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Article: Allogeneic bone marrow transplantation for infants with acute leukemia or myelodysplastic syndrome

TitleAllogeneic bone marrow transplantation for infants with acute leukemia or myelodysplastic syndrome
Authors
KeywordsInfant leukemia
Myelodysplastic syndrome
Allogeneic transplantation
Late sequelae
Issue Date2001
Citation
Bone Marrow Transplantation, 2001, v. 27, n. 7, p. 717-722 How to Cite?
AbstractThe objective of this study is to investigate the outcome of children 24 months or age or younger (infants) at the time of allogeneic bone marrow transplantation (BMT) for acute leukemia or myelodysplasia. We analyzed the survival rate, prognostic factors, incidences of late sequelae, and immune reconstitution in 22 infants who underwent allogeneic BMT. The 5-year event-free survival estimate was 45.5% (95% confidence interval (CI), 24.4% to 63.3%). Six patients died of transplant-related complications and six died of disease relapse. Remission status at the time of BMT was the most important prognostic factor (P = 0.005): no patient who received a transplant while their disease was not in remission survived, whereas the 5-year survival estimate for infants who underwent BMT during remission was 56% (95% CI, 31% to 75%). Long-term outcomes in the 10 infant survivors were compared with those of 10 older controls matched for diagnosis, disease status at the time of BMT, calendar year at the time of BMT, and source of stem cells. Immune function 1 year after transplantation and the incidences and spectra of late sequelae were similar for both groups during a median of 3.5 years (range, 1.5 to 7.2 years) of follow-up.
Persistent Identifierhttp://hdl.handle.net/10722/294405
ISSN
2023 Impact Factor: 4.5
2023 SCImago Journal Rankings: 1.318
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLeung, W.-
dc.contributor.authorPitts, N.-
dc.contributor.authorBurnette, K.-
dc.contributor.authorCunningham, J. M.-
dc.contributor.authorHorwitz, E. M.-
dc.contributor.authorBenaim, E.-
dc.contributor.authorHale, G.-
dc.contributor.authorWoodard, P.-
dc.contributor.authorPui, C. H.-
dc.contributor.authorBowman, L. C.-
dc.date.accessioned2020-12-03T08:22:39Z-
dc.date.available2020-12-03T08:22:39Z-
dc.date.issued2001-
dc.identifier.citationBone Marrow Transplantation, 2001, v. 27, n. 7, p. 717-722-
dc.identifier.issn0268-3369-
dc.identifier.urihttp://hdl.handle.net/10722/294405-
dc.description.abstractThe objective of this study is to investigate the outcome of children 24 months or age or younger (infants) at the time of allogeneic bone marrow transplantation (BMT) for acute leukemia or myelodysplasia. We analyzed the survival rate, prognostic factors, incidences of late sequelae, and immune reconstitution in 22 infants who underwent allogeneic BMT. The 5-year event-free survival estimate was 45.5% (95% confidence interval (CI), 24.4% to 63.3%). Six patients died of transplant-related complications and six died of disease relapse. Remission status at the time of BMT was the most important prognostic factor (P = 0.005): no patient who received a transplant while their disease was not in remission survived, whereas the 5-year survival estimate for infants who underwent BMT during remission was 56% (95% CI, 31% to 75%). Long-term outcomes in the 10 infant survivors were compared with those of 10 older controls matched for diagnosis, disease status at the time of BMT, calendar year at the time of BMT, and source of stem cells. Immune function 1 year after transplantation and the incidences and spectra of late sequelae were similar for both groups during a median of 3.5 years (range, 1.5 to 7.2 years) of follow-up.-
dc.languageeng-
dc.relation.ispartofBone Marrow Transplantation-
dc.subjectInfant leukemia-
dc.subjectMyelodysplastic syndrome-
dc.subjectAllogeneic transplantation-
dc.subjectLate sequelae-
dc.titleAllogeneic bone marrow transplantation for infants with acute leukemia or myelodysplastic syndrome-
dc.typeArticle-
dc.description.naturelink_to_OA_fulltext-
dc.identifier.doi10.1038/sj.bmt.1702998-
dc.identifier.pmid11360111-
dc.identifier.scopuseid_2-s2.0-17744377946-
dc.identifier.volume27-
dc.identifier.issue7-
dc.identifier.spage717-
dc.identifier.epage722-
dc.identifier.isiWOS:000168369900008-
dc.identifier.issnl0268-3369-

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