Systemic therapies for metastatic hormone‐sensitive prostate cancer: network meta‐analysis

Objectives To perform a systematic review and network meta‐analysis to compare the efficacy and safety of currently available treatments for the management of metastatic hormone‐sensitive prostate cancer (mHSPC), as there has been a paradigm shift with the use of next‐generation androgen receptor in...

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Veröffentlicht in:BJU international 2022-04, Vol.129 (4), p.423-433
Hauptverfasser: Mori, Keiichiro, Mostafaei, Hadi, Sari Motlagh, Reza, Pradere, Benjamin, Quhal, Fahad, Laukhtina, Ekaterina, Schuettfort, Victor M., Kramer, Gero, Abufaraj, Mohammad, Karakiewicz, Pierre I., Kimura, Takahiro, Egawa, Shin, Shariat, Shahrokh F.
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container_end_page 433
container_issue 4
container_start_page 423
container_title BJU international
container_volume 129
creator Mori, Keiichiro
Mostafaei, Hadi
Sari Motlagh, Reza
Pradere, Benjamin
Quhal, Fahad
Laukhtina, Ekaterina
Schuettfort, Victor M.
Kramer, Gero
Abufaraj, Mohammad
Karakiewicz, Pierre I.
Kimura, Takahiro
Egawa, Shin
Shariat, Shahrokh F.
description Objectives To perform a systematic review and network meta‐analysis to compare the efficacy and safety of currently available treatments for the management of metastatic hormone‐sensitive prostate cancer (mHSPC), as there has been a paradigm shift with the use of next‐generation androgen receptor inhibitors (ARIs) and docetaxel. Methods Multiple databases were searched for articles published before May 2020 according to the Preferred Reporting Items for Systematic Review and Meta‐analysis extension statement for network meta‐analysis. Studies comparing overall/progression‐free survival (OS/PFS) and/or adverse events (AEs) in patients with mHSPC were eligible. Results Nine studies (N = 9960) were selected, and formal network meta‐analyses were conducted. Abiraterone (hazard ratio [HR] 0.83, 95% credible interval [CrI] 0.76–0.90), docetaxel (HR 0.90, 95% CrI 0.82–0.98), and enzalutamide (HR 0.85, 95% CrI 0.73–0.99) were associated with significantly better OS than androgen‐deprivation therapy (ADT), and abiraterone emerged as the best option. Abiraterone (HR 0.71, 95% CrI 0.67–0.76), apalutamide (HR 0.73, 95% CrI 0.65–0.81), docetaxel (HR 0.84, 95% CrI 0.78–0.90), and enzalutamide (HR 0.67, 95% CrI 0.63–0.71) were associated with significantly better PFS than ADT, and enzalutamide emerged as the best option. Abiraterone (HR 0.85, 95% CrI 0.78–0.93), apalutamide (HR 0.87, 95% CrI 0.77–0.98), and enzalutamide (HR 0.80, 95% CrI 0.73–0.88) were significantly more effective than docetaxel. Regarding AEs, apalutamide was the likely best option among the three ARIs. In patients with low‐volume mHSPC, enzalutamide was the best option in terms of OS and PFS. Conclusions All three ARIs are effective therapies for mHSPC; apalutamide was the best tolerated. All three seemed more effective than docetaxel. These findings may facilitate individualised treatment strategies and inform future comparative trials.
