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Influence of KIT mutations on prognosis of pediatric patients with core-binding factor acute myeloid leukemia: a systematic review and meta-analysis

BACKGROUND: KIT mutations are common in children with core-binding factor (CBF) acute myeloid leukemia (AML). The relationship between KIT mutations and their prognostic value has generated intense attention during the past years. Although studies have evaluated the role of KIT mutations, their prog...

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Autores principales: Fan, Junjie, Gao, Li, Chen, Jing, Hu, Shaoyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7804481/
https://www.ncbi.nlm.nih.gov/pubmed/33457293
http://dx.doi.org/10.21037/tp-20-102
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author Fan, Junjie
Gao, Li
Chen, Jing
Hu, Shaoyan
author_facet Fan, Junjie
Gao, Li
Chen, Jing
Hu, Shaoyan
author_sort Fan, Junjie
collection PubMed
description BACKGROUND: KIT mutations are common in children with core-binding factor (CBF) acute myeloid leukemia (AML). The relationship between KIT mutations and their prognostic value has generated intense attention during the past years. Although studies have evaluated the role of KIT mutations, their prognostic implications remain unclear. To clarify this issue, we conducted this meta-analysis. METHODS: We electronically searched the PubMed, Embase and Cochrane Library databases. Twelve studies met our selection criteria. These studies involved 1,123 children with CBF-AML including 256 children with KIT mutations. We investigated the effects of KIT mutations on the complete remission (CR), relapse, event-free survival (EFS), disease-free survival (DFS), and overall survival (OS) rates of pediatric CBF-AML patients. RESULTS: KIT mutations were not associated with CR [relative risk: 1.01, 95% confidence interval (CI): 0.94–1.09, P=0.761], but were associated with higher relapse risk [hazard ratio (HR): 1.69, 95% CI: 1.32–2.16, P=0.000], lower OS (HR: 3.05, 95% CI: 1.23–7.60, P=0.016), lower DFS (HR: 1.65, 95% CI: 1.07–2.54, P=0.024), and lower EFS (HR: 3.08, 95% CI: 1.02–9.32, P=0.046). CONCLUSIONS: Our analysis suggested that KIT mutations had an adverse prognostic effect in pediatric CBF-AML patients. The initial diagnostic workup for these patients should include tests for the detection of KIT mutations, and the treatment may need to be adjusted when these mutations are found to be present.
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spelling pubmed-78044812021-01-15 Influence of KIT mutations on prognosis of pediatric patients with core-binding factor acute myeloid leukemia: a systematic review and meta-analysis Fan, Junjie Gao, Li Chen, Jing Hu, Shaoyan Transl Pediatr Original Article BACKGROUND: KIT mutations are common in children with core-binding factor (CBF) acute myeloid leukemia (AML). The relationship between KIT mutations and their prognostic value has generated intense attention during the past years. Although studies have evaluated the role of KIT mutations, their prognostic implications remain unclear. To clarify this issue, we conducted this meta-analysis. METHODS: We electronically searched the PubMed, Embase and Cochrane Library databases. Twelve studies met our selection criteria. These studies involved 1,123 children with CBF-AML including 256 children with KIT mutations. We investigated the effects of KIT mutations on the complete remission (CR), relapse, event-free survival (EFS), disease-free survival (DFS), and overall survival (OS) rates of pediatric CBF-AML patients. RESULTS: KIT mutations were not associated with CR [relative risk: 1.01, 95% confidence interval (CI): 0.94–1.09, P=0.761], but were associated with higher relapse risk [hazard ratio (HR): 1.69, 95% CI: 1.32–2.16, P=0.000], lower OS (HR: 3.05, 95% CI: 1.23–7.60, P=0.016), lower DFS (HR: 1.65, 95% CI: 1.07–2.54, P=0.024), and lower EFS (HR: 3.08, 95% CI: 1.02–9.32, P=0.046). CONCLUSIONS: Our analysis suggested that KIT mutations had an adverse prognostic effect in pediatric CBF-AML patients. The initial diagnostic workup for these patients should include tests for the detection of KIT mutations, and the treatment may need to be adjusted when these mutations are found to be present. AME Publishing Company 2020-12 /pmc/articles/PMC7804481/ /pubmed/33457293 http://dx.doi.org/10.21037/tp-20-102 Text en 2020 Translational Pediatrics. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Fan, Junjie
Gao, Li
Chen, Jing
Hu, Shaoyan
Influence of KIT mutations on prognosis of pediatric patients with core-binding factor acute myeloid leukemia: a systematic review and meta-analysis
title Influence of KIT mutations on prognosis of pediatric patients with core-binding factor acute myeloid leukemia: a systematic review and meta-analysis
title_full Influence of KIT mutations on prognosis of pediatric patients with core-binding factor acute myeloid leukemia: a systematic review and meta-analysis
title_fullStr Influence of KIT mutations on prognosis of pediatric patients with core-binding factor acute myeloid leukemia: a systematic review and meta-analysis
title_full_unstemmed Influence of KIT mutations on prognosis of pediatric patients with core-binding factor acute myeloid leukemia: a systematic review and meta-analysis
title_short Influence of KIT mutations on prognosis of pediatric patients with core-binding factor acute myeloid leukemia: a systematic review and meta-analysis
title_sort influence of kit mutations on prognosis of pediatric patients with core-binding factor acute myeloid leukemia: a systematic review and meta-analysis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7804481/
https://www.ncbi.nlm.nih.gov/pubmed/33457293
http://dx.doi.org/10.21037/tp-20-102
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