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Increasing completion of asparaginase treatment in childhood acute lymphoblastic leukaemia (ALL): summary of an expert panel discussion

Insufficient exposure to asparaginase therapy is a barrier to optimal treatment and survival in childhood acute lymphoblastic leukaemia (ALL). Three important reasons for inactivity or discontinuation of asparaginase therapy are infusion related reactions (IRRs), pancreatitis and life-threatening ce...

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Autores principales: Baruchel, André, Brown, Patrick, Rizzari, Carmelo, Silverman, Lewis, van der Sluis, Inge, Wolthers, Benjamin Ole, Schmiegelow, Kjeld
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7513670/
https://www.ncbi.nlm.nih.gov/pubmed/32967920
http://dx.doi.org/10.1136/esmoopen-2020-000977
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author Baruchel, André
Brown, Patrick
Rizzari, Carmelo
Silverman, Lewis
van der Sluis, Inge
Wolthers, Benjamin Ole
Schmiegelow, Kjeld
author_facet Baruchel, André
Brown, Patrick
Rizzari, Carmelo
Silverman, Lewis
van der Sluis, Inge
Wolthers, Benjamin Ole
Schmiegelow, Kjeld
author_sort Baruchel, André
collection PubMed
description Insufficient exposure to asparaginase therapy is a barrier to optimal treatment and survival in childhood acute lymphoblastic leukaemia (ALL). Three important reasons for inactivity or discontinuation of asparaginase therapy are infusion related reactions (IRRs), pancreatitis and life-threatening central nervous system (CNS). For IRRs, real-time therapeutic drug monitoring (TDM) and premedication are important aspects to be considered. For pancreatitis and CNS thrombosis one key question is if patients should be re-exposed to asparaginase after their occurrence. An expert panel met during the Congress of the International Society for Paediatric Oncology in Lyon in October 2019 to discuss strategies for diminishing the impact of these three toxicities. The panel agreed that TDM is particularly useful for optimising asparaginase treatment and that when a tight pharmacological monitoring programme is established premedication could be implemented more broadly to minimise the risk of IRR. Re-exposure to asparaginase needs to be balanced against the anticipated risk of leukemic relapse. However, more prospective data are needed to give clear recommendations if to re-expose patients to asparaginase after the occurrence of severe pancreatitis and CNS thrombosis.
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spelling pubmed-75136702020-10-05 Increasing completion of asparaginase treatment in childhood acute lymphoblastic leukaemia (ALL): summary of an expert panel discussion Baruchel, André Brown, Patrick Rizzari, Carmelo Silverman, Lewis van der Sluis, Inge Wolthers, Benjamin Ole Schmiegelow, Kjeld ESMO Open Review Insufficient exposure to asparaginase therapy is a barrier to optimal treatment and survival in childhood acute lymphoblastic leukaemia (ALL). Three important reasons for inactivity or discontinuation of asparaginase therapy are infusion related reactions (IRRs), pancreatitis and life-threatening central nervous system (CNS). For IRRs, real-time therapeutic drug monitoring (TDM) and premedication are important aspects to be considered. For pancreatitis and CNS thrombosis one key question is if patients should be re-exposed to asparaginase after their occurrence. An expert panel met during the Congress of the International Society for Paediatric Oncology in Lyon in October 2019 to discuss strategies for diminishing the impact of these three toxicities. The panel agreed that TDM is particularly useful for optimising asparaginase treatment and that when a tight pharmacological monitoring programme is established premedication could be implemented more broadly to minimise the risk of IRR. Re-exposure to asparaginase needs to be balanced against the anticipated risk of leukemic relapse. However, more prospective data are needed to give clear recommendations if to re-expose patients to asparaginase after the occurrence of severe pancreatitis and CNS thrombosis. BMJ Publishing Group 2020-09-23 /pmc/articles/PMC7513670/ /pubmed/32967920 http://dx.doi.org/10.1136/esmoopen-2020-000977 Text en © Author (s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. Published by BMJ on behalf of the European Society for Medical Oncology. http://creativecommons.org/licenses/by-nc/4.0/ http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, any changes made are indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Review
Baruchel, André
Brown, Patrick
Rizzari, Carmelo
Silverman, Lewis
van der Sluis, Inge
Wolthers, Benjamin Ole
Schmiegelow, Kjeld
Increasing completion of asparaginase treatment in childhood acute lymphoblastic leukaemia (ALL): summary of an expert panel discussion
title Increasing completion of asparaginase treatment in childhood acute lymphoblastic leukaemia (ALL): summary of an expert panel discussion
title_full Increasing completion of asparaginase treatment in childhood acute lymphoblastic leukaemia (ALL): summary of an expert panel discussion
title_fullStr Increasing completion of asparaginase treatment in childhood acute lymphoblastic leukaemia (ALL): summary of an expert panel discussion
title_full_unstemmed Increasing completion of asparaginase treatment in childhood acute lymphoblastic leukaemia (ALL): summary of an expert panel discussion
title_short Increasing completion of asparaginase treatment in childhood acute lymphoblastic leukaemia (ALL): summary of an expert panel discussion
title_sort increasing completion of asparaginase treatment in childhood acute lymphoblastic leukaemia (all): summary of an expert panel discussion
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7513670/
https://www.ncbi.nlm.nih.gov/pubmed/32967920
http://dx.doi.org/10.1136/esmoopen-2020-000977
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