A multicenter experience from Lebanon in childhood and adolescent acute myeloid leukemia

Background Acute myeloid leukemia (AML) is a disease with marked heterogeneity. Despite major improvement in outcome, it remains a life-threatening malignancy. Demographic and clinical data on pediatric AML is lacking among the Lebanese population. Purpose We aimed to identify clinical, molecular an...

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Main Author: Farhat, Hussein Z. (author)
Other Authors: Farah, Roula A. (author), Horkos, Jessy G. (author), Bustros, Youssef D. (author), Abla, Oussama (author)
Format: article
Published: 2015
Online Access:http://hdl.handle.net/10725/10527
http://dx.doi.org/10.4084/MJHID.2015.012
http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4283923/
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author Farhat, Hussein Z.
author2 Farah, Roula A.
Horkos, Jessy G.
Bustros, Youssef D.
Abla, Oussama
author2_role author
author
author
author
author_facet Farhat, Hussein Z.
Farah, Roula A.
Horkos, Jessy G.
Bustros, Youssef D.
Abla, Oussama
author_role author
dc.creator.none.fl_str_mv Farhat, Hussein Z.
Farah, Roula A.
Horkos, Jessy G.
Bustros, Youssef D.
Abla, Oussama
dc.date.none.fl_str_mv 2015
2019-05-03T06:57:07Z
2019-05-03T06:57:07Z
2019-05-03
dc.identifier.none.fl_str_mv 2035-3006
http://hdl.handle.net/10725/10527
http://dx.doi.org/10.4084/MJHID.2015.012
Farah, R. A., Horkos, J. G., Bustros, Y. D., Farhat, H. Z., & Abla, O. (2015). A multicenter experience from Lebanon in childhood and adolescent acute myeloid leukemia: high rate of early death in childhood acute promyelocytic leukemia. Mediterranean journal of hematology and infectious diseases, 7(1).
http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4283923/
dc.language.none.fl_str_mv en
dc.relation.none.fl_str_mv Mediterranean journal of hematology and infectious diseases
dc.rights.*.fl_str_mv info:eu-repo/semantics/openAccess
dc.title.none.fl_str_mv A multicenter experience from Lebanon in childhood and adolescent acute myeloid leukemia
high rate of early death in childhood acute promyelocytic leukemia
dc.type.none.fl_str_mv Article
info:eu-repo/semantics/publishedVersion
info:eu-repo/semantics/article
description Background Acute myeloid leukemia (AML) is a disease with marked heterogeneity. Despite major improvement in outcome, it remains a life-threatening malignancy. Demographic and clinical data on pediatric AML is lacking among the Lebanese population. Purpose We aimed to identify clinical, molecular and outcome data in children with AML in Lebanon. Methods A retrospective chart review of children with AML diagnosed in three Lebanese hospitals during the past 8 years was conducted. Results From May 2002 through March 2010, we identified 24 children with AML in Saint George Hospital University Medical Center, University Medical Center Rizk Hospital, and Abou-Jaoude Hospital. Males and females were equally represented; median age at diagnosis was 9 years (range 1–24) and median WBC at diagnosis was 31 × 109/L (range: 2.1–376 × 109/L). Twenty five percent of patients (6 out of 24) had acute promyelocytic leukemia (APL). Karyotype was normal in 33% of patients; t(8;21), inv (16), t(8;9), t(7;11), t(9;11), complex chromosomal abnormality, monosomy 7 and trisomy 8 were the most common cytogenetic abnormalities encountered. Patients were treated on different European and North American protocols. Twelve patients (50%) achieved morphologic CR after cycle 1, 6 of them (50%) had bone marrow relapse within 11 months from diagnosis. Nine patients underwent allogeneic stem cell transplant, and 3 of them are alive at 5 years post-transplant. Early death rate was 16.6% of patients, mainly those with APL and a presenting WBC > 10 × 109/L. Fifty per cent of APL patients had an early death due to DIC despite starting ATRA therapy. Overall, median survival for AML patients who died from disease progression was 25.8 months (range: 1–60 months). Overall disease-free survival was 30.4%. Patients < 10 years of age had a 50% survival rate compared to 0% in patients > 10 years. Conclusions Our report highlights the needs in Lebanon for better supportive care of children with APL, including faster ATRA administration and, aggressive transfusions, easy access to stem cell transplant for high-risk AML patients and the need for a national homogenous treatment strategy for children with AML.
