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Carboplatin and pegylated liposomal doxorubicin versus carboplatin and paclitaxel in very platinum-sensitive ovarian cancer patients: results from a subset analysis of the CALYPSO phase III trial.

Identifieur interne : 002E60 ( PubMed/Checkpoint ); précédent : 002E59; suivant : 002E61

Carboplatin and pegylated liposomal doxorubicin versus carboplatin and paclitaxel in very platinum-sensitive ovarian cancer patients: results from a subset analysis of the CALYPSO phase III trial.

Auteurs : Sven Mahner [Allemagne] ; Werner Meier [Allemagne] ; Andreas Du Bois [Allemagne] ; Chris Brown [Australie] ; Domenica Lorusso [Italie] ; Tiziana Dell'Anna [Italie] ; Jacques Cretin [France] ; Hanne Havsteen [Danemark] ; Paul Bessette [Canada] ; Alain G. Zeimet [Autriche] ; Ignace Vergote [Belgique] ; Paul Vasey [Australie] ; Eric Pujade-Lauraine [France] ; Laurence Gladieff [France] ; Annamaria Ferrero [Italie]

Source :

RBID : pubmed:25534295

Descripteurs français

English descriptors

Abstract

To perform a subset analysis of patients with very platinum-sensitive recurrent ovarian cancer (ROC) enrolled in the phase III CALYPSO trial.

DOI: 10.1016/j.ejca.2014.11.017
PubMed: 25534295


Affiliations:


