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Modelling of immune response in chronic myeloid leukemia patients suggests potential for treatment reduction prior to cessation
INTRODUCTION: Discontinuation of tyrosine kinase inhibitor (TKI) treatment is emerging as the main therapy goal for Chronic Myeloid Leukemia (CML) patients. The DESTINY trial showed that TKI dose reduction prior to cessation can lead to an increased number of patients achieving sustained treatment f...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9769401/ https://www.ncbi.nlm.nih.gov/pubmed/36568156 http://dx.doi.org/10.3389/fonc.2022.1028871 |
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author | Karg, Elena Baldow, Christoph Zerjatke, Thomas Clark, Richard E. Roeder, Ingo Fassoni, Artur C. Glauche, Ingmar |
author_facet | Karg, Elena Baldow, Christoph Zerjatke, Thomas Clark, Richard E. Roeder, Ingo Fassoni, Artur C. Glauche, Ingmar |
author_sort | Karg, Elena |
collection | PubMed |
description | INTRODUCTION: Discontinuation of tyrosine kinase inhibitor (TKI) treatment is emerging as the main therapy goal for Chronic Myeloid Leukemia (CML) patients. The DESTINY trial showed that TKI dose reduction prior to cessation can lead to an increased number of patients achieving sustained treatment free remission (TFR). However, there has been no systematic investigation to evaluate how dose reduction regimens can further improve the success of TKI stop trials. METHODS: Here, we apply an established mathematical model of CML therapy to investigate different TKI dose reduction schemes prior to therapy cessation and evaluate them with respect to the total amount of drug used and the expected TFR success. RESULTS: Our systematic analysis confirms clinical findings that the overall time of TKI treatment is a major determinant of TFR success, while highlighting that lower dose TKI treatment for the same duration is equally sufficient for many patients. Our results further suggest that a stepwise dose reduction prior to TKI cessation can increase the success rate of TFR, while substantially reducing the amount of administered TKI. DISCUSSION: Our findings illustrate the potential of dose reduction schemes prior to treatment cessation and suggest corresponding and clinically testable strategies that are applicable to many CML patients. |
format | Online Article Text |
id | pubmed-9769401 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97694012022-12-22 Modelling of immune response in chronic myeloid leukemia patients suggests potential for treatment reduction prior to cessation Karg, Elena Baldow, Christoph Zerjatke, Thomas Clark, Richard E. Roeder, Ingo Fassoni, Artur C. Glauche, Ingmar Front Oncol Oncology INTRODUCTION: Discontinuation of tyrosine kinase inhibitor (TKI) treatment is emerging as the main therapy goal for Chronic Myeloid Leukemia (CML) patients. The DESTINY trial showed that TKI dose reduction prior to cessation can lead to an increased number of patients achieving sustained treatment free remission (TFR). However, there has been no systematic investigation to evaluate how dose reduction regimens can further improve the success of TKI stop trials. METHODS: Here, we apply an established mathematical model of CML therapy to investigate different TKI dose reduction schemes prior to therapy cessation and evaluate them with respect to the total amount of drug used and the expected TFR success. RESULTS: Our systematic analysis confirms clinical findings that the overall time of TKI treatment is a major determinant of TFR success, while highlighting that lower dose TKI treatment for the same duration is equally sufficient for many patients. Our results further suggest that a stepwise dose reduction prior to TKI cessation can increase the success rate of TFR, while substantially reducing the amount of administered TKI. DISCUSSION: Our findings illustrate the potential of dose reduction schemes prior to treatment cessation and suggest corresponding and clinically testable strategies that are applicable to many CML patients. Frontiers Media S.A. 2022-12-06 /pmc/articles/PMC9769401/ /pubmed/36568156 http://dx.doi.org/10.3389/fonc.2022.1028871 Text en Copyright © 2022 Karg, Baldow, Zerjatke, Clark, Roeder, Fassoni and Glauche https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Karg, Elena Baldow, Christoph Zerjatke, Thomas Clark, Richard E. Roeder, Ingo Fassoni, Artur C. Glauche, Ingmar Modelling of immune response in chronic myeloid leukemia patients suggests potential for treatment reduction prior to cessation |
title | Modelling of immune response in chronic myeloid leukemia patients suggests potential for treatment reduction prior to cessation |
title_full | Modelling of immune response in chronic myeloid leukemia patients suggests potential for treatment reduction prior to cessation |
title_fullStr | Modelling of immune response in chronic myeloid leukemia patients suggests potential for treatment reduction prior to cessation |
title_full_unstemmed | Modelling of immune response in chronic myeloid leukemia patients suggests potential for treatment reduction prior to cessation |
title_short | Modelling of immune response in chronic myeloid leukemia patients suggests potential for treatment reduction prior to cessation |
title_sort | modelling of immune response in chronic myeloid leukemia patients suggests potential for treatment reduction prior to cessation |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9769401/ https://www.ncbi.nlm.nih.gov/pubmed/36568156 http://dx.doi.org/10.3389/fonc.2022.1028871 |
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