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        "resumen" => "<span class="elsevierStyleSectionTitle">Objetivo</span><p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Estudio retrospectivo de los resultados del trasplante de progenitores hematopoy&#233;ticos de sangre de cord&#243;n umbilical en Espa&#241;a&#46;</p> <span class="elsevierStyleSectionTitle">Pacientes y m&#233;todos</span><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Veintiocho ni&#241;os con edad media de 6&#44;5 a&#241;os y peso medio de 25 kg recibieron un trasplante de sangre de cord&#243;n umbilical entre julio de 1994 y mayo de 1998 en distintos centros pertenecientes al Grupo Espa&#241;ol para el Trasplan-te de Medula &#211;sea en ni&#241;os &#40;GETMON&#41;&#46;</p><p id="spar0110" class="elsevierStyleSimplePara elsevierViewall">El donante fue en 2 pacientes un hermano HLA-id&#233;ntico&#44; en otros 2 pacientes un familiar no id&#233;ntico y en los 24 restantes un donante no emparentado&#46; Entre &#233;stos&#44; la identidad antig&#233;nica HLA &#40;A&#44; B y DR&#41; 6&#47;6 s&#243;lo se observaba en 3 pacientes&#46; Los trasplantes se realizaron en su mayor&#237;a por leucemia &#40;21 pacientes&#44; 75&#37;&#41; y en fase avanzada&#46; Los restantes 7 pacientes se trasplantaron por una enfermedad gen&#233;tica&#44; en su mayor&#237;a inmunodeficiencia cong&#233;nita&#46; El tratamiento de acondicionamiento incluy&#243; irradiaci&#243;n corporal total en 10 pacientes y poliquimioterapia en los restantes&#46; La profilaxis de la enfermedad del injerto contra hu&#233;sped aguda se realiz&#243; con ciclosporina en todos los casos a&#241;adiendo corticoides o metotrexato en los trasplantes sin identidad HLA&#46; La media de c&#233;lulas perfun-didas fue de 53&#44;4&#215;10<span class="elsevierStyleSup">6</span>&#47;kg&#46;</p> <span class="elsevierStyleSectionTitle">Resultados</span><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">El fallo de implante de la sangre de cord&#243;n umbilical se observ&#243; en 9 pacientes&#46; Presentaron enfermedad del injerto contra hu&#233;sped aguda superior al grado II 18 pacientes &#40;64&#44;3&#37;&#41;&#46; Ocho &#40;28&#44;6&#37;&#41; presentaron EICH grave&#46; La supervivencia actuarial libre de enfermedad &#40;SLE&#41; de la serie global fue del 34&#44;4&#177;9&#37; a 3 a&#241;os&#44; con una media de seguimiento de 16&#44;6 meses&#46; Se observ&#243; una mejor SLE en las enfermedades cong&#233;nitas&#44; con una SLE del 71&#177;17&#37; y tambi&#233;n en los pacientes que recibieron trasplante de sangre de cord&#243;n umbilical con una identidad HLA A&#44; B y DR 6&#47;6&#44; en los que la SLE fue del 66&#177;19&#37;&#46;</p> <span class="elsevierStyleSectionTitle">Conclusiones</span><p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">Los mejores resultados se obtuvieron en las enfermeda-des gen&#233;ticas&#46; Se ha observado una correlaci&#243;n inversa en-tre la SLE y la disparidad antig&#233;nica HLA&#46; La incidencia relativamente alta de la enfermedad injerto contra hu&#233;sped aguda en esta serie&#44; podr&#237;a relacionarse con la escasa precisi&#243;n de la tipificaci&#243;n HLA efectuada en algunos pacientes&#46;</p>"
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        "resumen" => "<span class="elsevierStyleSectionTitle">Objective</span><p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">Retrospective study of the outcome of cord blood trans-plantation &#40;CBT&#41; in children in Spain&#46;</p> <span class="elsevierStyleSectionTitle">Patients and method</span><p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">Twenty-eight patients &#40;mean age 6&#46;5 years&#59; mean weight 25 kg&#41; received a CBT between July 1994 and May 1998 in several centres of the Spanish Pediatric Bone Marrow Transplant Group&#46; In 2 patients the donor was an identical human leukocyte antigen &#40;HLA&#41;-sibling and in two the donor was a mismatched family donor&#46; In 24 patients the donor was unrelated&#44; and 21 of these received an HLA-mismatched CBT&#46; Twenty-one patients &#40;75&#37;&#41; received a CBT for leukemia mainly in advanced phase&#46; Seven patients were transplanted for genetic disease&#46; Of