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dc.contributor.authorMorel, Pierre
dc.contributor.authorDuhamel, Alain
dc.contributor.authorGobbi, Paolo
dc.contributor.authorDimopoulos, Meletios A.
dc.contributor.authorDhodapkar, Madhav V.
dc.contributor.authorMcCoy, Jason
dc.contributor.authorCrowley, John
dc.contributor.authorOcio San Miguel, Enrique M.
dc.contributor.authorGarcía Sanz, Ramón 
dc.contributor.authorTreon, Steven P.
dc.contributor.authorLeblond, Veronique
dc.contributor.authorKyle, Robert A.
dc.contributor.authorBarlogie, Bart
dc.contributor.authorMerlini, Giampaolo
dc.date.accessioned2024-02-02T16:19:03Z
dc.date.available2024-02-02T16:19:03Z
dc.date.issued2009-04-30
dc.identifier.citationMorel, P., Duhamel, A., Gobbi, P., Dimopoulos, M. A., Dhodapkar, M. V., McCoy, J., ... & Merlini, G. (2009). International prognostic scoring system for Waldenström macroglobulinemia. Blood, The Journal of the American Society of Hematology, 113(18), 4163-4170. https://doi.org/10.1182/blood-2008-08-174961es_ES
dc.identifier.issn0006-4971
dc.identifier.urihttp://hdl.handle.net/10366/155235
dc.descriptionFue uno de los primeros pasos para lograr aunar al grupo internacional de MW, que ha proporcionado numerosos beneficios a los pacientes con esta enfermedad, transformando una neoplasia maligna en una enfermedad crónica con igual supervivencia que la población generales_ES
dc.description.abstract[EN]Recently, many new drugs have been developed for the treatment of Waldenström macroglobulinemia (WM). To optimize the treatment according to the prognosis and to facilitate the comparison of trials, we developed an International Prognostic Scoring System for WM in a series of 587 patients with clearly defined criteria for diagnosis and for initiation of treatment. The median survival after treatment initiation was 87 months. Five adverse covariates were identified: advanced age (>65 years), hemoglobin less than or equal to 11.5 g/dL, platelet count less than or equal to 100 x 10(9)/L, beta2-microglobulin more than 3 mg/L, and serum monoclonal protein concentration more than 7.0 g/dL. Low-risk patients (27%) presented with no or 1 of the adverse characteristics and advanced age, intermediate-risk patients (38%) with 2 adverse characteristics or only advanced age, and high-risk patients (35%) with more than 2 adverse characteristics. Five-year survival rates were 87%, 68%, and 36%, respectively (P < .001). The ISSWM retained its prognostic significance in subgroups defined by age, treatment with alkylating agent, and purine analog. Thus, the ISSWM may provide a means to design risk-adapted studies. However, independent validation and new biologic markers may enhance its significance.es_ES
dc.description.sponsorshipInerfnational Waldenstrom's Macoroglobulienmia Foundation Hospital Universitario de Salamanca Universidad de Salamancaes_ES
dc.language.isoenges_ES
dc.publisherAmerican Society of Hematologyes_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectWaldenstrom macroglobuliemiaes_ES
dc.subjectPrognosises_ES
dc.subjectSurvivales_ES
dc.subjectInternational Classificationes_ES
dc.subject.meshPrognosis *
dc.subject.meshAged *
dc.subject.meshValidation Studies as Topic *
dc.subject.meshTreatment Outcome *
dc.subject.meshHumans *
dc.subject.meshAntineoplastic Combined Chemotherapy Protocols *
dc.subject.meshSurvival Rate *
dc.subject.meshWaldenstrom Macroglobulinemia *
dc.titleInternational prognostic scoring system for Waldenstrom macroglobulinemiaes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publishversionhttps://doi.org/10.1182/blood-2008-08-174961es_ES
dc.subject.unesco3205.04 Hematologíaes_ES
dc.identifier.doi10.1182/blood-2008-08-174961
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.pmid19196866
dc.identifier.essn1528-0020
dc.journal.titleBloodes_ES
dc.volume.number113es_ES
dc.issue.number18es_ES
dc.page.initial4163es_ES
dc.page.final4170es_ES
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES
dc.subject.decspronóstico *
dc.subject.decsresultado del tratamiento *
dc.subject.decsprotocolos de quimioterapia antineoplásica combinada *
dc.subject.decsmacroglobulinemia de Waldenström *
dc.subject.decshumanos *
dc.subject.decsanciano *
dc.subject.decsestudios de validación como asunto *
dc.subject.decstasa de supervivencia *
dc.description.projectHospital Universitario de Salamancaes_ES


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