Serveur d'exploration sur les relations entre la France et l'Australie

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Changes in quality of life and disease-related symptoms in patients with polycythemia vera receiving ruxolitinib or standard therapy.

Identifieur interne : 002D97 ( Ncbi/Merge ); précédent : 002D96; suivant : 002D98

Changes in quality of life and disease-related symptoms in patients with polycythemia vera receiving ruxolitinib or standard therapy.

Auteurs : Ruben Mesa [États-Unis] ; Srdan Verstovsek [États-Unis] ; Jean-Jacques Kiladjian [France] ; Martin Griesshammer [Allemagne] ; Tamas Masszi [Hongrie] ; Simon Durrant [Australie] ; Francesco Passamonti [Italie] ; Claire N. Harrison [Royaume-Uni] ; Fabrizio Pane [Italie] ; Pierre Zachee [Belgique] ; Huiling Zhen [États-Unis] ; Mark M. Jones [États-Unis] ; Shreekant Parasuraman [États-Unis] ; Jingjin Li [États-Unis] ; Isabelle Côté [États-Unis] ; Dany Habr [États-Unis] ; Alessandro M. Vannucchi [Italie]

Source :

RBID : pubmed:26608702

Descripteurs français

English descriptors

Abstract

Polycythemia vera (PV)-related symptoms may not be adequately controlled with conventional therapy. This current analysis of the RESPONSE trial evaluated the effects of ruxolitinib compared with standard therapy on quality of life (QoL) and symptoms in patients with PV who were hydroxyurea resistant/intolerant.

