Improved survival in real‐world patients with advanced urothelial carcinoma: A multicenter propensity score‐matched cohort study comparing a period before the introduction of pembrolizumab (2003–2011) and a more recent period (2016–2020)
Objectives Although the treatment strategy for advanced urothelial carcinoma (aUC) has drastically changed since pembrolizumab was introduced in 2017, studies revealing current survival rates in aUC are lacking. This study aimed to assess (1) the improvement in survival among real‐world patients wit...
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Veröffentlicht in: | International journal of urology 2022-12, Vol.29 (12), p.1462-1469 |
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creator | Taguchi, Satoru Kawai, Taketo Nakagawa, Tohru Miyakawa, Jimpei Kishitani, Kenjiro Sugimoto, Kazuma Nakamura, Yu Kamei, Jun Obinata, Daisuke Yamaguchi, Kenya Kaneko, Tomoyuki Yoshida, Kanae Yamamoto, Sachi Kakutani, Shigenori Kanazawa, Koichiro Sugihara, Yuriko Tokunaga, Mayuko Matsumoto, Akihiko Uemura, Yukari Akiyama, Yoshiyuki Yamada, Yuta Sato, Yusuke Yamada, Daisuke Enomoto, Yutaka Nishimatsu, Hiroaki Ishikawa, Akira Tanaka, Yoshinori Nagase, Yasushi Fujimura, Tetsuya Fukuhara, Hiroshi Takahashi, Satoru Kume, Haruki |
description | Objectives
Although the treatment strategy for advanced urothelial carcinoma (aUC) has drastically changed since pembrolizumab was introduced in 2017, studies revealing current survival rates in aUC are lacking. This study aimed to assess (1) the improvement in survival among real‐world patients with aUC after the introduction of pembrolizumab and (2) the direct survival‐prolonging effect of pembrolizumab.
Methods
This multicenter retrospective study included 531 patients with aUC undergoing salvage chemotherapy, including 200 patients treated in the pre‐pembrolizumab era (2003–2011; earlier era) and 331 patients treated in a recent 5‐year period (2016–2020; recent era). Using propensity score matching (PSM), cancer‐specific survival (CSS) and overall survival (OS) were compared between the earlier and recent eras, in addition to between the recent era, both with and without pembrolizumab use, and the earlier era.
Results
After PSM, the recent era cohort had significantly longer CSS (21 months) and OS (19 months) than the earlier era cohort (CSS and OS: 12 months). In secondary analyses using PSM, patients treated with pembrolizumab had significantly longer CSS (25 months) and OS (24 months) than those in the earlier era cohort (CSS and OS: 11 months), whereas patients who did not receive pembrolizumab in the recent era had similar outcomes (CSS and OS: 14 months) as the earlier era cohort (CSS and OS: 12 months).
Conclusions
Patients with aUC treated in the recent era exhibited significantly longer survival than those treated before the introduction of pembrolizumab. The improved survival was primarily attributable to the use of pembrolizumab. |
doi_str_mv | 10.1111/iju.15014 |
format | Article |
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Although the treatment strategy for advanced urothelial carcinoma (aUC) has drastically changed since pembrolizumab was introduced in 2017, studies revealing current survival rates in aUC are lacking. This study aimed to assess (1) the improvement in survival among real‐world patients with aUC after the introduction of pembrolizumab and (2) the direct survival‐prolonging effect of pembrolizumab.
Methods
This multicenter retrospective study included 531 patients with aUC undergoing salvage chemotherapy, including 200 patients treated in the pre‐pembrolizumab era (2003–2011; earlier era) and 331 patients treated in a recent 5‐year period (2016–2020; recent era). Using propensity score matching (PSM), cancer‐specific survival (CSS) and overall survival (OS) were compared between the earlier and recent eras, in addition to between the recent era, both with and without pembrolizumab use, and the earlier era.
