| Literature DB >> 29303660 |
Anne-Charlotte Teyssier1, Hélène Lapillonne2, Marlene Pasquet3, Paola Ballerini2, André Baruchel4, Stephane Ducassou5, Odile Fenneteau6, Arnaud Petit7, Wendy Cuccuini8, Christine Ragu7, Claude Preudhomme9, Thomas Mercher10, Nicolas Sirvent1, Guy Leverger7.
Abstract
We report the outcome of 27 children with de novo acute megakaryoblastic leukemia (AMKL) (excluding Down syndrome) enrolled in the French multicenter prospective study ELAM02 (2005-2011). There was no difference in gender, initial leukocyte count, CNS involvement, and complete remission rate (88.9%), as compared to other acute myeloid leukemia (AML) subtypes. AMKL patients had a significantly poorer outcome (5-year overall survival 54% [CI 95% 33%-71%] than children with other AML subtypes (5-year overall survival 73% [CI 95% 68%-77%] p = 0.02). Gender, age, CNS leukemia, hyperleukocytosis, complete remission or cytogenetic subgroups were not significant prognostic factors of disease-free survival. AMKL (excluding Down syndrom) remains an AML subgroup with inferior outcome.Entities:
Keywords: AMKL; ELAM02; pediatric acute megakaryoblastic leukemia
Mesh:
Year: 2018 PMID: 29303660 DOI: 10.1080/08880018.2017.1414905
Source DB: PubMed Journal: Pediatr Hematol Oncol ISSN: 0888-0018 Impact factor: 1.969