doi_str_mv 10.1111/bju.15507
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Methods Multiple databases were searched for articles published before May 2020 according to the Preferred Reporting Items for Systematic Review and Meta‐analysis extension statement for network meta‐analysis. Studies comparing overall/progression‐free survival (OS/PFS) and/or adverse events (AEs) in patients with mHSPC were eligible. Results Nine studies (N = 9960) were selected, and formal network meta‐analyses were conducted. Abiraterone (hazard ratio [HR] 0.83, 95% credible interval [CrI] 0.76–0.90), docetaxel (HR 0.90, 95% CrI 0.82–0.98), and enzalutamide (HR 0.85, 95% CrI 0.73–0.99) were associated with significantly better OS than androgen‐deprivation therapy (ADT), and abiraterone emerged as the best option. Abiraterone (HR 0.71, 95% CrI 0.67–0.76), apalutamide (HR 0.73, 95% CrI 0.65–0.81), docetaxel (HR 0.84, 95% CrI 0.78–0.90), and enzalutamide (HR 0.67, 95% CrI 0.63–0.71) were associated with significantly better PFS than ADT, and enzalutamide emerged as the best option. Abiraterone (HR 0.85, 95% CrI 0.78–0.93), apalutamide (HR 0.87, 95% CrI 0.77–0.98), and enzalutamide (HR 0.80, 95% CrI 0.73–0.88) were significantly more effective than docetaxel. Regarding AEs, apalutamide was the likely best option among the three ARIs. In patients with low‐volume mHSPC, enzalutamide was the best option in terms of OS and PFS. Conclusions All three ARIs are effective therapies for mHSPC; apalutamide was the best tolerated. All three seemed more effective than docetaxel. These findings may facilitate individualised treatment strategies and inform future comparative trials.</description><identifier>ISSN: 1464-4096</identifier><identifier>EISSN: 1464-410X</identifier><identifier>DOI: 10.1111/bju.15507</identifier><identifier>PMID: 34171173</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Androgen Antagonists - adverse effects ; Androgen Receptor Antagonists ; androgen receptor inhibitors ; Androgen receptors ; Androgens ; Clinical trials ; docetaxel ; Docetaxel - therapeutic use ; Hormones ; Humans ; Male ; Meta-analysis ; Metastases ; Metastasis ; metastatic hormone‐sensitive prostate cancer ; Network Meta-Analysis ; Patients ; PCSM ; Prostate cancer ; ProstateCancer ; Prostatic Neoplasms - pathology ; Review ; Reviews ; Systematic review</subject><ispartof>BJU international, 2022-04, Vol.129 (4), p.423-433</ispartof><rights>2021 The Authors. published by John Wiley &amp; Sons Ltd on behalf of BJU International</rights><rights>2021 The Authors. BJU International published by John Wiley &amp; Sons Ltd on behalf of BJU International.</rights><rights>2021. This article is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5097-14f75b83595c7d5e1009fa10cdb137f4c3f77bc64e90bfb559495eaa87d2e093</citedby><cites>FETCH-LOGICAL-c5097-14f75b83595c7d5e1009fa10cdb137f4c3f77bc64e90bfb559495eaa87d2e093</cites><orcidid>0000-0002-6147-6569 ; 0000-0001-5596-1771 ; 0000-0002-8953-0272 ; 0000-0002-6603-6319 ; 0000-0002-3819-9911</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fbju.15507$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fbju.15507$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34171173$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mori, Keiichiro</creatorcontrib><creatorcontrib>Mostafaei, Hadi</creatorcontrib><creatorcontrib>Sari Motlagh, Reza</creatorcontrib><creatorcontrib>Pradere, Benjamin</creatorcontrib><creatorcontrib>Quhal, Fahad</creatorcontrib><creatorcontrib>Laukhtina, Ekaterina</creatorcontrib><creatorcontrib>Schuettfort, Victor M.</creatorcontrib><creatorcontrib>Kramer, Gero</creatorcontrib><creatorcontrib>Abufaraj, Mohammad</creatorcontrib><creatorcontrib>Karakiewicz, Pierre I.</creatorcontrib><creatorcontrib>Kimura, Takahiro</creatorcontrib><creatorcontrib>Egawa, Shin</creatorcontrib><creatorcontrib>Shariat, Shahrokh F.</creatorcontrib><title>Systemic therapies for metastatic hormone‐sensitive prostate cancer: network meta‐analysis</title><title>BJU international</title><addtitle>BJU Int</addtitle><description>Objectives To perform a systematic review and network meta‐analysis to compare the efficacy and safety of currently available treatments for the management of metastatic hormone‐sensitive prostate cancer (mHSPC), as there has been a paradigm shift with the use of next‐generation androgen receptor inhibitors (ARIs) and docetaxel. Methods Multiple databases were searched for articles published before May 2020 according to the Preferred Reporting Items for Systematic Review and Meta‐analysis extension statement for network meta‐analysis. Studies comparing overall/progression‐free survival (OS/PFS) and/or adverse events (AEs) in patients with mHSPC were eligible. Results Nine studies (N = 9960) were selected, and formal network meta‐analyses were conducted. Abiraterone (hazard ratio [HR] 0.83, 95% credible interval [CrI] 0.76–0.90), docetaxel (HR 0.90, 95% CrI 0.82–0.98), and enzalutamide (HR 0.85, 95% CrI 0.73–0.99) were associated with significantly better OS than androgen‐deprivation therapy (ADT), and abiraterone emerged as the best option. Abiraterone (HR 0.71, 95% CrI 0.67–0.76), apalutamide (HR 0.73, 95% CrI 0.65–0.81), docetaxel (HR 0.84, 95% CrI 0.78–0.90), and enzalutamide (HR 0.67, 95% CrI 0.63–0.71) were associated with significantly better PFS than ADT, and enzalutamide emerged as the best option. 