DOI: 10.1111/ejh.12707
PubMed: 26608702

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pubmed:26608702

Le document en format XML

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<name sortKey="Pane, Fabrizio" sort="Pane, Fabrizio" uniqKey="Pane F" first="Fabrizio" last="Pane">Fabrizio Pane</name>
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<name sortKey="Zachee, Pierre" sort="Zachee, Pierre" uniqKey="Zachee P" first="Pierre" last="Zachee">Pierre Zachee</name>
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<name sortKey="Vannucchi, Alessandro M" sort="Vannucchi, Alessandro M" uniqKey="Vannucchi A" first="Alessandro M" last="Vannucchi">Alessandro M. Vannucchi</name>
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<name sortKey="Passamonti, Francesco" sort="Passamonti, Francesco" uniqKey="Passamonti F" first="Francesco" last="Passamonti">Francesco Passamonti</name>
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<nlm:affiliation>Ospedale di Circolo e Fondazione Macchi, Varese, Italy.</nlm:affiliation>
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<name sortKey="Harrison, Claire N" sort="Harrison, Claire N" uniqKey="Harrison C" first="Claire N" last="Harrison">Claire N. Harrison</name>
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<nlm:affiliation>Guy's and St. Thomas' NHS Foundation Trust, London, UK.</nlm:affiliation>
<country xml:lang="fr">Royaume-Uni</country>
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<name sortKey="Pane, Fabrizio" sort="Pane, Fabrizio" uniqKey="Pane F" first="Fabrizio" last="Pane">Fabrizio Pane</name>
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<name sortKey="Zachee, Pierre" sort="Zachee, Pierre" uniqKey="Zachee P" first="Pierre" last="Zachee">Pierre Zachee</name>
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<nlm:affiliation>ZNA Stuivenberg, Antwerp, Belgium.</nlm:affiliation>
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<name sortKey="Zhen, Huiling" sort="Zhen, Huiling" uniqKey="Zhen H" first="Huiling" last="Zhen">Huiling Zhen</name>
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<nlm:affiliation>Incyte Corporation, Wilmington, DE, USA.</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
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<name sortKey="Jones, Mark M" sort="Jones, Mark M" uniqKey="Jones M" first="Mark M" last="Jones">Mark M. Jones</name>
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<nlm:affiliation>Incyte Corporation, Wilmington, DE, USA.</nlm:affiliation>
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<name sortKey="Parasuraman, Shreekant" sort="Parasuraman, Shreekant" uniqKey="Parasuraman S" first="Shreekant" last="Parasuraman">Shreekant Parasuraman</name>
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<country xml:lang="fr">États-Unis</country>
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<name sortKey="Cote, Isabelle" sort="Cote, Isabelle" uniqKey="Cote I" first="Isabelle" last="Côté">Isabelle Côté</name>
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<name sortKey="Habr, Dany" sort="Habr, Dany" uniqKey="Habr D" first="Dany" last="Habr">Dany Habr</name>
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<nlm:affiliation>Novartis Pharmaceuticals Corporation, East Hanover, NJ, USA.</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
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<name sortKey="Vannucchi, Alessandro M" sort="Vannucchi, Alessandro M" uniqKey="Vannucchi A" first="Alessandro M" last="Vannucchi">Alessandro M. Vannucchi</name>
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<nlm:affiliation>University of Florence, Florence, Italy.</nlm:affiliation>
<country xml:lang="fr">Italie</country>
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<title level="j">European journal of haematology</title>
<idno type="eISSN">1600-0609</idno>
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<term>Adult</term>
<term>Aged</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Patient Reported Outcome Measures</term>
<term>Polycythemia Vera (diagnosis)</term>
<term>Polycythemia Vera (epidemiology)</term>
<term>Polycythemia Vera (therapy)</term>
<term>Protein Kinase Inhibitors (administration & dosage)</term>
<term>Protein Kinase Inhibitors (adverse effects)</term>
<term>Protein Kinase Inhibitors (therapeutic use)</term>
<term>Pyrazoles (administration & dosage)</term>
<term>Pyrazoles (adverse effects)</term>
<term>Pyrazoles (therapeutic use)</term>
<term>Quality of Life</term>
<term>Standard of Care</term>
<term>Treatment Outcome</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Adulte</term>
<term>Adulte d'âge moyen</term>
<term>Femelle</term>
<term>Humains</term>
<term>Inhibiteurs de protéines kinases (administration et posologie)</term>
<term>Inhibiteurs de protéines kinases (effets indésirables)</term>
<term>Inhibiteurs de protéines kinases (usage thérapeutique)</term>
<term>Mesures des résultats rapportés par les patients</term>
<term>Mâle</term>
<term>Norme de soins</term>
<term>Polyglobulie primitive essentielle ()</term>
<term>Polyglobulie primitive essentielle (diagnostic)</term>
<term>Polyglobulie primitive essentielle (épidémiologie)</term>
<term>Pyrazoles (administration et posologie)</term>
<term>Pyrazoles (effets indésirables)</term>
<term>Pyrazoles (usage thérapeutique)</term>
<term>Qualité de vie</term>
<term>Résultat thérapeutique</term>
<term>Sujet âgé</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="administration & dosage" xml:lang="en">
<term>Protein Kinase Inhibitors</term>
<term>Pyrazoles</term>
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<keywords scheme="MESH" type="chemical" qualifier="adverse effects" xml:lang="en">
<term>Protein Kinase Inhibitors</term>
<term>Pyrazoles</term>
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<keywords scheme="MESH" qualifier="administration et posologie" xml:lang="fr">
<term>Inhibiteurs de protéines kinases</term>
<term>Pyrazoles</term>
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<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en">
<term>Polycythemia Vera</term>
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<term>Polyglobulie primitive essentielle</term>
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<keywords scheme="MESH" qualifier="effets indésirables" xml:lang="fr">
<term>Inhibiteurs de protéines kinases</term>
<term>Pyrazoles</term>
</keywords>
<keywords scheme="MESH" qualifier="epidemiology" xml:lang="en">
<term>Polycythemia Vera</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="therapeutic use" xml:lang="en">
<term>Protein Kinase Inhibitors</term>
<term>Pyrazoles</term>
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<term>Polycythemia Vera</term>
</keywords>
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<term>Inhibiteurs de protéines kinases</term>
<term>Pyrazoles</term>
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<term>Polyglobulie primitive essentielle</term>
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<term>Adult</term>
<term>Aged</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Patient Reported Outcome Measures</term>
<term>Quality of Life</term>
<term>Standard of Care</term>
<term>Treatment Outcome</term>
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<term>Adulte</term>
<term>Adulte d'âge moyen</term>
<term>Femelle</term>
<term>Humains</term>
<term>Mesures des résultats rapportés par les patients</term>
<term>Mâle</term>
<term>Norme de soins</term>
<term>Polyglobulie primitive essentielle</term>
<term>Qualité de vie</term>
<term>Résultat thérapeutique</term>
<term>Sujet âgé</term>
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<div type="abstract" xml:lang="en">Polycythemia vera (PV)-related symptoms may not be adequately controlled with conventional therapy. This current analysis of the RESPONSE trial evaluated the effects of ruxolitinib compared with standard therapy on quality of life (QoL) and symptoms in patients with PV who were hydroxyurea resistant/intolerant.</div>
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<Day>06</Day>
</DateCreated>
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<Year>2017</Year>
<Month>02</Month>
<Day>06</Day>
</DateCompleted>
<DateRevised>
<Year>2017</Year>
<Month>09</Month>
<Day>30</Day>
</DateRevised>
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<ISSN IssnType="Electronic">1600-0609</ISSN>
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<Volume>97</Volume>
<Issue>2</Issue>
<PubDate>
<Year>2016</Year>
<Month>Aug</Month>
</PubDate>
</JournalIssue>
<Title>European journal of haematology</Title>
<ISOAbbreviation>Eur. J. Haematol.</ISOAbbreviation>
</Journal>
<ArticleTitle>Changes in quality of life and disease-related symptoms in patients with polycythemia vera receiving ruxolitinib or standard therapy.</ArticleTitle>
<Pagination>
<MedlinePgn>192-200</MedlinePgn>
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<ELocationID EIdType="doi" ValidYN="Y">10.1111/ejh.12707</ELocationID>
<Abstract>
<AbstractText Label="OBJECTIVES" NlmCategory="OBJECTIVE">Polycythemia vera (PV)-related symptoms may not be adequately controlled with conventional therapy. This current analysis of the RESPONSE trial evaluated the effects of ruxolitinib compared with standard therapy on quality of life (QoL) and symptoms in patients with PV who were hydroxyurea resistant/intolerant.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">In the previously reported primary analysis, ruxolitinib achieved the primary composite endpoint of hematocrit control and ≥35% reduction in spleen volume at Week 32. The current analysis evaluated patient-reported outcomes using the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire-Core 30 (EORTC QLQ-C30), the Myeloproliferative Neoplasm Symptom Assessment Form (MPN-SAF), the Pruritus Symptom Impact Scale (PSIS), and the Patient Global Impression of Change (PGIC).</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Compared with standard therapy, ruxolitinib was associated with greater improvements in global health status/QoL, functional subscales, and individual symptom scores of the EORTC QLQ-C30. At Week 32, more patients in the ruxolitinib arm (44%) achieved a ≥10-point improvement in global health status/QoL vs. standard therapy (9%). Improvements in MPN-SAF symptom scores were consistent with improvements in EORTC QLQ-C30, PSIS, and PGIC scores.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">Ruxolitinib provides clinically relevant improvements in QoL and ameliorates symptom burden in patients with PV who are hydroxyurea resistant/intolerant.</AbstractText>
<CopyrightInformation>© 2016 The Authors. European Journal of Haematology Published by John Wiley & Sons Ltd.</CopyrightInformation>
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