Effects of thiazolidinedione in patients with active bladder cancer
Objective To examine the influence of perioperative thiazolidinedione (TZD) on cancer‐specific outcomes in patients with diabetes mellitus (DM) undergoing radical cystectomy (RC) for urothelial carcinoma (UC). Patients and Methods A retrospective cohort of 173 patients with DM undergoing RC from 200...
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creator | Li, Roger Metcalfe, Michael J. Ferguson, James E. Mokkapati, Sharada Nogueras González, Graciela M. Dinney, Colin P. Navai, Neema McConkey, David J. Sahai, Sunil K. Kamat, Ashish M. |
description | Objective
To examine the influence of perioperative thiazolidinedione (TZD) on cancer‐specific outcomes in patients with diabetes mellitus (DM) undergoing radical cystectomy (RC) for urothelial carcinoma (UC).
Patients and Methods
A retrospective cohort of 173 patients with DM undergoing RC from 2005 to 2010 was identified. Of those, 53 were on TZD treatment at the time of RC, with 33 patients taking pioglitazone. Baseline clinicopathological characteristics, as well as cancer‐specific survival (CSS), recurrence‐free survival (RFS), and overall survival (OS) were compared between the patients on and off TZD therapy at the time of RC. In subgroup analysis, outcomes in patients specifically taking pioglitazone at the time of RC were compared to those not on a TZD.
Results
Baseline clinicopathological characteristics were similar between patients on and off TZD therapy at the time of RC. Overall, the median CSS rate was not reached in either group (P = 0.7). The estimated 5‐year CSS was 67.8% in the non‐TZD group and 66.3% in the TZD group. On multivariate analysis incorporating patient age, pathological T‐staging, and adjuvant chemotherapy, TZD use was found not to be a significant predictor for CSS (hazard ratio 1.20, 95% confidence interval 0.66–2.17; P = 0.5). Additionally, RFS (P= 0.3) and OS (P = 0.2) were also similar between the two groups without adjusting for other variables. Comparison between patients taking pioglitazone vs patients not taking TZD yielded similar CSS (P = 0.2), RFS (P = 0.5), and OS (P= 0.2).
Conclusions
CSS, as well as RFS and OS after RC were not compromised in patients on TZD therapy at the time of RC. Additional investigation is warranted in patients with non‐muscle‐invasive bladder cancer and muscle‐invasive bladder cancer undergoing bladder‐sparing procedures to assess the safety of using TZD in the setting of active UC. |
doi_str_mv | 10.1111/bju.14009 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5780258</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1935812968</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4439-7e2a0e4db70fe8c89bc872add6abb3eaea4f1d67ab04315c702e2f687fe7b44e3</originalsourceid><addsrcrecordid>eNp1kU1LxDAURYMofowu_ANScKOL0aRNk3Qj6OAnghsFdyFJX5wMnWZM2hH99UZnFBXM5oXkcLiPi9AuwUcknWM96Y8IxbhaQZuEMjqkBD-uft1xxTbQVowTjNMDK9fRRi4EzzkXm2h0bi2YLmbeZt3YqTffuNq1UDvfQubabKY6B20CXlw3zpTp3Bwy3ai6hpAZ1RoI22jNqibCznIO0MPF-f3oanh7d3k9Or0dGkqLasghVxhorTm2IIyotEkpkogprQtQoKglNeNKY1qQ0nCcQ26Z4Ba4phSKATpZeGe9nkJtUqygGjkLbqrCq_TKyd8_rRvLJz-XJRc4L0USHCwFwT_3EDs5ddFA06gWfB8lqYpSkLxiH-j-H3Ti-9Cm9RIlKpHzgrFEHS4oE3yMAex3GILlRzUyVSM_q0ns3s_03-RXFwk4XgAvroHX_03y7OZhoXwHTCmZ0w</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1989827366</pqid></control><display><type>article</type><title>Effects of thiazolidinedione in patients with active bladder cancer</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Li, Roger ; Metcalfe, Michael J. ; Ferguson, James E. ; Mokkapati, Sharada ; Nogueras González, Graciela M. ; Dinney, Colin P. ; Navai, Neema ; McConkey, David J. ; Sahai, Sunil K. ; Kamat, Ashish M.</creator><creatorcontrib>Li, Roger ; Metcalfe, Michael J. ; Ferguson, James E. ; Mokkapati, Sharada ; Nogueras González, Graciela M. ; Dinney, Colin P. ; Navai, Neema ; McConkey, David J. ; Sahai, Sunil K. ; Kamat, Ashish M.</creatorcontrib><description>Objective
To examine the influence of perioperative thiazolidinedione (TZD) on cancer‐specific outcomes in patients with diabetes mellitus (DM) undergoing radical cystectomy (RC) for urothelial carcinoma (UC).