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Mostafaei, Hadi ; Sari Motlagh, Reza ; Pradere, Benjamin ; Quhal, Fahad ; Laukhtina, Ekaterina ; Schuettfort, Victor M. ; Kramer, Gero ; Abufaraj, Mohammad ; Karakiewicz, Pierre I. ; Kimura, Takahiro ; Egawa, Shin ; Shariat, Shahrokh F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5097-14f75b83595c7d5e1009fa10cdb137f4c3f77bc64e90bfb559495eaa87d2e093</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Androgen Antagonists - adverse effects</topic><topic>Androgen Receptor Antagonists</topic><topic>androgen receptor inhibitors</topic><topic>Androgen receptors</topic><topic>Androgens</topic><topic>Clinical trials</topic><topic>docetaxel</topic><topic>Docetaxel - therapeutic use</topic><topic>Hormones</topic><topic>Humans</topic><topic>Male</topic><topic>Meta-analysis</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>metastatic hormone‐sensitive prostate cancer</topic><topic>Network Meta-Analysis</topic><topic>Patients</topic><topic>PCSM</topic><topic>Prostate cancer</topic><topic>ProstateCancer</topic><topic>Prostatic Neoplasms - pathology</topic><topic>Review</topic><topic>Reviews</topic><topic>Systematic review</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mori, Keiichiro</creatorcontrib><creatorcontrib>Mostafaei, Hadi</creatorcontrib><creatorcontrib>Sari Motlagh, Reza</creatorcontrib><creatorcontrib>Pradere, Benjamin</creatorcontrib><creatorcontrib>Quhal, Fahad</creatorcontrib><creatorcontrib>Laukhtina, Ekaterina</creatorcontrib><creatorcontrib>Schuettfort, Victor M.</creatorcontrib><creatorcontrib>Kramer, Gero</creatorcontrib><creatorcontrib>Abufaraj, Mohammad</creatorcontrib><creatorcontrib>Karakiewicz, Pierre I.</creatorcontrib><creatorcontrib>Kimura, Takahiro</creatorcontrib><creatorcontrib>Egawa, Shin</creatorcontrib><creatorcontrib>Shariat, Shahrokh F.</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Wiley Online Library (Open Access Collection)</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium &amp; 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Methods Multiple databases were searched for articles published before May 2020 according to the Preferred Reporting Items for Systematic Review and Meta‐analysis extension statement for network meta‐analysis. Studies comparing overall/progression‐free survival (OS/PFS) and/or adverse events (AEs) in patients with mHSPC were eligible. Results Nine studies (N = 9960) were selected, and formal network meta‐analyses were conducted. Abiraterone (hazard ratio [HR] 0.83, 95% credible interval [CrI] 0.76–0.90), docetaxel (HR 0.90, 95% CrI 0.82–0.98), and enzalutamide (HR 0.85, 95% CrI 0.73–0.99) were associated with significantly better OS than androgen‐deprivation therapy (ADT), and abiraterone emerged as the best option. Abiraterone (HR 0.71, 95% CrI 0.67–0.76), apalutamide (HR 0.73, 95% CrI 0.65–0.81), docetaxel (HR 0.84, 95% CrI 0.78–0.90), and enzalutamide (HR 0.67, 95% CrI 0.63–0.71) were associated with significantly better PFS than ADT, and enzalutamide emerged as the best option. Abiraterone (HR 0.85, 95% CrI 0.78–0.93), apalutamide (HR 0.87, 95% CrI 0.77–0.98), and enzalutamide (HR 0.80, 95% CrI 0.73–0.88) were significantly more effective than docetaxel. Regarding AEs, apalutamide was the likely best option among the three ARIs. In patients with low‐volume mHSPC, enzalutamide was the best option in terms of OS and PFS. Conclusions All three ARIs are effective therapies for mHSPC; apalutamide was the best tolerated. All three seemed more effective than docetaxel. These findings may facilitate individualised treatment strategies and inform future comparative trials.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>34171173</pmid><doi>10.1111/bju.15507</doi><tpages>433</tpages><orcidid>https://orcid.org/0000-0002-6147-6569</orcidid><orcidid>https://orcid.org/0000-0001-5596-1771</orcidid><orcidid>https://orcid.org/0000-0002-8953-0272</orcidid><orcidid>https://orcid.org/0000-0002-6603-6319</orcidid><orcidid>https://orcid.org/0000-0002-3819-9911</orcidid><oa>free_for_read</oa></addata></record>
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subjects Androgen Antagonists - adverse effects
Androgen Receptor Antagonists
androgen receptor inhibitors
Androgen receptors
Androgens
Clinical trials
docetaxel
Docetaxel - therapeutic use
Hormones
Humans
Male
Meta-analysis
Metastases
Metastasis
metastatic hormone‐sensitive prostate cancer
Network Meta-Analysis
Patients
PCSM
Prostate cancer
ProstateCancer
Prostatic Neoplasms - pathology
Review
Reviews
Systematic review
title Systemic therapies for metastatic hormone‐sensitive prostate cancer: network meta‐analysis
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