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Increments in DNA-thioguanine level during thiopurine-enhanced maintenance therapy of acute lymphoblastic leukemia
Maintenance therapy containing methotrexate and 6-mercapto - purine is essential to cure acute lymphoblastic leukemia (ALL). Cytotoxicity is elicited by incorporation of thioguanine nucleotides into DNA (DNA-TG), and higher leukocyte DNA-TG is associated with increased relapse-free survival. As 6-th...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Fondazione Ferrata Storti
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8561300/ https://www.ncbi.nlm.nih.gov/pubmed/34047177 http://dx.doi.org/10.3324/haematol.2020.278166 |
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author | Larsen, Rikke Hebo Rank, Cecilie Utke Grell, Kathrine Møller, Lisbeth Nørgaard Overgaard, Ulrik Malthe Kampmann, Peter Nersting, Jacob Degn, Matilda Nielsen, Stine Nygaard Holst, Helle Albertsen, Birgitte Klug Wehner, Peder Skov Callesen, Michael Thude Kanerva, Jukka Frandsen, Thomas Leth Als-Nielsen, Bodil Hjalgrim, Lisa Lyngsie Schmiegelow, Kjeld |
author_facet | Larsen, Rikke Hebo Rank, Cecilie Utke Grell, Kathrine Møller, Lisbeth Nørgaard Overgaard, Ulrik Malthe Kampmann, Peter Nersting, Jacob Degn, Matilda Nielsen, Stine Nygaard Holst, Helle Albertsen, Birgitte Klug Wehner, Peder Skov Callesen, Michael Thude Kanerva, Jukka Frandsen, Thomas Leth Als-Nielsen, Bodil Hjalgrim, Lisa Lyngsie Schmiegelow, Kjeld |
author_sort | Larsen, Rikke Hebo |
collection | PubMed |
description | Maintenance therapy containing methotrexate and 6-mercapto - purine is essential to cure acute lymphoblastic leukemia (ALL). Cytotoxicity is elicited by incorporation of thioguanine nucleotides into DNA (DNA-TG), and higher leukocyte DNA-TG is associated with increased relapse-free survival. As 6-thioguanine provides 6- fold higher cytosolic levels of thioguanine nucleotides than does 6- mercapto purine, we added low-dose 6-thioguanine to methotrexate/6- mercapto purine maintenance therapy to explore if this combination results in significantly higher DNA-TG. The target population of the “Thiopurine Enhanced ALL Maintenance therapy” (TEAM) study was 30 patients with non-high-risk ALL, aged 1-45 years on methotrexate/6-mercaptopurine maintenance therapy receiving no other systemic chemotherapy. Incremental doses of 6-thioguanine were added to methotrexate/6-mercaptopurine maintenance therapy (starting 6-thioguanine dose: 2.5 mg/m(2)/day, maximum: 12.5 mg/m(2)/day). The primary endpoint was DNA-TG increments. Thirty-four patients were included, and 30 patients completed maintenance therapy according to the TEAM strategy. Of these 30 patients, 26 (87%) tolerated 10.0-12.5 mg/m(2)/day as the maximum 6-thioguanine dose. TEAM resulted in significantly higher DNA-TG levels compared to those in both TEAM patients before their inclusion in TEAM (on average 251 fmol/mg DNA higher [95% confidence interval: 160-341; P<0.0001]), and with historical patients receiving standard methotrexate/6-mercapto - purine maintenance therapy (on average 272 fmol/mg DNA higher [95% confidence interval: 147-398; P<0.0001]). TEAM did not increase myelotoxicity or hepatotoxicity. In conclusion, TEAM is an innovative and feasible approach to improve maintenance therapy and results in higher DNA-TG levels without inducing additional toxicity. It may therefore be an effective strategy to reduce the risk of ALL relapse through increased DNA-TG. This will be tested in a randomized ALLTogether-1 substudy. |
format | Online Article Text |
id | pubmed-8561300 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Fondazione Ferrata Storti |
record_format | MEDLINE/PubMed |
