Malignant melanoma in early-treated Parkinson's disease: the NET-PD trial.
Identifieur interne : 000663 ( PubMed/Curation ); précédent : 000662; suivant : 000664Malignant melanoma in early-treated Parkinson's disease: the NET-PD trial.
Auteurs : Radu Constantinescu [États-Unis] ; Jordan Elm ; Peggy Auinger ; Saloni Sharma ; Erika F. Augustine ; Laith Khadim ; Karl KieburtzSource :
- Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2014.
Descripteurs français
- Wicri :
- geographic : États-Unis.
English descriptors
- KwdEn :
- Adult, Aged, Aged, 80 and over, Cohort Studies, Double-Blind Method, Female, Humans, Incidence, Male, Melanoma (chemically induced), Melanoma (epidemiology), Middle Aged, National Institutes of Health (U.S.), Neuroprotective Agents (therapeutic use), Parkinson Disease (drug therapy), Parkinson Disease (epidemiology), Selegiline (therapeutic use), Skin Neoplasms (epidemiology), United States, Young Adult.
- MESH :
- chemical , therapeutic use : Neuroprotective Agents, Selegiline.
- geographic : United States.
- chemically induced : Melanoma.
- drug therapy : Parkinson Disease.
- epidemiology : Melanoma, Parkinson Disease, Skin Neoplasms.
- Adult, Aged, Aged, 80 and over, Cohort Studies, Double-Blind Method, Female, Humans, Incidence, Male, Middle Aged, National Institutes of Health (U.S.), Young Adult.
Abstract
The risk for malignant melanoma is higher than expected in Parkinson's disease (PD). The National Institutes of Health (NIH) Exploratory Trials in PD (NET-PD) Long-term Study 1 (LS-1) trial is a contemporary phase 3 study of subjects with early, treated PD. The objective of this work was to assess the incidence of malignant melanoma in a PD cohort.
DOI: 10.1002/mds.25734
PubMed: 24323565
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pubmed:24323565Le document en format XML
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<author><name sortKey="Constantinescu, Radu" sort="Constantinescu, Radu" uniqKey="Constantinescu R" first="Radu" last="Constantinescu">Radu Constantinescu</name>
<affiliation wicri:level="1"><nlm:affiliation>Center for Human Experimental Therapeutics, University of Rochester Medical Center, Rochester, New York, USA.</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Center for Human Experimental Therapeutics, University of Rochester Medical Center, Rochester, New York</wicri:regionArea>
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<author><name sortKey="Elm, Jordan" sort="Elm, Jordan" uniqKey="Elm J" first="Jordan" last="Elm">Jordan Elm</name>
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<author><name sortKey="Auinger, Peggy" sort="Auinger, Peggy" uniqKey="Auinger P" first="Peggy" last="Auinger">Peggy Auinger</name>
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<author><name sortKey="Sharma, Saloni" sort="Sharma, Saloni" uniqKey="Sharma S" first="Saloni" last="Sharma">Saloni Sharma</name>
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<author><name sortKey="Augustine, Erika F" sort="Augustine, Erika F" uniqKey="Augustine E" first="Erika F" last="Augustine">Erika F. Augustine</name>
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<author><name sortKey="Khadim, Laith" sort="Khadim, Laith" uniqKey="Khadim L" first="Laith" last="Khadim">Laith Khadim</name>
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<author><name sortKey="Kieburtz, Karl" sort="Kieburtz, Karl" uniqKey="Kieburtz K" first="Karl" last="Kieburtz">Karl Kieburtz</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Malignant melanoma in early-treated Parkinson's disease: the NET-PD trial.</title>
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<author><name sortKey="Elm, Jordan" sort="Elm, Jordan" uniqKey="Elm J" first="Jordan" last="Elm">Jordan Elm</name>
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<author><name sortKey="Auinger, Peggy" sort="Auinger, Peggy" uniqKey="Auinger P" first="Peggy" last="Auinger">Peggy Auinger</name>
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<author><name sortKey="Sharma, Saloni" sort="Sharma, Saloni" uniqKey="Sharma S" first="Saloni" last="Sharma">Saloni Sharma</name>
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<author><name sortKey="Augustine, Erika F" sort="Augustine, Erika F" uniqKey="Augustine E" first="Erika F" last="Augustine">Erika F. Augustine</name>
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<author><name sortKey="Khadim, Laith" sort="Khadim, Laith" uniqKey="Khadim L" first="Laith" last="Khadim">Laith Khadim</name>
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<author><name sortKey="Kieburtz, Karl" sort="Kieburtz, Karl" uniqKey="Kieburtz K" first="Karl" last="Kieburtz">Karl Kieburtz</name>
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<term>Double-Blind Method</term>
<term>Female</term>
<term>Humans</term>
<term>Incidence</term>
<term>Male</term>
<term>Melanoma (chemically induced)</term>
<term>Melanoma (epidemiology)</term>
<term>Middle Aged</term>
<term>National Institutes of Health (U.S.)</term>
<term>Neuroprotective Agents (therapeutic use)</term>
<term>Parkinson Disease (drug therapy)</term>
<term>Parkinson Disease (epidemiology)</term>
<term>Selegiline (therapeutic use)</term>
<term>Skin Neoplasms (epidemiology)</term>
<term>United States</term>
<term>Young Adult</term>
