Pemetrexed in combination with cisplatin versus cisplatin monotherapy in patients with recurrent or metastatic head and neck cancer
BACKGROUND: Recurrent or metastatic squamous cell carcinoma of the head and neck (SCCHN) is associated with poor survival. Platinum‐based chemotherapy is often a first‐line treatment. Pemetrexed has shown single‐agent activity in SCCHN and in combination with cisplatin for other tumors. This trial e...
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creator | Urba, Susan van Herpen, Carla M. L. Sahoo, Tarini Prasad Shin, Dong M. Licitra, Lisa Mezei, Klara Reuter, Christoph Hitt, Ricardo Russo, Francesca Chang, Shao‐Chun Hossain, Anwar M. Frimodt‐Moller, Bente Koustenis, Andrew Hong, Ruey‐Long |
description | BACKGROUND:
Recurrent or metastatic squamous cell carcinoma of the head and neck (SCCHN) is associated with poor survival. Platinum‐based chemotherapy is often a first‐line treatment. Pemetrexed has shown single‐agent activity in SCCHN and in combination with cisplatin for other tumors. This trial examined the efficacy of pemetrexed‐cisplatin for SCCHN.
METHODS:
In a double‐blind phase 3 trial, patients with recurrent or metastatic SCCHN and no prior systemic therapy for metastatic disease were randomized to pemetrexed (500 mg/m2) plus cisplatin (75 mg/m2; n = 398) or placebo plus cisplatin (75 mg/m2; n = 397) to assess overall survival (OS) and secondary endpoints.
RESULTS:
Median OS was 7.3 months in the pemetrexed‐cisplatin arm and 6.3 months in the placebo‐cisplatin arm (hazard ratio [HR], 0.87; 95% confidence interval [CI], 0.75‐1.02; P = .082). Median progression‐free survival (PFS, months) was similar in both treatment arms (pemetrexed‐cisplatin, 3.6; placebo‐cisplatin, 2.8; HR, 0.88; 95% CI, 0.76‐1.03; P = .166). Among patients with performance status 0 or 1, pemetrexed‐cisplatin (n = 347) led to longer OS and PFS than placebo‐cisplatin (n = 343; 8.4 vs 6.7 months; HR, 0.83; P = .026; 4.0 vs 3.0 months; HR, 0.84; P = .044, respectively). Among patients with oropharyngeal cancers, pemetrexed‐cisplatin (n = 86) resulted in longer OS and PFS than placebo‐cisplatin (n = 106; 9.9 vs 6.1 months; HR, 0.59; P = .002; 4.0 vs 3.4 months; HR, 0.73; P = .047, respectively). Pemetrexed‐cisplatin toxicity was consistent with studies in other tumors.
CONCLUSIONS:
Pemetrexed‐cisplatin compared with placebo‐cisplatin did not significantly improve survival for the intent‐to‐treat population. However, in a prespecified subgroup analysis, pemetrexed‐cisplatin showed OS and PFS advantage for patients with performance status 0 or 1 or oropharyngeal cancers. Cancer 2012. © 2012 American Cancer Society.
In a double‐blind, placebo‐controlled, phase 3 trial, patients with recurrent or metastatic squamous cell carcinoma of the head and neck are randomized to pemetrexed plus cisplatin or placebo plus cisplatin to assess overall survival and secondary endpoints. Pemetrexed‐cisplatin does not significantly improve survival for the intention‐to‐treat population. However, in a preplanned subgroup analysis, pemetrexed‐cisplatin leads to longer overall survival and progression‐free survival for patients with performance status 0 or 1 and patients with oropharyngeal cancers. |
doi_str_mv | 10.1002/cncr.27449 |
format | Article |