Results
After PSM, the recent era cohort had significantly longer CSS (21 months) and OS (19 months) than the earlier era cohort (CSS and OS: 12 months). In secondary analyses using PSM, patients treated with pembrolizumab had significantly longer CSS (25 months) and OS (24 months) than those in the earlier era cohort (CSS and OS: 11 months), whereas patients who did not receive pembrolizumab in the recent era had similar outcomes (CSS and OS: 14 months) as the earlier era cohort (CSS and OS: 12 months).
Conclusions
Patients with aUC treated in the recent era exhibited significantly longer survival than those treated before the introduction of pembrolizumab. The improved survival was primarily attributable to the use of pembrolizumab.</description><identifier>ISSN: 0919-8172</identifier><identifier>EISSN: 1442-2042</identifier><identifier>DOI: 10.1111/iju.15014</identifier><identifier>PMID: 35996761</identifier><language>eng</language><publisher>Australia: Wiley Subscription Services, Inc</publisher><subject>advanced ; bladder cancer ; Carcinoma, Transitional Cell - pathology ; Chemotherapy ; Cohort analysis ; Cohort Studies ; Humans ; metastatic ; Original : Clinical Investigation ; Pembrolizumab ; Propensity Score ; propensity score matching ; Retrospective Studies ; Survival ; Urinary Bladder Neoplasms - pathology ; Urothelial carcinoma</subject><ispartof>International journal of urology, 2022-12, Vol.29 (12), p.1462-1469</ispartof><rights>2022 The Authors. published by John Wiley & Sons Australia, Ltd on behalf of The Japanese Urological Association.</rights><rights>2022 The Authors. International Journal of Urology published by John Wiley & Sons Australia, Ltd on behalf of The Japanese Urological Association.</rights><rights>2022. This article is published under http://creativecommons.org/licenses/by/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-c4684-c074c614fcad8254057c7221948420be31317f1a65633cb2197ebfb0726669e43</citedby><cites>FETCH-LOGICAL-c4684-c074c614fcad8254057c7221948420be31317f1a65633cb2197ebfb0726669e43</cites><orcidid>0000-0002-1291-4294 ; 0000-0001-8632-4169 ; 0000-0002-0819-9478 ; 0000-0002-5762-7563 ; 0000-0002-3421-8273 ; 0000-0002-7279-2874</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%2Fiju.15014$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fiju.15014$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35996761$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Taguchi, Satoru</creatorcontrib><creatorcontrib>Kawai, Taketo</creatorcontrib><creatorcontrib>Nakagawa, Tohru</creatorcontrib><creatorcontrib>Miyakawa, Jimpei</creatorcontrib><creatorcontrib>Kishitani, Kenjiro</creatorcontrib><creatorcontrib>Sugimoto, Kazuma</creatorcontrib><creatorcontrib>Nakamura, Yu</creatorcontrib><creatorcontrib>Kamei, Jun</creatorcontrib><creatorcontrib>Obinata, Daisuke</creatorcontrib><creatorcontrib>Yamaguchi, Kenya</creatorcontrib><creatorcontrib>Kaneko, Tomoyuki</creatorcontrib><creatorcontrib>Yoshida, Kanae</creatorcontrib><creatorcontrib>Yamamoto, Sachi</creatorcontrib><creatorcontrib>Kakutani, Shigenori</creatorcontrib><creatorcontrib>Kanazawa, Koichiro</creatorcontrib><creatorcontrib>Sugihara, Yuriko</creatorcontrib><creatorcontrib>Tokunaga, Mayuko</creatorcontrib><creatorcontrib>Matsumoto, Akihiko</creatorcontrib><creatorcontrib>Uemura, Yukari