Patients and Methods
A retrospective cohort of 173 patients with DM undergoing RC from 2005 to 2010 was identified. Of those, 53 were on TZD treatment at the time of RC, with 33 patients taking pioglitazone. Baseline clinicopathological characteristics, as well as cancer‐specific survival (CSS), recurrence‐free survival (RFS), and overall survival (OS) were compared between the patients on and off TZD therapy at the time of RC. In subgroup analysis, outcomes in patients specifically taking pioglitazone at the time of RC were compared to those not on a TZD.
Results
Baseline clinicopathological characteristics were similar between patients on and off TZD therapy at the time of RC. Overall, the median CSS rate was not reached in either group (P = 0.7). The estimated 5‐year CSS was 67.8% in the non‐TZD group and 66.3% in the TZD group. On multivariate analysis incorporating patient age, pathological T‐staging, and adjuvant chemotherapy, TZD use was found not to be a significant predictor for CSS (hazard ratio 1.20, 95% confidence interval 0.66–2.17; P = 0.5). Additionally, RFS (P= 0.3) and OS (P = 0.2) were also similar between the two groups without adjusting for other variables. Comparison between patients taking pioglitazone vs patients not taking TZD yielded similar CSS (P = 0.2), RFS (P = 0.5), and OS (P= 0.2).
Conclusions
CSS, as well as RFS and OS after RC were not compromised in patients on TZD therapy at the time of RC. Additional investigation is warranted in patients with non‐muscle‐invasive bladder cancer and muscle‐invasive bladder cancer undergoing bladder‐sparing procedures to assess the safety of using TZD in the setting of active UC.</description><identifier>ISSN: 1464-4096</identifier><identifier>EISSN: 1464-410X</identifier><identifier>DOI: 10.1111/bju.14009</identifier><identifier>PMID: 28872778</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Aged ; BCG ; Bladder cancer ; BladderCancer ; Cancer therapies ; Carcinoma, Transitional Cell - complications ; Carcinoma, Transitional Cell - secondary ; Carcinoma, Transitional Cell - surgery ; Chemotherapy ; Cystectomy ; Diabetes mellitus ; Diabetes Mellitus - drug therapy ; Disease-Free Survival ; Female ; Humans ; Hypoglycemic Agents - therapeutic use ; Invasiveness ; Male ; Middle Aged ; Multivariate analysis ; Neoplasm Staging ; Pioglitazone ; PPARγ agonist ; Retrospective Studies ; Rosiglitazone ; Survival ; Survival Rate ; thiazolidinedione ; Thiazolidinediones - therapeutic use ; Urinary bladder ; Urinary Bladder Neoplasms - complications ; Urinary Bladder Neoplasms - pathology ; Urinary Bladder Neoplasms - surgery ; Urothelial carcinoma</subject><ispartof>BJU international, 2018-02, Vol.121 (2), p.244-251</ispartof><rights>2017 The Authors BJU International © 2017 BJU International Published by John Wiley & Sons Ltd</rights><rights>2017 The Authors BJU International © 2017 BJU International Published by John Wiley & Sons Ltd.</rights><rights>BJUI © 2018 BJU International</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4439-7e2a0e4db70fe8c89bc872add6abb3eaea4f1d67ab04315c702e2f687fe7b44e3</citedby><cites>FETCH-LOGICAL-c4439-7e2a0e4db70fe8c89bc872add6abb3eaea4f1d67ab04315c702e2f687fe7b44e3</cites><orcidid>0000-0003-1274-7200</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.14009$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fbju.14009$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,776,780,881,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28872778$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Roger</creatorcontrib><creatorcontrib>Metcalfe, Michael J.