fullrecord | <record><control><sourceid>wiley_pasca</sourceid><recordid>TN_cdi_pascalfrancis_primary_26379520</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>CNCR27449</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2349-a10112761f6d2e855b7ed0bd992b03786e42c80a07ea28d5b8d6e7f19565f05f3</originalsourceid><addsrcrecordid>eNpNUE1LxDAQDaLgunrxF-TiseskbZr2KItfsKiIgreSJlM22qYl6bru2T9udlfE08z7mHnwCDlnMGMA_FI77WdcZll5QCYMSpkAy_ghmQBAkYgsfTsmJyG8Ryi5SCfk-wk7HD1-oaHWUd13tXVqtL2jazsuqbZhaCN29BN9WIV_RNe7flyiV8NmezpEEt0Y9nce9cr7iGnvaUxQYYy6pktUhipnqEP9QbVyGv0pOWpUG_Dsd07J6831y_wuWTze3s-vFonmaVYmigFjXOasyQ3HQohaooHalCWvIZVFjhnXBSiQqHhhRF2YHGXDSpGLBkSTTsnF_u-gglZt42O6DdXgbaf8puJ5KkvBIfrY3re2LW7-dAbVtuNq23G167iaP8yfd1v6A8nFdMU</addsrcrecordid><sourcetype>Index Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Pemetrexed in combination with cisplatin versus cisplatin monotherapy in patients with recurrent or metastatic head and neck cancer</title><source>Access via Wiley Online Library</source><source>Wiley Online Library (Open Access Collection)</source><source>Alma/SFX Local Collection</source><source>EZB Electronic Journals Library</source><creator>Urba, Susan ; van Herpen, Carla M. L. ; Sahoo, Tarini Prasad ; Shin, Dong M. ; Licitra, Lisa ; Mezei, Klara ; Reuter, Christoph ; Hitt, Ricardo ; Russo, Francesca ; Chang, Shao‐Chun ; Hossain, Anwar M. ; Frimodt‐Moller, Bente ; Koustenis, Andrew ; Hong, Ruey‐Long</creator><creatorcontrib>Urba, Susan ; van Herpen, Carla M. L. ; Sahoo, Tarini Prasad ; Shin, Dong M. ; Licitra, Lisa ; Mezei, Klara ; Reuter, Christoph ; Hitt, Ricardo ; Russo, Francesca ; Chang, Shao‐Chun ; Hossain, Anwar M. ; Frimodt‐Moller, Bente ; Koustenis, Andrew ; Hong, Ruey‐Long</creatorcontrib><description>BACKGROUND:
Recurrent or metastatic squamous cell carcinoma of the head and neck (SCCHN) is associated with poor survival. Platinum‐based chemotherapy is often a first‐line treatment. Pemetrexed has shown single‐agent activity in SCCHN and in combination with cisplatin for other tumors. This trial examined the efficacy of pemetrexed‐cisplatin for SCCHN.
METHODS:
In a double‐blind phase 3 trial, patients with recurrent or metastatic SCCHN and no prior systemic therapy for metastatic disease were randomized to pemetrexed (500 mg/m2) plus cisplatin (75 mg/m2; n = 398) or placebo plus cisplatin (75 mg/m2; n = 397) to assess overall survival (OS) and secondary endpoints.
RESULTS:
Median OS was 7.3 months in the pemetrexed‐cisplatin arm and 6.3 months in the placebo‐cisplatin arm (hazard ratio [HR], 0.87; 95% confidence interval [CI], 0.75‐1.02; P = .082). Median progression‐free survival (PFS, months) was similar in both treatment arms (pemetrexed‐cisplatin, 3.6; placebo‐cisplatin, 2.8; HR, 0.88; 95% CI, 0.76‐1.03; P = .166). Among patients with performance status 0 or 1, pemetrexed‐cisplatin (n = 347) led to longer OS and PFS than placebo‐cisplatin (n = 343; 8.4 vs 6.7 months; HR, 0.83; P = .026; 4.0 vs 3.0 months; HR, 0.84; P = .044, respectively). Among patients with oropharyngeal cancers, pemetrexed‐cisplatin (n = 86) resulted in longer OS and PFS than placebo‐cisplatin (n = 106; 9.9 vs 6.1 months; HR, 0.59; P = .002; 4.0 vs 3.4 months; HR, 0.73; P = .047, respectively). Pemetrexed‐cisplatin toxicity was consistent with studies in other tumors.
CONCLUSIONS:
Pemetrexed‐cisplatin compared with placebo‐cisplatin did not significantly improve survival for the intent‐to‐treat population. However, in a prespecified subgroup analysis, pemetrexed‐cisplatin showed OS and PFS advantage for patients with performance status 0 or 1 or oropharyngeal cancers. Cancer 2012. © 2012 American Cancer Society.
