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Metronomic chemotherapy

Toxic effects and chemoresistance are major hurdles in chemotherapy and to avoid these problems caused by traditional chemotherapeutic regimens, a new modality of drug administration called “metronomic chemotherapy” has emerged. Such regimen involves the frequent administration of conventional chemo...

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Detalles Bibliográficos
Autor principal: Maiti, Rituparna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4156829/
https://www.ncbi.nlm.nih.gov/pubmed/25210398
http://dx.doi.org/10.4103/0976-500X.136098
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author Maiti, Rituparna
author_facet Maiti, Rituparna
author_sort Maiti, Rituparna
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description Toxic effects and chemoresistance are major hurdles in chemotherapy and to avoid these problems caused by traditional chemotherapeutic regimens, a new modality of drug administration called “metronomic chemotherapy” has emerged. Such regimen involves the frequent administration of conventional chemotherapeutic agents at very low doses to target activated endothelial cells in tumors, the advantages of which include minimal adverse effects and a rare chance of developing acquired drug resistance. Previously it was thought that they act by targeting angiogenesis, but recently additional mechanisms have been discovered which has established metronomic chemotherapy as a type of multi-targeted therapy. The knowledge gained from the preclinical studies of metronomic chemotherapy, along with clinical experience, will help to design better therapeutic protocols against cancer. Detailed pharmacogenomic and pharmacoproteomic studies on tumor endothelial cells and large multi-centered clinical trials, integrating bio-marker analyzes, are needed to investigate and validate the best treatment combinations for each tumor type and patient population.
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spelling pubmed-41568292014-09-10 Metronomic chemotherapy Maiti, Rituparna J Pharmacol Pharmacother Review Article Toxic effects and chemoresistance are major hurdles in chemotherapy and to avoid these problems caused by traditional chemotherapeutic regimens, a new modality of drug administration called “metronomic chemotherapy” has emerged. Such regimen involves the frequent administration of conventional chemotherapeutic agents at very low doses to target activated endothelial cells in tumors, the advantages of which include minimal adverse effects and a rare chance of developing acquired drug resistance. Previously it was thought that they act by targeting angiogenesis, but recently additional mechanisms have been discovered which has established metronomic chemotherapy as a type of multi-targeted therapy. The knowledge gained from the preclinical studies of metronomic chemotherapy, along with clinical experience, will help to design better therapeutic protocols against cancer. Detailed pharmacogenomic and pharmacoproteomic studies on tumor endothelial cells and large multi-centered clinical trials, integrating bio-marker analyzes, are needed to investigate and validate the best treatment combinations for each tumor type and patient population. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4156829/ /pubmed/25210398 http://dx.doi.org/10.4103/0976-500X.136098 Text en Copyright: © Journal of Pharmacology and Pharmacotherapeutics http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Maiti, Rituparna
Metronomic chemotherapy
title Metronomic chemotherapy
title_full Metronomic chemotherapy
title_fullStr Metronomic chemotherapy
title_full_unstemmed Metronomic chemotherapy
title_short Metronomic chemotherapy
title_sort metronomic chemotherapy
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4156829/
https://www.ncbi.nlm.nih.gov/pubmed/25210398
http://dx.doi.org/10.4103/0976-500X.136098
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