</creatorcontrib><creatorcontrib>Ferguson, James E.</creatorcontrib><creatorcontrib>Mokkapati, Sharada</creatorcontrib><creatorcontrib>Nogueras González, Graciela M.</creatorcontrib><creatorcontrib>Dinney, Colin P.</creatorcontrib><creatorcontrib>Navai, Neema</creatorcontrib><creatorcontrib>McConkey, David J.</creatorcontrib><creatorcontrib>Sahai, Sunil K.</creatorcontrib><creatorcontrib>Kamat, Ashish M.</creatorcontrib><title>Effects of thiazolidinedione in patients with active bladder cancer</title><title>BJU international</title><addtitle>BJU Int</addtitle><description>Objective
To examine the influence of perioperative thiazolidinedione (TZD) on cancer‐specific outcomes in patients with diabetes mellitus (DM) undergoing radical cystectomy (RC) for urothelial carcinoma (UC).
Patients and Methods
A retrospective cohort of 173 patients with DM undergoing RC from 2005 to 2010 was identified. Of those, 53 were on TZD treatment at the time of RC, with 33 patients taking pioglitazone. Baseline clinicopathological characteristics, as well as cancer‐specific survival (CSS), recurrence‐free survival (RFS), and overall survival (OS) were compared between the patients on and off TZD therapy at the time of RC. In subgroup analysis, outcomes in patients specifically taking pioglitazone at the time of RC were compared to those not on a TZD.
Results
Baseline clinicopathological characteristics were similar between patients on and off TZD therapy at the time of RC. Overall, the median CSS rate was not reached in either group (P = 0.7). The estimated 5‐year CSS was 67.8% in the non‐TZD group and 66.3% in the TZD group. On multivariate analysis incorporating patient age, pathological T‐staging, and adjuvant chemotherapy, TZD use was found not to be a significant predictor for CSS (hazard ratio 1.20, 95% confidence interval 0.66–2.17; P = 0.5). Additionally, RFS (P= 0.3) and OS (P = 0.2) were also similar between the two groups without adjusting for other variables. Comparison between patients taking pioglitazone vs patients not taking TZD yielded similar CSS (P = 0.2), RFS (P = 0.5), and OS (P= 0.2).
Conclusions
CSS, as well as RFS and OS after RC were not compromised in patients on TZD therapy at the time of RC. Additional investigation is warranted in patients with non‐muscle‐invasive bladder cancer and muscle‐invasive bladder cancer undergoing bladder‐sparing procedures to assess the safety of using TZD in the setting of active UC.</description><subject>Aged</subject><subject>BCG</subject><subject>Bladder cancer</subject><subject>BladderCancer</subject><subject>Cancer therapies</subject><subject>Carcinoma, Transitional Cell - complications</subject><subject>Carcinoma, Transitional Cell - secondary</subject><subject>Carcinoma, Transitional Cell - surgery</subject><subject>Chemotherapy</subject><subject>Cystectomy</subject><subject>Diabetes mellitus</subject><subject>Diabetes Mellitus - drug therapy</subject><subject>Disease-Free Survival</subject><subject>Female</subject><subject>Humans</subject><subject>Hypoglycemic Agents - therapeutic use</subject><subject>Invasiveness</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Multivariate analysis</subject><subject>Neoplasm Staging</subject><subject>Pioglitazone</subject><subject>PPARγ agonist</subject><subject>Retrospective Studies</subject><subject>Rosiglitazone</subject><subject>Survival</subject><subject>Survival Rate</subject><subject>thiazolidinedione</subject><subject>Thiazolidinediones - therapeutic use</subject><subject>Urinary