditioning</subject><subject>Transplantation, Homologous</subject><subject>Young Adult</subject><issn>0006-4971</issn><issn>1528-0020</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU1vEzEQhi1ERUPhHyDkI5cFf6w_9oKEqhaQKnGgnC3HHidGXjusvY3677tpQoELp_HIM--8Mw9Cbyh5T6lmH9apFN8xQlVHhk4T1Wv1DK2oYLojhJHnaEUIkV0_KHqOXtb6kxDacyZeoHM2MDVwoVZo_312DmoNc8Jlbq6MgENJqexj3mC7PDaQITq8hdG2sisR2pLVBiN2kBJuk811l2xutsWScczY-jm1ivexbfFuiqOd7nEcxzkXDyG6CNndv0JnwaYKr0_xAv24vrq9_NLdfPv89fLTTed6yVsngK6DUjbo3g_SCq18oF6yPljGnCPgrKRBQQ9cSy3WmhMtpVTc00FxrvkF-njU3c3rEbyDvBhO5mTLFBvNvz85bs2m3BnJmFg0F4F3J4Gp_JqhNjPGetjcZihzNXTQlAjBOF9K-2Opm0qtE4SnMZSYAzPzyMwcmBkymCOzpe3t3xafmn5D-rMDLIe6izCZ-nhE8HEC14wv8f8THgCz962D</recordid><startdate>20180222</startdate><enddate>20180222</enddate><creator>Fox, Thomas A.</creator><creator>Chakraverty, Ronjon</creator><creator>Burns, Siobhan</creator><creator>Carpenter, Benjamin</creator><creator>Thomson, Kirsty</creator><creator>Lowe, David</creator><creator>Fielding, Adele</creator><creator>Peggs, Karl</creator><creator>Kottaridis, Panagiotis</creator><creator>Uttenthal, Benjamin</creator><creator>Bigley, Venetia</creator><creator>Buckland, Matthew</creator><creator>Grandage, Victoria</creator><creator>Denovan, Shari</creator><creator>Grace, Sarah</creator><creator>Dahlstrom, Julia</creator><creator>Workman, Sarita</creator><creator>Symes, Andrew</creator><creator>Mackinnon, Stephen</creator><creator>Hough, Rachael</creator><creator>Morris, Emma</creator><general>Elsevier Inc</general><general>American Society of Hematology</general><scope>6I.</scope><scope>AAFTH</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><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-4834-1130</orcidid></search><sort><creationdate>20180222</creationdate><title>Successful outcome following allogeneic hematopoietic stem cell transplantation in adults with primary immunodeficiency</title><author>Fox, Thomas A. ; Chakraverty, Ronjon ; Burns, Siobhan ; Carpenter, Benjamin ; Thomson, Kirsty ; Lowe, David ; Fielding, Adele ; Peggs, Karl ; Kottaridis, Panagiotis ; Uttenthal, Benjamin ; Bigley, Venetia ; Buckland, Matthew ; Grandage, Victoria ; Denovan, Shari ; Grace, Sarah ; Dahlstrom, Julia ; Workman, Sarita ; Symes, Andrew ; Mackinnon, Stephen ; Hough, Rachael ; Morris, Emma</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c463t-5e1bf77af84d96a587df1d624fa22cc0eca61f7e4e38685b830866673d1973383</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Cohort Studies</topic><topic>Female</topic><topic>Hematopoietic Stem Cell Transplantation - mortality</topic><topic>Humans</topic><topic>Immunologic Deficiency Syndromes - mortality</topic><topic>Immunologic Deficiency Syndromes - pathology</topic><topic>Immunologic Deficiency Syndromes - therapy</topic><topic>Middle Aged</topic><topic>Prognosis</topic><topic>Survival Rate</topic><topic>Transplantation</topic><topic>Transplantation Conditioning</topic><topic>Transplantation, Homologous</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fox, Thomas A.</creatorcontrib><creatorcontrib>Chakraverty, Ronjon</creatorcontrib><creatorcontrib>Burns, Siobhan</creatorcontrib><creatorcontrib>Carpenter, Benjamin</creatorcontrib><creatorcontrib>Thomson, Kirsty</creatorcontrib><creatorcontrib>Lowe, David</creatorcontrib><creatorcontrib>Fielding, Adele</creatorcontrib><creatorcontrib>Peggs, Karl</creatorcontrib><creatorcontrib>Kottaridis, Panagiotis</creatorcontrib><creatorcontrib>Uttenthal, Benjamin</creatorcontrib><creatorcontrib>Bigley, Venetia</creatorcontrib><creatorcontrib>Buckland, Matthew</creatorcontrib><creatorcontrib>Grandage, Victoria</creatorcontrib><creatorcontrib>Denovan, Shari</creatorcontrib><creatorcontrib>Grace, Sarah</creatorcontrib><creatorcontrib>Dahlstrom, Julia</creatorcontrib><creatorcontrib>Workman, Sarita</creatorcontrib><creatorcontrib>Symes, Andrew</creatorcontrib><creatorcontrib>Mackinnon, Stephen</creatorcontrib><creatorcontrib>Hough, Rachael</creatorcontrib><creatorcontrib>Morris, Emma</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Blood</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fox, Thomas A.