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Overcoming PARP inhibitor resistance in ovarian cancer: what are the most promising strategies?
PURPOSE: Ovarian cancer is the most lethal gynaecological malignancy. Despite the introduction of bevacizumab, standard chemotherapy has remained largely unchanged and the vast majority of patients will relapse within the first two years of diagnosis. However, results from recent clinical trials dem...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7524817/ https://www.ncbi.nlm.nih.gov/pubmed/32833070 http://dx.doi.org/10.1007/s00404-020-05677-1 |
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author | Klotz, Daniel Martin Wimberger, Pauline |
author_facet | Klotz, Daniel Martin Wimberger, Pauline |
author_sort | Klotz, Daniel Martin |
collection | PubMed |
description | PURPOSE: Ovarian cancer is the most lethal gynaecological malignancy. Despite the introduction of bevacizumab, standard chemotherapy has remained largely unchanged and the vast majority of patients will relapse within the first two years of diagnosis. However, results from recent clinical trials demonstrating clinical benefits of PARP inhibitor treatment are rapidly changing therapeutic options for many patients with ovarian cancer. METHODS: Given the introduction of new therapeutic options in the treatment of ovarian cancer, we critically review key clinical trials, areas of scientific research and its clinical relevance. RESULTS: Most notably, patients with BRCA1/2 mutant ovarian cancer benefit from maintenance treatment with PARP inhibitors after (complete or partial) response to platinum-based chemotherapy. Here, we discuss the mechanism of PARP inhibition, multiple drug resistance mechanisms, including BRCA reverse mutations, altered PARP expression, changes in DNA repair pathways, kinase activation and additional drug targets that may augment PARP inhibition. CONCLUSION: Although the use of PARP inhibitors is a huge step forward, it is apparent that patients, both with and without BRCA-mutant ovarian cancer, will eventually become resistant to PARP inhibitors. Therefore, novel combination therapies may enhance PARP inhibitor efficacy and overcome resistance mechanisms. |
format | Online Article Text |
id | pubmed-7524817 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-75248172020-10-14 Overcoming PARP inhibitor resistance in ovarian cancer: what are the most promising strategies? Klotz, Daniel Martin Wimberger, Pauline Arch Gynecol Obstet Review PURPOSE: Ovarian cancer is the most lethal gynaecological malignancy. Despite the introduction of bevacizumab, standard chemotherapy has remained largely unchanged and the vast majority of patients will relapse within the first two years of diagnosis. However, results from recent clinical trials demonstrating clinical benefits of PARP inhibitor treatment are rapidly changing therapeutic options for many patients with ovarian cancer. METHODS: Given the introduction of new therapeutic options in the treatment of ovarian cancer, we critically review key clinical trials, areas of scientific research and its clinical relevance. RESULTS: Most notably, patients with BRCA1/2 mutant ovarian cancer benefit from maintenance treatment with PARP inhibitors after (complete or partial) response to platinum-based chemotherapy. Here, we discuss the mechanism of PARP inhibition, multiple drug resistance mechanisms, including BRCA reverse mutations, altered PARP expression, changes in DNA repair pathways, kinase activation and additional drug targets that may augment PARP inhibition. CONCLUSION: Although the use of PARP inhibitors is a huge step forward, it is apparent that patients, both with and without BRCA-mutant ovarian cancer, will eventually become resistant to PARP inhibitors. Therefore, novel combination therapies may enhance PARP inhibitor efficacy and overcome resistance mechanisms. Springer Berlin Heidelberg 2020-08-24 2020 /pmc/articles/PMC7524817/ /pubmed/32833070 http://dx.doi.org/10.1007/s00404-020-05677-1 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Review Klotz, Daniel Martin Wimberger, Pauline Overcoming PARP inhibitor resistance in ovarian cancer: what are the most promising strategies? |
title | Overcoming PARP inhibitor resistance in ovarian cancer: what are the most promising strategies? |
title_full | Overcoming PARP inhibitor resistance in ovarian cancer: what are the most promising strategies? |
title_fullStr | Overcoming PARP inhibitor resistance in ovarian cancer: what are the most promising strategies? |
title_full_unstemmed | Overcoming PARP inhibitor resistance in ovarian cancer: what are the most promising strategies? |
title_short | Overcoming PARP inhibitor resistance in ovarian cancer: what are the most promising strategies? |
title_sort | overcoming parp inhibitor resistance in ovarian cancer: what are the most promising strategies? |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7524817/ https://www.ncbi.nlm.nih.gov/pubmed/32833070 http://dx.doi.org/10.1007/s00404-020-05677-1 |
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