</creatorcontrib><creatorcontrib>Akiyama, Yoshiyuki</creatorcontrib><creatorcontrib>Yamada, Yuta</creatorcontrib><creatorcontrib>Sato, Yusuke</creatorcontrib><creatorcontrib>Yamada, Daisuke</creatorcontrib><creatorcontrib>Enomoto, Yutaka</creatorcontrib><creatorcontrib>Nishimatsu, Hiroaki</creatorcontrib><creatorcontrib>Ishikawa, Akira</creatorcontrib><creatorcontrib>Tanaka, Yoshinori</creatorcontrib><creatorcontrib>Nagase, Yasushi</creatorcontrib><creatorcontrib>Fujimura, Tetsuya</creatorcontrib><creatorcontrib>Fukuhara, Hiroshi</creatorcontrib><creatorcontrib>Takahashi, Satoru</creatorcontrib><creatorcontrib>Kume, Haruki</creatorcontrib><title>Improved survival in real‐world patients with advanced urothelial carcinoma: A multicenter propensity score‐matched cohort study comparing a period before the introduction of pembrolizumab (2003–2011) and a more recent period (2016–2020)</title><title>International journal of urology</title><addtitle>Int J Urol</addtitle><description>Objectives
Although the treatment strategy for advanced urothelial carcinoma (aUC) has drastically changed since pembrolizumab was introduced in 2017, studies revealing current survival rates in aUC are lacking. This study aimed to assess (1) the improvement in survival among real‐world patients with aUC after the introduction of pembrolizumab and (2) the direct survival‐prolonging effect of pembrolizumab.
Methods
This multicenter retrospective study included 531 patients with aUC undergoing salvage chemotherapy, including 200 patients treated in the pre‐pembrolizumab era (2003–2011; earlier era) and 331 patients treated in a recent 5‐year period (2016–2020; recent era). Using propensity score matching (PSM), cancer‐specific survival (CSS) and overall survival (OS) were compared between the earlier and recent eras, in addition to between the recent era, both with and without pembrolizumab use, and the earlier era.
Results
After PSM, the recent era cohort had significantly longer CSS (21 months) and OS (19 months) than the earlier era cohort (CSS and OS: 12 months). In secondary analyses using PSM, patients treated with pembrolizumab had significantly longer CSS (25 months) and OS (24 months) than those in the earlier era cohort (CSS and OS: 11 months), whereas patients who did not receive pembrolizumab in the recent era had similar outcomes (CSS and OS: 14 months) as the earlier era cohort (CSS and OS: 12 months).
Conclusions
Patients with aUC treated in the recent era exhibited significantly longer survival than those treated before the introduction of pembrolizumab. The improved survival was primarily attributable to the use of pembrolizumab.</description><subject>advanced</subject><subject>bladder cancer</subject><subject>Carcinoma, Transitional Cell - pathology</subject><subject>Chemotherapy</subject><subject>Cohort analysis</subject><subject>Cohort Studies</subject><subject>Humans</subject><subject>metastatic</subject><subject>Original : Clinical Investigation</subject><subject>Pembrolizumab</subject><subject>Propensity Score</subject><subject>propensity score matching</subject><subject>Retrospective Studies</subject><subject>Survival</subject><subject>Urinary Bladder Neoplasms - pathology</subject><subject>Urothelial