these&#44; five had congenital immunodeficiency&#46; The conditioning treatment included total body irradiation in ten patients and combined chemotherapy in the remaining patients&#46; In all patients graft-versus-host disease &#40;GVHD&#41; prophylaxis was performed with cyclosporine&#44; and corticosteroids or methotrexate were added in patients with HLA-mismatched donors&#46; The mean number of nucleated cells infused was 53&#46;4&#215;10<span class="elsevierStyleSup">6</span>&#47;kg&#46;</p> <span class="elsevierStyleSectionTitle">Results</span><p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">Graft failure was observed in nine patients&#46; Eighteen patients &#40;64&#46;3&#37;&#41; developed grade II-IV acute GVHD&#46; Eight patients &#40;28&#46;6&#37;&#41; developed severe GVHD&#46; Actuarial event-free survival &#40;EFS&#41; of all the patients was 34&#46;4&#177;69&#37; at 3 years&#44; with a mean followup of 16&#46;6 months&#46; EFS was more favorable in patients with genetic disease &#40;71&#177;17&#37;&#41; and in those with an HLA &#40;A&#44; B and DR&#41; identical donor &#40;6&#47;6&#41; &#40;66&#177;19&#37;&#41;&#46;</p> <span class="elsevierStyleSectionTitle">Conclusions</span><p id="spar0040" class="elsevierStyleSimplePara elsevierViewall">The most favorable results were obtained in patients with genetic diseases&#46; We observed an inverse correlation between EFS and patients with HLA-identical donors&#46; The high incidence of severe acute GVHD could have been related to a lack of accuracy in the HLA-typography of some patients&#46;</p>"
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Trasplante de progenitores hematopoyéticos de sangre de cordón umbilical en niños
Transplantation of umbilical cord blood hematopoietic progenitor cells in children
I. Badell Serraa,
Autor para correspondencia
ibadell@hsp.santpau.es

Correspondencia:Dra. I. Badell Serra. Servicio de Pediatría. Hospital de la Santa Creu i Sant Pau. Avda. Sant Antoni M. Claret, 167. 08025 Barcelona.
, T. Olivé Oliverasb, L. Madero Lópezc, A. Muñoz Villad, A. Martínez Rubioe, A. Verdeguer Mirallesf, C. Díaz de Heredia Rubiob, M.A. Díaz Perezc, J. Cubells Rieróa, M.S. Maldonado Regaladod, J.J. Ortega Aramburub, por el Grupo Español para el Trasplante de Medula Ósea en niños (GETMON)
a Servicios de Pediatría.Hospital de la Santa Creu i Sant Pau y
b Hospital Vall d’Hebron. Barcelona.
c Hospital Niño Jesús,
d Hospital Ramón y Cajal y
e Hospital La Paz. Madrid.
f Hospital La Fe. Valencia
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        "resumen" => "<span class="elsevierStyleSectionTitle">Objetivo</span><p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Estudio retrospectivo de los resultados del trasplante de progenitores hematopoy&#233;ticos de sangre de cord&#243;n umbilical en Espa&#241;a&#46;</p> <span class="elsevierStyleSectionTitle">Pacientes y m&#233;todos</span><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Veintiocho ni&#241;os con edad media de 6&#44;5 a&#241;os y peso medio de 25 kg recibieron un trasplante de sangre de cord&#243;n umbilical entre julio de 1994 y mayo de 1998 en distintos centros pertenecientes al Grupo Espa&#241;ol para el Trasplan-te de Medula &#211;sea en ni&#241;os &#40;GETMON&#41;&#46;</p><p id="spar0110" class="elsevierStyleSimplePara elsevierViewall">El donante fue en 2 pacientes un hermano HLA-id&#233;ntico&#44; en otros 2 pacientes un familiar no id&#233;ntico y en los 24 restantes un donante no emparentado&#46; Entre &#233;stos&#44; la identidad antig&#233;nica HLA &#40;A&#44; B y DR&#41; 6&#47;6 s&#243;lo se observaba en 3 pacientes&#46; Los trasplantes se realizaron en su mayor&#237;a por leucemia &#40;21 pacientes&#44; 75&#37;&#41; y en fase avanzada&#46; Los restantes 7 pacientes se trasplantaron por una enfermedad gen&#233;tica&#44; en su mayor&#237;a inmunodeficiencia cong&#233;nita&#46; El tratamiento de acondicionamiento incluy&#243; irradiaci&#243;n corporal total en 10 pacientes y poliquimioterapia en los restantes&#46; La profilaxis de la enfermedad del injerto contra hu&#233;sped aguda se realiz&#243; con ciclosporina en todos los casos a&#241;adiendo corticoides o metotrexato en los trasplantes sin identidad HLA&#46; La media de