Plerixafor for the Treatment of WHIM Syndrome

Detalhes bibliográficos
Autor(a) principal: McDermott, DH
Data de Publicação: 2019
Outros Autores: Pastrana, DV, Calvo, KR, Pittaluga, S, Velez, D, Cho, E, Liu, Q, Trout, HH, Farela Neves, J, Gardner, PJ, Bianchi, DA, Blair, EA, Landon, EM, Silva, SL, Buck, CB, Murphy, PM
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.17/4730
Resumo: WHIM syndrome (warts, hypogammaglobulinemia, infections, and myelokathexis), a primary immunodeficiency disorder involving panleukopenia, is caused by autosomal dominant gain-of-function mutations in CXC chemokine receptor 4 (CXCR4). Myelokathexis is neutropenia caused by neutrophil retention in bone marrow. Patients with WHIM syndrome are often treated with granulocyte colony-stimulating factor (G-CSF), which can increase neutrophil counts but does not affect cytopenias other than neutropenia. In this investigator-initiated, open-label study, three severely affected patients with WHIM syndrome who could not receive G-CSF were treated with low-dose plerixafor, a CXCR4 antagonist, for 19 to 52 months. Myelofibrosis, panleukopenia, anemia, and thrombocytopenia were ameliorated, the wart burden and frequency of infection declined, human papillomavirus-associated oropharyngeal squamous-cell carcinoma stabilized, and quality of life improved markedly. Adverse events were mainly infections attributable to the underlying immunodeficiency. One patient died from complications of elective reconstructive surgery. (Funded by the National Institutes of Health.).
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spelling Plerixafor for the Treatment of WHIM SyndromeBenzylaminesBone Marrow / pathology*Bone Marrow ExaminationCyclamsFatal OutcomeHeterocyclic Compounds / therapeutic use*Immunologic Deficiency Syndromes / drug therapy*Immunologic Deficiency Syndromes / pathologyMiddle AgedNeoplasms, Squamous Cell / drug therapyNeoplasms, Squamous Cell / geneticsPhenotypePrimary Immunodeficiency DiseasesPrimary Myelofibrosis / drug therapyPrimary Myelofibrosis / pathologyReceptors, CXCR4 / antagonists & inhibitors*Receptors, CXCR4 / geneticsWarts / drug therapy*Warts / pathologyHDE INF PEDWHIM syndrome (warts, hypogammaglobulinemia, infections, and myelokathexis), a primary immunodeficiency disorder involving panleukopenia, is caused by autosomal dominant gain-of-function mutations in CXC chemokine receptor 4 (CXCR4). Myelokathexis is neutropenia caused by neutrophil retention in bone marrow. Patients with WHIM syndrome are often treated with granulocyte colony-stimulating factor (G-CSF), which can increase neutrophil counts but does not affect cytopenias other than neutropenia. In this investigator-initiated, open-label study, three severely affected patients with WHIM syndrome who could not receive G-CSF were treated with low-dose plerixafor, a CXCR4 antagonist, for 19 to 52 months. Myelofibrosis, panleukopenia, anemia, and thrombocytopenia were ameliorated, the wart burden and frequency of infection declined, human papillomavirus-associated oropharyngeal squamous-cell carcinoma stabilized, and quality of life improved markedly. Adverse events were mainly infections attributable to the underlying immunodeficiency. One patient died from complications of elective reconstructive surgery. (Funded by the National Institutes of Health.).NEJM GroupRepositório do Centro Hospitalar Universitário de Lisboa Central, EPEMcDermott, DHPastrana, DVCalvo, KRPittaluga, SVelez, DCho, ELiu, QTrout, HHFarela Neves, JGardner, PJBianchi, DABlair, EALandon, EMSilva, SLBuck, CBMurphy, PM2023-11-03T11:33:48Z20192019-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.17/4730engN Engl J Med . 2019 Jan 10;380(2):163-17010.1056/NEJMoa1808575info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-11-05T06:33:13Zoai:repositorio.chlc.min-saude.pt:10400.17/4730Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:26:50.106621Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Plerixafor for the Treatment of WHIM Syndrome
title Plerixafor for the Treatment of WHIM Syndrome
spellingShingle Plerixafor for the Treatment of WHIM Syndrome
McDermott, DH
Benzylamines
Bone Marrow / pathology*
Bone Marrow Examination
Cyclams
Fatal Outcome
Heterocyclic Compounds / therapeutic use*