carcinoma</subject><issn>0919-8172</issn><issn>1442-2042</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>EIF</sourceid><recordid>eNp1ks1u1DAYRSMEokNhwQsgS2zaxbS24zgJm6qq-BlUiQ1dW47jdDxy7OCfGQ2rPgISb9h3YM83nbYCJLKJIp97fCPdonhN8AmB59Ss8gmpMGFPihlhjM4pZvRpMcMtaecNqelB8SLGFcakpKR5XhyUVdvympNZ8WsxTsGvdY9iDmuzlhYZh4KW9vbmx8YH26NJJqNdimhj0hLJfi2dAj4Hn5baGkgoGZRxfpTv0Dkas01GQUAHBOpJu2jSFkXlgwbnKJNaQlz5pQ8JxZT7LXyMkwzGXSOJJh2M71GnBwgguAIKpeD7rJLxDvkBiLEL3prveZQdOqIYl7c3Pykm5BhJ14Nj3EWD3rV48AFG-B1G8fHL4tkgbdSv7t-HxdWH918vPs0vv3xcXJxfzhXjDZsrXDPFCRuU7BtaMVzVqqaUtKxhFHe6JCWpByJ5xctSdXBQ627ocE05561m5WFxtvdOuRt1v-sTpBVTMKMMW-GlEX-fOLMU134tCMZNzUgJhqN7Q_Dfso5JjCYqba102ucoaA2lKoL5Dn37D7ryOTj4P6AqVpUtTAOo4z2lgo8x6OGxDcFityYBaxJ3awL2zZ_1H8mH-QBwugc2xurt_01i8flqr_wN4mrauw</recordid><startdate>202212</startdate><enddate>202212</enddate><creator>Taguchi, Satoru</creator><creator>Kawai, Taketo</creator><creator>Nakagawa, Tohru</creator><creator>Miyakawa, Jimpei</creator><creator>Kishitani, Kenjiro</creator><creator>Sugimoto, Kazuma</creator><creator>Nakamura, Yu</creator><creator>Kamei, Jun</creator><creator>Obinata, Daisuke</creator><creator>Yamaguchi, Kenya</creator><creator>Kaneko, Tomoyuki</creator><creator>Yoshida, Kanae</creator><creator>Yamamoto, Sachi</creator><creator>Kakutani, Shigenori</creator><creator>Kanazawa, Koichiro</creator><creator>Sugihara, Yuriko</creator><creator>Tokunaga, Mayuko</creator><creator>Matsumoto, Akihiko</creator><creator>Uemura, Yukari</creator><creator>Akiyama, Yoshiyuki</creator><creator>Yamada, Yuta</creator><creator>Sato, Yusuke</creator><creator>Yamada, Daisuke</creator><creator>Enomoto, Yutaka</creator><creator>Nishimatsu, Hiroaki</creator><creator>Ishikawa, Akira</creator><creator>Tanaka, Yoshinori</creator><creator>Nagase, Yasushi</creator><creator>Fujimura, Tetsuya</creator><creator>Fukuhara, Hiroshi</creator><creator>Takahashi, Satoru</creator><creator>Kume, Haruki</creator><general>Wiley Subscription Services, Inc</general><general>John Wiley and Sons Inc</general><scope>24P</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/0000-0002-1291-4294</orcidid><orcidid>https://orcid.org/0000-0001-8632-4169</orcidid><orcidid>https://orcid.org/0000-0002-0819-9478</orcidid><orcidid>https://orcid.org/0000-0002-5762-7563</orcidid><orcidid>https://orcid.org/0000-0002-3421-8273</orcidid><orcidid>https://orcid.org/0000-0002-7279-2874</orcidid></search><sort><creationdate>202212</creationdate><title>Improved survival in real‐world patients with advanced urothelial carcinoma: A multicenter propensity score‐matched cohort study comparing a period before the introduction of pembrolizumab (2003–2011) and a more recent period (2016–2020)</title><author>Taguchi, Satoru ; Kawai, Taketo ; Nakagawa, Tohru ; Miyakawa, Jimpei ; Kishitani, Kenjiro ; Sugimoto, Kazuma ; Nakamura, Yu ; Kamei, Jun ; Obinata, Daisuke ; Yamaguchi, Kenya ; Kaneko, Tomoyuki ; Yoshida, Kanae ; Yamamoto, Sachi ; Kakutani, Shigenori ; Kanazawa, Koichiro ; Sugihara, Yuriko ; Tokunaga, Mayuko ; Matsumoto, Akihiko ; Uemura, Yukari ; Akiyama, Yoshiyuki ; Yamada, Yuta ; Sato, Yusuke ; Yamada, Daisuke ; Enomoto, Yutaka ; Nishimatsu, Hiroaki ; Ishikawa, Akira ; Tanaka, Yoshinori ; Nagase, Yasushi ; Fujimura, Tetsuya ; Fukuhara, Hiroshi ; Takahashi, Satoru ; Kume, Haruki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4684-c074c614fcad8254057c7221948420be31317f1a65633cb2197ebfb0726669e43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>advanced</topic><topic>bladder