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Radiation therapy dose and androgen deprivation therapy in localized prostate cancer: a meta-regression of 5-year outcomes in phase III randomized controlled trials

BACKGROUND: While multiple randomized trials have evaluated the benefit of radiation therapy (RT) dose escalation and the use and prolongation of androgen deprivation therapy (ADT) in the treatment of prostate cancer, few studies have evaluated the relative benefit of either form of treatment intens...

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Autores principales: Jiang, Tommy, Markovic, Daniela, Patel, Jay, Juarez, Jesus E., Ma, Ting Martin, Shabsovich, David, Nickols, Nicholas G., Reiter, Robert E., Elashoff, David, Rettig, Matthew B., Zaorsky, Nicholas G., Spratt, Daniel E., Kishan, Amar U.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9018418/
https://www.ncbi.nlm.nih.gov/pubmed/34400799
http://dx.doi.org/10.1038/s41391-021-00432-2
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author Jiang, Tommy
Markovic, Daniela
Patel, Jay
Juarez, Jesus E.
Ma, Ting Martin
Shabsovich, David
Nickols, Nicholas G.
Reiter, Robert E.
Elashoff, David
Rettig, Matthew B.
Zaorsky, Nicholas G.
Spratt, Daniel E.
Kishan, Amar U.
author_facet Jiang, Tommy
Markovic, Daniela
Patel, Jay
Juarez, Jesus E.
Ma, Ting Martin
Shabsovich, David
Nickols, Nicholas G.
Reiter, Robert E.
Elashoff, David
Rettig, Matthew B.
Zaorsky, Nicholas G.
Spratt, Daniel E.
Kishan, Amar U.
author_sort Jiang, Tommy
collection PubMed
description BACKGROUND: While multiple randomized trials have evaluated the benefit of radiation therapy (RT) dose escalation and the use and prolongation of androgen deprivation therapy (ADT) in the treatment of prostate cancer, few studies have evaluated the relative benefit of either form of treatment intensification with each other. Many trials have included treatment strategies that incorporate either high or low dose RT, or short-term or long-term ADT (STADT or LTADT), in one or more trial arms. We sought to compare different forms of treatment intensification of RT in the context of localized prostate cancer. METHODS: Using preferred reporting items for systemic reviews and meta-analyses (PRISMA) guidelines, we collected over 40 phases III clinical trials comparing different forms of RT for localized prostate cancer. We performed a meta-regression of 40 individual trials with 21,429 total patients to allow a comparison of the rates and cumulative proportions of 5-year overall survival (OS), prostate cancer-specific mortality (PCSM), and distant metastasis (DM) for each treatment arm of every trial. RESULTS: Dose-escalation either in the absence or presence of STADT failed to significantly improve any 5-year outcome. In contrast, adding LTADT to low dose RT significantly improved 5-year PCSM (Odds ratio [OR] 0.34, 95% confidence interval [CI] 0.22–0.54, p < 0.001) and DM (OR 0.35, 95% CI 0.20–0.63. p < 0.001) over low dose RT alone. Adding STADT also significantly improved 5-year PCSM over low dose RT alone (OR 0.55, 95% CI 0.41–0.75, p < 0.001). CONCLUSION: While limited by between-study heterogeneity and a lack of individual patient data, this meta-analysis suggests that adding ADT, versus increasing RT dose alone, offers a more consistent improvement in clinical endpoints.
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spelling pubmed-90184182022-04-29 Radiation therapy dose and androgen deprivation therapy in localized prostate cancer: a meta-regression of 5-year outcomes in phase III randomized controlled trials Jiang, Tommy Markovic, Daniela Patel, Jay Juarez, Jesus E. Ma, Ting Martin Shabsovich, David Nickols, Nicholas G. Reiter, Robert E. Elashoff, David Rettig, Matthew B. Zaorsky, Nicholas G. Spratt, Daniel E. Kishan, Amar U. Prostate Cancer Prostatic Dis Brief Communication BACKGROUND: While multiple randomized trials have evaluated the benefit of radiation therapy (RT) dose escalation and the use and prolongation of androgen deprivation therapy (ADT) in the treatment of prostate cancer, few studies have evaluated the relative benefit of either form of treatment intensification with each other. Many trials have included treatment strategies that incorporate either high or low dose RT, or short-term or long-term ADT (STADT or LTADT), in one or more trial arms. We sought to compare different forms of treatment intensification of RT in the context of localized prostate cancer. METHODS: Using preferred reporting items for systemic reviews and meta-analyses (PRISMA) guidelines, we collected over 40 phases III clinical trials comparing different forms of RT for localized prostate cancer. We performed a meta-regression of 40 individual trials with 21,429 total patients to allow a comparison of the rates and cumulative proportions of 5-year overall survival (OS), prostate cancer-specific mortality (PCSM), and distant metastasis (DM) for each treatment arm of every trial. RESULTS: Dose-escalation either in the absence or presence of STADT failed to significantly improve any 5-year outcome. In contrast, adding LTADT to low dose RT significantly improved 5-year PCSM (Odds ratio [OR] 0.34, 95% confidence interval [CI] 0.22–0.54, p < 0.001) and DM (OR 0.35, 95% CI 0.20–0.63. p < 0.001) over low dose RT alone. Adding STADT also significantly improved 5-year PCSM over low dose RT alone (OR 0.55, 95% CI 0.41–0.75, p < 0.001). CONCLUSION: While limited by between-study heterogeneity and a lack of individual patient data, this meta-analysis suggests that adding ADT, versus increasing RT dose alone, offers a more consistent improvement in clinical endpoints. Nature Publishing Group UK 2021-08-16 2022 /pmc/articles/PMC9018418/ /pubmed/34400799 http://dx.doi.org/10.1038/s41391-021-00432-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Brief Communication
Jiang, Tommy
Markovic, Daniela
Patel, Jay
Juarez, Jesus E.
Ma, Ting Martin
Shabsovich, David
Nickols, Nicholas G.
Reiter, Robert E.
Elashoff, David
Rettig, Matthew B.
Zaorsky, Nicholas G.
Spratt, Daniel E.
Kishan, Amar U.
Radiation therapy dose and androgen deprivation therapy in localized prostate cancer: a meta-regression of 5-year outcomes in phase III randomized controlled trials
title Radiation therapy dose and androgen deprivation therapy in localized prostate cancer: a meta-regression of 5-year outcomes in phase III randomized controlled trials
title_full Radiation therapy dose and androgen deprivation therapy in localized prostate cancer: a meta-regression of 5-year outcomes in phase III randomized controlled trials
title_fullStr Radiation therapy dose and androgen deprivation therapy in localized prostate cancer: a meta-regression of 5-year outcomes in phase III randomized controlled trials
title_full_unstemmed Radiation therapy dose and androgen deprivation therapy in localized prostate cancer: a meta-regression of 5-year outcomes in phase III randomized controlled trials
title_short Radiation therapy dose and androgen deprivation therapy in localized prostate cancer: a meta-regression of 5-year outcomes in phase III randomized controlled trials
title_sort radiation therapy dose and androgen deprivation therapy in localized prostate cancer: a meta-regression of 5-year outcomes in phase iii randomized controlled trials
topic Brief Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9018418/
https://www.ncbi.nlm.nih.gov/pubmed/34400799
http://dx.doi.org/10.1038/s41391-021-00432-2
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