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Impact of secondary cytoreductive surgery on survival in patients with platinum sensitive recurrent ovarian cancer: analysis of the CALYPSO trial.

Identifieur interne : 003042 ( PubMed/Curation ); précédent : 003041; suivant : 003043

Impact of secondary cytoreductive surgery on survival in patients with platinum sensitive recurrent ovarian cancer: analysis of the CALYPSO trial.

Auteurs : Chee Khoon Lee [Australie] ; Sarah Lord [Australie] ; Tami Grunewald [Australie] ; Val Gebski [Australie] ; Anne-Claire Hardy-Bessard [France] ; Jalid Sehouli [Allemagne] ; Kathrine Woie [Norvège] ; Mark Heywood [Canada] ; Christian Schauer [Autriche] ; Ignace Vergote [Belgique] ; Giovanni Scambia [Italie] ; Annamaria Ferrero [Italie] ; Philipp Harter [Allemagne] ; Eric Pujade-Lauraine [France] ; Michael Friedlander [Australie]

Source :

RBID : pubmed:25281492

Descripteurs français

English descriptors

Abstract

The role of secondary cytoreductive surgery (SCR) in platinum-sensitive recurrent ovarian cancer (ROC) remains controversial. The overall survival (OS) benefits for surgery reported in observational studies may be due to the selection of patients with better prognosis.

