| Literature DB >> 20535148 |
A C Lankester1, M B Bierings, E R van Wering, A J M Wijkhuijs, R A de Weger, J T Wijnen, J M Vossen, B Versluys, R M Egeler, M J D van Tol, H Putter, T Révész, J J M van Dongen, V H J van der Velden, M W Schilham.
Abstract
Relapse of pediatric acute lymphoblastic leukemia (ALL) remains the main cause of treatment failure after allogeneic stem cell transplantation (alloSCT). A high level of minimal residual disease (MRD) before alloSCT has been shown to predict these relapses. Patients at risk might benefit from a preemptive alloimmune intervention. In this first prospective, MRD-guided intervention study, 48 patients were stratified according to pre-SCT MRD level. Eighteen children with MRD level >or=1 x 10(-4) were eligible for intervention, consisting of early cyclosporine A tapering followed by consecutive, incremental donor lymphocyte infusions (n=1-4). The intervention was associated with graft versus host disease >or=grade II in only 23% of patients. Event-free survival in the intervention group was 19%. However, in contrast with the usual early recurrence of leukemia, relapses were delayed up to 3 years after SCT. In addition, several relapses presented at unusual extramedullary sites suggesting that the immune intervention may have altered the pattern of leukemia recurrence. In 8 out of 11 evaluable patients, relapse was preceded by MRD recurrence (median 9 weeks, range 0-30). We conclude that in children with high-risk ALL, immunotherapy-based regimens after SCT are feasible and may need to be further intensified to achieve total eradication of residual leukemic cells.Entities:
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Year: 2010 PMID: 20535148 DOI: 10.1038/leu.2010.133
Source DB: PubMed Journal: Leukemia ISSN: 0887-6924 Impact factor: 11.528