PARAMOUNT: Final Overall Survival Results of the Phase III Study of Maintenance Pemetrexed Versus Placebo Immediately After Induction Treatment With Pemetrexed Plus Cisplatin for Advanced Nonsquamous Non–Small-Cell Lung Cancer

In the phase III PARAMOUNT trial, pemetrexed continuation maintenance therapy reduced the risk of disease progression versus placebo (hazard ratio [HR], 0.62; 95% CI, 0.49 to 0.79; P < .001). Here we report final overall survival (OS) and updated safety data. In all, 939 patients with advanced no...

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Veröffentlicht in:Journal of clinical oncology 2013-08, Vol.31 (23), p.2895-2902
Hauptverfasser: PAZ-ARES, Luis G, DE MARINIS, Filippo, CORRAL, Jesús, MELEMED, Symantha, JOHN, William, CHOUAKI, Nadia, ZIMMERMANN, Annamaria H, VISSEREN-GRUL, Carla, GRIDELLI, Cesare, DEDIU, Mircea, THOMAS, Michael, PUJOL, Jean-Louis, BIDOLI, Paolo, MOLINIER, Olivier, TARINI PRASAD SAHOO, LAACK, Eckart, RECK, Martin
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container_end_page 2902
container_issue 23
container_start_page 2895
container_title Journal of clinical oncology
container_volume 31
creator PAZ-ARES, Luis G
DE MARINIS, Filippo
CORRAL, Jesús
MELEMED, Symantha
JOHN, William
CHOUAKI, Nadia
ZIMMERMANN, Annamaria H
VISSEREN-GRUL, Carla
GRIDELLI, Cesare
DEDIU, Mircea
THOMAS, Michael
PUJOL, Jean-Louis
BIDOLI, Paolo
MOLINIER, Olivier
TARINI PRASAD SAHOO
LAACK, Eckart
RECK, Martin
description In the phase III PARAMOUNT trial, pemetrexed continuation maintenance therapy reduced the risk of disease progression versus placebo (hazard ratio [HR], 0.62; 95% CI, 0.49 to 0.79; P < .001). Here we report final overall survival (OS) and updated safety data. In all, 939 patients with advanced nonsquamous non-small-cell lung cancer (NSCLC) received four cycles of pemetrexed-cisplatin induction therapy; then, 539 patients with no disease progression and Eastern Cooperative Oncology Group performance status 0 or 1 were randomly assigned (2:1) to maintenance pemetrexed (500 mg/m(2) on day 1 of 21-day cycles; n = 359) or placebo (n = 180). Log-rank test compared OS between arms as measured from random assignment (α = .0498). The mean number of maintenance cycles was 7.9 (range, one to 44) for pemetrexed and 5.0 (range, one to 38) for placebo. After 397 deaths (pemetrexed, 71%; placebo, 78%) and a median follow-up of 24.3 months for alive patients (95% CI, 23.2 to 25.1 months), pemetrexed therapy resulted in a statistically significant 22% reduction in the risk of death (HR, 0.78; 95% CI, 0.64 to 0.96; P = .0195; median OS: pemetrexed, 13.9 months; placebo, 11.0 months). Survival on pemetrexed was consistently improved for all patient subgroups, including induction response: complete/partial responders (n = 234) OS HR, 0.81; 95% CI, 0.59 to 1.11 and stable disease (n = 285) OS HR, 0.76; 95% CI, 0.57 to 1.01). Postdiscontinuation therapy use was similar: pemetrexed, 64%; placebo, 72%. No new safety findings emerged. Drug-related grade 3 to 4 anemia, fatigue, and neutropenia were significantly higher in pemetrexed-treated patients. Pemetrexed continuation maintenance therapy is well-tolerated and offers superior OS compared with placebo, further demonstrating that it is an efficacious treatment strategy for patients with advanced nonsquamous NSCLC and good performance status who did not progress during pemetrexed-cisplatin induction therapy.
