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dc.contributor.authorGarcía Sanz, Ramón 
dc.contributor.authorGonzález Porras, José Ramón 
dc.contributor.authorHernández, J. M.
dc.contributor.authorPolo-Zarzuela, M
dc.contributor.authorSureda, Anna
dc.contributor.authorBarrenetxea, C
dc.contributor.authorPalomera, Luis
dc.contributor.authorLópez, R
dc.contributor.authorGrande-García, C
dc.contributor.authorAlegre, Adrian
dc.contributor.authorVargas-Pabón, M
dc.contributor.authorGutiérrez, O N
dc.contributor.authorRodríguez, J A
dc.contributor.authorSan Miguel Izquierdo, Jesús Fernando
dc.date.accessioned2024-02-02T11:53:28Z
dc.date.available2024-02-02T11:53:28Z
dc.date.issued2004
dc.identifier.citationGarcia-Sanz, R., Gonzalez-Porras, J. R., Hernandez, J. M., Polo-Zarzuela, M., Sureda, A., Barrenetxea, C., ... & San Miguel, J. F. (2004). The oral combination of thalidomide, cyclophosphamide and dexamethasone (ThaCyDex) is effective in relapsed/refractory multiple myeloma. Leukemia, 18(4), 856-863. doi:10.1038/sj.leu.2403322es_ES
dc.identifier.issn0887-6924
dc.identifier.urihttp://hdl.handle.net/10366/155215
dc.descriptionFue el trabajo que ha permitido tratar con éxito a muchos pacientes con mieloma múltiple resis-tente. Ha sido citado múltiples veces y es una referencia esencial en el tratamiento con asocia-ciones de inmunomoduladores y alquilantes Fue utilizado por el grupo inglés como referencia para el ensayo MRC IX, que incluyó casi 2000 pacientes.es_ES
dc.description.abstract[EN]We evaluate the efficacy of the oral combination of thalidomide, cyclophosphamide and dexamethasone (ThaCyDex) in 71 refractory/relapsed multiple myeloma patients, including a prognostic analysis to predict both response and survival. Patients received thalidomide at escalating doses (200-800 mg/day), daily cyclophosphamide (50 mg/day) and pulsed dexamethasone (40 mg/day, 4 days every 3 weeks). On an intention-to-treat basis and using the EBMT response criteria, 2% patients reached complete response (CR), 55% partial response (PR) and 26% minor response (MR) yielding a total response (CR+PR+MR) rate of 83% after 3 months of therapy. After 6 months of therapy, responses were maintained including a 10% CR. The 2-year progression free and overall survival were 57 and 66%, respectively. A favorable response was associated with beta2 microglobulin < or =4 mg/dl, platelets >80 x 10(9)/l and nonrefractory disease. Regarding survival, low beta2 microglobulin (< or =4 mg/dl), age (< or =65 years) and absence of extramedullary myelomatous lesion were associated with a longer survival. Major adverse effects included constipation (24%), somnolence (18%), fatigue (17%) and infection (13%). Only 7% of patients developed a thrombo-embolic event. ThaCyDex is an oral regimen that induces a high response rate and long remissions, particularly in relapsing patients with beta2 microglobulin < or =4 mg/dl and < or =65 years.es_ES
dc.description.sponsorshipGrupo Español de Mieloma (GEM/PETHEMA) Hospital Universitario de Salamanca Universidad de Salamancaes_ES
dc.language.isoenges_ES
dc.publisherSpringer Naturees_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional
dc.subjectMyelomaes_ES
dc.subjectThalidomidees_ES
dc.subjectCyclophosphamidees_ES
dc.subjectDexamethasonees_ES
dc.subject.meshbeta 2-Microglobulin *
dc.subject.meshAged *
dc.subject.meshCyclophosphamide *
dc.subject.meshHumans *
dc.subject.meshAntineoplastic Combined Chemotherapy Protocols *
dc.subject.meshMiddle Aged *
dc.subject.meshPrognosis *
dc.subject.meshMultiple Myeloma *
dc.subject.meshSalvage Therapy *
dc.subject.meshThalidomide *
dc.subject.meshTreatment Outcome *
dc.subject.meshRemission Induction *
dc.subject.meshSurvival Analysis *
dc.subject.meshDexamethasone *
dc.titleThe oral combination of thalidomide, cyclophosphamide and dexamethasone (ThaCyDex) is effective in relapsed/refractory multiple myelomaes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publishversionhttps://www.nature.com/articles/2403322es_ES
dc.identifier.doi10.1038/sj.leu.2403322
dc.relation.projectIDGrupo Español de Mieloma (GEM)es_ES
dc.relation.projectIDRed Española de Mieloma G03/136es_ES
dc.relation.projectIDFIS-SS PI-02/0905es_ES
dc.rights.accessRightsinfo:eu-repo/semantics/embargoedAccesses_ES
dc.identifier.pmid14973508
dc.identifier.essn1476-5551
dc.journal.titleLeukemiaes_ES
dc.volume.number18es_ES
dc.issue.number4es_ES
dc.page.initial856es_ES
dc.page.final863es_ES
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES
dc.subject.decstalidomida *
dc.subject.decsprotocolos de quimioterapia antineoplásica combinada *
dc.subject.decsdexametasona *
dc.subject.decshumanos *
dc.subject.decsinducción de remisión *
dc.subject.decsanciano *
dc.subject.decsciclofosfamida *
dc.subject.decsmediana edad *
dc.subject.decsmieloma múltiple *
dc.subject.decspronóstico *
dc.subject.decsmicroglobulina-beta 2 *
dc.subject.decsresultado del tratamiento *
dc.subject.decsanálisis de supervivencia *
dc.subject.decstratamiento de última línea *
dc.description.projectHospital Universitario de Salamancaes_ES


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