Delivery of perioperative chemotherapy for bladder cancer in routine clinical practice
Few articles have documented regimens and timing of perioperative chemotherapy for bladder cancer in routine practice. Here, we describe practice patterns in the general population of Ontario, Canada. In this retrospective cohort study, treatment and physician billing records were linked to the Onta...
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Veröffentlicht in: | Annals of oncology 2014-09, Vol.25 (9), p.1783-1788 |
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description | Few articles have documented regimens and timing of perioperative chemotherapy for bladder cancer in routine practice. Here, we describe practice patterns in the general population of Ontario, Canada.
In this retrospective cohort study, treatment and physician billing records were linked to the Ontario Cancer Registry to describe use of neoadjuvant (NACT) and adjuvant (ACT) chemotherapy among all patients with muscle-invasive bladder cancer treated with cystectomy in Ontario 1994–2008. Time to initiation of ACT (TTAC) was measured from cystectomy. Multivariate Cox regression was used to identify factors associated with overall (OS) and cancer-specific survival (CSS).
Of 2944 patients undergoing cystectomy, 4% (129/2944) and 19% (571/2944) were treated with NACT and ACT, respectively. Five-year OS was 25% [95% confidence interval (CI) 17% to 34%] for NACT, 29% (95% CI 25% to 33%) for ACT cases. Among patients with identifiable drug regimens, cisplatin was used in 82% (253/308) and carboplatin in 14% (43/308). The most common regimens were gemcitabine–cisplatin (54%, 166/308) and methotrexate, vinblastine, doxorubicin, cisplatin (MVAC) (21%, 66/308). Mean TTAC was 10 weeks; 23% of patients had TTAC >12 weeks. TTAC >12 weeks was associated with inferior OS [hazard ratio (HR) 1.28, 95% CI 1.00–1.62] and CSS (HR 1.30, 95% CI 1.00–1.69). In adjusted analyses, OS and CSS were lower among patients treated with carboplatin compared with those treated with cisplatin; OS HR 2.14 (95% CI 1.40–3.29) and CSS HR 2.06 (95% CI 1.26–3.37).
Most patients in the general population receive cisplatin, and this may be associated with superior outcomes to carboplatin. Initiation of ACT beyond 12 weeks is associated with inferior survival. Patients should start ACT as soon as they are medically fit to do so. |
doi_str_mv | 10.1093/annonc/mdu204 |
format | Article |
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In this retrospective cohort study, treatment and physician billing records were linked to the Ontario Cancer Registry to describe use of neoadjuvant (NACT) and adjuvant (ACT) chemotherapy among all patients with muscle-invasive bladder cancer treated with cystectomy in Ontario 1994–2008. Time to initiation of ACT (TTAC) was measured from cystectomy. Multivariate Cox regression was used to identify factors associated with overall (OS) and cancer-specific survival (CSS).
Of 2944 patients undergoing cystectomy, 4% (129/2944) and 19% (571/2944) were treated with NACT and ACT, respectively. Five-year OS was 25% [95% confidence interval (CI) 17% to 34%] for NACT, 29% (95% CI 25% to 33%) for ACT cases. Among patients with identifiable drug regimens, cisplatin was used in 82% (253/308) and carboplatin in 14% (43/308). The most common regimens were gemcitabine–cisplatin (54%, 166/308) and methotrexate, vinblastine, doxorubicin, cisplatin (MVAC) (21%, 66/308). Mean TTAC was 10 weeks; 23% of patients had TTAC >12 weeks. TTAC >12 weeks was associated with inferior OS [hazard ratio (HR) 1.28, 95% CI 1.00–1.62] and CSS (HR 1.30, 95% CI 1.00–1.69). In adjusted analyses, OS and CSS were lower among patients treated with carboplatin compared with those treated with cisplatin; OS HR 2.14 (95% CI 1.40–3.29) and CSS HR 2.06 (95% CI 1.26–3.37).
