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Outcome of transplantation for acute lymphoblastic leukemia in children with Down syndrome.

dc.contributor.author Hitzler, Johann K
dc.contributor.author He, Wensheng
dc.contributor.author Doyle, John
dc.contributor.author Cairo, Mitchell
dc.contributor.author Camitta, Bruce M
dc.contributor.author Chan, Ka Wah
dc.contributor.author Diaz Perez, Miguel A
dc.contributor.author Fraser, Christopher
dc.contributor.author Gross, Thomas G
dc.contributor.author Horan, John T
dc.contributor.author Kennedy-Nasser, Alana A
dc.contributor.author Kitko, Carrie
dc.contributor.author Kurtzberg, Joanne
dc.contributor.author Lehmann, Leslie
dc.contributor.author O'Brien, Tracey
dc.contributor.author Pulsipher, Michael A
dc.contributor.author Smith, Franklin O
dc.contributor.author Zhang, Mei-Jie
dc.contributor.author Eapen, Mary
dc.contributor.author Carpenter, Paul A
dc.contributor.author CIBMTR Pediatric Cancer Working Committee
dc.date.accessioned 2022-03-23T19:29:52Z
dc.date.available 2022-03-23T19:29:52Z
dc.date.issued 2014-06
dc.identifier.issn 1545-5009
dc.identifier.issn 1545-5017
dc.identifier.uri https://hdl.handle.net/10161/24654
dc.description.abstract We report on 27 patients with Down syndrome (DS) and acute lymphoblastic leukemia (ALL) who received allogeneic hematopoietic cell transplantation (HCT) between 2000 and 2009. Seventy-eight percent of patients received myeloablative conditioning and 52% underwent transplantation in second remission. Disease-free survival (DFS) was 24% at a median of 3 years. Post-transplant leukemic relapse was more frequent than expected for children with DS-ALL (54%) than for non-DS ALL. These data suggest leukemic relapse rather than transplant toxicity is the most important cause of treatment failure. Advancements in leukemia control are especially needed for improvement in HCT outcomes for DS-ALL.
dc.language eng
dc.publisher Wiley
dc.relation.ispartof Pediatric blood & cancer
dc.relation.isversionof 10.1002/pbc.24918
dc.subject CIBMTR Pediatric Cancer Working Committee
dc.subject Humans
dc.subject Down Syndrome
dc.subject Graft vs Host Disease
dc.subject Genetic Predisposition to Disease
dc.subject Recurrence
dc.subject Tacrolimus
dc.subject Cyclosporine
dc.subject Antineoplastic Combined Chemotherapy Protocols
dc.subject Immunosuppressive Agents
dc.subject Myeloablative Agonists
dc.subject Disease-Free Survival
dc.subject Treatment Outcome
dc.subject Transplantation Conditioning
dc.subject Combined Modality Therapy
dc.subject Salvage Therapy
dc.subject Whole-Body Irradiation
dc.subject Remission Induction
dc.subject Bone Marrow Transplantation
dc.subject Hematopoietic Stem Cell Transplantation
dc.subject Registries
dc.subject Retrospective Studies
dc.subject Adolescent
dc.subject Adult
dc.subject Child
dc.subject Child, Preschool
dc.subject Infant
dc.subject Living Donors
dc.subject Precursor Cell Lymphoblastic Leukemia-Lymphoma
dc.subject Kaplan-Meier Estimate
dc.subject Allografts
dc.title Outcome of transplantation for acute lymphoblastic leukemia in children with Down syndrome.
dc.type Journal article
duke.contributor.id Kurtzberg, Joanne|0097203
dc.date.updated 2022-03-23T19:29:52Z
pubs.begin-page 1126
pubs.end-page 1128
pubs.issue 6
pubs.organisational-group Duke
pubs.organisational-group School of Medicine
pubs.organisational-group Clinical Science Departments
pubs.organisational-group Institutes and Centers
pubs.organisational-group Pathology
pubs.organisational-group Pediatrics
pubs.organisational-group Duke Cancer Institute
pubs.organisational-group Institutes and Provost's Academic Units
pubs.organisational-group Initiatives
pubs.organisational-group Duke Innovation & Entrepreneurship
pubs.organisational-group Pediatrics, Transplant and Cellular Therapy
pubs.publication-status Published
pubs.volume 61
duke.contributor.orcid Kurtzberg, Joanne|0000-0002-3370-0703


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