cancer</topic><topic>Carcinoma, Transitional Cell - pathology</topic><topic>Chemotherapy</topic><topic>Cohort analysis</topic><topic>Cohort Studies</topic><topic>Humans</topic><topic>metastatic</topic><topic>Original : Clinical Investigation</topic><topic>Pembrolizumab</topic><topic>Propensity Score</topic><topic>propensity score matching</topic><topic>Retrospective Studies</topic><topic>Survival</topic><topic>Urinary Bladder Neoplasms - pathology</topic><topic>Urothelial carcinoma</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Taguchi, Satoru</creatorcontrib><creatorcontrib>Kawai, Taketo</creatorcontrib><creatorcontrib>Nakagawa, Tohru</creatorcontrib><creatorcontrib>Miyakawa, Jimpei</creatorcontrib><creatorcontrib>Kishitani, Kenjiro</creatorcontrib><creatorcontrib>Sugimoto, Kazuma</creatorcontrib><creatorcontrib>Nakamura, Yu</creatorcontrib><creatorcontrib>Kamei, Jun</creatorcontrib><creatorcontrib>Obinata, Daisuke</creatorcontrib><creatorcontrib>Yamaguchi, Kenya</creatorcontrib><creatorcontrib>Kaneko, Tomoyuki</creatorcontrib><creatorcontrib>Yoshida, Kanae</creatorcontrib><creatorcontrib>Yamamoto, Sachi</creatorcontrib><creatorcontrib>Kakutani, Shigenori</creatorcontrib><creatorcontrib>Kanazawa, Koichiro</creatorcontrib><creatorcontrib>Sugihara, Yuriko</creatorcontrib><creatorcontrib>Tokunaga, Mayuko</creatorcontrib><creatorcontrib>Matsumoto, Akihiko</creatorcontrib><creatorcontrib>Uemura, Yukari</creatorcontrib><creatorcontrib>Akiyama, Yoshiyuki</creatorcontrib><creatorcontrib>Yamada, Yuta</creatorcontrib><creatorcontrib>Sato, Yusuke</creatorcontrib><creatorcontrib>Yamada, Daisuke</creatorcontrib><creatorcontrib>Enomoto, Yutaka</creatorcontrib><creatorcontrib>Nishimatsu, Hiroaki</creatorcontrib><creatorcontrib>Ishikawa, Akira</creatorcontrib><creatorcontrib>Tanaka, Yoshinori</creatorcontrib><creatorcontrib>Nagase, Yasushi</creatorcontrib><creatorcontrib>Fujimura, Tetsuya</creatorcontrib><creatorcontrib>Fukuhara, Hiroshi</creatorcontrib><creatorcontrib>Takahashi, Satoru</creatorcontrib><creatorcontrib>Kume, Haruki</creatorcontrib><collection>Wiley Online Library Open Access</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>International journal of urology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Taguchi, Satoru</au><au>Kawai, Taketo</au><au>Nakagawa, Tohru</au><au>Miyakawa, Jimpei</au><au>Kishitani, Kenjiro</au><au>Sugimoto, Kazuma</au><au>Nakamura, Yu</au><au>Kamei, Jun</au><au>Obinata, Daisuke</au><au>Yamaguchi, Kenya</au><au>Kaneko, Tomoyuki</au><au>Yoshida, Kanae</au><au>Yamamoto, Sachi</au><au>Kakutani, Shigenori</au><au>Kanazawa, Koichiro</au><au>Sugihara, Yuriko</au><au>Tokunaga, Mayuko</au><au>Matsumoto, Akihiko</au><au>Uemura, Yukari</au><au>Akiyama, Yoshiyuki</au><au>Yamada, Yuta</au><au>Sato, Yusuke</au><au>Yamada, Daisuke</au><au>Enomoto, Yutaka</au><au>Nishimatsu, Hiroaki</au><au>Ishikawa, Akira</au><au>Tanaka, Yoshinori</au><au>Nagase, Yasushi</au><au>Fujimura, Tetsuya</au><au>Fukuhara, Hiroshi</au><au>Takahashi, Satoru</au><au>Kume, Haruki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Improved survival in real‐world patients with advanced urothelial carcinoma: A multicenter propensity score‐matched cohort study comparing a period before the introduction of pembrolizumab (2003–2011) and a more recent period (2016–2020)</atitle><jtitle>International journal of urology</jtitle><addtitle>Int J Urol</addtitle><date>2022-12</date><risdate>2022</risdate><volume>29</volume><issue>12</issue><spage>1462</spage><epage>1469</epage><pages>1462-1469</pages><issn>0919-8172</issn><eissn>1442-2042</eissn><abstract>Objectives