DOI: 10.1016/j.ygyno.2014.09.017
PubMed: 25281492

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pubmed:25281492

Le document en format XML

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<keywords scheme="MESH" qualifier="traitement médicamenteux" xml:lang="fr">
<term>Récidive tumorale locale</term>
<term>Tumeurs de l'ovaire</term>
</keywords>
<keywords scheme="MESH" qualifier="usage thérapeutique" xml:lang="fr">
<term>Protocoles de polychimiothérapie antinéoplasique</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Adolescent</term>
<term>Adult</term>
<term>Aged</term>
<term>Aged, 80 and over</term>
<term>Combined Modality Therapy</term>
<term>Disease-Free Survival</term>
<term>Female</term>
<term>Humans</term>
<term>Middle Aged</term>
<term>Prognosis</term>
<term>Survival Rate</term>
<term>Young Adult</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Adolescent</term>
<term>Adulte</term>
<term>Adulte d'âge moyen</term>
<term>Association thérapeutique</term>
<term>Femelle</term>
<term>Humains</term>
<term>Jeune adulte</term>
<term>Pronostic</term>
<term>Récidive tumorale locale</term>
<term>Sujet âgé</term>
<term>Sujet âgé de 80 ans ou plus</term>
<term>Survie sans rechute</term>
<term>Taux de survie</term>
<term>Tumeurs de l'ovaire</term>
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</textClass>
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<front>
<div type="abstract" xml:lang="en">The role of secondary cytoreductive surgery (SCR) in platinum-sensitive recurrent ovarian cancer (ROC) remains controversial. The overall survival (OS) benefits for surgery reported in observational studies may be due to the selection of patients with better prognosis.</div>
</front>
</TEI>
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<PMID Version="1">25281492</PMID>
<DateCreated>
<Year>2015</Year>
<Month>01</Month>
<Day>02</Day>
</DateCreated>
<DateCompleted>
<Year>2015</Year>
<Month>03</Month>
<Day>02</Day>
</DateCompleted>
<DateRevised>
<Year>2015</Year>
<Month>11</Month>
<Day>19</Day>
</DateRevised>
<Article PubModel="Print-Electronic">
<Journal>
<ISSN IssnType="Electronic">1095-6859</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>136</Volume>
<Issue>1</Issue>
<PubDate>
<Year>2015</Year>
<Month>Jan</Month>
</PubDate>
</JournalIssue>
<Title>Gynecologic oncology</Title>
<ISOAbbreviation>Gynecol. Oncol.</ISOAbbreviation>
</Journal>
<ArticleTitle>Impact of secondary cytoreductive surgery on survival in patients with platinum sensitive recurrent ovarian cancer: analysis of the CALYPSO trial.</ArticleTitle>
<Pagination>
<MedlinePgn>18-24</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1016/j.ygyno.2014.09.017</ELocationID>
<ELocationID EIdType="pii" ValidYN="Y">S0090-8258(14)01344-4</ELocationID>
<Abstract>
<AbstractText Label="OBJECTIVE" NlmCategory="OBJECTIVE">The role of secondary cytoreductive surgery (SCR) in platinum-sensitive recurrent ovarian cancer (ROC) remains controversial. The overall survival (OS) benefits for surgery reported in observational studies may be due to the selection of patients with better prognosis.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">Using data from the CALYPSO trial, OS of patients who had SCR was compared to those treated with chemotherapy alone. Multivariate analyses were performed to adjust for prognostic factors. We also tested for an interaction between baseline prognostic groupings and the benefit of surgery.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Of the 975 patients randomised in CALYPSO, 19% had SCR and 80% had chemotherapy alone. OS was longer for the SCR group than for chemotherapy alone (median, 49.9 vs. 29.7 months; adjusted hazard ratio (HR), 0.68; P = 0.004). For patients with SCR, the 3-year OS was 72% for those with no measurable disease, and 28% if residual tumour was larger than 5 cm. Patients with good prognostic features benefited the most from SCR (HR 0.43; P < 0.001). The benefit of SCR was less in patients with poorer prognostic features (test of trend P < 0.001).</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">SCR was associated with improved OS in platinum-sensitive ROC, particularly in patients with favourable prognostic characteristics. However, these findings may be due to selection bias, and hence randomised trials are still essential.</AbstractText>
<CopyrightInformation>Copyright © 2014 Elsevier Inc. All rights reserved.</CopyrightInformation>
</Abstract>
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<Author ValidYN="Y">
<LastName>Lee</LastName>
<ForeName>Chee Khoon</ForeName>
<Initials>CK</Initials>
<AffiliationInfo>
<Affiliation>National Health and Medical Research Council Clinical Trials Centre, The University of Sydney, Locked Bag 77, Camperdown, NSW 1450, Australia; Cancer Care Centre, St George Hospital, Grey Street, Kogarah, NSW 2230, Australia. Electronic address: chee.lee@ctc.usyd.edu.au.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Lord</LastName>
<ForeName>Sarah</ForeName>
<Initials>S</Initials>
<AffiliationInfo>
<Affiliation>National Health and Medical Research Council Clinical Trials Centre, The University of Sydney, Locked Bag 77, Camperdown, NSW 1450, Australia.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Grunewald</LastName>
<ForeName>Tami</ForeName>
<Initials>T</Initials>
<AffiliationInfo>
<Affiliation>Cancer Care Centre, St George Hospital, Grey Street, Kogarah, NSW 2230, Australia.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Gebski</LastName>
<ForeName>Val</ForeName>
<Initials>V</Initials>
<AffiliationInfo>