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pubmed:25534295

Le document en format XML

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<title level="j">European journal of cancer (Oxford, England : 1990)</title>
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<term>Adult</term>
<term>Aged</term>
<term>Aged, 80 and over</term>
<term>Carboplatin (administration & dosage)</term>
<term>Carboplatin (adverse effects)</term>
<term>Chemotherapy, Adjuvant</term>
<term>Cystadenocarcinoma, Serous (drug therapy)</term>
<term>Cystadenocarcinoma, Serous (epidemiology)</term>
<term>Doxorubicin (administration & dosage)</term>
<term>Doxorubicin (adverse effects)</term>
<term>Doxorubicin (analogs & derivatives)</term>
<term>Drug Resistance, Neoplasm (drug effects)</term>
<term>Drug-Related Side Effects and Adverse Reactions (epidemiology)</term>
<term>Female</term>
<term>Humans</term>
<term>Middle Aged</term>
<term>Ovarian Neoplasms (drug therapy)</term>
<term>Ovarian Neoplasms (epidemiology)</term>
<term>Paclitaxel (administration & dosage)</term>
<term>Paclitaxel (adverse effects)</term>
<term>Platinum Compounds (therapeutic use)</term>
<term>Polyethylene Glycols (administration & dosage)</term>
<term>Polyethylene Glycols (adverse effects)</term>
<term>Recurrence</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Adulte</term>
<term>Adulte d'âge moyen</term>
<term>Carboplatine (administration et posologie)</term>
<term>Carboplatine (effets indésirables)</term>
<term>Composés du platine (usage thérapeutique)</term>
<term>Cystadénocarcinome séreux (traitement médicamenteux)</term>
<term>Cystadénocarcinome séreux (épidémiologie)</term>
<term>Doxorubicine (administration et posologie)</term>
<term>Doxorubicine (analogues et dérivés)</term>
<term>Doxorubicine (effets indésirables)</term>
<term>Effets secondaires indésirables des médicaments (épidémiologie)</term>
<term>Femelle</term>
<term>Humains</term>
<term>Paclitaxel (administration et posologie)</term>
<term>Paclitaxel (effets indésirables)</term>
<term>Polyéthylène glycols (administration et posologie)</term>
<term>Polyéthylène glycols (effets indésirables)</term>
<term>Récidive</term>
<term>Résistance aux médicaments antinéoplasiques ()</term>
<term>Sujet âgé</term>
<term>Sujet âgé de 80 ans ou plus</term>
<term>Traitement médicamenteux adjuvant</term>
<term>Tumeurs de l'ovaire (traitement médicamenteux)</term>
<term>Tumeurs de l'ovaire (épidémiologie)</term>
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<term>Carboplatin</term>
<term>Doxorubicin</term>
<term>Paclitaxel</term>
<term>Polyethylene Glycols</term>
</keywords>
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<term>Carboplatin</term>
<term>Doxorubicin</term>
<term>Paclitaxel</term>
<term>Polyethylene Glycols</term>
</keywords>
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<term>Doxorubicin</term>
</keywords>
<keywords scheme="MESH" qualifier="administration et posologie" xml:lang="fr">
<term>Carboplatine</term>
<term>Doxorubicine</term>
<term>Paclitaxel</term>
<term>Polyéthylène glycols</term>
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<term>Doxorubicine</term>
</keywords>
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<term>Drug Resistance, Neoplasm</term>
</keywords>
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<term>Cystadenocarcinoma, Serous</term>
<term>Ovarian Neoplasms</term>
</keywords>
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<term>Carboplatine</term>
<term>Doxorubicine</term>
<term>Paclitaxel</term>
<term>Polyéthylène glycols</term>
</keywords>
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<term>Cystadenocarcinoma, Serous</term>
<term>Drug-Related Side Effects and Adverse Reactions</term>
<term>Ovarian Neoplasms</term>
</keywords>
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<term>Platinum Compounds</term>
</keywords>
<keywords scheme="MESH" qualifier="traitement médicamenteux" xml:lang="fr">
<term>Cystadénocarcinome séreux</term>
<term>Tumeurs de l'ovaire</term>
</keywords>
<keywords scheme="MESH" qualifier="usage thérapeutique" xml:lang="fr">
<term>Composés du platine</term>
</keywords>
<keywords scheme="MESH" qualifier="épidémiologie" xml:lang="fr">
<term>Cystadénocarcinome séreux</term>
<term>Effets secondaires indésirables des médicaments</term>
<term>Tumeurs de l'ovaire</term>
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<term>Adult</term>
<term>Aged</term>
<term>Aged, 80 and over</term>
<term>Chemotherapy, Adjuvant</term>
<term>Female</term>
<term>Humans</term>
<term>Middle Aged</term>
<term>Recurrence</term>
</keywords>
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<term>Adulte</term>
<term>Adulte d'âge moyen</term>
<term>Femelle</term>
<term>Humains</term>
<term>Récidive</term>
<term>Résistance aux médicaments antinéoplasiques</term>
<term>Sujet âgé</term>
<term>Sujet âgé de 80 ans ou plus</term>
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<front>
<div type="abstract" xml:lang="en">To perform a subset analysis of patients with very platinum-sensitive recurrent ovarian cancer (ROC) enrolled in the phase III CALYPSO trial.</div>
</front>
</TEI>
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<MedlineCitation Status="MEDLINE" Owner="NLM">
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<DateCreated>
<Year>2015</Year>
<Month>02</Month>
<Day>04</Day>
</DateCreated>
<DateCompleted>
<Year>2015</Year>
<Month>04</Month>
<Day>15</Day>
</DateCompleted>
<DateRevised>
<Year>2015</Year>
<Month>11</Month>
<Day>19</Day>
</DateRevised>
<Article PubModel="Print-Electronic">
<Journal>
<ISSN IssnType="Electronic">1879-0852</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>51</Volume>
<Issue>3</Issue>
<PubDate>
<Year>2015</Year>
<Month>Feb</Month>
</PubDate>
</JournalIssue>
<Title>European journal of cancer (Oxford, England : 1990)</Title>
<ISOAbbreviation>Eur. J. Cancer</ISOAbbreviation>
</Journal>
<ArticleTitle>Carboplatin and pegylated liposomal doxorubicin versus carboplatin and paclitaxel in very platinum-sensitive ovarian cancer patients: results from a subset analysis of the CALYPSO phase III trial.</ArticleTitle>
<Pagination>
<MedlinePgn>352-8</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1016/j.ejca.2014.11.017</ELocationID>
<ELocationID EIdType="pii" ValidYN="Y">S0959-8049(14)01142-3</ELocationID>
<Abstract>
<AbstractText Label="AIM" NlmCategory="OBJECTIVE">To perform a subset analysis of patients with very platinum-sensitive recurrent ovarian cancer (ROC) enrolled in the phase III CALYPSO trial.</AbstractText>