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<keywords scheme="MESH" type="chemical" qualifier="therapeutic use" xml:lang="en"><term>Neuroprotective Agents</term>
<term>Selegiline</term>
</keywords>
<keywords scheme="MESH" type="geographic" xml:lang="en"><term>United States</term>
</keywords>
<keywords scheme="MESH" qualifier="chemically induced" xml:lang="en"><term>Melanoma</term>
</keywords>
<keywords scheme="MESH" qualifier="drug therapy" xml:lang="en"><term>Parkinson Disease</term>
</keywords>
<keywords scheme="MESH" qualifier="epidemiology" xml:lang="en"><term>Melanoma</term>
<term>Parkinson Disease</term>
<term>Skin Neoplasms</term>
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<term>Aged</term>
<term>Aged, 80 and over</term>
<term>Cohort Studies</term>
<term>Double-Blind Method</term>
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<term>Humans</term>
<term>Incidence</term>
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<front><div type="abstract" xml:lang="en">The risk for malignant melanoma is higher than expected in Parkinson's disease (PD). The National Institutes of Health (NIH) Exploratory Trials in PD (NET-PD) Long-term Study 1 (LS-1) trial is a contemporary phase 3 study of subjects with early, treated PD. The objective of this work was to assess the incidence of malignant melanoma in a PD cohort.</div>
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<DateCreated><Year>2014</Year>
<Month>03</Month>
<Day>04</Day>
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<DateCompleted><Year>2014</Year>
<Month>10</Month>
<Day>29</Day>
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<DateRevised><Year>2015</Year>
<Month>10</Month>
<Day>04</Day>
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<Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1531-8257</ISSN>
<JournalIssue CitedMedium="Internet"><Volume>29</Volume>
<Issue>2</Issue>
<PubDate><Year>2014</Year>
<Month>Feb</Month>
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<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
<ISOAbbreviation>Mov. Disord.</ISOAbbreviation>
</Journal>
<ArticleTitle>Malignant melanoma in early-treated Parkinson's disease: the NET-PD trial.</ArticleTitle>
<Pagination><MedlinePgn>263-5</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1002/mds.25734</ELocationID>
<Abstract><AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">The risk for malignant melanoma is higher than expected in Parkinson's disease (PD). The National Institutes of Health (NIH) Exploratory Trials in PD (NET-PD) Long-term Study 1 (LS-1) trial is a contemporary phase 3 study of subjects with early, treated PD. The objective of this work was to assess the incidence of malignant melanoma in a PD cohort.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">Incident melanoma cases were identified from the adverse events log. The expected number of cases was calculated, using the expected incidence rates and the number of person-years.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">A total of 618 females and 1119 males were followed for 6452 person-years; 19 new melanoma cases were observed. The expected number was 5.29. The standardized event ratio compared to the general population was 3.6 (95% confidence interval, 2.2-5.6).</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">The risk for developing melanoma was higher than expected in the NET-PD LS-1 cohort and was similar to the risk reported in earlier comparable clinical trial cohorts. Dermatologic screening may be useful in Parkinson's disease to identify melanoma at an early stage.</AbstractText>
<CopyrightInformation>© 2013 Movement Disorder Society.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Constantinescu</LastName>
<ForeName>Radu</ForeName>
<Initials>R</Initials>
<AffiliationInfo><Affiliation>Center for Human Experimental Therapeutics, University of Rochester Medical Center, Rochester, New York, USA.</Affiliation>
</AffiliationInfo>
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<Author ValidYN="Y"><LastName>Sharma</LastName>
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<CommentsCorrectionsList><CommentsCorrections RefType="Cites"><RefSource>Mov Disord. 2010 Sep 15;25(12):1801-8</RefSource>
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<CommentsCorrections RefType="Cites"><RefSource>Neurology. 2011 Jun 7;76(23):2002-9</RefSource>
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<CommentsCorrections RefType="Cites"><RefSource>PLoS One. 2012;7(9):e45183</RefSource>
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<CommentsCorrections RefType="Cites"><RefSource>Mov Disord. 2012 Oct;27(12):1513-21</RefSource>
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<CommentsCorrections RefType="Cites"><RefSource>J Am Acad Dermatol. 2013 Jun;68(6):e169-75</RefSource>
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</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Curr Opin Cell Biol. 2000 Dec;12(6):719-24</RefSource>
<PMID Version="1">11063938</PMID>
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<CommentsCorrections RefType="Cites"><RefSource>Mov Disord. 2007 Apr 15;22(5):720-2</RefSource>
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</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Cancer Causes Control. 2010 May;21(5):697-707</RefSource>
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