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Outcome after intensive reinduction therapy and allogeneic stem cell transplant in paediatric relapsed acute myeloid leukaemia.

Authors :
Karlsson, Lene
Forestier, Erik
Hasle, Henrik
Jahnukainen, Kirsi
Jónsson, Ólafur G.
Lausen, Birgitte
Norén Nyström, Ulrika
Palle, Josefine
Tierens, Anne
Zeller, Bernward
Abrahamsson, Jonas
Source :
British Journal of Haematology. Aug2017, Vol. 178 Issue 4, p592-602. 11p.
Publication Year :
2017

Abstract

Given that 30-40% of children with acute myeloid leukaemia ( AML) relapse after primary therapy it is important to define prognostic factors and identify optimal therapy. From 1993 to 2012, 543 children from the Nordic countries were treated according to two consecutive protocols: 208 children relapsed. The influence of disease characteristics, first line treatment, relapse therapy and duration of first remission on outcome was analysed. Second complete remission ( CR2) was achieved in 146 (70%) patients. Estimated 5-year overall survival ( OS5y) was 39 ± 4% for the whole group and 43 ± 4% for the 190 patients given re-induction therapy, of whom 76% received regimens that included fludarabine, cytarabine ( FLA) ± anthracyclines, 18% received Nordic Society for Paediatric Haematology and Oncology ( NOPHO) upfront blocks and 5% received other regimens. Late relapse ≥1 year from diagnosis, no allogeneic stem cell transplantation ( SCT) in first remission and core binding factor AML were independent favourable prognostic factors for survival. For the 128 children (124 in CR2) that received SCT as consolidation therapy after relapse, OS5y was 61 ± 5%. Four of 19 children (21%) survived without receiving SCT as part of relapse therapy. Our data show that intensive re-induction followed by SCT can give cure rates of 40% in children with relapsed AML. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00071048
Volume :
178
Issue :
4
Database :
Academic Search Index
Journal :
British Journal of Haematology
Publication Type :
Academic Journal
Accession number :
124486027
Full Text :
https://doi.org/10.1111/bjh.14720