Serveur d'exploration sur le lymphœdème

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Lanreotide Autogel 90 mg and lymphorrhea prevention after axillary node dissection in breast cancer: a phase III double blind, randomized, placebo-controlled trial.

Identifieur interne : 002079 ( PubMed/Curation ); précédent : 002078; suivant : 002080

Lanreotide Autogel 90 mg and lymphorrhea prevention after axillary node dissection in breast cancer: a phase III double blind, randomized, placebo-controlled trial.

Auteurs : T. Gauthier [France] ; A. Garuchet-Bigot ; B. Marin ; J. Mollard ; O. Loum ; V. Fermeaux ; I. Jammet ; D. Kanoun ; A. Maubon ; Y. Aubard

Source :

RBID : pubmed:22703757

Descripteurs français

English descriptors

Abstract

The aim of this study was to assess the efficacy of Lanreotide Autogel 90 mg PR to prevent lymphorrhea after axillary dissection in breast cancer.

DOI: 10.1016/j.ejso.2012.05.009
PubMed: 22703757

Links toward previous steps (curation, corpus...)


Links to Exploration step

pubmed:22703757

Le document en format XML

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<term>Aged, 80 and over</term>
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<term>Double-Blind Method</term>
<term>Female</term>
<term>Follow-Up Studies</term>
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<div type="abstract" xml:lang="en">The aim of this study was to assess the efficacy of Lanreotide Autogel 90 mg PR to prevent lymphorrhea after axillary dissection in breast cancer.</div>
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<DateCreated>
<Year>2012</Year>
<Month>09</Month>
<Day>18</Day>
</DateCreated>
<DateCompleted>
<Year>2012</Year>
<Month>11</Month>
<Day>28</Day>
</DateCompleted>
<DateRevised>
<Year>2016</Year>
<Month>11</Month>
<Day>25</Day>
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<Journal>
<ISSN IssnType="Electronic">1532-2157</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>38</Volume>
<Issue>10</Issue>
<PubDate>
<Year>2012</Year>
<Month>Oct</Month>
</PubDate>
</JournalIssue>
<Title>European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology</Title>
<ISOAbbreviation>Eur J Surg Oncol</ISOAbbreviation>
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<ArticleTitle>Lanreotide Autogel 90 mg and lymphorrhea prevention after axillary node dissection in breast cancer: a phase III double blind, randomized, placebo-controlled trial.</ArticleTitle>
<Pagination>
<MedlinePgn>902-9</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1016/j.ejso.2012.05.009</ELocationID>
<ELocationID EIdType="pii" ValidYN="Y">S0748-7983(12)00329-0</ELocationID>
<Abstract>
<AbstractText Label="AIM" NlmCategory="OBJECTIVE">The aim of this study was to assess the efficacy of Lanreotide Autogel 90 mg PR to prevent lymphorrhea after axillary dissection in breast cancer.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">A Phase III double-blind, randomized, placebo-controlled trial was performed between April 1st, 2008, and December 31st, 2010. The primary endpoint was the lymphorrhea volume (ml) in the axillary drain during the first four postoperative days. The secondary end points were the number of days until axillary drain removal, hospital stay duration (days), lymphorrhea volume (ml) up to days 15, 30 and 180, number of cases with seroma aspiration and number of seroma aspirations, evaluation of wound, arm pain and mobility on days 15, 30 and 180.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">A total of 148 patients were recruited for the study. Altogether 145 patients were randomized and analysed on an intention-to-treat basis. On the day before surgery 73 patients received the placebo and 72 patients received lanreotide. At four postoperative days, there was a tendency towards a reduction of the lymphorrhea volume in the lanreotide group (median 292 ml, range 1-965 ml) as compared to the placebo group (median 337 ml, range 0-1230 ml), although it was not statistically significant (p = 0.18). There was no significant difference for the secondary end points. In the group with axillary dissection performed alone (n = 24), the lymphorrhea volume was shown to be significantly reduced in the lanreotide group, (p = 0.035) as compared to the placebo group.</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">Our study did not identify any overall significant reduction of lymphorrhea on lanreotide.</AbstractText>
<CopyrightInformation>Copyright © 2012 Elsevier Ltd. All rights reserved.</CopyrightInformation>
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<Country>England</Country>
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<Chemical>
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<NameOfSubstance UI="C060347">lanreotide</NameOfSubstance>
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<Chemical>
<RegistryNumber>51110-01-1</RegistryNumber>
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