In a double‐blind, placebo‐controlled, phase 3 trial, patients with recurrent or metastatic squamous cell carcinoma of the head and neck are randomized to pemetrexed plus cisplatin or placebo plus cisplatin to assess overall survival and secondary endpoints. Pemetrexed‐cisplatin does not significantly improve survival for the intention‐to‐treat population. However, in a preplanned subgroup analysis, pemetrexed‐cisplatin leads to longer overall survival and progression‐free survival for patients with performance status 0 or 1 and patients with oropharyngeal cancers.</description><identifier>ISSN: 0008-543X</identifier><identifier>EISSN: 1097-0142</identifier><identifier>DOI: 10.1002/cncr.27449</identifier><identifier>CODEN: CANCAR</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Biological and medical sciences ; cisplatin ; clinical trial ; head and neck cancer ; Medical sciences ; Otorhinolaryngology (head neck, general aspects and miscellaneous) ; Otorhinolaryngology. Stomatology ; pemetrexed ; phase 3 ; Tumors</subject><ispartof>Cancer, 2012-10, Vol.118 (19), p.4694-4705</ispartof><rights>Copyright © 2012 American Cancer Society</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2349-a10112761f6d2e855b7ed0bd992b03786e42c80a07ea28d5b8d6e7f19565f05f3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fcncr.27449$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fcncr.27449$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,781,785,1418,1434,27926,27927,45576,45577,46411,46835</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26379520$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Urba, Susan</creatorcontrib><creatorcontrib>van Herpen, Carla M. L.</creatorcontrib><creatorcontrib>Sahoo, Tarini Prasad</creatorcontrib><creatorcontrib>Shin, Dong M.</creatorcontrib><creatorcontrib>Licitra, Lisa</creatorcontrib><creatorcontrib>Mezei, Klara</creatorcontrib><creatorcontrib>Reuter, Christoph</creatorcontrib><creatorcontrib>Hitt, Ricardo</creatorcontrib><creatorcontrib>Russo, Francesca</creatorcontrib><creatorcontrib>Chang, Shao‐Chun</creatorcontrib><creatorcontrib>Hossain, Anwar M.</creatorcontrib><creatorcontrib>Frimodt‐Moller, Bente</creatorcontrib><creatorcontrib>Koustenis, Andrew</creatorcontrib><creatorcontrib>Hong, Ruey‐Long</creatorcontrib><title>Pemetrexed in combination with cisplatin versus cisplatin monotherapy in patients with recurrent or metastatic head and neck cancer</title><title>Cancer</title><description>BACKGROUND:
Recurrent or metastatic squamous cell carcinoma of the head and neck (SCCHN) is associated with poor survival. Platinum‐based chemotherapy is often a first‐line treatment. Pemetrexed has shown single‐agent activity in SCCHN and in combination with cisplatin for other tumors. This trial examined the efficacy of pemetrexed‐cisplatin for SCCHN.
METHODS:
In a double‐blind phase 3 trial, patients with recurrent or metastatic SCCHN and no prior systemic therapy for metastatic disease were randomized to pemetrexed (500 mg/m2) plus cisplatin (75 mg/m2; n = 398) or placebo plus cisplatin (75 mg/m2; n = 397) to assess overall survival (OS) and secondary endpoints.
RESULTS:
Median OS was 7.3 months in the pemetrexed‐cisplatin arm and 6.3 months in the placebo‐cisplatin arm (hazard ratio [HR], 0.87; 95% confidence interval [CI], 0.75‐1.02; P = .082). Median progression‐free survival (PFS, months) was similar in both treatment arms (pemetrexed‐cisplatin, 3.6; placebo‐cisplatin, 2.8; HR, 0.88; 95% CI, 0.76‐1.03; P = .166). Among patients with performance status 0 or 1, pemetrexed‐cisplatin (n = 347) led to longer OS and PFS than placebo‐cisplatin (n = 343; 8.4 vs 6.7 months; HR, 0.83; P = .026; 4.0 vs 3.0 months; HR, 0.84; P = .044, respectively). Among patients with oropharyngeal cancers, pemetrexed‐cisplatin (n = 86) resulted in longer OS and PFS than placebo‐cisplatin (n = 106; 9.9 vs 6.1 months; HR, 0.59; P = .002; 4.0 vs 3.4 months; HR, 0.73; P = .047, respectively). Pemetrexed‐cisplatin toxicity was consistent with studies in other tumors.
CONCLUSIONS:
Pemetrexed‐cisplatin compared with placebo‐cisplatin did not significantly improve survival for the intent‐to‐treat population. However, in a prespecified subgroup analysis, pemetrexed‐cisplatin showed OS and PFS advantage for patients with performance status 0 or 1 or oropharyngeal cancers. Cancer 2012. © 2012 American Cancer Society.
