Effect of upfront intensive therapy on oncological outcomes in older patients with high tumor burden metastatic castration‐sensitive prostate cancer: A multicenter retrospective study

Background The effect of upfront intensive therapy on the prognosis of older patients with metastatic castration‐sensitive prostate cancer (mCSPC) remains unclear. Thus, we assessed the impact of older age (≥75 years) on oncological outcomes in mCSPC patients with a high tumor burden. Methods This m...

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Veröffentlicht in:The Prostate 2022-09, Vol.82 (13), p.1304-1312
Hauptverfasser: Miura, Yuki, Hatakeyama, Shingo, Narita, Shintaro, Kimura, Takahiro, Hata, Kenichi, Yanagisawa, Takafumi, Tanaka, Toshikazu, Ishi, Noritaka, Kawamura, Sadafumi, Hoshi, Senji, Ishidoya, Shigeto, Mitsuzuka, Koji, Ito, Akihiro, Tsuchiya, Norihiko, Egawa, Shin, Habuchi, Tomonori, Ohyama, Chikara
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container_issue 13
container_start_page 1304
container_title The Prostate
container_volume 82
creator Miura, Yuki
Hatakeyama, Shingo
Narita, Shintaro
Kimura, Takahiro
Hata, Kenichi
Yanagisawa, Takafumi
Tanaka, Toshikazu
Ishi, Noritaka
Kawamura, Sadafumi
Hoshi, Senji
Ishidoya, Shigeto
Mitsuzuka, Koji
Ito, Akihiro
Tsuchiya, Norihiko
Egawa, Shin
Habuchi, Tomonori
Ohyama, Chikara
description Background The effect of upfront intensive therapy on the prognosis of older patients with metastatic castration‐sensitive prostate cancer (mCSPC) remains unclear. Thus, we assessed the impact of older age (≥75 years) on oncological outcomes in mCSPC patients with a high tumor burden. Methods This multicenter retrospective study included 252 patients aged ≥75 years treated with either upfront or conventional therapy between 2014 and 2021. We compared castration‐resistant prostate cancer (CRPC)‐free survival (FS) and overall survival (OS) between patients with androgen deprivation therapy (ADT) plus upfront intensive therapy (docetaxel [DTX] or abiraterone acetate [ABI] plus prednisolone) and conventional therapy (ADT monotherapy or ADT combined with bicalutamide). We evaluated the effect of upfront intensive therapy on prognosis by multivariable Cox regression analysis. Results The 231 patients enrolled in our study were classified in the conventional group (n = 148) or the upfront group (n = 104; DTX = 27 and ABI = 77). The upfront group had significantly prolonged CRPC‐FS and OS compared with the conventional group, and this was also the case in the background‐adjusted multivariable Cox regression analysis. Conclusion Patients aged ≥75 years who received upfront intensive therapy had significantly longer CRPC‐FS and OS compared with similar age patients treated with conventional therapy in real‐world practice. The oncological benefit may not diminish in this older population.
