| Literature DB >> 31578451 |
Martin G Sauer1, Peter J Lang2, Michael H Albert3, Peter Bader4, Ursula Creutzig5, Matthias Eyrich6, Johann Greil7, Bernd Gruhn8, Wolfgang Holter9, Thomas Klingebiel4, Bernhard Kremens10, Heiko von der Leyen11, Christine Mauz-Körholz12, Roland Meisel13, Kirsten Mischke5, Ingo Müller14, Charlotte M Niemeyer15, Christina Peters9, Christine Pohler11, Dirk Reinhardt10, Birgit Burkhardt16, Paul G Schlegel6, Ansgar S Schulz17, Johanna Schrum14, Petr Sedlacek18,19, Brigitte Strahm15, Wilhelm Woessmann12, Rupert Handgretinger2, Martin Zimmermann5, Arndt Borkhardt13.
Abstract
AML SCT-BFM 2007 was the first hematopoietic stem cell transplantation (HCT) trial in Germany to comply with the European Clinical Trials Directive, and aimed to standardize pediatric HCT for acute myeloid leukemia (AML) across centers in Germany, Austria, and the Czech Republic. Children with high-risk features and a good early response achieving a complete first remission (CR-1) and those in CR-2 after a first relapse were stratified to receive HCT from a matched donor after myeloablative conditioning consisting of busulfan, cyclophosphamide, and melphalan. Four-year EFS and OS were 61 and 70%. Cumulative incidence of relapse (CIR) was 22%. TRM was 15% and correlated with age reaching 9% (SE 3%) in children younger than 12 years and 31% (SE 9%) in older children and adolescents. Children with poorly responding primary disease or relapse were allocated to receive early HCT after a cytoreductive regimen with fludarabine, amsacrine, and cytarabine, followed by reduced intensity conditioning and prophylactic donor lymphocyte infusions. Four-year EFS and OS were 49 and 53%. CIR was 38% and TRM 11%. For patients with primary poor response disease, early use of RIC HCT followed by prophylactic DLI can induce long-term remissions in more than 50% (EFS 46% (SE 9%)).Entities:
Year: 2019 PMID: 31578451 DOI: 10.1038/s41375-019-0584-8
Source DB: PubMed Journal: Leukemia ISSN: 0887-6924 Impact factor: 11.528