Cargando…
Improved outcome of pediatric patients with acute megakaryoblastic leukemia in the AML-BFM 04 trial
Despite recent advances in the treatment of children with acute megakaryoblastic leukemia (AMKL) using intensified treatment protocols, clear prognostic indicators, and treatment recommendations for this acute myeloid leukemia (AML) subgroup are yet to be defined. Here, we report the outcome of 97 p...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4488462/ https://www.ncbi.nlm.nih.gov/pubmed/25913479 http://dx.doi.org/10.1007/s00277-015-2383-2 |
_version_ | 1782379163147042816 |
---|---|
author | Schweitzer, Jana Zimmermann, Martin Rasche, Mareike von Neuhoff, Christine Creutzig, Ursula Dworzak, Michael Reinhardt, Dirk Klusmann, Jan-Henning |
author_facet | Schweitzer, Jana Zimmermann, Martin Rasche, Mareike von Neuhoff, Christine Creutzig, Ursula Dworzak, Michael Reinhardt, Dirk Klusmann, Jan-Henning |
author_sort | Schweitzer, Jana |
collection | PubMed |
description | Despite recent advances in the treatment of children with acute megakaryoblastic leukemia (AMKL) using intensified treatment protocols, clear prognostic indicators, and treatment recommendations for this acute myeloid leukemia (AML) subgroup are yet to be defined. Here, we report the outcome of 97 pediatric patients with de novo AMKL (excluding Down syndrome [DS]) enrolled in the prospective multicenter studies AML-BFM 98 and AML-BFM 04 (1998-2014). AMKL occurred in 7.4 % of pediatric AML cases, at younger age (median 1.44 years) and with lower white blood cell count (mean 16.5 × 10(9)/L) as compared to other AML subgroups. With 60 ± 5 %, children with AMKL had a lower 5-year overall survival (5-year OS; vs. 68 ± 1 %, P(log rank) = 0.038). Yet, we achieved an improved 5-year OS in AML-BFM 04 compared to AML-BFM 98 (70 ± 6 % vs. 45 ± 8 %, P(log rank) = 0.041). Allogeneic hematopoietic stem cell transplantation in first remission did not provide a significant survival benefit (5-year OS 70 ± 11 % vs. 63 ± 6 %; P(Mantel-Byar) = 0.85). Cytogenetic data were available for n = 78 patients. AMKL patients with gain of chromosome 21 had a superior 5-year OS (80 ± 9 %, P(log rank) = 0.034), whereas translocation t(1;22)(p13;q13) was associated with an inferior 5-year event-free survival (38 ± 17 %, P(log rank) = 0.04). However, multivariate analysis showed that treatment response (bone marrow morphology on day 15 and 28) was the only independent prognostic marker (RR = 4.39; 95 % CI, 1.97–9.78). Interestingly, GATA1-mutations were detected in six patients (11 %) without previously known trisomy 21. Thus, AMKL (excluding DS) remains an AML subgroup with inferior outcome. Nevertheless, with intensive therapy regimens, a steep increase in the survival rates was achieved. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00277-015-2383-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4488462 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-44884622015-07-07 Improved outcome of pediatric patients with acute megakaryoblastic leukemia in the AML-BFM 04 trial Schweitzer, Jana Zimmermann, Martin Rasche, Mareike von Neuhoff, Christine Creutzig, Ursula Dworzak, Michael Reinhardt, Dirk Klusmann, Jan-Henning Ann Hematol Original Article Despite recent advances in the treatment of children with acute megakaryoblastic leukemia (AMKL) using intensified treatment protocols, clear prognostic indicators, and treatment recommendations for this acute myeloid leukemia (AML) subgroup are yet to be defined. Here, we report the outcome of 97 pediatric patients with de novo AMKL (excluding Down syndrome [DS]) enrolled in the prospective