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Outcome of relapse after allogeneic HSCT in children with ALL enrolled in the ALL-SCT 2003/2007 trial.

Authors :
Kuhlen M
Willasch AM
Dalle JH
Wachowiak J
Yaniv I
Ifversen M
Sedlacek P
Guengoer T
Lang P
Bader P
Sufliarska S
Balduzzi A
Strahm B
von Luettichau I
Hoell JI
Borkhardt A
Klingebiel T
Schrappe M
von Stackelberg A
Glogova E
Poetschger U
Meisel R
Peters C
Source :
British journal of haematology [Br J Haematol] 2018 Jan; Vol. 180 (1), pp. 82-89. Date of Electronic Publication: 2017 Nov 28.
Publication Year :
2018

Abstract

Relapse remains the major cause of treatment failure in children with high-risk acute lymphoblastic leukaemia (ALL) undergoing allogeneic haematopoietic stem-cell transplantation (allo-SCT). Prognosis is considered dismal but data on risk factors and outcome are lacking from prospective studies. We analysed 242 children with recurrence of ALL after first allo-SCT enrolled in the Berlin-Frankfurt-Munster (BFM) ALL-SCT-BFM 2003 and ALL-SCT-BFM international 2007 studies. Median time from allo-SCT to relapse was 7·7 months; median follow-up from relapse after allo-SCT until last follow-up was 3·4 years. The 3-year event-free survival (EFS) was 15% and overall survival (OS) was 20%. The main cause of death was disease progression or relapse (86·5%). The majority of children (48%) received salvage therapy without second allo-SCT, 26% of the children underwent a second allo-SCT and 25% received palliative treatment only. In multivariate analyses, age, site of relapse, time to relapse and type of salvage therapy were identified as significant prognostic factors for OS and EFS, whereas factors associated with first SCT were not statistically significant. Combined approaches incorporating novel immunotherapeutic treatment options and second allo-SCT hold promise to improve outcome in children with post allo-SCT relapse.<br /> (© 2017 John Wiley & Sons Ltd.)

Details

Language :
English
ISSN :
1365-2141
Volume :
180
Issue :
1
Database :
MEDLINE
Journal :
British journal of haematology
Publication Type :
Academic Journal
Accession number :
29193007
Full Text :
https://doi.org/10.1111/bjh.14965