Although the treatment strategy for advanced urothelial carcinoma (aUC) has drastically changed since pembrolizumab was introduced in 2017, studies revealing current survival rates in aUC are lacking. This study aimed to assess (1) the improvement in survival among real‐world patients with aUC after the introduction of pembrolizumab and (2) the direct survival‐prolonging effect of pembrolizumab.
Methods
This multicenter retrospective study included 531 patients with aUC undergoing salvage chemotherapy, including 200 patients treated in the pre‐pembrolizumab era (2003–2011; earlier era) and 331 patients treated in a recent 5‐year period (2016–2020; recent era). Using propensity score matching (PSM), cancer‐specific survival (CSS) and overall survival (OS) were compared between the earlier and recent eras, in addition to between the recent era, both with and without pembrolizumab use, and the earlier era.
Results
After PSM, the recent era cohort had significantly longer CSS (21 months) and OS (19 months) than the earlier era cohort (CSS and OS: 12 months). In secondary analyses using PSM, patients treated with pembrolizumab had significantly longer CSS (25 months) and OS (24 months) than those in the earlier era cohort (CSS and OS: 11 months), whereas patients who did not receive pembrolizumab in the recent era had similar outcomes (CSS and OS: 14 months) as the earlier era cohort (CSS and OS: 12 months).
Conclusions
Patients with aUC treated in the recent era exhibited significantly longer survival than those treated before the introduction of pembrolizumab. The improved survival was primarily attributable to the use of pembrolizumab.</abstract><cop>Australia</cop><pub>Wiley Subscription Services, Inc</pub><pmid>35996761</pmid><doi>10.1111/iju.15014</doi><tpages>1469</tpages><orcidid>https://orcid.org/0000-0002-1291-4294</orcidid><orcidid>https://orcid.org/0000-0001-8632-4169</orcidid><orcidid>https://orcid.org/0000-0002-0819-9478</orcidid><orcidid>https://orcid.org/0000-0002-5762-7563</orcidid><orcidid>https://orcid.org/0000-0002-3421-8273</orcidid><orcidid>https://orcid.org/0000-0002-7279-2874</orcidid><oa>free_for_read</oa></addata></record> |
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recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10087413 |
source | MEDLINE; Wiley Online Library Journals Frontfile Complete |
subjects | advanced bladder cancer Carcinoma, Transitional Cell - pathology Chemotherapy Cohort analysis Cohort Studies Humans metastatic Original : Clinical Investigation Pembrolizumab Propensity Score propensity score matching Retrospective Studies Survival Urinary Bladder Neoplasms - pathology Urothelial carcinoma |
title | Improved survival in real‐world patients with advanced urothelial carcinoma: A multicenter propensity score‐matched cohort study comparing a period before the introduction of pembrolizumab (2003–2011) and a more recent period (2016–2020) |
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