Exchange Transfusion and Leukapheresis in Pediatric Patients with AML With High Risk of Early Death by Bleeding and Leukostasis
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články
PubMed
26670831
DOI
10.1002/pbc.25855
Knihovny.cz E-zdroje
- Klíčová slova
- bleeding, early death, exchange transfusion, leukapheresis, leukostasis, pediatric AML,
- MeSH
- akutní myeloidní leukemie komplikace mortalita terapie MeSH
- dítě MeSH
- kojenec MeSH
- krevní transfuze * MeSH
- krvácení etiologie mortalita prevence a kontrola MeSH
- leukaferéza * MeSH
- leukostáza etiologie mortalita prevence a kontrola MeSH
- lidé MeSH
- předškolní dítě MeSH
- proporcionální rizikové modely MeSH
- rizikové faktory MeSH
- Check Tag
- dítě MeSH
- kojenec MeSH
- lidé MeSH
- mužské pohlaví MeSH
- předškolní dítě MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
BACKGROUND: The risk of early death (ED) by bleeding/leukostasis is high in patients with AML with hyperleukocytosis (>100,000/μl). Within the pediatric AML-BFM (Berlin-Frankfurt-Münster) 98/04 studies, emergency strategies for these children included exchange transfusion (ET) or leukapheresis (LPh). Risk factors for ED and interventions performed were analyzed. PATIENTS: Two hundred thirty-eight of 1,251 (19%) patients with AML presented with hyperleukocytosis; 23 of 1,251 (1.8%) patients died of bleeding/leukostasis. RESULTS: ED due to bleeding/leukostasis was highest at white blood cell (WBC) count >200,000/μl (14.3%). ED rates were even higher (20%) in patients with FAB (French-American-British) M4/M5 and hyperleukocytosis >200,000/μl. Patients with WBC >200,000/μl did slightly better with ET/LPh compared to those without ET/LPh (ED rate 7.5% vs. 21.2%, P = 0.055). Multivariate WBC >200,000/μl was of strongest prognostic significance for ED (P(χ(2) ) <0.0001). CONCLUSION: Our data confirm the high risk of bleeding/leukostasis in patients with hyperleukocytosis. ET/LPh shows a trend toward reduced ED rate due to bleeding/leukostasis and is recommended at WBC >200,000/μl, and in FAB M4/M5 even at lower WBC.
Department of Pediatric Hematology and Oncology Justus Liebig University Giessen Germany
Department of Pediatric Hematology Oncology University of Duisburg Essen Essen Germany
Department of Pediatric Oncology Hematology Charité University Medical Center Berlin Berlin Germany
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