Most patients in the general population receive cisplatin, and this may be associated with superior outcomes to carboplatin. Initiation of ACT beyond 12 weeks is associated with inferior survival. Patients should start ACT as soon as they are medically fit to do so.</description><identifier>ISSN: 0923-7534</identifier><identifier>EISSN: 1569-8041</identifier><identifier>DOI: 10.1093/annonc/mdu204</identifier><identifier>PMID: 24915872</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Antineoplastic agents ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Biological and medical sciences ; bladder cancer ; Canada ; Carboplatin - therapeutic use ; chemotherapy ; Chemotherapy, Adjuvant ; Cisplatin - therapeutic use ; Cohort Studies ; Cystectomy ; Deoxycytidine - analogs & derivatives ; Deoxycytidine - therapeutic use ; Doxorubicin - therapeutic use ; Female ; Gemcitabine ; General aspects ; Humans ; Male ; Medical sciences ; Methotrexate - therapeutic use ; Middle Aged ; Neoadjuvant Therapy ; Nephrology. Urinary tract diseases ; outcomes ; Pharmacology. Drug treatments ; quality of care ; Retrospective Studies ; surgery ; Treatment Outcome ; Tumors of the urinary system ; Urinary Bladder - pathology ; Urinary Bladder - surgery ; Urinary Bladder Neoplasms - drug therapy ; Urinary Bladder Neoplasms - surgery ; Urinary system involvement in other diseases. Miscellaneous ; Urinary tract. Prostate gland ; Vinblastine - therapeutic use ; Young Adult</subject><ispartof>Annals of oncology, 2014-09, Vol.25 (9), p.1783-1788</ispartof><rights>2014 European Society for Medical Oncology</rights><rights>2015 INIST-CNRS</rights><rights>The Author 2014. Published by Oxford University Press on behalf of the European Society for Medical Oncology. All rights reserved. For permissions, please email: journals.permissions@oup.com.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c410t-cd472ca76f242a9c570091beb1d918868cff7f7eb46b17e92f570f8c62dd7f183</citedby><cites>FETCH-LOGICAL-c410t-cd472ca76f242a9c570091beb1d918868cff7f7eb46b17e92f570f8c62dd7f183</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28752616$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24915872$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Booth, C.M.</creatorcontrib><creatorcontrib>Siemens, D.R.</creatorcontrib><creatorcontrib>Peng, Y.</creatorcontrib><creatorcontrib>Tannock, I.F.</creatorcontrib><creatorcontrib>Mackillop, W.J.</creatorcontrib><title>Delivery of perioperative chemotherapy for bladder cancer in routine clinical practice</title><title>Annals of oncology</title><addtitle>Ann Oncol</addtitle><description>Few articles have documented regimens and timing of perioperative chemotherapy for bladder cancer in routine practice. Here, we describe practice patterns in the general population of Ontario, Canada.
In this retrospective cohort study, treatment and physician billing records were linked to the Ontario Cancer Registry to describe use of neoadjuvant (NACT) and adjuvant (ACT) chemotherapy among all patients with muscle-invasive bladder cancer treated with cystectomy in Ontario 1994–2008. Time to initiation of ACT (TTAC) was measured from cystectomy. Multivariate Cox regression was used to identify factors associated with overall (OS) and cancer-specific survival (CSS).
Of 2944 patients undergoing cystectomy, 4% (129/2944) and 19% (571/2944) were treated with NACT and ACT, respectively. Five-year OS was 25% [95% confidence interval (CI) 17% to 34%] for NACT, 29% (95% CI 25% to 33%) for ACT cases. Among patients with identifiable drug regimens, cisplatin was used in 82% (253/308) and carboplatin in 14% (43/308). The most common regimens were gemcitabine–cisplatin (54%, 166/308) and methotrexate, vinblastine, doxorubicin, cisplatin (MVAC) (21%, 66/308). Mean TTAC was 10 weeks; 23% of patients had TTAC >12 weeks. TTAC >12 weeks was associated with inferior OS [hazard ratio (HR) 1.28, 95% CI 1.00–1.62] and CSS (HR 1.30, 95% CI 1.00–1.69). In adjusted analyses, OS and CSS were lower among patients treated with carboplatin compared with those treated with cisplatin; OS HR 2.14 (95% CI 1.40–3.29) and CSS HR 2.06 (95% CI 1.26–3.37).
