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Mortality Risk for Docetaxel-Treated, High-Grade Prostate Cancer With Low PSA Levels: A Meta-Analysis

IMPORTANCE: Patients with high-grade prostate cancer with low levels of prostate-specific antigen (PSA; <4 ng/mL) are at high risk of mortality, necessitating an improved treatment paradigm. OBJECTIVE: To assess for these patients whether adding docetaxel to standard of care (SOC) treatment is as...

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Autores principales: Mahal, Brandon A., Kwak, Lucia, Xie, Wanling, Eastham, James A., James, Nicholas D., Sandler, Howard M., Feng, Felix Y., Brihoum, Meryem, Fizazi, Karim, Sweeney, Christopher, Ravi, Praful, D’Amico, Anthony V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Medical Association 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10620614/
https://www.ncbi.nlm.nih.gov/pubmed/37910103
http://dx.doi.org/10.1001/jamanetworkopen.2023.40787
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author Mahal, Brandon A.
Kwak, Lucia
Xie, Wanling
Eastham, James A.
James, Nicholas D.
Sandler, Howard M.
Feng, Felix Y.
Brihoum, Meryem
Fizazi, Karim
Sweeney, Christopher
Ravi, Praful
D’Amico, Anthony V.
author_facet Mahal, Brandon A.
Kwak, Lucia
Xie, Wanling
Eastham, James A.
James, Nicholas D.
Sandler, Howard M.
Feng, Felix Y.
Brihoum, Meryem
Fizazi, Karim
Sweeney, Christopher
Ravi, Praful
D’Amico, Anthony V.
author_sort Mahal, Brandon A.
collection PubMed
description IMPORTANCE: Patients with high-grade prostate cancer with low levels of prostate-specific antigen (PSA; <4 ng/mL) are at high risk of mortality, necessitating an improved treatment paradigm. OBJECTIVE: To assess for these patients whether adding docetaxel to standard of care (SOC) treatment is associated with decreased prostate cancer–specific mortality (PCSM) and all-cause mortality (ACM). DATA SOURCES: PubMed search from 2000 to 2022. STUDY SELECTION: Five prospective randomized clinical trials (RCTs) performed in the US, France, and the United Kingdom evaluating SOC treatment with radiotherapy and androgen deprivation therapy (ADT) or with radical prostatectomy vs SOC plus docetaxel. DATA EXTRACTION AND SYNTHESIS: Individual data were included from patients with nonmetastatic prostate cancer, a PSA level of less than 4 ng/mL, and a Gleason score of 8 to 10. Patients initiated treatment between February 21, 2006, and December 31, 2015 (median follow-up, 7.1 [IQR, 5.4-9.9] years). Data were analyzed on December 16, 2022. MAIN OUTCOMES AND MEASURES: Hazard ratio (HR) of ACM and subdistribution HR (sHR) of PCSM adjusted for performance status (1 vs 0 or good health), Gleason score (9 or 10 vs 8), tumor category (T3-T4 vs T1-T2 or TX), and duration of ADT (2 years vs 4-6 months). RESULTS: From a cohort of 2184 patients, 145 patients (6.6%) in 4 RCTs were eligible (median age, 63 [IQR, 46-67] years). Thirty-one patients died, and of these deaths, 22 were due to prostate cancer. Performance status was 0 for 139 patients (95.9%) and 1 for 6 patients (4.1%). A reduced but nonsignificant risk of ACM (HR, 0.51 [95% CI, 0.24-1.09]) and PCSM (sHR, 0.42 [95% CI, 0.17-1.02]) was associated with patients randomized to SOC plus docetaxel compared with SOC. The risk reduction in ACM (HR, 0.46 [95% CI, 0.21-1.02]) was more pronounced among patients with a performance status of 0 and was significant for PCSM (sHR, 0.30 [95% CI, 0.11-0.86]). CONCLUSIONS AND RELEVANCE: Adding docetaxel to SOC treatment for patients who are in otherwise good health with a PSA level of less than 4 ng/mL and a Gleason score of 8 to 10 was associated with a significant reduction in PCSM and therefore has the potential to improve prognosis.
