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 : 002D98Changes 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 :
- European journal of haematology [ 1600-0609 ] ; 2016.
Descripteurs français
- KwdFr :
- Adulte, Adulte d'âge moyen, Femelle, Humains, Inhibiteurs de protéines kinases (administration et posologie), Inhibiteurs de protéines kinases (effets indésirables), Inhibiteurs de protéines kinases (usage thérapeutique), Mesures des résultats rapportés par les patients, Mâle, Norme de soins, Polyglobulie primitive essentielle (), Polyglobulie primitive essentielle (diagnostic), Polyglobulie primitive essentielle (épidémiologie), Pyrazoles (administration et posologie), Pyrazoles (effets indésirables), Pyrazoles (usage thérapeutique), Qualité de vie, Résultat thérapeutique, Sujet âgé.
- MESH :
- administration et posologie : Inhibiteurs de protéines kinases, Pyrazoles.
- diagnostic : Polyglobulie primitive essentielle.
- effets indésirables : Inhibiteurs de protéines kinases, Pyrazoles.
- usage thérapeutique : Inhibiteurs de protéines kinases, Pyrazoles.
- épidémiologie : Polyglobulie primitive essentielle.
- Adulte, Adulte d'âge moyen, Femelle, Humains, Mesures des résultats rapportés par les patients, Mâle, Norme de soins, Polyglobulie primitive essentielle, Qualité de vie, Résultat thérapeutique, Sujet âgé.
English descriptors
- KwdEn :
- Adult, Aged, Female, Humans, Male, Middle Aged, Patient Reported Outcome Measures, Polycythemia Vera (diagnosis), Polycythemia Vera (epidemiology), Polycythemia Vera (therapy), Protein Kinase Inhibitors (administration & dosage), Protein Kinase Inhibitors (adverse effects), Protein Kinase Inhibitors (therapeutic use), Pyrazoles (administration & dosage), Pyrazoles (adverse effects), Pyrazoles (therapeutic use), Quality of Life, Standard of Care, Treatment Outcome.
- MESH :
- chemical , administration & dosage : Protein Kinase Inhibitors, Pyrazoles.
- chemical , adverse effects : Protein Kinase Inhibitors, Pyrazoles.
- diagnosis : Polycythemia Vera.
- epidemiology : Polycythemia Vera.
- chemical , therapeutic use : Protein Kinase Inhibitors, Pyrazoles.
- therapy : Polycythemia Vera.
- Adult, Aged, Female, Humans, Male, Middle Aged, Patient Reported Outcome Measures, Quality of Life, Standard of Care, Treatment Outcome.
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:26608702Le document en format XML
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Changes in quality of life and disease-related symptoms in patients with polycythemia vera receiving ruxolitinib or standard therapy.</title>
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<author><name sortKey="Passamonti, Francesco" sort="Passamonti, Francesco" uniqKey="Passamonti F" first="Francesco" last="Passamonti">Francesco Passamonti</name>
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<author><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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<author><name sortKey="Pane, Fabrizio" sort="Pane, Fabrizio" uniqKey="Pane F" first="Fabrizio" last="Pane">Fabrizio Pane</name>
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<author><name sortKey="Zachee, Pierre" sort="Zachee, Pierre" uniqKey="Zachee P" first="Pierre" last="Zachee">Pierre Zachee</name>
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<author><name sortKey="Zhen, Huiling" sort="Zhen, Huiling" uniqKey="Zhen H" first="Huiling" last="Zhen">Huiling Zhen</name>
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<author><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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<author><name sortKey="Parasuraman, Shreekant" sort="Parasuraman, Shreekant" uniqKey="Parasuraman S" first="Shreekant" last="Parasuraman">Shreekant Parasuraman</name>
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<author><name sortKey="Li, Jingjin" sort="Li, Jingjin" uniqKey="Li J" first="Jingjin" last="Li">Jingjin Li</name>
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<author><name sortKey="Cote, Isabelle" sort="Cote, Isabelle" uniqKey="Cote I" first="Isabelle" last="Côté">Isabelle Côté</name>
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<author><name sortKey="Habr, Dany" sort="Habr, Dany" uniqKey="Habr D" first="Dany" last="Habr">Dany Habr</name>
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<author><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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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><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>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="adverse effects" xml:lang="en"><term>Protein Kinase Inhibitors</term>
<term>Pyrazoles</term>
</keywords>
<keywords scheme="MESH" qualifier="administration et posologie" xml:lang="fr"><term>Inhibiteurs de protéines kinases</term>
<term>Pyrazoles</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Polycythemia Vera</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnostic" xml:lang="fr"><term>Polyglobulie primitive essentielle</term>
</keywords>
<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>
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<term>Pyrazoles</term>
</keywords>
<keywords scheme="MESH" qualifier="therapy" xml:lang="en"><term>Polycythemia Vera</term>
</keywords>
<keywords scheme="MESH" qualifier="usage thérapeutique" xml:lang="fr"><term>Inhibiteurs de protéines kinases</term>
<term>Pyrazoles</term>
</keywords>
<keywords scheme="MESH" qualifier="épidémiologie" xml:lang="fr"><term>Polyglobulie primitive essentielle</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><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>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><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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<front><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>
