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Adjuvant androgen deprivation therapy for prostate cancer treated with radiation therapy

Radiation therapy is a commonly used curative modality for prostate cancer. The addition of androgen deprivation therapy (ADT) increases the curative potential of prostate radiotherapy (RT) in multiple subsets of patients. In addition to having an independent cytotoxic effect, current evidence sugge...

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Detalles Bibliográficos
Autores principales: Siddiqui, Zaid A., Krauss, Daniel J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6043751/
https://www.ncbi.nlm.nih.gov/pubmed/30050798
http://dx.doi.org/10.21037/tau.2018.01.06
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author Siddiqui, Zaid A.
Krauss, Daniel J.
author_facet Siddiqui, Zaid A.
Krauss, Daniel J.
author_sort Siddiqui, Zaid A.
collection PubMed
description Radiation therapy is a commonly used curative modality for prostate cancer. The addition of androgen deprivation therapy (ADT) increases the curative potential of prostate radiotherapy (RT) in multiple subsets of patients. In addition to having an independent cytotoxic effect, current evidence suggests that androgen deprivation synergistically works with radiation therapy by preventing DNA repair. Given the wide-ranging toxicities of this therapy, clinicians must judiciously choose which patients may benefit from ADT and also consider the appropriate length of treatment. With recent advances in RT delivery, higher doses of radiation are currently used when compared with the dose used in historic trials, leading to the unanswered question of how RT dose interacts with ADT. Current and future clinical studies are attempting to further define the appropriate indications and patient populations for which ADT represents a clinically appropriate addition to prostate RT.
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spelling pubmed-60437512018-07-26 Adjuvant androgen deprivation therapy for prostate cancer treated with radiation therapy Siddiqui, Zaid A. Krauss, Daniel J. Transl Androl Urol Review Article Radiation therapy is a commonly used curative modality for prostate cancer. The addition of androgen deprivation therapy (ADT) increases the curative potential of prostate radiotherapy (RT) in multiple subsets of patients. In addition to having an independent cytotoxic effect, current evidence suggests that androgen deprivation synergistically works with radiation therapy by preventing DNA repair. Given the wide-ranging toxicities of this therapy, clinicians must judiciously choose which patients may benefit from ADT and also consider the appropriate length of treatment. With recent advances in RT delivery, higher doses of radiation are currently used when compared with the dose used in historic trials, leading to the unanswered question of how RT dose interacts with ADT. Current and future clinical studies are attempting to further define the appropriate indications and patient populations for which ADT represents a clinically appropriate addition to prostate RT. AME Publishing Company 2018-06 /pmc/articles/PMC6043751/ /pubmed/30050798 http://dx.doi.org/10.21037/tau.2018.01.06 Text en 2018 Translational Andrology and Urology. All rights reserved.
spellingShingle Review Article
Siddiqui, Zaid A.
Krauss, Daniel J.
Adjuvant androgen deprivation therapy for prostate cancer treated with radiation therapy
title Adjuvant androgen deprivation therapy for prostate cancer treated with radiation therapy
title_full Adjuvant androgen deprivation therapy for prostate cancer treated with radiation therapy
title_fullStr Adjuvant androgen deprivation therapy for prostate cancer treated with radiation therapy
title_full_unstemmed Adjuvant androgen deprivation therapy for prostate cancer treated with radiation therapy
title_short Adjuvant androgen deprivation therapy for prostate cancer treated with radiation therapy
title_sort adjuvant androgen deprivation therapy for prostate cancer treated with radiation therapy
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6043751/
https://www.ncbi.nlm.nih.gov/pubmed/30050798
http://dx.doi.org/10.21037/tau.2018.01.06
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