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 |
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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 |
format | Article |
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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.</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 & Sons Ltd on behalf of BJU International</rights><rights>2021 The Authors. BJU International published by John Wiley & 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. 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><subject>Androgen Antagonists - adverse effects</subject><subject>Androgen Receptor Antagonists</subject><subject>androgen receptor inhibitors</subject><subject>Androgen receptors</subject><subject>Androgens</subject><subject>Clinical trials</subject><subject>docetaxel</subject><subject>Docetaxel - therapeutic use</subject><subject>Hormones</subject><subject>Humans</subject><subject>Male</subject><subject>Meta-analysis</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>metastatic hormone‐sensitive prostate cancer</subject><subject>Network Meta-Analysis</subject><subject>Patients</subject><subject>PCSM</subject><subject>Prostate cancer</subject><subject>ProstateCancer</subject><subject>Prostatic Neoplasms - pathology</subject><subject>Review</subject><subject>Reviews</subject><subject>Systematic review</subject><issn>1464-4096</issn><issn>1464-410X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><sourceid>EIF</sourceid><recordid>eNp1kc1OAyEUhYnR-FNd-AJmEje6qMIMDMWFiRp_Y-JCTVxJGHrHUmeGCkxNdz6Cz-iTSK0aNZHNJZyPw70chNYJ3iFx7RbDdocwhvkcWiY0p11K8N381x6LfAmteD_EOB7kbBEtZZRwQni2jO6vJz5AbXQSBuDUyIBPSuuSGoLyQYUoDKyrbQNvL68eGm-CGUMycnaqQqJVo8HtJQ2EZ-seP-5FUjWqmnjjV9FCqSoPa5-1g25Ojm-OzrqXV6fnRweXXc2w4F1CS86KXsYE07zPgGAsSkWw7hck4yXVWcl5oXMKAhdlwZiggoFSPd5PAYusg_ZntqO2qKGvoQlOVXLkTK3cRFpl5G-lMQP5YMdSpIL0WBYNtj4NnH1qwQdZG6-hqlQDtvUyZTQ-SnhkO2jzDzq0rYvzRiqnNKWsl06p7Rml4095B-V3MwTLaWgyhiY_Qovsxs_uv8mvlCKwOwOeTQWT_53k4cXtzPIdfxGlZw</recordid><startdate>202204</startdate><enddate>202204</enddate><creator>Mori, Keiichiro</creator><creator>Mostafaei, Hadi</creator><creator>Sari Motlagh, Reza</creator><creator>Pradere, Benjamin</creator><creator>Quhal, Fahad</creator><creator>Laukhtina, Ekaterina</creator><creator>Schuettfort, Victor M.</creator><creator>Kramer, Gero</creator><creator>Abufaraj, Mohammad</creator><creator>Karakiewicz, Pierre I.</creator><creator>Kimura, Takahiro</creator><creator>Egawa, Shin</creator><creator>Shariat, Shahrokh F.</creator><general>Wiley Subscription Services, Inc</general><general>John Wiley and Sons Inc</general><scope>24P</scope><scope>WIN</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7X8</scope><scope>5PM</scope><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></search><sort><creationdate>202204</creationdate><title>Systemic therapies for metastatic hormone‐sensitive prostate cancer: network meta‐analysis</title><author>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.</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 & Calcified Tissue Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>BJU international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mori, Keiichiro</au><au>Mostafaei, Hadi</au><au>Sari Motlagh, Reza</au><au>Pradere, Benjamin</au><au>Quhal, Fahad</au><au>Laukhtina, Ekaterina</au><au>Schuettfort, Victor M.</au><au>Kramer, Gero</au><au>Abufaraj, Mohammad</au><au>Karakiewicz, Pierre I.</au><au>Kimura, Takahiro</au><au>Egawa, Shin</au><au>Shariat, Shahrokh F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Systemic therapies for metastatic hormone‐sensitive prostate cancer: network meta‐analysis</atitle><jtitle>BJU international</jtitle><addtitle>BJU Int</addtitle><date>2022-04</date><risdate>2022</risdate><volume>129</volume><issue>4</issue><spage>423</spage><epage>433</epage><pages>423-433</pages><issn>1464-4096</issn><eissn>1464-410X</eissn><abstract>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.</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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