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PARP inhibitor combinations in prostate cancer

Polyadenosine-diphosphate-ribose polymerase (PARP) inhibitors cause deoxyribonucleic acid (DNA) damage that can be lethal to cells with deficient repair mechanisms. A number of PARP inhibitors are being tested as treatments for men with prostate cancer, both as monotherapies and in combinations that...

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Autor principal: Pezaro, Carmel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7081465/
https://www.ncbi.nlm.nih.gov/pubmed/32215055
http://dx.doi.org/10.1177/1758835919897537
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author Pezaro, Carmel
author_facet Pezaro, Carmel
author_sort Pezaro, Carmel
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description Polyadenosine-diphosphate-ribose polymerase (PARP) inhibitors cause deoxyribonucleic acid (DNA) damage that can be lethal to cells with deficient repair mechanisms. A number of PARP inhibitors are being tested as treatments for men with prostate cancer, both as monotherapies and in combinations that are based on purported synergies in treatment effect. While the initial single-agent development focused on men with identified deficiencies in DNA-repair pathways, broader patient populations are being considered for combination approaches. This review summarizes the current clinical development of PARP inhibitors and explores the rationale for novel combination strategies.
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spelling pubmed-70814652020-03-25 PARP inhibitor combinations in prostate cancer Pezaro, Carmel Ther Adv Med Oncol Challenging Dogma: New Evidence to Guide Practice in Urologic Oncology Polyadenosine-diphosphate-ribose polymerase (PARP) inhibitors cause deoxyribonucleic acid (DNA) damage that can be lethal to cells with deficient repair mechanisms. A number of PARP inhibitors are being tested as treatments for men with prostate cancer, both as monotherapies and in combinations that are based on purported synergies in treatment effect. While the initial single-agent development focused on men with identified deficiencies in DNA-repair pathways, broader patient populations are being considered for combination approaches. This review summarizes the current clinical development of PARP inhibitors and explores the rationale for novel combination strategies. SAGE Publications 2020-03-18 /pmc/articles/PMC7081465/ /pubmed/32215055 http://dx.doi.org/10.1177/1758835919897537 Text en © The Author(s), 2020 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Challenging Dogma: New Evidence to Guide Practice in Urologic Oncology
Pezaro, Carmel
PARP inhibitor combinations in prostate cancer
title PARP inhibitor combinations in prostate cancer
title_full PARP inhibitor combinations in prostate cancer
title_fullStr PARP inhibitor combinations in prostate cancer
title_full_unstemmed PARP inhibitor combinations in prostate cancer
title_short PARP inhibitor combinations in prostate cancer
title_sort parp inhibitor combinations in prostate cancer
topic Challenging Dogma: New Evidence to Guide Practice in Urologic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7081465/
https://www.ncbi.nlm.nih.gov/pubmed/32215055
http://dx.doi.org/10.1177/1758835919897537
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