</front>
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<pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">26608702</PMID>
<DateCreated><Year>2016</Year>
<Month>07</Month>
<Day>06</Day>
</DateCreated>
<DateCompleted><Year>2017</Year>
<Month>02</Month>
<Day>06</Day>
</DateCompleted>
<DateRevised><Year>2017</Year>
<Month>09</Month>
<Day>30</Day>
</DateRevised>
<Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1600-0609</ISSN>
<JournalIssue CitedMedium="Internet"><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>
</Pagination>
<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>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Mesa</LastName>
<ForeName>Ruben</ForeName>
<Initials>R</Initials>
<AffiliationInfo><Affiliation>Mayo Clinic Cancer Center, Scottsdale, AZ, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Verstovsek</LastName>
<ForeName>Srdan</ForeName>
<Initials>S</Initials>
<AffiliationInfo><Affiliation>The University of Texas MD Anderson Cancer Center, Houston, TX, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Kiladjian</LastName>
<ForeName>Jean-Jacques</ForeName>
<Initials>JJ</Initials>
<AffiliationInfo><Affiliation>Hôpital Saint-Louis et Université Paris Diderot, Paris, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Griesshammer</LastName>
<ForeName>Martin</ForeName>
<Initials>M</Initials>
<AffiliationInfo><Affiliation>Johannes Wesling Clinic, Minden, Germany.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Masszi</LastName>
<ForeName>Tamas</ForeName>
<Initials>T</Initials>
<AffiliationInfo><Affiliation>St. István and St. László Hospital, Budapest, Hungary.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Semmelweis University, Budapest, Hungary.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Durrant</LastName>
<ForeName>Simon</ForeName>
<Initials>S</Initials>
<AffiliationInfo><Affiliation>Royal Brisbane & Women's Hospital, Brisbane, Qld, Australia.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Passamonti</LastName>
<ForeName>Francesco</ForeName>
<Initials>F</Initials>
<AffiliationInfo><Affiliation>Ospedale di Circolo e Fondazione Macchi, Varese, Italy.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Harrison</LastName>
<ForeName>Claire N</ForeName>
<Initials>CN</Initials>
<AffiliationInfo><Affiliation>Guy's and St. Thomas' NHS Foundation Trust, London, UK.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Pane</LastName>
<ForeName>Fabrizio</ForeName>
<Initials>F</Initials>
<AffiliationInfo><Affiliation>University of Naples Federico II, Naples, Italy.</Affiliation>
</AffiliationInfo>
</Author>
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<ForeName>Pierre</ForeName>
<Initials>P</Initials>
<AffiliationInfo><Affiliation>ZNA Stuivenberg, Antwerp, Belgium.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Zhen</LastName>
<ForeName>Huiling</ForeName>
<Initials>H</Initials>
<AffiliationInfo><Affiliation>Incyte Corporation, Wilmington, DE, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Jones</LastName>
<ForeName>Mark M</ForeName>
<Initials>MM</Initials>
<AffiliationInfo><Affiliation>Incyte Corporation, Wilmington, DE, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Parasuraman</LastName>
<ForeName>Shreekant</ForeName>
<Initials>S</Initials>
<AffiliationInfo><Affiliation>Incyte Corporation, Wilmington, DE, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Li</LastName>
<ForeName>Jingjin</ForeName>
<Initials>J</Initials>
<AffiliationInfo><Affiliation>Novartis Pharmaceuticals Corporation, East Hanover, NJ, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Côté</LastName>
<ForeName>Isabelle</ForeName>
<Initials>I</Initials>
<AffiliationInfo><Affiliation>Novartis Pharmaceuticals Corporation, East Hanover, NJ, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Habr</LastName>
<ForeName>Dany</ForeName>
<Initials>D</Initials>
<AffiliationInfo><Affiliation>Novartis Pharmaceuticals Corporation, East Hanover, NJ, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Vannucchi</LastName>
<ForeName>Alessandro M</ForeName>
<Initials>AM</Initials>
<AffiliationInfo><Affiliation>University of Florence, Florence, Italy.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList><PublicationType UI="D017428">Clinical Trial, Phase III</PublicationType>
<PublicationType UI="D016428">Journal Article</PublicationType>
<PublicationType UI="D016448">Multicenter Study</PublicationType>
<PublicationType UI="D016449">Randomized Controlled Trial</PublicationType>
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<ArticleDate DateType="Electronic"><Year>2016</Year>
<Month>01</Month>
<Day>03</Day>
</ArticleDate>
</Article>
<MedlineJournalInfo><Country>England</Country>
<MedlineTA>Eur J Haematol</MedlineTA>
<NlmUniqueID>8703985</NlmUniqueID>
<ISSNLinking>0902-4441</ISSNLinking>
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<ChemicalList><Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="C540383">INCB018424</NameOfSubstance>
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<MeshHeadingList><MeshHeading><DescriptorName UI="D000328" MajorTopicYN="N">Adult</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D000368" MajorTopicYN="N">Aged</DescriptorName>
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<MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName>
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<MeshHeading><DescriptorName UI="D011087" MajorTopicYN="N">Polycythemia Vera</DescriptorName>
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<KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">polycythemia vera</Keyword>
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<PubmedData><History><PubMedPubDate PubStatus="accepted"><Year>2015</Year>
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