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
Hauptverfasser: 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
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container_end_page 931
container_issue 8
container_start_page 917
container_title Blood
container_volume 131
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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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><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. 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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. 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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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