eu_rights_str_mv openAccess
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id LAURepo_f168853c2a0121f74ea09f8f76a83ca2
identifier_str_mv 2035-3006
Farah, R. A., Horkos, J. G., Bustros, Y. D., Farhat, H. Z., & Abla, O. (2015). A multicenter experience from Lebanon in childhood and adolescent acute myeloid leukemia: high rate of early death in childhood acute promyelocytic leukemia. Mediterranean journal of hematology and infectious diseases, 7(1).
language_invalid_str_mv en
network_acronym_str LAURepo
network_name_str Lebanese American University repository
oai_identifier_str oai:laur.lau.edu.lb:10725/10527
publishDate 2015
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spelling A multicenter experience from Lebanon in childhood and adolescent acute myeloid leukemiahigh rate of early death in childhood acute promyelocytic leukemiaFarhat, Hussein Z.Farah, Roula A.Horkos, Jessy G.Bustros, Youssef D.Abla, OussamaBackground Acute myeloid leukemia (AML) is a disease with marked heterogeneity. Despite major improvement in outcome, it remains a life-threatening malignancy. Demographic and clinical data on pediatric AML is lacking among the Lebanese population. Purpose We aimed to identify clinical, molecular and outcome data in children with AML in Lebanon. Methods A retrospective chart review of children with AML diagnosed in three Lebanese hospitals during the past 8 years was conducted. Results From May 2002 through March 2010, we identified 24 children with AML in Saint George Hospital University Medical Center, University Medical Center Rizk Hospital, and Abou-Jaoude Hospital. Males and females were equally represented; median age at diagnosis was 9 years (range 1–24) and median WBC at diagnosis was 31 × 109/L (range: 2.1–376 × 109/L). Twenty five percent of patients (6 out of 24) had acute promyelocytic leukemia (APL). Karyotype was normal in 33% of patients; t(8;21), inv (16), t(8;9), t(7;11), t(9;11), complex chromosomal abnormality, monosomy 7 and trisomy 8 were the most common cytogenetic abnormalities encountered. Patients were treated on different European and North American protocols. Twelve patients (50%) achieved morphologic CR after cycle 1, 6 of them (50%) had bone marrow relapse within 11 months from diagnosis. Nine patients underwent allogeneic stem cell transplant, and 3 of them are alive at 5 years post-transplant. Early death rate was 16.6% of patients, mainly those with APL and a presenting WBC > 10 × 109/L. Fifty per cent of APL patients had an early death due to DIC despite starting ATRA therapy. Overall, median survival for AML patients who died from disease progression was 25.8 months (range: 1–60 months). Overall disease-free survival was 30.4%. Patients < 10 years of age had a 50% survival rate compared to 0% in patients > 10 years. Conclusions Our report highlights the needs in Lebanon for better supportive care of children with APL, including faster ATRA administration and, aggressive transfusions, easy access to stem cell transplant for high-risk AML patients and the need for a national homogenous treatment strategy for children with AML.PublishedN/A2019-05-03T06:57:07Z2019-05-03T06:57:07Z20152019-05-03Articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article2035-3006http://hdl.handle.net/10725/10527http://dx.doi.org/10.4084/MJHID.2015.012Farah, R. A., Horkos, J. G., Bustros, Y. D., Farhat, H. Z., & Abla, O. (2015). A multicenter experience from Lebanon in childhood and adolescent acute myeloid leukemia: high rate of early death in childhood acute promyelocytic leukemia. Mediterranean journal of hematology and infectious diseases, 7(1).http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.phphttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4283923/enMediterranean journal of hematology and infectious diseasesinfo:eu-repo/semantics/openAccessoai:laur.lau.edu.lb:10725/105272021-03-19T10:47:34Z
spellingShingle A multicenter experience from Lebanon in childhood and adolescent acute myeloid leukemia
Farhat, Hussein Z.
status_str publishedVersion
title A multicenter experience from Lebanon in childhood and adolescent acute myeloid leukemia
title_full A multicenter experience from Lebanon in childhood and adolescent acute myeloid leukemia
title_fullStr A multicenter experience from Lebanon in childhood and adolescent acute myeloid leukemia
title_full_unstemmed A multicenter experience from Lebanon in childhood and adolescent acute myeloid leukemia
title_short A multicenter experience from Lebanon in childhood and adolescent acute myeloid leukemia
title_sort A multicenter experience from Lebanon in childhood and adolescent acute myeloid leukemia
url http://hdl.handle.net/10725/10527
http://dx.doi.org/10.4084/MJHID.2015.012
http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4283923/