In a double‐blind, placebo‐controlled, phase 3 trial, patients with recurrent or metastatic squamous cell carcinoma of the head and neck are randomized to pemetrexed plus cisplatin or placebo plus cisplatin to assess overall survival and secondary endpoints. Pemetrexed‐cisplatin does not significantly improve survival for the intention‐to‐treat population. However, in a preplanned subgroup analysis, pemetrexed‐cisplatin leads to longer overall survival and progression‐free survival for patients with performance status 0 or 1 and patients with oropharyngeal cancers.</description><subject>Biological and medical sciences</subject><subject>cisplatin</subject><subject>clinical trial</subject><subject>head and neck cancer</subject><subject>Medical sciences</subject><subject>Otorhinolaryngology (head neck, general aspects and miscellaneous)</subject><subject>Otorhinolaryngology. Stomatology</subject><subject>pemetrexed</subject><subject>phase 3</subject><subject>Tumors</subject><issn>0008-543X</issn><issn>1097-0142</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNpNUE1LxDAQDaLgunrxF-TiseskbZr2KItfsKiIgreSJlM22qYl6bru2T9udlfE08z7mHnwCDlnMGMA_FI77WdcZll5QCYMSpkAy_ghmQBAkYgsfTsmJyG8Ryi5SCfk-wk7HD1-oaHWUd13tXVqtL2jazsuqbZhaCN29BN9WIV_RNe7flyiV8NmezpEEt0Y9nce9cr7iGnvaUxQYYy6pktUhipnqEP9QbVyGv0pOWpUG_Dsd07J6831y_wuWTze3s-vFonmaVYmigFjXOasyQ3HQohaooHalCWvIZVFjhnXBSiQqHhhRF2YHGXDSpGLBkSTTsnF_u-gglZt42O6DdXgbaf8puJ5KkvBIfrY3re2LW7-dAbVtuNq23G167iaP8yfd1v6A8nFdMU</recordid><startdate>20121001</startdate><enddate>20121001</enddate><creator>Urba, Susan</creator><creator>van Herpen, Carla M. L.</creator><creator>Sahoo, Tarini Prasad</creator><creator>Shin, Dong M.</creator><creator>Licitra, Lisa</creator><creator>Mezei, Klara</creator><creator>Reuter, Christoph</creator><creator>Hitt, Ricardo</creator><creator>Russo, Francesca</creator><creator>Chang, Shao‐Chun</creator><creator>Hossain, Anwar M.</creator><creator>Frimodt‐Moller, Bente</creator><creator>Koustenis, Andrew</creator><creator>Hong, Ruey‐Long</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Blackwell</general><scope>IQODW</scope></search><sort><creationdate>20121001</creationdate><title>Pemetrexed in combination with cisplatin versus cisplatin monotherapy in patients with recurrent or metastatic head and neck cancer</title><author>Urba, Susan ; van Herpen, Carla M. L. ; Sahoo, Tarini Prasad ; Shin, Dong M. ; Licitra, Lisa ; Mezei, Klara ; Reuter, Christoph ; Hitt, Ricardo ; Russo, Francesca ; Chang, Shao‐Chun ; Hossain, Anwar M. ; Frimodt‐Moller, Bente ; Koustenis, Andrew ; Hong, Ruey‐Long</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2349-a10112761f6d2e855b7ed0bd992b03786e42c80a07ea28d5b8d6e7f19565f05f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Biological and medical sciences</topic><topic>cisplatin</topic><topic>clinical trial</topic><topic>head and neck cancer</topic><topic>Medical sciences</topic><topic>Otorhinolaryngology (head neck, general aspects and miscellaneous)</topic><topic>Otorhinolaryngology. Stomatology</topic><topic>pemetrexed</topic><topic>phase 3</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Urba, Susan</creatorcontrib><creatorcontrib>van Herpen, Carla M. L.</creatorcontrib><creatorcontrib>Sahoo, Tarini Prasad</creatorcontrib><creatorcontrib>Shin, Dong M.</creatorcontrib><creatorcontrib>Licitra, Lisa</creatorcontrib><creatorcontrib>Mezei, Klara</creatorcontrib><creatorcontrib>Reuter, Christoph</creatorcontrib><creatorcontrib>Hitt, Ricardo</creatorcontrib><creatorcontrib>Russo, Francesca</creatorcontrib><creatorcontrib>Chang, Shao‐Chun</creatorcontrib><creatorcontrib>Hossain, Anwar M.</creatorcontrib><creatorcontrib>Frimodt‐Moller, Bente</creatorcontrib><creatorcontrib>Koustenis, Andrew</creatorcontrib><creatorcontrib>Hong, Ruey‐Long</creatorcontrib><collection>Pascal-Francis</collection><jtitle>Cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Urba, Susan</au><au>van Herpen, Carla M. L.