</au><au>Chakraverty, Ronjon</au><au>Burns, Siobhan</au><au>Carpenter, Benjamin</au><au>Thomson, Kirsty</au><au>Lowe, David</au><au>Fielding, Adele</au><au>Peggs, Karl</au><au>Kottaridis, Panagiotis</au><au>Uttenthal, Benjamin</au><au>Bigley, Venetia</au><au>Buckland, Matthew</au><au>Grandage, Victoria</au><au>Denovan, Shari</au><au>Grace, Sarah</au><au>Dahlstrom, Julia</au><au>Workman, Sarita</au><au>Symes, Andrew</au><au>Mackinnon, Stephen</au><au>Hough, Rachael</au><au>Morris, Emma</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Successful outcome following allogeneic hematopoietic stem cell transplantation in adults with primary immunodeficiency</atitle><jtitle>Blood</jtitle><addtitle>Blood</addtitle><date>2018-02-22</date><risdate>2018</risdate><volume>131</volume><issue>8</issue><spage>917</spage><epage>931</epage><pages>917-931</pages><issn>0006-4971</issn><eissn>1528-0020</eissn><abstract>The primary immunodeficiencies (PIDs), rare inherited diseases characterized by severe dysfunction of immunity, have been successfully treated by allogeneic hematopoietic stem cell transplantation (Allo-HSCT) in childhood. Controversy exists regarding optimal timing and use of Allo-HSCT in adults, due to lack of experience and previous poor outcomes. Twenty-nine consecutive adult patients, with a mean age at transplant of 24 years (range, 17-50 years), underwent Allo-HSCT. Reduced-intensity conditioning (RIC) included fludarabine (Flu)/melphalan/alemtuzumab (n = 20), Flu/busulfan (Bu)/alemtuzumab (n = 8), and Flu/Bu/antithymocyte globulin (n = 1). Stem cell donors were matched unrelated donors or mismatched unrelated donors (n = 18) and matched related donors (n = 11). Overall survival (OS), event-free survival, transplant-related mortality (TRM), acute and chronic graft-versus-host disease incidence and severity, time to engraftment, lineage-specific chimerism, immune reconstitution, and discontinuation of immunoglobulin replacement therapy were recorded. OS at 3 years for the whole cohort was 85.2%. The rarer PID patients without chronic granulomatous disease (CGD) achieved an OS at 3 years of 88.9% (n = 18), compared with 81.8% for CGD patients (n = 11). TRM was low with only 4 deaths observed at a median follow-up of 3.5 years. There were no cases of early or late rejection. In all surviving patients, either stable mixed chimerism or full donor chimerism were observed. At last follow-up, 87% of the surviving patients had no evidence of persistent or recurrent infections. Allo-HSCT is safe and effective in young adult patients with severe PID and should be considered the treatment of choice where an appropriate donor is available.
•Allo-HSCT with RIC is safe and effective in younger adults with severe PID.•Referral triggers should include severe infections, autoimmunity, malignancy, and disease progression despite conservative management.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>29279357</pmid><doi>10.1182/blood-2017-09-807487</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0003-4834-1130</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Cohort Studies Female Hematopoietic Stem Cell Transplantation - mortality Humans Immunologic Deficiency Syndromes - mortality Immunologic Deficiency Syndromes - pathology Immunologic Deficiency Syndromes - therapy Middle Aged Prognosis Survival Rate Transplantation Transplantation Conditioning Transplantation, Homologous Young Adult |
title | Successful outcome following allogeneic hematopoietic stem cell transplantation in adults with primary immunodeficiency |
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