c&#233;lulas perfun-didas fue de 53&#44;4&#215;10<span class="elsevierStyleSup">6</span>&#47;kg&#46;</p> <span class="elsevierStyleSectionTitle">Resultados</span><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">El fallo de implante de la sangre de cord&#243;n umbilical se observ&#243; en 9 pacientes&#46; Presentaron enfermedad del injerto contra hu&#233;sped aguda superior al grado II 18 pacientes &#40;64&#44;3&#37;&#41;&#46; Ocho &#40;28&#44;6&#37;&#41; presentaron EICH grave&#46; La supervivencia actuarial libre de enfermedad &#40;SLE&#41; de la serie global fue del 34&#44;4&#177;9&#37; a 3 a&#241;os&#44; con una media de seguimiento de 16&#44;6 meses&#46; Se observ&#243; una mejor SLE en las enfermedades cong&#233;nitas&#44; con una SLE del 71&#177;17&#37; y tambi&#233;n en los pacientes que recibieron trasplante de sangre de cord&#243;n umbilical con una identidad HLA A&#44; B y DR 6&#47;6&#44; en los que la SLE fue del 66&#177;19&#37;&#46;</p> <span class="elsevierStyleSectionTitle">Conclusiones</span><p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">Los mejores resultados se obtuvieron en las enfermeda-des gen&#233;ticas&#46; Se ha observado una correlaci&#243;n inversa en-tre la SLE y la disparidad antig&#233;nica HLA&#46; La incidencia relativamente alta de la enfermedad injerto contra hu&#233;sped aguda en esta serie&#44; podr&#237;a relacionarse con la escasa precisi&#243;n de la tipificaci&#243;n HLA efectuada en algunos pacientes&#46;</p>"
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        "resumen" => "<span class="elsevierStyleSectionTitle">Objective</span><p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">Retrospective study of the outcome of cord blood trans-plantation &#40;CBT&#41; in children in Spain&#46;</p> <span class="elsevierStyleSectionTitle">Patients and method</span><p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">Twenty-eight patients &#40;mean age 6&#46;5 years&#59; mean weight 25 kg&#41; received a CBT between July 1994 and May 1998 in several centres of the Spanish Pediatric Bone Marrow Transplant Group&#46; In 2 patients the donor was an identical human leukocyte antigen &#40;HLA&#41;-sibling and in two the donor was a mismatched family donor&#46; In 24 patients the donor was unrelated&#44; and 21 of these received an HLA-mismatched CBT&#46; Twenty-one patients &#40;75&#37;&#41; received a CBT for leukemia mainly in advanced phase&#46; Seven patients were transplanted for genetic disease&#46; Of these&#44; five had congenital immunodeficiency&#46; The conditioning treatment included total body irradiation in ten patients and combined chemotherapy in the remaining patients&#46; In all patients graft-versus-host disease &#40;GVHD&#41; prophylaxis was performed with cyclosporine&#44; and corticosteroids or methotrexate were added in patients with HLA-mismatched donors&#46; The mean number of nucleated cells infused was 53&#46;4&#215;10<span class="elsevierStyleSup">6</span>&#47;kg&#46;</p> <span class="elsevierStyleSectionTitle">Results</span><p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">Graft failure was observed in nine patients&#46; Eighteen patients &#40;64&#46;3&#37;&#41; developed grade II-IV acute GVHD&#46; Eight patients &#40;28&#46;6&#37;&#41; developed severe GVHD&#46; Actuarial event-free survival &#40;EFS&#41; of all the patients was 34&#46;4&#177;69&#37; at 3 years&#44; with a mean followup of 16&#46;6 months&#46; EFS was more favorable in patients with genetic disease &#40;71&#177;17&#37;&#41; and in those with an HLA &#40;A&#44; B and DR&#41; identical donor &#40;6&#47;6&#41; &#40;66&#177;19&#37;&#41;&#46;</p> <span class="elsevierStyleSectionTitle">Conclusions</span><p id="spar0040" class="elsevierStyleSimplePara elsevierViewall">The most favorable results were obtained in patients with genetic diseases&#46; We observed an inverse correlation between EFS and patients with HLA-identical donors&#46; The high incidence of severe acute GVHD could have been related to a lack of accuracy in the HLA-typography of some patients&#46;</p>"
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Información del artículo
ISSN: 16954033
Idioma original: Español
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