<Affiliation>National Health and Medical Research Council Clinical Trials Centre, The University of Sydney, Locked Bag 77, Camperdown, NSW 1450, Australia.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Hardy-Bessard</LastName>
<ForeName>Anne-Claire</ForeName>
<Initials>AC</Initials>
<AffiliationInfo>
<Affiliation>Clinique Armoricaine de Radiologie, 21 Rue du Vieux Séminaire, 22015 Saint-Brieuc Cedex, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Sehouli</LastName>
<ForeName>Jalid</ForeName>
<Initials>J</Initials>
<AffiliationInfo>
<Affiliation>Department of Gynecology, European Competence Center for Ovarian Cancer, Charité-University Medicine of Berlin, Augustenburger Platz 1, 13353, Berlin, Germany.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Woie</LastName>
<ForeName>Kathrine</ForeName>
<Initials>K</Initials>
<AffiliationInfo>
<Affiliation>Department of Obstetrics and Gynecology, Haukeland University Hospital, N-5021 Bergen, Norway.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Heywood</LastName>
<ForeName>Mark</ForeName>
<Initials>M</Initials>
<AffiliationInfo>
<Affiliation>Vancouver Acute Department of Gynaecology, Rm 6207D Diamond Health Care Centre, 2775 Laurel St., Vancouver, BC V5Z 1M9, Canada.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Schauer</LastName>
<ForeName>Christian</ForeName>
<Initials>C</Initials>
<AffiliationInfo>
<Affiliation>Barmherzige Brüder Graz, Marschallgasse 12, 8020 Graz, Austria.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Vergote</LastName>
<ForeName>Ignace</ForeName>
<Initials>I</Initials>
<AffiliationInfo>
<Affiliation>Division of Gynaecological Oncology, Department of Obstetrics and Gynaecology, Leuven Cancer Institute, University Hospital Leuven, Herestraat 49, B-3000 Leuven, Belgium.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Scambia</LastName>
<ForeName>Giovanni</ForeName>
<Initials>G</Initials>
<AffiliationInfo>
<Affiliation>Department of Obstetrics and Gynecology, Division of Gynecologic Oncology, Catholic University of the Sacred Heart, Largo Agostino Gemelli 8, 00168 Rome, Italy.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Ferrero</LastName>
<ForeName>Annamaria</ForeName>
<Initials>A</Initials>
<AffiliationInfo>
<Affiliation>Academic Department Gynecologic Oncology, Mauriziano Hospital, Largo Turati 62, 10128 Torino, Italy.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Harter</LastName>
<ForeName>Philipp</ForeName>
<Initials>P</Initials>
<AffiliationInfo>
<Affiliation>Department of Gynecology & Gynecologic Oncology, Klinikum Essen Mitte, Henricistrasse 92, 45136 Essen, Germany.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Pujade-Lauraine</LastName>
<ForeName>Eric</ForeName>
<Initials>E</Initials>
<AffiliationInfo>
<Affiliation>Université Paris Descartes, AP-HP, Hôpitaux Universitaires Paris Centre, Site Hôtel-Dieu, Oncologie, 1 Place du Parvis Notre-Dame, 75004 Paris, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Friedlander</LastName>
<ForeName>Michael</ForeName>
<Initials>M</Initials>
<AffiliationInfo>
<Affiliation>Medical Oncology, Prince of Wales Hospital, Barker Street, Randwick, NSW 2013, Australia.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
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<PublicationType UI="D017428">Clinical Trial, Phase III</PublicationType>
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<PublicationType UI="D016448">Multicenter Study</PublicationType>
<PublicationType UI="D016449">Randomized Controlled Trial</PublicationType>
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<ArticleDate DateType="Electronic">
<Year>2014</Year>
<Month>10</Month>
<Day>02</Day>
</ArticleDate>
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<Country>United States</Country>
<MedlineTA>Gynecol Oncol</MedlineTA>
<NlmUniqueID>0365304</NlmUniqueID>
<ISSNLinking>0090-8258</ISSNLinking>
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<NameOfSubstance UI="C506643">liposomal doxorubicin</NameOfSubstance>
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<NameOfSubstance UI="D011092">Polyethylene Glycols</NameOfSubstance>
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<NameOfSubstance UI="D004317">Doxorubicin</NameOfSubstance>
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<MeshHeading>
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<MeshHeading>
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<QualifierName UI="Q000601" MajorTopicYN="Y">surgery</QualifierName>
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<QualifierName UI="Q000008" MajorTopicYN="N">administration & dosage</QualifierName>
<QualifierName UI="Q000009" MajorTopicYN="N">adverse effects</QualifierName>
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<DescriptorName UI="D011092" MajorTopicYN="N">Polyethylene Glycols</DescriptorName>
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<QualifierName UI="Q000009" MajorTopicYN="N">adverse effects</QualifierName>
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<MeshHeading>
<DescriptorName UI="D011379" MajorTopicYN="N">Prognosis</DescriptorName>
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<DescriptorName UI="D055815" MajorTopicYN="N">Young Adult</DescriptorName>
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</MeshHeadingList>
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<Keyword MajorTopicYN="N">Observational study</Keyword>
<Keyword MajorTopicYN="N">Platinum sensitive</Keyword>
<Keyword MajorTopicYN="N">Prognosis</Keyword>
<Keyword MajorTopicYN="N">Recurrent ovarian cancer</Keyword>
<Keyword MajorTopicYN="N">Secondary cytoreductive surgery</Keyword>
<Keyword MajorTopicYN="N">Selection bias</Keyword>
</KeywordList>
</MedlineCitation>
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