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Efficacy of imatinib mesylate-based front-line therapy in pediatric chronic myelogenous leukemia
PURPOSE: Despite the established role of imatinib (IM) in chronic myelogenous leukemia (CML) in adults, there are few reports on its efficacy in children. In this study, we compared the outcomes of children with CML before and after the advent of IM-based treatment. METHODS: The study cohort consist...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Pediatric Society
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3764259/ https://www.ncbi.nlm.nih.gov/pubmed/24019845 http://dx.doi.org/10.3345/kjp.2013.56.8.343 |
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author | Oh, Hyun Jin Cho, Mun Sung Lee, Jae Wook Jang, Pil-Sang Chung, Nack-Gyun Cho, Bin Kim, Hack-Ki |
author_facet | Oh, Hyun Jin Cho, Mun Sung Lee, Jae Wook Jang, Pil-Sang Chung, Nack-Gyun Cho, Bin Kim, Hack-Ki |
author_sort | Oh, Hyun Jin |
collection | PubMed |
description | PURPOSE: Despite the established role of imatinib (IM) in chronic myelogenous leukemia (CML) in adults, there are few reports on its efficacy in children. In this study, we compared the outcomes of children with CML before and after the advent of IM-based treatment. METHODS: The study cohort consisted of 52 patients treated for CML at the Department of Pediatrics, The Catholic University of Korea from January 1995 to October 2010. Patients were divided and analyzed according to the preImatinib group (pre-IMG) and imatinib group (IMG). RESULTS: Median age at diagnosis for the overall cohort (pre-IMG, n=27; IMG, n=25) was 9 years, with a median follow-up duration of survivors of 84 months. Except for 5 patients in the IMG, all were diagnosed in chronic phase (CP). The overall survival (OS) of patients diagnosed in CP was 45.7% and 89.7% for pre-IMG and IMG, respectively (P=0.025). The OS of hematopoietic stem cell transplantation (HSCT) recipients in the 2 groups was similar, but the OS of patients diagnosed in CP who did not receive HSCT was superior in IMG (91.7% vs. 16.7%, P=0.014). Of the 12 patients in IMG who remained on IM without HSCT, 2 showed disease progression, compared to 11 of 12 in pre-IMG. No difference was observed in the progression free survival (PFS) of matched donor HSCT recipients and IM-based treatment recipients. CONCLUSION: Similar PFS of patients treated with IM and those who received matched donor HSCT underscore the potential of IM as effective first-line treatment in childhood CML. |
format | Online Article Text |
id | pubmed-3764259 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | The Korean Pediatric Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-37642592013-09-09 Efficacy of imatinib mesylate-based front-line therapy in pediatric chronic myelogenous leukemia Oh, Hyun Jin Cho, Mun Sung Lee, Jae Wook Jang, Pil-Sang Chung, Nack-Gyun Cho, Bin Kim, Hack-Ki Korean J Pediatr Original Article PURPOSE: Despite the established role of imatinib (IM) in chronic myelogenous leukemia (CML) in adults, there are few reports on its efficacy in children. In this study, we compared the outcomes of children with CML before and after the advent of IM-based treatment. METHODS: The study cohort consisted of 52 patients treated for CML at the Department of Pediatrics, The Catholic University of Korea from January 1995 to October 2010. Patients were divided and analyzed according to the preImatinib group (pre-IMG) and imatinib group (IMG). RESULTS: Median age at diagnosis for the overall cohort (pre-IMG, n=27; IMG, n=25) was 9 years, with a median follow-up duration of survivors of 84 months. Except for 5 patients in the IMG, all were diagnosed in chronic phase (CP). The overall survival (OS) of patients diagnosed in CP was 45.7% and 89.7% for pre-IMG and IMG, respectively (P=0.025). The OS of hematopoietic stem cell transplantation (HSCT) recipients in the 2 groups was similar, but the OS of patients diagnosed in CP who did not receive HSCT was superior in IMG (91.7% vs. 16.7%, P=0.014). Of the 12 patients in IMG who remained on IM without HSCT, 2 showed disease progression, compared to 11 of 12 in pre-IMG. No difference was observed in the progression free survival (PFS) of matched donor HSCT recipients and IM-based treatment recipients. CONCLUSION: Similar PFS of patients treated with IM and those who received matched donor HSCT underscore the potential of IM as effective first-line treatment in childhood CML. The Korean Pediatric Society 2013-08 2013-08-27 /pmc/articles/PMC3764259/ /pubmed/24019845 http://dx.doi.org/10.3345/kjp.2013.56.8.343 Text en Copyright © 2013 by The Korean Pediatric Society http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Oh, Hyun Jin Cho, Mun Sung Lee, Jae Wook Jang, Pil-Sang Chung, Nack-Gyun Cho, Bin Kim, Hack-Ki Efficacy of imatinib mesylate-based front-line therapy in pediatric chronic myelogenous leukemia |
title | Efficacy of imatinib mesylate-based front-line therapy in pediatric chronic myelogenous leukemia |
title_full | Efficacy of imatinib mesylate-based front-line therapy in pediatric chronic myelogenous leukemia |
title_fullStr | Efficacy of imatinib mesylate-based front-line therapy in pediatric chronic myelogenous leukemia |
title_full_unstemmed | Efficacy of imatinib mesylate-based front-line therapy in pediatric chronic myelogenous leukemia |
title_short | Efficacy of imatinib mesylate-based front-line therapy in pediatric chronic myelogenous leukemia |
title_sort | efficacy of imatinib mesylate-based front-line therapy in pediatric chronic myelogenous leukemia |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3764259/ https://www.ncbi.nlm.nih.gov/pubmed/24019845 http://dx.doi.org/10.3345/kjp.2013.56.8.343 |
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