spelling | pubmed-85613002021-11-10 Increments in DNA-thioguanine level during thiopurine-enhanced maintenance therapy of acute lymphoblastic leukemia Larsen, Rikke Hebo Rank, Cecilie Utke Grell, Kathrine Møller, Lisbeth Nørgaard Overgaard, Ulrik Malthe Kampmann, Peter Nersting, Jacob Degn, Matilda Nielsen, Stine Nygaard Holst, Helle Albertsen, Birgitte Klug Wehner, Peder Skov Callesen, Michael Thude Kanerva, Jukka Frandsen, Thomas Leth Als-Nielsen, Bodil Hjalgrim, Lisa Lyngsie Schmiegelow, Kjeld Haematologica Article Maintenance therapy containing methotrexate and 6-mercapto - purine is essential to cure acute lymphoblastic leukemia (ALL). Cytotoxicity is elicited by incorporation of thioguanine nucleotides into DNA (DNA-TG), and higher leukocyte DNA-TG is associated with increased relapse-free survival. As 6-thioguanine provides 6- fold higher cytosolic levels of thioguanine nucleotides than does 6- mercapto purine, we added low-dose 6-thioguanine to methotrexate/6- mercapto purine maintenance therapy to explore if this combination results in significantly higher DNA-TG. The target population of the “Thiopurine Enhanced ALL Maintenance therapy” (TEAM) study was 30 patients with non-high-risk ALL, aged 1-45 years on methotrexate/6-mercaptopurine maintenance therapy receiving no other systemic chemotherapy. Incremental doses of 6-thioguanine were added to methotrexate/6-mercaptopurine maintenance therapy (starting 6-thioguanine dose: 2.5 mg/m(2)/day, maximum: 12.5 mg/m(2)/day). The primary endpoint was DNA-TG increments. Thirty-four patients were included, and 30 patients completed maintenance therapy according to the TEAM strategy. Of these 30 patients, 26 (87%) tolerated 10.0-12.5 mg/m(2)/day as the maximum 6-thioguanine dose. TEAM resulted in significantly higher DNA-TG levels compared to those in both TEAM patients before their inclusion in TEAM (on average 251 fmol/mg DNA higher [95% confidence interval: 160-341; P<0.0001]), and with historical patients receiving standard methotrexate/6-mercapto - purine maintenance therapy (on average 272 fmol/mg DNA higher [95% confidence interval: 147-398; P<0.0001]). TEAM did not increase myelotoxicity or hepatotoxicity. In conclusion, TEAM is an innovative and feasible approach to improve maintenance therapy and results in higher DNA-TG levels without inducing additional toxicity. It may therefore be an effective strategy to reduce the risk of ALL relapse through increased DNA-TG. This will be tested in a randomized ALLTogether-1 substudy. Fondazione Ferrata Storti 2021-05-27 /pmc/articles/PMC8561300/ /pubmed/34047177 http://dx.doi.org/10.3324/haematol.2020.278166 Text en Copyright© 2021 Ferrata Storti Foundation https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution Noncommercial License (by-nc 4.0) which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Article Larsen, Rikke Hebo Rank, Cecilie Utke Grell, Kathrine Møller, Lisbeth Nørgaard Overgaard, Ulrik Malthe Kampmann, Peter Nersting, Jacob Degn, Matilda Nielsen, Stine Nygaard Holst, Helle Albertsen, Birgitte Klug Wehner, Peder Skov Callesen, Michael Thude Kanerva, Jukka Frandsen, Thomas Leth Als-Nielsen, Bodil Hjalgrim, Lisa Lyngsie Schmiegelow, Kjeld Increments in DNA-thioguanine level during thiopurine-enhanced maintenance therapy of acute lymphoblastic leukemia |
title | Increments in DNA-thioguanine level during thiopurine-enhanced maintenance therapy of acute lymphoblastic leukemia |
title_full | Increments in DNA-thioguanine level during thiopurine-enhanced maintenance therapy of acute lymphoblastic leukemia |
title_fullStr | Increments in DNA-thioguanine level during thiopurine-enhanced maintenance therapy of acute lymphoblastic leukemia |
title_full_unstemmed | Increments in DNA-thioguanine level during thiopurine-enhanced maintenance therapy of acute lymphoblastic leukemia |
title_short | Increments in DNA-thioguanine level during thiopurine-enhanced maintenance therapy of acute lymphoblastic leukemia |
title_sort | increments in dna-thioguanine level during thiopurine-enhanced maintenance therapy of acute lymphoblastic leukemia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8561300/ https://www.ncbi.nlm.nih.gov/pubmed/34047177 http://dx.doi.org/10.3324/haematol.2020.278166 |
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