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Pediatric haematopoiesis and related malignancies

Survival after acute paediatric (0–14 years), adolescent (15–19 years) and young adult (20–39 years) leukaemia has improved substantially over the last five decades, particularly for acute lymphoblastic leukaemia (ALL) and acute promyelocytic leukaemia. This progress represents one of the most succe...

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Detalles Bibliográficos
Autores principales: Jin, Mingwei, Xu, Shumei, An, Qi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5494839/
https://www.ncbi.nlm.nih.gov/pubmed/28693128
http://dx.doi.org/10.3892/ol.2017.6106
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author Jin, Mingwei
Xu, Shumei
An, Qi
author_facet Jin, Mingwei
Xu, Shumei
An, Qi
author_sort Jin, Mingwei
collection PubMed
description Survival after acute paediatric (0–14 years), adolescent (15–19 years) and young adult (20–39 years) leukaemia has improved substantially over the last five decades, particularly for acute lymphoblastic leukaemia (ALL) and acute promyelocytic leukaemia. This progress represents one of the most successful achievements in the history of medicine and has been attributed to the development of effective chemotherapy regimens, improvement in supportive care, better risk stratification, use of targeted therapies, and advances in haematopoietic stem cell transplantation. Recent studies have revealed improvement in survival over time for all age groups and subtypes of leukaemia. However, these outcomes varied widely by age and are associated with sociodemographic and clinical factors. The present review concludes that survival and early death after acute leukaemia has greatly improved among young patients. However, inequalities in outcomes remain and are likely a result of multiple factors.
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spelling pubmed-54948392017-07-07 Pediatric haematopoiesis and related malignancies Jin, Mingwei Xu, Shumei An, Qi Oncol Lett Review Survival after acute paediatric (0–14 years), adolescent (15–19 years) and young adult (20–39 years) leukaemia has improved substantially over the last five decades, particularly for acute lymphoblastic leukaemia (ALL) and acute promyelocytic leukaemia. This progress represents one of the most successful achievements in the history of medicine and has been attributed to the development of effective chemotherapy regimens, improvement in supportive care, better risk stratification, use of targeted therapies, and advances in haematopoietic stem cell transplantation. Recent studies have revealed improvement in survival over time for all age groups and subtypes of leukaemia. However, these outcomes varied widely by age and are associated with sociodemographic and clinical factors. The present review concludes that survival and early death after acute leukaemia has greatly improved among young patients. However, inequalities in outcomes remain and are likely a result of multiple factors. D.A. Spandidos 2017-07 2017-04-28 /pmc/articles/PMC5494839/ /pubmed/28693128 http://dx.doi.org/10.3892/ol.2017.6106 Text en Copyright: © Jin et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Review
Jin, Mingwei
Xu, Shumei
An, Qi
Pediatric haematopoiesis and related malignancies
title Pediatric haematopoiesis and related malignancies
title_full Pediatric haematopoiesis and related malignancies
title_fullStr Pediatric haematopoiesis and related malignancies
title_full_unstemmed Pediatric haematopoiesis and related malignancies
title_short Pediatric haematopoiesis and related malignancies
title_sort pediatric haematopoiesis and related malignancies
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5494839/
https://www.ncbi.nlm.nih.gov/pubmed/28693128
http://dx.doi.org/10.3892/ol.2017.6106
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