Immunologic Deficiency Syndromes / drug therapy*
Immunologic Deficiency Syndromes / pathology
Middle Aged
Neoplasms, Squamous Cell / drug therapy
Neoplasms, Squamous Cell / genetics
Phenotype
Primary Immunodeficiency Diseases
Primary Myelofibrosis / drug therapy
Primary Myelofibrosis / pathology
Receptors, CXCR4 / antagonists & inhibitors*
Receptors, CXCR4 / genetics
Warts / drug therapy*
Warts / pathology
HDE INF PED
title_short Plerixafor for the Treatment of WHIM Syndrome
title_full Plerixafor for the Treatment of WHIM Syndrome
title_fullStr Plerixafor for the Treatment of WHIM Syndrome
title_full_unstemmed Plerixafor for the Treatment of WHIM Syndrome
title_sort Plerixafor for the Treatment of WHIM Syndrome
author McDermott, DH
author_facet McDermott, DH
Pastrana, DV
Calvo, KR
Pittaluga, S
Velez, D
Cho, E
Liu, Q
Trout, HH
Farela Neves, J
Gardner, PJ
Bianchi, DA
Blair, EA
Landon, EM
Silva, SL
Buck, CB
Murphy, PM
author_role author
author2 Pastrana, DV
Calvo, KR
Pittaluga, S
Velez, D
Cho, E
Liu, Q
Trout, HH
Farela Neves, J
Gardner, PJ
Bianchi, DA
Blair, EA
Landon, EM
Silva, SL
Buck, CB
Murphy, PM
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Repositório do Centro Hospitalar Universitário de Lisboa Central, EPE
dc.contributor.author.fl_str_mv McDermott, DH
Pastrana, DV
Calvo, KR
Pittaluga, S
Velez, D
Cho, E
Liu, Q
Trout, HH
Farela Neves, J
Gardner, PJ
Bianchi, DA
Blair, EA
Landon, EM
Silva, SL
Buck, CB
Murphy, PM
dc.subject.por.fl_str_mv Benzylamines
Bone Marrow / pathology*
Bone Marrow Examination
Cyclams
Fatal Outcome
Heterocyclic Compounds / therapeutic use*
Immunologic Deficiency Syndromes / drug therapy*
Immunologic Deficiency Syndromes / pathology
Middle Aged
Neoplasms, Squamous Cell / drug therapy
Neoplasms, Squamous Cell / genetics
Phenotype
Primary Immunodeficiency Diseases
Primary Myelofibrosis / drug therapy
Primary Myelofibrosis / pathology
Receptors, CXCR4 / antagonists & inhibitors*
Receptors, CXCR4 / genetics
Warts / drug therapy*
Warts / pathology
HDE INF PED
topic Benzylamines
Bone Marrow / pathology*
Bone Marrow Examination
Cyclams
Fatal Outcome
Heterocyclic Compounds / therapeutic use*
Immunologic Deficiency Syndromes / drug therapy*
Immunologic Deficiency Syndromes / pathology
Middle Aged
Neoplasms, Squamous Cell / drug therapy
Neoplasms, Squamous Cell / genetics
Phenotype
Primary Immunodeficiency Diseases
Primary Myelofibrosis / drug therapy
Primary Myelofibrosis / pathology
Receptors, CXCR4 / antagonists & inhibitors*
Receptors, CXCR4 / genetics
Warts / drug therapy*
Warts / pathology
HDE INF PED
description WHIM syndrome (warts, hypogammaglobulinemia, infections, and myelokathexis), a primary immunodeficiency disorder involving panleukopenia, is caused by autosomal dominant gain-of-function mutations in CXC chemokine receptor 4 (CXCR4). Myelokathexis is neutropenia caused by neutrophil retention in bone marrow. Patients with WHIM syndrome are often treated with granulocyte colony-stimulating factor (G-CSF), which can increase neutrophil counts but does not affect cytopenias other than neutropenia. In this investigator-initiated, open-label study, three severely affected patients with WHIM syndrome who could not receive G-CSF were treated with low-dose plerixafor, a CXCR4 antagonist, for 19 to 52 months. Myelofibrosis, panleukopenia, anemia, and thrombocytopenia were ameliorated, the wart burden and frequency of infection declined, human papillomavirus-associated oropharyngeal squamous-cell carcinoma stabilized, and quality of life improved markedly. Adverse events were mainly infections attributable to the underlying immunodeficiency. One patient died from complications of elective reconstructive surgery. (Funded by the National Institutes of Health.).
publishDate 2019
dc.date.none.fl_str_mv 2019
2019-01-01T00:00:00Z
2023-11-03T11:33:48Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.17/4730
url http://hdl.handle.net/10400.17/4730
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv N Engl J Med . 2019 Jan 10;380(2):163-170
10.1056/NEJMoa1808575
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv NEJM Group
publisher.none.fl_str_mv NEJM Group
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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