<AbstractText Label="PATIENTS AND METHODS" NlmCategory="METHODS">The international non-inferiority trial enrolled women with ROC that relapsed >6 months following first- or second-line platinum- and paclitaxel-based therapies. Patients were randomised to CD [carboplatin-pegylated liposomal doxorubicin (PLD)] or CP (carboplatin-paclitaxel) and stratified by treatment-free interval (TFI). In this analysis, patients with a TFI>24 months were analysed separately for progression free survival (PFS), the primary endpoint of CALYPSO, overall survival (OS) and safety.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">A total of 259 very platinum-sensitive patients were included (n=131, CD; n=128, CP). Median PFS was 12.0 months for the CD arm and 12.3 months for CP [HR=1.05 (95% CI, 0.79-1.40); P=0.73 for superiority] and median OS was 40.2 months for CD and 43.9 for CP [HR=1.18 (95% CI 0.85-1.63); P=0.33 for superiority]. Overall response rates were 42% and 38%, respectively (P=0.46). Toxicities were more common with CP versus CD, including grade 3/4 neutropenia (40.8% versus 27.5%; P=0.025), nausea (4.8% versus 3.1%; P=0.47), allergic reaction (8% versus 3.1%; P=0.082) sensory neuropathy (4.8% versus 2.3%; P=0.27) and grade 2 alopecia (88% versus 9.2%; P<0.001). Grade 3/4 thrombocytopenia (12.2% versus 3.2%; P=0.007) and mucositis (2.3% versus 0%; P=0.089) were more common with CD. Grade 3/4 hand-foot syndrome occurred rarely with CD (3 patients versus 0 in CP arm; P=0.089).</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">CP and CD were equally effective treatment regimens for patients with very platinum-sensitive ROC. The favourable risk-benefit profile suggests carboplatin-PLD as treatment of choice for these patients.</AbstractText>
<CopyrightInformation>Copyright © 2014 Elsevier Ltd. All rights reserved.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y">
<Author ValidYN="Y">
<LastName>Mahner</LastName>
<ForeName>Sven</ForeName>
<Initials>S</Initials>
<AffiliationInfo>
<Affiliation>Arbeitsgemeinschaft Gynäkologische Onkologie, AGO Study Group (AGO) and University Medical Center Hamburg-Eppendorf, Germany. Electronic address: Sven.Mahner@gmx.de.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Meier</LastName>
<ForeName>Werner</ForeName>
<Initials>W</Initials>
<AffiliationInfo>
<Affiliation>Arbeitsgemeinschaft Gynäkologische Onkologie, AGO Study Group (AGO) and Evangelisches Krankenhaus Düsseldorf, Germany.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>du Bois</LastName>
<ForeName>Andreas</ForeName>
<Initials>A</Initials>
<AffiliationInfo>
<Affiliation>Arbeitsgemeinschaft Gynäkologische Onkologie, AGO Study Group (AGO) and Kliniken Essen-Mitte, Germany.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Brown</LastName>
<ForeName>Chris</ForeName>
<Initials>C</Initials>
<AffiliationInfo>
<Affiliation>ANZGOG-NHMRC, Sydney, Australia.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Lorusso</LastName>
<ForeName>Domenica</ForeName>
<Initials>D</Initials>
<AffiliationInfo>
<Affiliation>Multicenter Italian Trials in Ovarian Cancer and gynecologic malignancies group (MITO) and Istituto Nazionale dei Tumori, Milan, Italy.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Dell'Anna</LastName>
<ForeName>Tiziana</ForeName>
<Initials>T</Initials>
<AffiliationInfo>
<Affiliation>Mario Negri Gynecologic Oncology Group (MANGO) and Ospedale San Gerardo, Monza, Italy.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Cretin</LastName>
<ForeName>Jacques</ForeName>
<Initials>J</Initials>
<AffiliationInfo>
<Affiliation>Group d'Investigateurs Nationaux pour l'Etude des Cancers Ovariens (GINECO) and Clinique Valdegourue, Nimes, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Havsteen</LastName>
<ForeName>Hanne</ForeName>
<Initials>H</Initials>
<AffiliationInfo>
<Affiliation>Nordic Society of Gynecological Oncology (NSGO) and Copenhagen University, Copenhagen, Denmark.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Bessette</LastName>
<ForeName>Paul</ForeName>
<Initials>P</Initials>
<AffiliationInfo>
<Affiliation>National Cancer Institute of Canada Clinical Trials Group (NCIC-CTG) and Universite de Sherbrooke, Sherbrooke, Canada.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Zeimet</LastName>
<ForeName>Alain G</ForeName>
<Initials>AG</Initials>
<AffiliationInfo>
<Affiliation>Arbeitsgemeinschaft Gynäkologische Onkologie Österreich (AGO-Austria) and Innsbruck University, Innsbruck, Austria.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Vergote</LastName>
<ForeName>Ignace</ForeName>
<Initials>I</Initials>
<AffiliationInfo>
<Affiliation>European Organisation for Research and Treatment of Cancer (EORTC) and University Hospital Leuven, Leuven, Belgium.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Vasey</LastName>
<ForeName>Paul</ForeName>
<Initials>P</Initials>
<AffiliationInfo>
<Affiliation>Australia New Zealand Gynecological Oncology Group (ANZGOG) and Wesley Medical Centre, Brisbane, Australia.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Pujade-Lauraine</LastName>
<ForeName>Eric</ForeName>
<Initials>E</Initials>
<AffiliationInfo>
<Affiliation>Group d'Investigateurs Nationaux pour l'Etude des Cancers Ovariens (GINECO) and Universite Paris Descartes, Paris, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Gladieff</LastName>
<ForeName>Laurence</ForeName>
<Initials>L</Initials>
<AffiliationInfo>
<Affiliation>Group d'Investigateurs Nationaux pour l'Etude des Cancers Ovariens (GINECO) and Institut Claudius Regaud, Toulouse, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Ferrero</LastName>
<ForeName>Annamaria</ForeName>
<Initials>A</Initials>
<AffiliationInfo>
<Affiliation>Mario Negri Gynecologic Oncology Group (MANGO) and Ospedale Ordine Mauriziano di Torino, Turin, Italy.</Affiliation>
</AffiliationInfo>
</Author>
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<Language>eng</Language>
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<PublicationType UI="D017428">Clinical Trial, Phase III</PublicationType>
<PublicationType UI="D016428">Journal Article</PublicationType>
<PublicationType UI="D016448">Multicenter Study</PublicationType>
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<Month>12</Month>
<Day>17</Day>
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<Country>England</Country>
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<country name="Belgique">
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<name sortKey="Vergote, Ignace" sort="Vergote, Ignace" uniqKey="Vergote I" first="Ignace" last="Vergote">Ignace Vergote</name>
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{{Explor lien
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