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...
Gespeichert in:
Veröffentlicht in: | Journal of clinical oncology 2013-08, Vol.31 (23), p.2895-2902 |
---|---|
Hauptverfasser: | , , , , , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
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 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1419343850</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1419343850</sourcerecordid><originalsourceid>FETCH-LOGICAL-c403t-51442d65f4ca203f7c09fa4d71e015be65e16778c770e5ebb713376bf2cffb93</originalsourceid><addsrcrecordid>eNpNkcuO0zAUhiMEYsrAnhXyBg2bFF-SOmUXRQwEdabVtFx2luMcTz3KpWM7he54B94Q8SA4armsjnX8nd-_zx9FzwmeEorx6w_FckoxodOETwnB9EE0ISnlMedp-jCaYM5oTDL25Sx64twdxiTJWPo4OqMsVI75JPq1ym_yq-XH680bdGk62aDlHqxsGrQe7N7sQ-MG3NB4h3qN_BbQaisdoLIs0doP9WFsX0nTeehkp8I1tOAtfIMafQLrBodWjVRQ9ahsW6iN9NAcUK49WFR29aC86Tu0sSB9C51Hn43f_i-yaoJEYdyukd50SPcW5fV-fKpG133n7gfZ9gEJ55_ff6zbYD0uIPhfDN0tKkbQPo0eadk4eHaq59Hm8u2meB8vlu_KIl_EKsHMxylJElrPUp0oSTHTXOG5lknNCWCSVjBLgcw4zxTnGFKoKk4Y47NKU6V1NWfn0auj7M729wM4L1rjVPAiOwgWBUnInCUsS3FA8RFVtnfOghY7a1ppD4JgMUYrQrRijFYkXIzRhpEXJ_WhCov8O_AnywC8PAHSKdloG_5u3D-Oz3hG5lngLo7c1txuvxoLwo1bC7JU3KmekSApaDZP2W-F0r2r</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1419343850</pqid></control><display><type>article</type><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><source>MEDLINE</source><source>American Society of Clinical Oncology Online Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Alma/SFX Local Collection</source><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</creator><creatorcontrib>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</creatorcontrib><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.</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. Solid tumors. Tumors in childhood (general aspects) ; Pemetrexed ; Pneumology ; Remission Induction ; Survival Analysis ; Treatment Outcome ; Tumors ; Tumors of the respiratory system and mediastinum]]></subject><ispartof>Journal of clinical oncology, 2013-08, Vol.31 (23), p.2895-2902</ispartof><rights>2014 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c403t-51442d65f4ca203f7c09fa4d71e015be65e16778c770e5ebb713376bf2cffb93</citedby><cites>FETCH-LOGICAL-c403t-51442d65f4ca203f7c09fa4d71e015be65e16778c770e5ebb713376bf2cffb93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3716,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=27678198$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23835707$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>PAZ-ARES, Luis G</creatorcontrib><creatorcontrib>DE MARINIS, Filippo</creatorcontrib><creatorcontrib>CORRAL, Jesús</creatorcontrib><creatorcontrib>MELEMED, Symantha</creatorcontrib><creatorcontrib>JOHN, William</creatorcontrib><creatorcontrib>CHOUAKI, Nadia</creatorcontrib><creatorcontrib>ZIMMERMANN, Annamaria H</creatorcontrib><creatorcontrib>VISSEREN-GRUL, Carla</creatorcontrib><creatorcontrib>GRIDELLI, Cesare</creatorcontrib><creatorcontrib>DEDIU, Mircea</creatorcontrib><creatorcontrib>THOMAS, Michael</creatorcontrib><creatorcontrib>PUJOL, Jean-Louis</creatorcontrib><creatorcontrib>BIDOLI, Paolo</creatorcontrib><creatorcontrib>MOLINIER, Olivier</creatorcontrib><creatorcontrib>TARINI PRASAD SAHOO</creatorcontrib><creatorcontrib>LAACK, Eckart</creatorcontrib><creatorcontrib>RECK, Martin</creatorcontrib><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><title>Journal of clinical oncology</title><addtitle>J Clin Oncol</addtitle><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.