Most patients in the general population receive cisplatin, and this may be associated with superior outcomes to carboplatin. Initiation of ACT beyond 12 weeks is associated with inferior survival. Patients should start ACT as soon as they are medically fit to do so.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antineoplastic agents</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>bladder cancer</subject><subject>Canada</subject><subject>Carboplatin - therapeutic use</subject><subject>chemotherapy</subject><subject>Chemotherapy, Adjuvant</subject><subject>Cisplatin - therapeutic use</subject><subject>Cohort Studies</subject><subject>Cystectomy</subject><subject>Deoxycytidine - analogs & derivatives</subject><subject>Deoxycytidine - therapeutic use</subject><subject>Doxorubicin - therapeutic use</subject><subject>Female</subject><subject>Gemcitabine</subject><subject>General aspects</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Methotrexate - therapeutic use</subject><subject>Middle Aged</subject><subject>Neoadjuvant Therapy</subject><subject>Nephrology. Urinary tract diseases</subject><subject>outcomes</subject><subject>Pharmacology. Drug treatments</subject><subject>quality of care</subject><subject>Retrospective Studies</subject><subject>surgery</subject><subject>Treatment Outcome</subject><subject>Tumors of the urinary system</subject><subject>Urinary Bladder - pathology</subject><subject>Urinary Bladder - surgery</subject><subject>Urinary Bladder Neoplasms - drug therapy</subject><subject>Urinary Bladder Neoplasms - surgery</subject><subject>Urinary system involvement in other diseases. Miscellaneous</subject><subject>Urinary tract. Prostate gland</subject><subject>Vinblastine - therapeutic use</subject><subject>Young Adult</subject><issn>0923-7534</issn><issn>1569-8041</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10M1PwyAYBnBiNG5Oj14NF491QGmBo_E7WeJFvTYUXjJMVxroluy_F9OpJy-84c0vhOdB6JKSG0pUudR9H3qz3NgtI_wIzWlVq0ISTo_RnChWFqIq-QydpfRJCKkVU6doxriilRRsjj7uofM7iHscHB4g-pAPPeYVNmvYhHGdr8MeuxBx22lrIWKje5OH73EM29H3mXa-90Z3eIjajN7AOTpxuktwcZgL9P748Hb3XKxen17ubleF4ZSMhbFcMKNF7RhnWplKEKJoCy21ikpZS-OccAJaXrdUgGIuCydNzawVjspygYrpXRNDShFcM0S_0XHfUNJ899NM_TRTP9lfTX7Ythuwv_qnkAyuD0CnHMjFnNWnPydFxWpaZycmBzndzkNskvGQe7E-ghkbG_w_X_gCq6uFnQ</recordid><startdate>20140901</startdate><enddate>20140901</enddate><creator>Booth, C.M.</creator><creator>Siemens, D.R.</creator><creator>Peng, Y.</creator><creator>Tannock, I.F.</creator><creator>Mackillop, W.J.</creator><general>Elsevier Ltd</general><general>Oxford University Press</general><scope>6I.</scope><scope>AAFTH</scope><scope>IQODW</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></search><sort><creationdate>20140901</creationdate><title>Delivery of perioperative chemotherapy for bladder cancer in routine clinical practice</title><author>Booth, C.M. ; Siemens, D.R. ; Peng, Y. ; Tannock, I.F. ; Mackillop, W.J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c410t-cd472ca76f242a9c570091beb1d918868cff7f7eb46b17e92f570f8c62dd7f183</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Antineoplastic agents</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>bladder cancer</topic><topic>Canada</topic><topic>Carboplatin - therapeutic use</topic><topic>chemotherapy</topic><topic>Chemotherapy, Adjuvant</topic><topic>Cisplatin - therapeutic use</topic><topic>Cohort Studies</topic><topic>Cystectomy</topic><topic>Deoxycytidine - analogs & derivatives</topic><topic>Deoxycytidine - therapeutic use</topic><topic>Doxorubicin - therapeutic use</topic><topic>Female</topic><topic>Gemcitabine</topic><topic>General aspects</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Methotrexate - therapeutic use</topic><topic>Middle Aged</topic><topic>Neoadjuvant Therapy</topic><topic>Nephrology. Urinary tract diseases</topic><topic>outcomes</topic><topic>Pharmacology. Drug treatments</topic><topic>quality of care</topic><topic>Retrospective Studies</topic><topic>surgery</topic><topic>Treatment Outcome</topic><topic>Tumors of the urinary system</topic><topic>Urinary Bladder - pathology</topic><topic>Urinary Bladder - surgery</topic><topic>Urinary Bladder Neoplasms - drug therapy</topic><topic>Urinary Bladder Neoplasms - surgery</topic><topic>Urinary system involvement in other diseases. Miscellaneous</topic><topic>Urinary tract. Prostate gland</topic><topic>Vinblastine - therapeutic use</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Booth, C.M.