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dc.contributor.authorMateos Manteca, María Victoria 
dc.contributor.authorMartinez-Lopez, Joaquin
dc.contributor.authorHernández, Miguel-Teodoro
dc.contributor.authorOcio San Miguel, Enrique M.
dc.contributor.authorRosiñol, Laura
dc.contributor.authorMartinez, Rafael
dc.contributor.authorTeruel, Ana-Isabel
dc.contributor.authorGutiérrez Gutiérrez, Norma Carmen 
dc.contributor.authorMartín-Ramos, María-Luisa
dc.contributor.authorOriol, Albert
dc.contributor.authorBargay, Joan
dc.contributor.authorBengoechea, Enrique
dc.contributor.authorGonzález, Yolanda
dc.contributor.authorPérez de Oteyza, Jaime
dc.contributor.authorGironella, Mercedes
dc.contributor.authorEncinas, Cristina
dc.contributor.authorMartín, Jesús
dc.contributor.authorCabrera, Carmen
dc.contributor.authorLourenço Paiva, Bruno
dc.contributor.authorCedena, Maria-Teresa
dc.contributor.authorPuig Morón, Noemí
dc.contributor.authorBladé, Joan
dc.contributor.authorLahuerta, Juan José
dc.contributor.authorSan Miguel Izquierdo, Jesús Fernando
dc.date.accessioned2024-01-19T15:35:53Z
dc.date.available2024-01-19T15:35:53Z
dc.date.issued2016-01-28
dc.identifier.citationMateos MV, Martínez-López J, Hernández MT, Ocio EM, Rosiñol L, Martínez R, Teruel AI, Gutiérrez NC, Martín Ramos ML, Oriol A, Bargay J, Bengoechea E, González Y, Pérez de Oteyza J, Gironella M, Encinas C, Martín J, Cabrera C, Paiva B, Cedena MT, Puig N, Bladé J, Lahuerta JJ, San-Miguel J. Sequential vs alternating administration of VMP and Rd in elderly patients with newly diagnosed MM. Blood. 2016 Jan 28;127(4):420-5. doi: 10.1182/blood-2015-08-666537. Epub 2015 Oct 23. PMID: 26500339.es_ES
dc.identifier.issn0006-4971
dc.identifier.urihttp://hdl.handle.net/10366/154452
dc.description.abstract[EN]Bortezomib plus melphalan and prednisone (VMP) and lenalidomide plus low-dose dexamethasone (Rd) are 2 standards of care for elderly untreated multiple myeloma (MM) patients. We planned to use VMP and Rd for 18 cycles in a sequential or alternating scheme. Patients (233) with untreated MM, >65 years, were randomized to receive 9 cycles of VMP followed by 9 cycles of Rd (sequential scheme; n 5 118) vs 1 cycle of VMP followed by 1 cycle of Rd, and so on, up to 18 cycles (alternating scheme; n 5 115). VMP consisted of one 6-week cycle of bortezomib using a biweekly schedule, followed by eight 5-week cycles of once-weekly VMP. Rd included nine 4-week cycles of Rd. The primary end points were 18-month progression free survival (PFS) and safety profile of both schemes. The 18-month PFS was 74% and 80% in the sequential and alternating arms, respectively (P 5 .21). The sequential and alternating groups exhibited similar hematologic and nonhematologic toxicity. Both arms yielded similar complete response rate (42% and 40%), median PFS (32 months vs 34 months, P 5 .65), and 3-year overall survival (72% vs 74%, P 5 .63). The benefit of both schemes was remarkable in patients aged 65 to 75 years. In addition, achieving complete and immunophenotypic response was associated with better outcome. The present approach, based on VMP and Rd, is associated with high efficacy and acceptable toxicity profile with no differences between the sequential and alternating regimenses_ES
dc.publisherAmerican Society of Hematologyes_ES
dc.subjectVMPes_ES
dc.subjectMieloma múltiplees_ES
dc.subject.meshMultiple Myeloma *
dc.subject.meshAged *
dc.titleSequential vs alternating administration of VMP and Rd in elderly patients with newly diagnosed MMes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publishversionhttps://doi.org/10.1182/blood-2015-08-666537es_ES
dc.identifier.doi10.1182/blood-2015-08-666537
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.essn1528-0020
dc.journal.titleBloodes_ES
dc.volume.number127es_ES
dc.issue.number4es_ES
dc.page.initial420es_ES
dc.page.final425es_ES
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES
dc.subject.decsanciano *
dc.subject.decsmieloma múltiple *


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