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Topoisomerase I inhibitors: the relevance of prolonged exposure for present clinical development.
Topoisomerase I inhibitors constitute a new class of anti-cancer agents. Recently, topotecan and irinotecan were registered for clinical use in ovarian cancer and colorectal cancer respectively. Cytotoxicity of topoisomerase I inhibitors is S-phase specific, and in vitro and in vivo studies have sug...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1997
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2228255/ https://www.ncbi.nlm.nih.gov/pubmed/9328159 |
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author | Gerrits, C. J. de Jonge, M. J. Schellens, J. H. Stoter, G. Verweij, J. |
author_facet | Gerrits, C. J. de Jonge, M. J. Schellens, J. H. Stoter, G. Verweij, J. |
author_sort | Gerrits, C. J. |
collection | PubMed |
description | Topoisomerase I inhibitors constitute a new class of anti-cancer agents. Recently, topotecan and irinotecan were registered for clinical use in ovarian cancer and colorectal cancer respectively. Cytotoxicity of topoisomerase I inhibitors is S-phase specific, and in vitro and in vivo studies have suggested that, for efficacy, prolonged exposure might be more important than short-term exposure to high concentration. Clinical development of those topoisomerase I inhibitors that have reached this stage is also focused on schedules aiming to achieve prolonged exposure. In this review, we summarize all published preclinical studies on this topic for topoisomerase I inhibitors in clinical development, namely 20-S-camptothecin, 9-nitro-camptothecin, 9-amino-camptothecin, topotecan, irinotecan and GI147211. In addition, preliminary data on clinical studies concerning this topic are also reviewed. The data suggest that prolonged exposure may indeed be relevant for anti-tumour activity. However, the optimal schedule is yet to be determined. Finally, clinical data are yet too immature to draw definitive conclusions. |
format | Text |
id | pubmed-2228255 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1997 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-22282552009-09-10 Topoisomerase I inhibitors: the relevance of prolonged exposure for present clinical development. Gerrits, C. J. de Jonge, M. J. Schellens, J. H. Stoter, G. Verweij, J. Br J Cancer Research Article Topoisomerase I inhibitors constitute a new class of anti-cancer agents. Recently, topotecan and irinotecan were registered for clinical use in ovarian cancer and colorectal cancer respectively. Cytotoxicity of topoisomerase I inhibitors is S-phase specific, and in vitro and in vivo studies have suggested that, for efficacy, prolonged exposure might be more important than short-term exposure to high concentration. Clinical development of those topoisomerase I inhibitors that have reached this stage is also focused on schedules aiming to achieve prolonged exposure. In this review, we summarize all published preclinical studies on this topic for topoisomerase I inhibitors in clinical development, namely 20-S-camptothecin, 9-nitro-camptothecin, 9-amino-camptothecin, topotecan, irinotecan and GI147211. In addition, preliminary data on clinical studies concerning this topic are also reviewed. The data suggest that prolonged exposure may indeed be relevant for anti-tumour activity. However, the optimal schedule is yet to be determined. Finally, clinical data are yet too immature to draw definitive conclusions. Nature Publishing Group 1997 /pmc/articles/PMC2228255/ /pubmed/9328159 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Research Article Gerrits, C. J. de Jonge, M. J. Schellens, J. H. Stoter, G. Verweij, J. Topoisomerase I inhibitors: the relevance of prolonged exposure for present clinical development. |
title | Topoisomerase I inhibitors: the relevance of prolonged exposure for present clinical development. |
title_full | Topoisomerase I inhibitors: the relevance of prolonged exposure for present clinical development. |
title_fullStr | Topoisomerase I inhibitors: the relevance of prolonged exposure for present clinical development. |
title_full_unstemmed | Topoisomerase I inhibitors: the relevance of prolonged exposure for present clinical development. |
title_short | Topoisomerase I inhibitors: the relevance of prolonged exposure for present clinical development. |
title_sort | topoisomerase i inhibitors: the relevance of prolonged exposure for present clinical development. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2228255/ https://www.ncbi.nlm.nih.gov/pubmed/9328159 |
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