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Updates on drug discovery in ovarian cancer

Drug discovery in the ovarian cancer arena continues to launch important new clinical trials. Many biologic agents are being studied in phase II and phase III clinical trials for recurrent disease. These agents include compounds that disrupt angiogenesis through a variety of mechanisms. Other oncoge...

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Detalles Bibliográficos
Autores principales: Gibson, Steven J, Tewari, Krishnansu S, Monk, Bradley J, Chase, Dana M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4878024/
https://www.ncbi.nlm.nih.gov/pubmed/27231556
http://dx.doi.org/10.1186/2053-6844-1-3
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author Gibson, Steven J
Tewari, Krishnansu S
Monk, Bradley J
Chase, Dana M
author_facet Gibson, Steven J
Tewari, Krishnansu S
Monk, Bradley J
Chase, Dana M
author_sort Gibson, Steven J
collection PubMed
description Drug discovery in the ovarian cancer arena continues to launch important new clinical trials. Many biologic agents are being studied in phase II and phase III clinical trials for recurrent disease. These agents include compounds that disrupt angiogenesis through a variety of mechanisms. Other oncogenic pathways are also specifically targeted such as PARP, MEK, and topoisomerase inhibitors which are currently being studied in phase III trials. Various cytotoxic agents, as well as therapeutic vaccines, are also under investigation, and continue to demonstrate promising new data. The relevant agents in the treatment of ovarian cancer which have demonstrated positive phase II activity will be discussed. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/2053-6844-1-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-48780242016-05-26 Updates on drug discovery in ovarian cancer Gibson, Steven J Tewari, Krishnansu S Monk, Bradley J Chase, Dana M Gynecol Oncol Res Pract Review Drug discovery in the ovarian cancer arena continues to launch important new clinical trials. Many biologic agents are being studied in phase II and phase III clinical trials for recurrent disease. These agents include compounds that disrupt angiogenesis through a variety of mechanisms. Other oncogenic pathways are also specifically targeted such as PARP, MEK, and topoisomerase inhibitors which are currently being studied in phase III trials. Various cytotoxic agents, as well as therapeutic vaccines, are also under investigation, and continue to demonstrate promising new data. The relevant agents in the treatment of ovarian cancer which have demonstrated positive phase II activity will be discussed. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/2053-6844-1-3) contains supplementary material, which is available to authorized users. BioMed Central 2014-09-30 /pmc/articles/PMC4878024/ /pubmed/27231556 http://dx.doi.org/10.1186/2053-6844-1-3 Text en © Gibson et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Gibson, Steven J
Tewari, Krishnansu S
Monk, Bradley J
Chase, Dana M
Updates on drug discovery in ovarian cancer
title Updates on drug discovery in ovarian cancer
title_full Updates on drug discovery in ovarian cancer
title_fullStr Updates on drug discovery in ovarian cancer
title_full_unstemmed Updates on drug discovery in ovarian cancer
title_short Updates on drug discovery in ovarian cancer
title_sort updates on drug discovery in ovarian cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4878024/
https://www.ncbi.nlm.nih.gov/pubmed/27231556
http://dx.doi.org/10.1186/2053-6844-1-3
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