doi_str_mv 10.1002/pros.24404
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Thus, we assessed the impact of older age (≥75 years) on oncological outcomes in mCSPC patients with a high tumor burden. Methods This multicenter retrospective study included 252 patients aged ≥75 years treated with either upfront or conventional therapy between 2014 and 2021. We compared castration‐resistant prostate cancer (CRPC)‐free survival (FS) and overall survival (OS) between patients with androgen deprivation therapy (ADT) plus upfront intensive therapy (docetaxel [DTX] or abiraterone acetate [ABI] plus prednisolone) and conventional therapy (ADT monotherapy or ADT combined with bicalutamide). We evaluated the effect of upfront intensive therapy on prognosis by multivariable Cox regression analysis. Results The 231 patients enrolled in our study were classified in the conventional group (n = 148) or the upfront group (n = 104; DTX = 27 and ABI = 77). The upfront group had significantly prolonged CRPC‐FS and OS compared with the conventional group, and this was also the case in the background‐adjusted multivariable Cox regression analysis. Conclusion Patients aged ≥75 years who received upfront intensive therapy had significantly longer CRPC‐FS and OS compared with similar age patients treated with conventional therapy in real‐world practice. The oncological benefit may not diminish in this older population.</description><identifier>ISSN: 0270-4137</identifier><identifier>EISSN: 1097-0045</identifier><identifier>DOI: 10.1002/pros.24404</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc</publisher><subject>Acetic acid ; Castration ; castration‐resistant prostate cancer ; castration‐sensitive prostate cancer ; Medical prognosis ; Metastases ; Metastasis ; older age ; Prednisolone ; Prognosis ; Prostate cancer ; Regression analysis ; Survival ; Tumors ; upfront intensive therapy</subject><ispartof>The Prostate, 2022-09, Vol.82 (13), p.1304-1312</ispartof><rights>2022 Wiley Periodicals LLC.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3344-dc22da03704a96e56338dd8fba242f8dd676dbb70dd088c3bf7df2eef8408c23</citedby><cites>FETCH-LOGICAL-c3344-dc22da03704a96e56338dd8fba242f8dd676dbb70dd088c3bf7df2eef8408c23</cites><orcidid>0000-0002-0026-4079 ; 0000-0002-7410-0712</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fpros.24404$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fpros.24404$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,781,785,1418,27926,27927,45576,45577</link.rule.ids></links><search><creatorcontrib>Miura, Yuki</creatorcontrib><creatorcontrib>Hatakeyama, Shingo</creatorcontrib><creatorcontrib>Narita, Shintaro</creatorcontrib><creatorcontrib>Kimura, Takahiro</creatorcontrib><creatorcontrib>Hata, Kenichi</creatorcontrib><creatorcontrib>Yanagisawa, Takafumi</creatorcontrib><creatorcontrib>Tanaka, Toshikazu</creatorcontrib><creatorcontrib>Ishi, Noritaka</creatorcontrib><creatorcontrib>Kawamura, Sadafumi</creatorcontrib><creatorcontrib>Hoshi, Senji</creatorcontrib><creatorcontrib>Ishidoya, Shigeto</creatorcontrib><creatorcontrib>Mitsuzuka, Koji</creatorcontrib><creatorcontrib>Ito, Akihiro</creatorcontrib><creatorcontrib>Tsuchiya, Norihiko</creatorcontrib><creatorcontrib>Egawa, Shin</creatorcontrib><creatorcontrib>Habuchi, Tomonori</creatorcontrib><creatorcontrib>Ohyama, Chikara</creatorcontrib><title>Effect of upfront intensive therapy on oncological outcomes in older patients with high tumor burden metastatic castration‐sensitive prostate cancer: A multicenter retrospective study</title><title>The Prostate</title><description>Background The effect of upfront intensive therapy on the prognosis of older patients with metastatic castration‐sensitive prostate cancer (mCSPC) remains unclear. Thus, we assessed the impact of older age (≥75 years) on oncological outcomes in mCSPC patients with a high tumor burden. Methods This multicenter retrospective study included 252 patients aged ≥75 years treated with either upfront or conventional therapy between 2014 and 2021. We compared castration‐resistant prostate cancer (CRPC)‐free survival (FS) and overall survival (OS) between patients with androgen deprivation therapy (ADT) plus upfront intensive therapy (docetaxel [DTX] or abiraterone acetate [ABI] plus prednisolone) and conventional therapy (ADT monotherapy or ADT combined with bicalutamide). We evaluated the effect of upfront intensive therapy on prognosis by multivariable Cox regression analysis. Results The 231 patients enrolled in our study were classified in the conventional group (n = 148) or the upfront group (n = 104; DTX = 27 and ABI = 77). The upfront group had significantly prolonged CRPC‐FS and OS compared with the conventional group, and this was also the case in the background‐adjusted multivariable Cox regression analysis. Conclusion Patients aged ≥75 years who received upfront intensive therapy had significantly longer CRPC‐FS and OS compared with similar age patients treated with conventional therapy in real‐world practice. 