doi_str_mv 10.1200/JCO.2012.47.1102
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Here we report final overall survival (OS) and updated safety data. In all, 939 patients with advanced nonsquamous non-small-cell lung cancer (NSCLC) received four cycles of pemetrexed-cisplatin induction therapy; then, 539 patients with no disease progression and Eastern Cooperative Oncology Group performance status 0 or 1 were randomly assigned (2:1) to maintenance pemetrexed (500 mg/m(2) on day 1 of 21-day cycles; n = 359) or placebo (n = 180). Log-rank test compared OS between arms as measured from random assignment (α = .0498). The mean number of maintenance cycles was 7.9 (range, one to 44) for pemetrexed and 5.0 (range, one to 38) for placebo. After 397 deaths (pemetrexed, 71%; placebo, 78%) and a median follow-up of 24.3 months for alive patients (95% CI, 23.2 to 25.1 months), pemetrexed therapy resulted in a statistically significant 22% reduction in the risk of death (HR, 0.78; 95% CI, 0.64 to 0.96; P = .0195; median OS: pemetrexed, 13.9 months; placebo, 11.0 months). Survival on pemetrexed was consistently improved for all patient subgroups, including induction response: complete/partial responders (n = 234) OS HR, 0.81; 95% CI, 0.59 to 1.11 and stable disease (n = 285) OS HR, 0.76; 95% CI, 0.57 to 1.01). Postdiscontinuation therapy use was similar: pemetrexed, 64%; placebo, 72%. No new safety findings emerged. Drug-related grade 3 to 4 anemia, fatigue, and neutropenia were significantly higher in pemetrexed-treated patients. Pemetrexed continuation maintenance therapy is well-tolerated and offers superior OS compared with placebo, further demonstrating that it is an efficacious treatment strategy for patients with advanced nonsquamous NSCLC and good performance status who did not progress during pemetrexed-cisplatin induction therapy.</description><identifier>ISSN: 0732-183X</identifier><identifier>EISSN: 1527-7755</identifier><identifier>DOI: 10.1200/JCO.2012.47.1102</identifier><identifier>PMID: 23835707</identifier><language>eng</language><publisher>Alexandria, VA: American Society of Clinical Oncology</publisher><subject><![CDATA[Antimetabolites, Antineoplastic - administration & dosage ; Antimetabolites, Antineoplastic - adverse effects ; Antimetabolites, Antineoplastic - therapeutic use ; Antineoplastic Combined Chemotherapy Protocols - administration & dosage ; Antineoplastic Combined Chemotherapy Protocols - adverse effects ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Biological and medical sciences ; Carcinoma, Non-Small-Cell Lung - drug therapy ; Carcinoma, Non-Small-Cell Lung - pathology ; Cisplatin - administration & dosage ; Cisplatin - adverse effects ; Disease-Free Survival ; Double-Blind Method ; Female ; Glutamates - administration & dosage ; Glutamates - adverse effects ; Glutamates - therapeutic use ; Guanine - administration & dosage ; Guanine - adverse effects ; Guanine - analogs & derivatives ; Guanine - therapeutic use ; Humans ; Induction Chemotherapy ; Lung Neoplasms - drug therapy ; Lung Neoplasms - pathology ; Male ; Medical sciences ; Middle Aged ; Multiple tumors. 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Survival on pemetrexed was consistently improved for all patient subgroups, including induction response: complete/partial responders (n = 234) OS HR, 0.81; 95% CI, 0.59 to 1.11 and stable disease (n = 285) OS HR, 0.76; 95% CI, 0.57 to 1.01). Postdiscontinuation therapy use was similar: pemetrexed, 64%; placebo, 72%. No new safety findings emerged. Drug-related grade 3 to 4 anemia, fatigue, and neutropenia were significantly higher in pemetrexed-treated patients. Pemetrexed continuation maintenance therapy is well-tolerated and offers superior OS compared with placebo, further demonstrating that it is an efficacious treatment strategy for patients with advanced nonsquamous NSCLC and good performance status who did not progress during pemetrexed-cisplatin induction therapy.