| dc.contributor.author | Morel, Pierre | |
| dc.contributor.author | Duhamel, Alain | |
| dc.contributor.author | Gobbi, Paolo | |
| dc.contributor.author | Dimopoulos, Meletios A. | |
| dc.contributor.author | Dhodapkar, Madhav V. | |
| dc.contributor.author | McCoy, Jason | |
| dc.contributor.author | Crowley, John | |
| dc.contributor.author | Ocio San Miguel, Enrique M. | |
| dc.contributor.author | García Sanz, Ramón | |
| dc.contributor.author | Treon, Steven P. | |
| dc.contributor.author | Leblond, Veronique | |
| dc.contributor.author | Kyle, Robert A. | |
| dc.contributor.author | Barlogie, Bart | |
| dc.contributor.author | Merlini, Giampaolo | |
| dc.date.accessioned | 2024-02-02T16:19:03Z | |
| dc.date.available | 2024-02-02T16:19:03Z | |
| dc.date.issued | 2009-04-30 | |
| dc.identifier.citation | Morel, 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-2008-08-174961 | es_ES |
| dc.identifier.issn | 0006-4971 | |
| dc.identifier.uri | http://hdl.handle.net/10366/155235 | |
| dc.description | Fue 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 general | es_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.sponsorship | Inerfnational Waldenstrom's Macoroglobulienmia Foundation Hospital Universitario de Salamanca Universidad de Salamanca | es_ES |
| dc.language.iso | eng | es_ES |
| dc.publisher | American Society of Hematology | es_ES |
| dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 Internacional | * |
| dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | * |
| dc.subject | Waldenstrom macroglobuliemia | es_ES |
| dc.subject | Prognosis | es_ES |
| dc.subject | Survival | es_ES |
| dc.subject | International Classification | es_ES |
| dc.subject.mesh | Prognosis | * |
| dc.subject.mesh | Aged | * |
| dc.subject.mesh | Validation Studies as Topic | * |
| dc.subject.mesh | Treatment Outcome | * |
| dc.subject.mesh | Humans | * |
| dc.subject.mesh | Antineoplastic Combined Chemotherapy Protocols | * |
| dc.subject.mesh | Survival Rate | * |
| dc.subject.mesh | Waldenstrom Macroglobulinemia | * |
| dc.title | International prognostic scoring system for Waldenstrom macroglobulinemia | es_ES |
| dc.type | info:eu-repo/semantics/article | es_ES |
| dc.relation.publishversion | https://doi.org/10.1182/blood-2008-08-174961 | es_ES |
| dc.subject.unesco | 3205.04 Hematología | es_ES |
| dc.identifier.doi | 10.1182/blood-2008-08-174961 | |
| dc.rights.accessRights | info:eu-repo/semantics/openAccess | es_ES |
| dc.identifier.pmid | 19196866 | |
| dc.identifier.essn | 1528-0020 | |
| dc.journal.title | Blood | es_ES |
| dc.volume.number | 113 | es_ES |
| dc.issue.number | 18 | es_ES |
| dc.page.initial | 4163 | es_ES |
| dc.page.final | 4170 | es_ES |
| dc.type.hasVersion | info:eu-repo/semantics/publishedVersion | es_ES |
| dc.subject.decs | pronóstico | * |
| dc.subject.decs | resultado del tratamiento | * |
| dc.subject.decs | protocolos de quimioterapia antineoplásica combinada | * |
| dc.subject.decs | macroglobulinemia de Waldenström | * |
| dc.subject.decs | humanos | * |
| dc.subject.decs | anciano | * |
| dc.subject.decs | estudios de validación como asunto | * |
| dc.subject.decs | tasa de supervivencia | * |
| dc.description.project | Hospital Universitario de Salamanca | es_ES |
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