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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Veröffentlicht in:Cancer 2012-10, Vol.118 (19), p.4694-4705
Hauptverfasser: 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
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container_end_page 4705
container_issue 19
container_start_page 4694
container_title Cancer
container_volume 118
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.
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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. 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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. 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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. 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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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