</au><au>Sahoo, Tarini Prasad</au><au>Shin, Dong M.</au><au>Licitra, Lisa</au><au>Mezei, Klara</au><au>Reuter, Christoph</au><au>Hitt, Ricardo</au><au>Russo, Francesca</au><au>Chang, Shao‐Chun</au><au>Hossain, Anwar M.</au><au>Frimodt‐Moller, Bente</au><au>Koustenis, Andrew</au><au>Hong, Ruey‐Long</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pemetrexed in combination with cisplatin versus cisplatin monotherapy in patients with recurrent or metastatic head and neck cancer</atitle><jtitle>Cancer</jtitle><date>2012-10-01</date><risdate>2012</risdate><volume>118</volume><issue>19</issue><spage>4694</spage><epage>4705</epage><pages>4694-4705</pages><issn>0008-543X</issn><eissn>1097-0142</eissn><coden>CANCAR</coden><abstract>BACKGROUND:
Recurrent or metastatic squamous cell carcinoma of the head and neck (SCCHN) is associated with poor survival. Platinum‐based chemotherapy is often a first‐line treatment. Pemetrexed has shown single‐agent activity in SCCHN and in combination with cisplatin for other tumors. This trial examined the efficacy of pemetrexed‐cisplatin for SCCHN.
METHODS:
In a double‐blind phase 3 trial, patients with recurrent or metastatic SCCHN and no prior systemic therapy for metastatic disease were randomized to pemetrexed (500 mg/m2) plus cisplatin (75 mg/m2; n = 398) or placebo plus cisplatin (75 mg/m2; n = 397) to assess overall survival (OS) and secondary endpoints.
RESULTS:
Median OS was 7.3 months in the pemetrexed‐cisplatin arm and 6.3 months in the placebo‐cisplatin arm (hazard ratio [HR], 0.87; 95% confidence interval [CI], 0.75‐1.02; P = .082). Median progression‐free survival (PFS, months) was similar in both treatment arms (pemetrexed‐cisplatin, 3.6; placebo‐cisplatin, 2.8; HR, 0.88; 95% CI, 0.76‐1.03; P = .166). Among patients with performance status 0 or 1, pemetrexed‐cisplatin (n = 347) led to longer OS and PFS than placebo‐cisplatin (n = 343; 8.4 vs 6.7 months; HR, 0.83; P = .026; 4.0 vs 3.0 months; HR, 0.84; P = .044, respectively). Among patients with oropharyngeal cancers, pemetrexed‐cisplatin (n = 86) resulted in longer OS and PFS than placebo‐cisplatin (n = 106; 9.9 vs 6.1 months; HR, 0.59; P = .002; 4.0 vs 3.4 months; HR, 0.73; P = .047, respectively). Pemetrexed‐cisplatin toxicity was consistent with studies in other tumors.
CONCLUSIONS:
Pemetrexed‐cisplatin compared with placebo‐cisplatin did not significantly improve survival for the intent‐to‐treat population. However, in a prespecified subgroup analysis, pemetrexed‐cisplatin showed OS and PFS advantage for patients with performance status 0 or 1 or oropharyngeal cancers. Cancer 2012. © 2012 American Cancer Society.
In a double‐blind, placebo‐controlled, phase 3 trial, patients with recurrent or metastatic squamous cell carcinoma of the head and neck are randomized to pemetrexed plus cisplatin or placebo plus cisplatin to assess overall survival and secondary endpoints. Pemetrexed‐cisplatin does not significantly improve survival for the intention‐to‐treat population. However, in a preplanned subgroup analysis, pemetrexed‐cisplatin leads to longer overall survival and progression‐free survival for patients with performance status 0 or 1 and patients with oropharyngeal cancers.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><doi>10.1002/cncr.27449</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Biological and medical sciences cisplatin clinical trial head and neck cancer Medical sciences Otorhinolaryngology (head neck, general aspects and miscellaneous) Otorhinolaryngology. Stomatology pemetrexed phase 3 Tumors |
title | Pemetrexed in combination with cisplatin versus cisplatin monotherapy in patients with recurrent or metastatic head and neck cancer |
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