</description><subject>Antimetabolites, Antineoplastic - administration &amp; dosage</subject><subject>Antimetabolites, Antineoplastic - adverse effects</subject><subject>Antimetabolites, Antineoplastic - therapeutic use</subject><subject>Antineoplastic Combined Chemotherapy Protocols - administration &amp; dosage</subject><subject>Antineoplastic Combined Chemotherapy Protocols - adverse effects</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Carcinoma, Non-Small-Cell Lung - drug therapy</subject><subject>Carcinoma, Non-Small-Cell Lung - pathology</subject><subject>Cisplatin - administration &amp; dosage</subject><subject>Cisplatin - adverse effects</subject><subject>Disease-Free Survival</subject><subject>Double-Blind Method</subject><subject>Female</subject><subject>Glutamates - administration &amp; dosage</subject><subject>Glutamates - adverse effects</subject><subject>Glutamates - therapeutic use</subject><subject>Guanine - administration &amp; dosage</subject><subject>Guanine - adverse effects</subject><subject>Guanine - analogs &amp; derivatives</subject><subject>Guanine - therapeutic use</subject><subject>Humans</subject><subject>Induction Chemotherapy</subject><subject>Lung Neoplasms - drug therapy</subject><subject>Lung Neoplasms - pathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Multiple tumors. Solid tumors. Tumors in childhood (general aspects)</subject><subject>Pemetrexed</subject><subject>Pneumology</subject><subject>Remission Induction</subject><subject>Survival Analysis</subject><subject>Treatment Outcome</subject><subject>Tumors</subject><subject>Tumors of the respiratory system and mediastinum</subject><issn>0732-183X</issn><issn>1527-7755</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkcuO0zAUhiMEYsrAnhXyBg2bFF-SOmUXRQwEdabVtFx2luMcTz3KpWM7he54B94Q8SA4armsjnX8nd-_zx9FzwmeEorx6w_FckoxodOETwnB9EE0ISnlMedp-jCaYM5oTDL25Sx64twdxiTJWPo4OqMsVI75JPq1ym_yq-XH680bdGk62aDlHqxsGrQe7N7sQ-MG3NB4h3qN_BbQaisdoLIs0doP9WFsX0nTeehkp8I1tOAtfIMafQLrBodWjVRQ9ahsW6iN9NAcUK49WFR29aC86Tu0sSB9C51Hn43f_i-yaoJEYdyukd50SPcW5fV-fKpG133n7gfZ9gEJ55_ff6zbYD0uIPhfDN0tKkbQPo0eadk4eHaq59Hm8u2meB8vlu_KIl_EKsHMxylJElrPUp0oSTHTXOG5lknNCWCSVjBLgcw4zxTnGFKoKk4Y47NKU6V1NWfn0auj7M729wM4L1rjVPAiOwgWBUnInCUsS3FA8RFVtnfOghY7a1ppD4JgMUYrQrRijFYkXIzRhpEXJ_WhCov8O_AnywC8PAHSKdloG_5u3D-Oz3hG5lngLo7c1txuvxoLwo1bC7JU3KmekSApaDZP2W-F0r2r</recordid><startdate>20130810</startdate><enddate>20130810</enddate><creator>PAZ-ARES, Luis G</creator><creator>DE MARINIS, Filippo</creator><creator>CORRAL, Jesús</creator><creator>MELEMED, Symantha</creator><creator>JOHN, William</creator><creator>CHOUAKI, Nadia</creator><creator>ZIMMERMANN, Annamaria H</creator><creator>VISSEREN-GRUL, Carla</creator><creator>GRIDELLI, Cesare</creator><creator>DEDIU, Mircea</creator><creator>THOMAS, Michael</creator><creator>PUJOL, Jean-Louis</creator><creator>BIDOLI, Paolo</creator><creator>MOLINIER, Olivier</creator><creator>TARINI PRASAD SAHOO</creator><creator>LAACK, Eckart</creator><creator>RECK, Martin</creator><general>American Society of Clinical Oncology</general><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><scope>7X8</scope></search><sort><creationdate>20130810</creationdate><title>PARAMOUNT: Final Overall Survival Results of the Phase III Study of Maintenance Pemetrexed Versus Placebo Immediately After Induction Treatment With Pemetrexed Plus Cisplatin for Advanced Nonsquamous Non–Small-Cell Lung Cancer</title><author>PAZ-ARES, Luis G ; DE MARINIS, Filippo ; CORRAL, Jesús ; MELEMED, Symantha ; JOHN, William ; CHOUAKI, Nadia ; ZIMMERMANN, Annamaria H ; VISSEREN-GRUL, Carla ; GRIDELLI, Cesare ; DEDIU, Mircea ; THOMAS, Michael ; PUJOL, Jean-Louis ; BIDOLI, Paolo ; MOLINIER, Olivier ; TARINI PRASAD SAHOO ; LAACK, Eckart ; RECK, Martin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c403t-51442d65f4ca203f7c09fa4d71e015be65e16778c770e5ebb713376bf2cffb93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Antimetabolites, Antineoplastic - administration &amp; dosage</topic><topic>Antimetabolites, Antineoplastic - adverse effects</topic><topic>Antimetabolites, Antineoplastic - therapeutic use</topic><topic>Antineoplastic Combined Chemotherapy Protocols - administration &amp; dosage</topic><topic>Antineoplastic Combined Chemotherapy Protocols - adverse effects</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Carcinoma, Non-Small-Cell Lung - drug therapy</topic><topic>Carcinoma, Non-Small-Cell Lung - pathology</topic><topic>Cisplatin - administration &amp; dosage</topic><topic>Cisplatin - adverse effects</topic><topic>Disease-Free Survival</topic><topic>Double-Blind Method</topic><topic>Female</topic><topic>Glutamates - administration &amp; dosage</topic><topic>Glutamates - adverse effects</topic><topic>Glutamates - therapeutic use</topic><topic>Guanine - administration &amp; dosage</topic><topic>Guanine - adverse effects</topic><topic>Guanine - analogs &amp; derivatives</topic><topic>Guanine - therapeutic use</topic><topic>Humans</topic><topic>Induction Chemotherapy</topic><topic>Lung Neoplasms - drug therapy</topic><topic>Lung Neoplasms - pathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Multiple tumors. 