Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/107440
Citations
Scopus Web of Science® Altmetric
?
?
Full metadata record
DC FieldValueLanguage
dc.contributor.authorPui, C.-H.-
dc.contributor.authorMullighan, C.-
dc.contributor.authorEvans, W.-
dc.contributor.authorRelling, M.-
dc.date.issued2012-
dc.identifier.citationBlood, 2012; 120(6):1165-1174-
dc.identifier.issn0006-4971-
dc.identifier.issn1528-0020-
dc.identifier.urihttp://hdl.handle.net/2440/107440-
dc.description.abstractImproved supportive care, more precise risk stratification, and personalized chemotherapy based on the characteristics of leukemic cells and hosts (eg, pharmacokinetics and pharmacogenetics) have pushed the cure rate of childhood acute lymphoblastic leukemia to near 90%. Further increase in cure rate can be expected from the discovery of additional recurrent molecular lesions, coupled with the development of novel targeted treatment through high-throughput genomics and innovative drug-screening systems. We discuss specific areas of research that promise to further refine current treatment and to improve the cure rate and quality of life of the patients.-
dc.description.statementofresponsibilityChing-Hon Pui, Charles G. Mullighan, William E. Evans and Mary V. Relling-
dc.language.isoen-
dc.publisherAmerican Society of Hematology-
dc.rights© 2012 by The American Society of Hematology-
dc.source.urihttp://dx.doi.org/10.1182/blood-2012-05-378943-
dc.subjectYoung adult-
dc.titlePediatric acute lymphoblastic leukemia: where are we going and how do we get there?-
dc.typeJournal article-
dc.identifier.doi10.1182/blood-2012-05-378943-
pubs.publication-statusPublished-
dc.identifier.orcidMullighan, C. [0000-0002-1871-1850]-
Appears in Collections:Aurora harvest 3
Paediatrics publications

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.