Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/118938
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dc.contributor.authorScarisbrick, Julia J.-
dc.contributor.authorPrince, H Miles-
dc.contributor.authorVermeer, Maarten H.-
dc.contributor.authorQuaglino, Pietro-
dc.contributor.authorHorwitz, Steven-
dc.contributor.authorPorcu, Pierluigi-
dc.contributor.authorStadler, Rudolf-
dc.contributor.authorWood, Gary-
dc.contributor.authorBeylot-Barry, Marie-
dc.contributor.authorPham-Ledard, Anne-
dc.contributor.authorFoss, Francine-
dc.contributor.authorGirardi, Michael-
dc.contributor.authorBagot, Martine-
dc.contributor.authorMichel, Laurence-
dc.contributor.authorBattistella, Maxime-
dc.contributor.authorGuitart, Joan-
dc.contributor.authorKuzel, Timothy M.-
dc.contributor.authorMartinez-Escala, Maria Estela-
dc.contributor.authorEstrach Panella, Ma. Teresa (María Teresa)-
dc.contributor.authorPapadavid, Evangelia-
dc.contributor.authorAntoniou, Christina-
dc.contributor.authorRigopoulos, Dimitis-
dc.contributor.authorNikolaou, Vassilki-
dc.contributor.authorSugaya, Makoto-
dc.contributor.authorMiyagaki, Tomomitsu-
dc.contributor.authorGniadecki, Robert-
dc.contributor.authorSanches, José Antonio-
dc.contributor.authorCury-Martins, Jade-
dc.contributor.authorMiyashiro, Denis-
dc.contributor.authorServitje Bedate, Octavio-
dc.contributor.authorMuniesa Montserrat, Cristina-
dc.contributor.authorBerti, Emilio-
dc.contributor.authorOnida, Francesco-
dc.contributor.authorCorti, Laura-
dc.contributor.authorHodak, Emilia-
dc.contributor.authorAmitay-Laish, Iris-
dc.contributor.authorOrtiz Romero, Pablo L.-
dc.contributor.authorRodríguez Peralto, José Luis-
dc.contributor.authorKnobler, Robert-
dc.contributor.authorPorkert, Stefanie-
dc.date.accessioned2018-01-10T08:50:30Z-
dc.date.available2018-01-10T08:50:30Z-
dc.date.issued2015-10-05-
dc.identifier.issn0732-183X-
dc.identifier.urihttp://hdl.handle.net/2445/118938-
dc.description.abstractAdvanced-stage mycosis fungoides (MF; stage IIB to IV) and Sézary syndrome (SS) are aggressive lymphomas with a median survival of 1 to 5 years. Clinical management is stage based; however, there is wide range of outcome within stages. Published prognostic studies in MF/SS have been single-center trials. Because of the rarity of MF/SS, only a large collaboration would power a study to identify independent prognostic markers. PATIENTS AND METHODS: Literature review identified the following 10 candidate markers: stage, age, sex, cutaneous histologic features of folliculotropism, CD30 positivity, proliferation index, large-cell transformation, WBC/lymphocyte count, serum lactate dehydrogenase, and identical T-cell clone in blood and skin. Data were collected at specialist centers on patients diagnosed with advanced-stage MF/SS from 2007. Each parameter recorded at diagnosis was tested against overall survival (OS). RESULTS: Staging data on 1,275 patients with advanced MF/SS from 29 international sites were included for survival analysis. The median OS was 63 months, with 2- and 5-year survival rates of 77% and 52%, respectively. The median OS for patients with stage IIB disease was 68 months, but patients diagnosed with stage III disease had slightly improved survival compared with patients with stage IIB, although patients diagnosed with stage IV disease had significantly worse survival (48 months for stage IVA and 33 months for stage IVB). Of the 10 variables tested, four (stage IV, age > 60 years, large-cell transformation, and increased lactate dehydrogenase) were independent prognostic markers for a worse survival. Combining these four factors in a prognostic index model identified the following three risk groups across stages with significantly different 5-year survival rates: low risk (68%), intermediate risk (44%), and high risk (28%). CONCLUSION: To our knowledge, this study includes the largest cohort of patients with advanced-stage MF/SS and identifies markers with independent prognostic value, which, used together in a prognostic index, may be useful to stratify advanced-stage patients.-
dc.format.extent13 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherAmerican Society of Clinical Oncology-
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1200/JCO.2015.61.7142-
dc.relation.ispartofJournal of Clinical Oncology, 2015, vol. 33, num. 32, p. 3766-3773-
dc.relation.urihttps://doi.org/10.1200/JCO.2015.61.7142-
dc.rights(c) American Society of Clinical Oncology, 2015-
dc.sourceArticles publicats en revistes (Ciències Clíniques)-
dc.subject.classificationLimfomes-
dc.subject.classificationMalalties de la pell-
dc.subject.classificationMicosi-
dc.subject.classificationOncologia-
dc.subject.classificationEstudi de casos-
dc.subject.otherLymphomas-
dc.subject.otherSkin diseases-
dc.subject.otherMycosis-
dc.subject.otherOncology-
dc.subject.otherCase studies-
dc.titleCutaneous lymphoma international consortium study of outcome in advanced stages of mycosis fungoides and Sézary syndrome: effect of specific prognostic markers on survival and development of a prognostic model-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.identifier.idgrec654944-
dc.date.updated2018-01-10T08:50:30Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.pmid26438120-
Appears in Collections:Articles publicats en revistes (Medicina)
Articles publicats en revistes (Ciències Clíniques)
Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

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