</creatorcontrib><creatorcontrib>Siemens, D.R.</creatorcontrib><creatorcontrib>Peng, Y.</creatorcontrib><creatorcontrib>Tannock, I.F.</creatorcontrib><creatorcontrib>Mackillop, W.J.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Annals of oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Booth, C.M.</au><au>Siemens, D.R.</au><au>Peng, Y.</au><au>Tannock, I.F.</au><au>Mackillop, W.J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Delivery of perioperative chemotherapy for bladder cancer in routine clinical practice</atitle><jtitle>Annals of oncology</jtitle><addtitle>Ann Oncol</addtitle><date>2014-09-01</date><risdate>2014</risdate><volume>25</volume><issue>9</issue><spage>1783</spage><epage>1788</epage><pages>1783-1788</pages><issn>0923-7534</issn><eissn>1569-8041</eissn><abstract>Few articles have documented regimens and timing of perioperative chemotherapy for bladder cancer in routine practice. Here, we describe practice patterns in the general population of Ontario, Canada.
In this retrospective cohort study, treatment and physician billing records were linked to the Ontario Cancer Registry to describe use of neoadjuvant (NACT) and adjuvant (ACT) chemotherapy among all patients with muscle-invasive bladder cancer treated with cystectomy in Ontario 1994–2008. Time to initiation of ACT (TTAC) was measured from cystectomy. Multivariate Cox regression was used to identify factors associated with overall (OS) and cancer-specific survival (CSS).
Of 2944 patients undergoing cystectomy, 4% (129/2944) and 19% (571/2944) were treated with NACT and ACT, respectively. Five-year OS was 25% [95% confidence interval (CI) 17% to 34%] for NACT, 29% (95% CI 25% to 33%) for ACT cases. Among patients with identifiable drug regimens, cisplatin was used in 82% (253/308) and carboplatin in 14% (43/308). The most common regimens were gemcitabine–cisplatin (54%, 166/308) and methotrexate, vinblastine, doxorubicin, cisplatin (MVAC) (21%, 66/308). Mean TTAC was 10 weeks; 23% of patients had TTAC >12 weeks. TTAC >12 weeks was associated with inferior OS [hazard ratio (HR) 1.28, 95% CI 1.00–1.62] and CSS (HR 1.30, 95% CI 1.00–1.69). In adjusted analyses, OS and CSS were lower among patients treated with carboplatin compared with those treated with cisplatin; OS HR 2.14 (95% CI 1.40–3.29) and CSS HR 2.06 (95% CI 1.26–3.37).
Most patients in the general population receive cisplatin, and this may be associated with superior outcomes to carboplatin. Initiation of ACT beyond 12 weeks is associated with inferior survival. Patients should start ACT as soon as they are medically fit to do so.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>24915872</pmid><doi>10.1093/annonc/mdu204</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Aged, 80 and over Antineoplastic agents Antineoplastic Combined Chemotherapy Protocols - therapeutic use Biological and medical sciences bladder cancer Canada Carboplatin - therapeutic use chemotherapy Chemotherapy, Adjuvant Cisplatin - therapeutic use Cohort Studies Cystectomy Deoxycytidine - analogs & derivatives Deoxycytidine - therapeutic use Doxorubicin - therapeutic use Female Gemcitabine General aspects Humans Male Medical sciences Methotrexate - therapeutic use Middle Aged Neoadjuvant Therapy Nephrology. Urinary tract diseases outcomes Pharmacology. Drug treatments quality of care Retrospective Studies surgery Treatment Outcome Tumors of the urinary system Urinary Bladder - pathology Urinary Bladder - surgery Urinary Bladder Neoplasms - drug therapy Urinary Bladder Neoplasms - surgery Urinary system involvement in other diseases. Miscellaneous Urinary tract. Prostate gland Vinblastine - therapeutic use Young Adult |
title | Delivery of perioperative chemotherapy for bladder cancer in routine clinical practice |
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