bladder</subject><subject>Urinary Bladder Neoplasms - complications</subject><subject>Urinary Bladder Neoplasms - pathology</subject><subject>Urinary Bladder Neoplasms - surgery</subject><subject>Urothelial carcinoma</subject><issn>1464-4096</issn><issn>1464-410X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kU1LxDAURYMofowu_ANScKOL0aRNk3Qj6OAnghsFdyFJX5wMnWZM2hH99UZnFBXM5oXkcLiPi9AuwUcknWM96Y8IxbhaQZuEMjqkBD-uft1xxTbQVowTjNMDK9fRRi4EzzkXm2h0bi2YLmbeZt3YqTffuNq1UDvfQubabKY6B20CXlw3zpTp3Bwy3ai6hpAZ1RoI22jNqibCznIO0MPF-f3oanh7d3k9Or0dGkqLasghVxhorTm2IIyotEkpkogprQtQoKglNeNKY1qQ0nCcQ26Z4Ba4phSKATpZeGe9nkJtUqygGjkLbqrCq_TKyd8_rRvLJz-XJRc4L0USHCwFwT_3EDs5ddFA06gWfB8lqYpSkLxiH-j-H3Ti-9Cm9RIlKpHzgrFEHS4oE3yMAex3GILlRzUyVSM_q0ns3s_03-RXFwk4XgAvroHX_03y7OZhoXwHTCmZ0w</recordid><startdate>201802</startdate><enddate>201802</enddate><creator>Li, Roger</creator><creator>Metcalfe, Michael J.</creator><creator>Ferguson, James E.</creator><creator>Mokkapati, Sharada</creator><creator>Nogueras González, Graciela M.</creator><creator>Dinney, Colin P.</creator><creator>Navai, Neema</creator><creator>McConkey, David J.</creator><creator>Sahai, Sunil K.</creator><creator>Kamat, Ashish M.</creator><general>Wiley Subscription Services, Inc</general><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/0000-0003-1274-7200</orcidid></search><sort><creationdate>201802</creationdate><title>Effects of thiazolidinedione in patients with active bladder cancer</title><author>Li, Roger ; Metcalfe, Michael J. ; Ferguson, James E. ; Mokkapati, Sharada ; Nogueras González, Graciela M. ; Dinney, Colin P. ; Navai, Neema ; McConkey, David J. ; Sahai, Sunil K. ; Kamat, Ashish M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4439-7e2a0e4db70fe8c89bc872add6abb3eaea4f1d67ab04315c702e2f687fe7b44e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Aged</topic><topic>BCG</topic><topic>Bladder cancer</topic><topic>BladderCancer</topic><topic>Cancer therapies</topic><topic>Carcinoma, Transitional Cell - complications</topic><topic>Carcinoma, Transitional Cell - secondary</topic><topic>Carcinoma, Transitional Cell - surgery</topic><topic>Chemotherapy</topic><topic>Cystectomy</topic><topic>Diabetes mellitus</topic><topic>Diabetes Mellitus - drug therapy</topic><topic>Disease-Free Survival</topic><topic>Female</topic><topic>Humans</topic><topic>Hypoglycemic Agents - therapeutic use</topic><topic>Invasiveness</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Multivariate analysis</topic><topic>Neoplasm Staging</topic><topic>Pioglitazone</topic><topic>PPARγ agonist</topic><topic>Retrospective Studies</topic><topic>Rosiglitazone</topic><topic>Survival</topic><topic>Survival Rate</topic><topic>thiazolidinedione</topic><topic>Thiazolidinediones - therapeutic use</topic><topic>Urinary bladder</topic><topic>Urinary Bladder Neoplasms - complications</topic><topic>Urinary Bladder Neoplasms - pathology</topic><topic>Urinary Bladder Neoplasms - surgery</topic><topic>Urothelial carcinoma</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Roger</creatorcontrib><creatorcontrib>Metcalfe, Michael J.</creatorcontrib><creatorcontrib>Ferguson, James E.</creatorcontrib><creatorcontrib>Mokkapati, Sharada</creatorcontrib><creatorcontrib>Nogueras González, Graciela M.</creatorcontrib><creatorcontrib>Dinney, Colin P.</creatorcontrib><creatorcontrib>Navai, Neema</creatorcontrib><creatorcontrib>McConkey, David J.</creatorcontrib><creatorcontrib>Sahai, Sunil K.</creatorcontrib><creatorcontrib>Kamat, Ashish M.