| Literature DB >> 29193007 |
Michaela Kuhlen1, Andre M Willasch2, Jean-Hugues Dalle3, Jacek Wachowiak4, Isaac Yaniv5,6, Marianne Ifversen7, Petr Sedlacek8, Tayfun Guengoer9, Peter Lang10, Peter Bader2, Sabina Sufliarska11, Adriana Balduzzi12, Brigitte Strahm13, Irene von Luettichau14,15, Jessica I Hoell1, Arndt Borkhardt1, Thomas Klingebiel2, Martin Schrappe16, Arend von Stackelberg17, Evgenia Glogova18, Ulrike Poetschger18, Roland Meisel1, Christina Peters18.
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.Entities:
Keywords: children; leukaemia; relapse; stem cell transplantation
Mesh:
Year: 2017 PMID: 29193007 DOI: 10.1111/bjh.14965
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998