multicenter studies AML-BFM 98 and AML-BFM 04 (1998-2014). AMKL occurred in 7.4 % of pediatric AML cases, at younger age (median 1.44 years) and with lower white blood cell count (mean 16.5 × 10(9)/L) as compared to other AML subgroups. With 60 ± 5 %, children with AMKL had a lower 5-year overall survival (5-year OS; vs. 68 ± 1 %, P(log rank) = 0.038). Yet, we achieved an improved 5-year OS in AML-BFM 04 compared to AML-BFM 98 (70 ± 6 % vs. 45 ± 8 %, P(log rank) = 0.041). Allogeneic hematopoietic stem cell transplantation in first remission did not provide a significant survival benefit (5-year OS 70 ± 11 % vs. 63 ± 6 %; P(Mantel-Byar) = 0.85). Cytogenetic data were available for n = 78 patients. AMKL patients with gain of chromosome 21 had a superior 5-year OS (80 ± 9 %, P(log rank) = 0.034), whereas translocation t(1;22)(p13;q13) was associated with an inferior 5-year event-free survival (38 ± 17 %, P(log rank) = 0.04). However, multivariate analysis showed that treatment response (bone marrow morphology on day 15 and 28) was the only independent prognostic marker (RR = 4.39; 95 % CI, 1.97–9.78). Interestingly, GATA1-mutations were detected in six patients (11 %) without previously known trisomy 21. Thus, AMKL (excluding DS) remains an AML subgroup with inferior outcome. Nevertheless, with intensive therapy regimens, a steep increase in the survival rates was achieved. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00277-015-2383-2) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2015-04-28 2015 /pmc/articles/PMC4488462/ /pubmed/25913479 http://dx.doi.org/10.1007/s00277-015-2383-2 Text en © The Author(s) 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Schweitzer, Jana Zimmermann, Martin Rasche, Mareike von Neuhoff, Christine Creutzig, Ursula Dworzak, Michael Reinhardt, Dirk Klusmann, Jan-Henning Improved outcome of pediatric patients with acute megakaryoblastic leukemia in the AML-BFM 04 trial |
title | Improved outcome of pediatric patients with acute megakaryoblastic leukemia in the AML-BFM 04 trial |
title_full | Improved outcome of pediatric patients with acute megakaryoblastic leukemia in the AML-BFM 04 trial |
title_fullStr | Improved outcome of pediatric patients with acute megakaryoblastic leukemia in the AML-BFM 04 trial |
title_full_unstemmed | Improved outcome of pediatric patients with acute megakaryoblastic leukemia in the AML-BFM 04 trial |
title_short | Improved outcome of pediatric patients with acute megakaryoblastic leukemia in the AML-BFM 04 trial |
title_sort | improved outcome of pediatric patients with acute megakaryoblastic leukemia in the aml-bfm 04 trial |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4488462/ https://www.ncbi.nlm.nih.gov/pubmed/25913479 http://dx.doi.org/10.1007/s00277-015-2383-2 |
work_keys_str_mv | AT schweitzerjana improvedoutcomeofpediatricpatientswithacutemegakaryoblasticleukemiaintheamlbfm04trial AT zimmermannmartin improvedoutcomeofpediatricpatientswithacutemegakaryoblasticleukemiaintheamlbfm04trial AT raschemareike improvedoutcomeofpediatricpatientswithacutemegakaryoblasticleukemiaintheamlbfm04trial AT vonneuhoffchristine improvedoutcomeofpediatricpatientswithacutemegakaryoblasticleukemiaintheamlbfm04trial AT creutzigursula improvedoutcomeofpediatricpatientswithacutemegakaryoblasticleukemiaintheamlbfm04trial AT dworzakmichael improvedoutcomeofpediatricpatientswithacutemegakaryoblasticleukemiaintheamlbfm04trial AT reinhardtdirk improvedoutcomeofpediatricpatientswithacutemegakaryoblasticleukemiaintheamlbfm04trial AT klusmannjanhenning improvedoutcomeofpediatricpatientswithacutemegakaryoblasticleukemiaintheamlbfm04trial |