</description><subject>Antimetabolites, Antineoplastic - administration & dosage</subject><subject>Antimetabolites, Antineoplastic - adverse effects</subject><subject>Antimetabolites, Antineoplastic - therapeutic use</subject><subject>Antineoplastic Combined Chemotherapy Protocols - administration & 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 & dosage</subject><subject>Cisplatin - adverse effects</subject><subject>Disease-Free Survival</subject><subject>Double-Blind Method</subject><subject>Female</subject><subject>Glutamates - administration & dosage</subject><subject>Glutamates - adverse effects</subject><subject>Glutamates - therapeutic use</subject><subject>Guanine - administration & dosage</subject><subject>Guanine - adverse effects</subject><subject>Guanine - analogs & 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 & dosage</topic><topic>Antimetabolites, Antineoplastic - adverse effects</topic><topic>Antimetabolites, Antineoplastic - therapeutic use</topic><topic>Antineoplastic Combined Chemotherapy Protocols - administration & 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 & dosage</topic><topic>Cisplatin - adverse effects</topic><topic>Disease-Free Survival</topic><topic>Double-Blind Method</topic><topic>Female</topic><topic>Glutamates - administration & dosage</topic><topic>Glutamates - adverse effects</topic><topic>Glutamates - therapeutic use</topic><topic>Guanine - administration & dosage</topic><topic>Guanine - adverse effects</topic><topic>Guanine - analogs & 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. Solid tumors. Tumors in childhood (general aspects)</topic><topic>Pemetrexed</topic><topic>Pneumology</topic><topic>Remission Induction</topic><topic>Survival Analysis</topic><topic>Treatment Outcome</topic><topic>Tumors</topic><topic>Tumors of the respiratory system and mediastinum</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>PAZ-ARES, Luis G</creatorcontrib><creatorcontrib>DE MARINIS, Filippo</creatorcontrib><creatorcontrib>CORRAL, Jesús</creatorcontrib><creatorcontrib>MELEMED, Symantha</creatorcontrib><creatorcontrib>JOHN, William</creatorcontrib><creatorcontrib>CHOUAKI, Nadia</creatorcontrib><creatorcontrib>ZIMMERMANN, Annamaria H</creatorcontrib><creatorcontrib>VISSEREN-GRUL, Carla</creatorcontrib><creatorcontrib>GRIDELLI, Cesare</creatorcontrib><creatorcontrib>DEDIU, Mircea</creatorcontrib><creatorcontrib>THOMAS, Michael</creatorcontrib><creatorcontrib>PUJOL, Jean-Louis</creatorcontrib><creatorcontrib>BIDOLI, Paolo</creatorcontrib><creatorcontrib>MOLINIER, Olivier</creatorcontrib><creatorcontrib>TARINI PRASAD SAHOO</creatorcontrib><creatorcontrib>LAACK, Eckart</creatorcontrib><creatorcontrib>RECK, Martin</creatorcontrib><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><collection>MEDLINE - Academic</collection><jtitle>Journal of clinical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>PAZ-ARES, Luis G</au><au>DE MARINIS, Filippo</au><au>CORRAL, Jesús</au><au>MELEMED, Symantha</au><au>JOHN, William</au><au>CHOUAKI, Nadia</au><au>ZIMMERMANN, Annamaria H</au><au>VISSEREN-GRUL, Carla</au><au>GRIDELLI, Cesare</au><au>DEDIU, Mircea</au><au>THOMAS, Michael</au><au>PUJOL, Jean-Louis</au><au>BIDOLI, Paolo</au><au>MOLINIER, Olivier</au><au>TARINI PRASAD SAHOO</au><au>LAACK, Eckart</au><au>RECK, Martin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>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</atitle><jtitle>Journal of clinical oncology</jtitle><addtitle>J Clin Oncol</addtitle><date>2013-08-10</date><risdate>2013</risdate><volume>31</volume><issue>23</issue><spage>2895</spage><epage>2902</epage><pages>2895-2902</pages><issn>0732-183X</issn><eissn>1527-7755</eissn><abstract>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.</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> |
fulltext | fulltext |
identifier | ISSN: 0732-183X |
ispartof | Journal of clinical oncology, 2013-08, Vol.31 (23), p.2895-2902 |
issn | 0732-183X 1527-7755 |
language | eng |
recordid | cdi_proquest_miscellaneous_1419343850 |
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 |