</creatorcontrib><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>Li, Roger</au><au>Metcalfe, Michael J.</au><au>Ferguson, James E.</au><au>Mokkapati, Sharada</au><au>Nogueras González, Graciela M.</au><au>Dinney, Colin P.</au><au>Navai, Neema</au><au>McConkey, David J.</au><au>Sahai, Sunil K.</au><au>Kamat, Ashish M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of thiazolidinedione in patients with active bladder cancer</atitle><jtitle>BJU international</jtitle><addtitle>BJU Int</addtitle><date>2018-02</date><risdate>2018</risdate><volume>121</volume><issue>2</issue><spage>244</spage><epage>251</epage><pages>244-251</pages><issn>1464-4096</issn><eissn>1464-410X</eissn><abstract>Objective
To examine the influence of perioperative thiazolidinedione (TZD) on cancer‐specific outcomes in patients with diabetes mellitus (DM) undergoing radical cystectomy (RC) for urothelial carcinoma (UC).
Patients and Methods
A retrospective cohort of 173 patients with DM undergoing RC from 2005 to 2010 was identified. Of those, 53 were on TZD treatment at the time of RC, with 33 patients taking pioglitazone. Baseline clinicopathological characteristics, as well as cancer‐specific survival (CSS), recurrence‐free survival (RFS), and overall survival (OS) were compared between the patients on and off TZD therapy at the time of RC. In subgroup analysis, outcomes in patients specifically taking pioglitazone at the time of RC were compared to those not on a TZD.
Results
Baseline clinicopathological characteristics were similar between patients on and off TZD therapy at the time of RC. Overall, the median CSS rate was not reached in either group (P = 0.7). The estimated 5‐year CSS was 67.8% in the non‐TZD group and 66.3% in the TZD group. On multivariate analysis incorporating patient age, pathological T‐staging, and adjuvant chemotherapy, TZD use was found not to be a significant predictor for CSS (hazard ratio 1.20, 95% confidence interval 0.66–2.17; P = 0.5). Additionally, RFS (P= 0.3) and OS (P = 0.2) were also similar between the two groups without adjusting for other variables. Comparison between patients taking pioglitazone vs patients not taking TZD yielded similar CSS (P = 0.2), RFS (P = 0.5), and OS (P= 0.2).
Conclusions
CSS, as well as RFS and OS after RC were not compromised in patients on TZD therapy at the time of RC. Additional investigation is warranted in patients with non‐muscle‐invasive bladder cancer and muscle‐invasive bladder cancer undergoing bladder‐sparing procedures to assess the safety of using TZD in the setting of active UC.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>28872778</pmid><doi>10.1111/bju.14009</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-1274-7200</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Aged BCG Bladder cancer BladderCancer Cancer therapies Carcinoma, Transitional Cell - complications Carcinoma, Transitional Cell - secondary Carcinoma, Transitional Cell - surgery Chemotherapy Cystectomy Diabetes mellitus Diabetes Mellitus - drug therapy Disease-Free Survival Female Humans Hypoglycemic Agents - therapeutic use Invasiveness Male Middle Aged Multivariate analysis Neoplasm Staging Pioglitazone PPARγ agonist Retrospective Studies Rosiglitazone Survival Survival Rate thiazolidinedione Thiazolidinediones - therapeutic use Urinary bladder Urinary Bladder Neoplasms - complications Urinary Bladder Neoplasms - pathology Urinary Bladder Neoplasms - surgery Urothelial carcinoma |
title | Effects of thiazolidinedione in patients with active bladder cancer |
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