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Hatakeyama, Shingo ; Narita, Shintaro ; Kimura, Takahiro ; Hata, Kenichi ; Yanagisawa, Takafumi ; Tanaka, Toshikazu ; Ishi, Noritaka ; Kawamura, Sadafumi ; Hoshi, Senji ; Ishidoya, Shigeto ; Mitsuzuka, Koji ; Ito, Akihiro ; Tsuchiya, Norihiko ; Egawa, Shin ; Habuchi, Tomonori ; Ohyama, Chikara</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3344-dc22da03704a96e56338dd8fba242f8dd676dbb70dd088c3bf7df2eef8408c23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Acetic acid</topic><topic>Castration</topic><topic>castration‐resistant prostate cancer</topic><topic>castration‐sensitive prostate cancer</topic><topic>Medical prognosis</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>older age</topic><topic>Prednisolone</topic><topic>Prognosis</topic><topic>Prostate cancer</topic><topic>Regression analysis</topic><topic>Survival</topic><topic>Tumors</topic><topic>upfront intensive therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Miura, Yuki</creatorcontrib><creatorcontrib>Hatakeyama, Shingo</creatorcontrib><creatorcontrib>Narita, Shintaro</creatorcontrib><creatorcontrib>Kimura, Takahiro</creatorcontrib><creatorcontrib>Hata, Kenichi</creatorcontrib><creatorcontrib>Yanagisawa, Takafumi</creatorcontrib><creatorcontrib>Tanaka, Toshikazu</creatorcontrib><creatorcontrib>Ishi, Noritaka</creatorcontrib><creatorcontrib>Kawamura, Sadafumi</creatorcontrib><creatorcontrib>Hoshi, Senji</creatorcontrib><creatorcontrib>Ishidoya, Shigeto</creatorcontrib><creatorcontrib>Mitsuzuka, Koji</creatorcontrib><creatorcontrib>Ito, Akihiro</creatorcontrib><creatorcontrib>Tsuchiya, Norihiko</creatorcontrib><creatorcontrib>Egawa, Shin</creatorcontrib><creatorcontrib>Habuchi, Tomonori</creatorcontrib><creatorcontrib>Ohyama, Chikara</creatorcontrib><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; 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Thus, we assessed the impact of older age (≥75 years) on oncological outcomes in mCSPC patients with a high tumor burden. Methods This multicenter retrospective study included 252 patients aged ≥75 years treated with either upfront or conventional therapy between 2014 and 2021. We compared castration‐resistant prostate cancer (CRPC)‐free survival (FS) and overall survival (OS) between patients with androgen deprivation therapy (ADT) plus upfront intensive therapy (docetaxel [DTX] or abiraterone acetate [ABI] plus prednisolone) and conventional therapy (ADT monotherapy or ADT combined with bicalutamide). We evaluated the effect of upfront intensive therapy on prognosis by multivariable Cox regression analysis. Results The 231 patients enrolled in our study were classified in the conventional group (n = 148) or the upfront group (n = 104; DTX = 27 and ABI = 77). The upfront group had significantly prolonged CRPC‐FS and OS compared with the conventional group, and this was also the case in the background‐adjusted multivariable Cox regression analysis. Conclusion Patients aged ≥75 years who received upfront intensive therapy had significantly longer CRPC‐FS and OS compared with similar age patients treated with conventional therapy in real‐world practice. The oncological benefit may not diminish in this older population.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/pros.24404</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-0026-4079</orcidid><orcidid>https://orcid.org/0000-0002-7410-0712</orcidid></addata></record>
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subjects Acetic acid
Castration
castration‐resistant prostate cancer
castration‐sensitive prostate cancer
Medical prognosis
Metastases
Metastasis
older age
Prednisolone
Prognosis
Prostate cancer
Regression analysis
Survival
Tumors
upfront intensive therapy
title Effect of upfront intensive therapy on oncological outcomes in older patients with high tumor burden metastatic castration‐sensitive prostate cancer: A multicenter retrospective study
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