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spelling pubmed-106206142023-11-03 Mortality Risk for Docetaxel-Treated, High-Grade Prostate Cancer With Low PSA Levels: A Meta-Analysis Mahal, Brandon A. Kwak, Lucia Xie, Wanling Eastham, James A. James, Nicholas D. Sandler, Howard M. Feng, Felix Y. Brihoum, Meryem Fizazi, Karim Sweeney, Christopher Ravi, Praful D’Amico, Anthony V. JAMA Netw Open Original Investigation IMPORTANCE: Patients with high-grade prostate cancer with low levels of prostate-specific antigen (PSA; <4 ng/mL) are at high risk of mortality, necessitating an improved treatment paradigm. OBJECTIVE: To assess for these patients whether adding docetaxel to standard of care (SOC) treatment is associated with decreased prostate cancer–specific mortality (PCSM) and all-cause mortality (ACM). DATA SOURCES: PubMed search from 2000 to 2022. STUDY SELECTION: Five prospective randomized clinical trials (RCTs) performed in the US, France, and the United Kingdom evaluating SOC treatment with radiotherapy and androgen deprivation therapy (ADT) or with radical prostatectomy vs SOC plus docetaxel. DATA EXTRACTION AND SYNTHESIS: Individual data were included from patients with nonmetastatic prostate cancer, a PSA level of less than 4 ng/mL, and a Gleason score of 8 to 10. Patients initiated treatment between February 21, 2006, and December 31, 2015 (median follow-up, 7.1 [IQR, 5.4-9.9] years). Data were analyzed on December 16, 2022. MAIN OUTCOMES AND MEASURES: Hazard ratio (HR) of ACM and subdistribution HR (sHR) of PCSM adjusted for performance status (1 vs 0 or good health), Gleason score (9 or 10 vs 8), tumor category (T3-T4 vs T1-T2 or TX), and duration of ADT (2 years vs 4-6 months). RESULTS: From a cohort of 2184 patients, 145 patients (6.6%) in 4 RCTs were eligible (median age, 63 [IQR, 46-67] years). Thirty-one patients died, and of these deaths, 22 were due to prostate cancer. Performance status was 0 for 139 patients (95.9%) and 1 for 6 patients (4.1%). A reduced but nonsignificant risk of ACM (HR, 0.51 [95% CI, 0.24-1.09]) and PCSM (sHR, 0.42 [95% CI, 0.17-1.02]) was associated with patients randomized to SOC plus docetaxel compared with SOC. The risk reduction in ACM (HR, 0.46 [95% CI, 0.21-1.02]) was more pronounced among patients with a performance status of 0 and was significant for PCSM (sHR, 0.30 [95% CI, 0.11-0.86]). CONCLUSIONS AND RELEVANCE: Adding docetaxel to SOC treatment for patients who are in otherwise good health with a PSA level of less than 4 ng/mL and a Gleason score of 8 to 10 was associated with a significant reduction in PCSM and therefore has the potential to improve prognosis. American Medical Association 2023-11-01 /pmc/articles/PMC10620614/ /pubmed/37910103 http://dx.doi.org/10.1001/jamanetworkopen.2023.40787 Text en Copyright 2023 Mahal BA et al. JAMA Network Open. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the CC-BY License.
spellingShingle Original Investigation
Mahal, Brandon A.
Kwak, Lucia
Xie, Wanling
Eastham, James A.
James, Nicholas D.
Sandler, Howard M.
Feng, Felix Y.
Brihoum, Meryem
Fizazi, Karim
Sweeney, Christopher
Ravi, Praful
D’Amico, Anthony V.
Mortality Risk for Docetaxel-Treated, High-Grade Prostate Cancer With Low PSA Levels: A Meta-Analysis
title Mortality Risk for Docetaxel-Treated, High-Grade Prostate Cancer With Low PSA Levels: A Meta-Analysis
title_full Mortality Risk for Docetaxel-Treated, High-Grade Prostate Cancer With Low PSA Levels: A Meta-Analysis
title_fullStr Mortality Risk for Docetaxel-Treated, High-Grade Prostate Cancer With Low PSA Levels: A Meta-Analysis
title_full_unstemmed Mortality Risk for Docetaxel-Treated, High-Grade Prostate Cancer With Low PSA Levels: A Meta-Analysis
title_short Mortality Risk for Docetaxel-Treated, High-Grade Prostate Cancer With Low PSA Levels: A Meta-Analysis
title_sort mortality risk for docetaxel-treated, high-grade prostate cancer with low psa levels: a meta-analysis
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10620614/
https://www.ncbi.nlm.nih.gov/pubmed/37910103
http://dx.doi.org/10.1001/jamanetworkopen.2023.40787
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