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Here we report final overall survival (OS) and updated safety data. In all, 939 patients with advanced nonsquamous non-small-cell lung cancer (NSCLC) received four cycles of pemetrexed-cisplatin induction therapy; then, 539 patients with no disease progression and Eastern Cooperative Oncology Group performance status 0 or 1 were randomly assigned (2:1) to maintenance pemetrexed (500 mg/m(2) on day 1 of 21-day cycles; n = 359) or placebo (n = 180). Log-rank test compared OS between arms as measured from random assignment (α = .0498). The mean number of maintenance cycles was 7.9 (range, one to 44) for pemetrexed and 5.0 (range, one to 38) for placebo. After 397 deaths (pemetrexed, 71%; placebo, 78%) and a median follow-up of 24.3 months for alive patients (95% CI, 23.2 to 25.1 months), pemetrexed therapy resulted in a statistically significant 22% reduction in the risk of death (HR, 0.78; 95% CI, 0.64 to 0.96; P = .0195; median OS: pemetrexed, 13.9 months; placebo, 11.0 months). Survival on pemetrexed was consistently improved for all patient subgroups, including induction response: complete/partial responders (n = 234) OS HR, 0.81; 95% CI, 0.59 to 1.11 and stable disease (n = 285) OS HR, 0.76; 95% CI, 0.57 to 1.01). Postdiscontinuation therapy use was similar: pemetrexed, 64%; placebo, 72%. No new safety findings emerged. Drug-related grade 3 to 4 anemia, fatigue, and neutropenia were significantly higher in pemetrexed-treated patients. Pemetrexed continuation maintenance therapy is well-tolerated and offers superior OS compared with placebo, further demonstrating that it is an efficacious treatment strategy for patients with advanced nonsquamous NSCLC and good performance status who did not progress during pemetrexed-cisplatin induction therapy.</abstract><cop>Alexandria, VA</cop><pub>American Society of Clinical Oncology</pub><pmid>23835707</pmid><doi>10.1200/JCO.2012.47.1102</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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ispartof Journal of clinical oncology, 2013-08, Vol.31 (23), p.2895-2902
issn 0732-183X
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source MEDLINE; American Society of Clinical Oncology Online Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection
subjects Antimetabolites, Antineoplastic - administration & dosage
Antimetabolites, Antineoplastic - adverse effects
Antimetabolites, Antineoplastic - therapeutic use
Antineoplastic Combined Chemotherapy Protocols - administration & dosage
Antineoplastic Combined Chemotherapy Protocols - adverse effects
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Biological and medical sciences
Carcinoma, Non-Small-Cell Lung - drug therapy
Carcinoma, Non-Small-Cell Lung - pathology
Cisplatin - administration & dosage
Cisplatin - adverse effects
Disease-Free Survival
Double-Blind Method
Female
Glutamates - administration & dosage
Glutamates - adverse effects
Glutamates - therapeutic use
Guanine - administration & dosage
Guanine - adverse effects
Guanine - analogs & derivatives
Guanine - therapeutic use
Humans
Induction Chemotherapy
Lung Neoplasms - drug therapy
Lung Neoplasms - pathology
Male
Medical sciences
Middle Aged
Multiple tumors. Solid tumors. Tumors in childhood (general aspects)
Pemetrexed
Pneumology
Remission Induction
Survival Analysis
Treatment Outcome
Tumors
Tumors of the respiratory system and mediastinum
title PARAMOUNT: Final Overall Survival Results of the Phase III Study of Maintenance Pemetrexed Versus Placebo Immediately After Induction Treatment With Pemetrexed Plus Cisplatin for Advanced Nonsquamous Non–Small-Cell Lung Cancer
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-02T16%3A53%3A17IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=PARAMOUNT:%20Final%20Overall%20Survival%20Results%20of%20the%20Phase%20III%20Study%20of%20Maintenance%20Pemetrexed%20Versus%20Placebo%20Immediately%20After%20Induction%20Treatment%20With%20Pemetrexed%20Plus%20Cisplatin%20for%20Advanced%20Nonsquamous%20Non%E2%80%93Small-Cell%20Lung%20Cancer&rft.jtitle=Journal%20of%20clinical%20oncology&rft.au=PAZ-ARES,%20Luis%20G&rft.date=2013-08-10&rft.volume=31&rft.issue=23&rft.spage=2895&rft.epage=2902&rft.pages=2895-2902&rft.issn=0732-183X&rft.eissn=1527-7755&rft_id=info:doi/10.1200/JCO.2012.47.1102&rft_dat=%3Cproquest_cross%3E1419343850%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1419343850&rft_id=info:pmid/23835707&rfr_iscdi=true