Identifier to cite or link to this item: http://hdl.handle.net/20.500.13003/17257
Tandem Autologous Stem Cell Transplantation Improves Outcomes in Newly Diagnosed Multiple Myeloma with Extramedullary Disease and High-Risk Cytogenetics: A Study from the Chronic Malignancies Working Party of the European Society for Blood and Marrow Transplantation
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ISSN: 1083-8791
eISSN: 1523-6536
WOS ID: 000500077400003
Scopus EID: 2-s2.0-85070201442
PMID: 31288095
Embase PUI: L2002510511
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Gagelmann, Nico; Eikema, Diderik-Jan; Koster, Linda; Caillot, Denis; Pioltelli, Pietro; Lleonart, Juan Bargay; Remenyi, Peter; Blaise, Didier; Schaap, Nicolaas; Trneny, Marek; Passweg, Jakob; Parody Porras, Rocio; Cahn, Jean Yves; Musso, Maurizio; Poire, Xavier; Fenk, Roland; Itala-Remes, Maija; Pavone, Vincenzo; Fouillard, Loic; Maertens, Johan; Bron, Dominique; Pouli, Anastasia; Schroyens, Wilfried; Schoenland, Stefan; Garderet, Laurent; Yakoub-Agha, Ibrahim; Kroeger, NicolausPublication date
2019-11Document type
research articleCitation
Gagelmann N, Eikema DJ, Koster L, Caillot D, Pioltelli P, Bargay Lleonart J, et al. Tandem Autologous Stem Cell Transplantation Improves Outcomes in Newly Diagnosed Multiple Myeloma with Extramedullary Disease and High-Risk Cytogenetics: A Study from the Chronic Malignancies Working Party of the European Society for Blood and Marrow Transplantation. Biol Blood Marrow Transplant. 2019 Nov;25(11):2134-42. Epub 2019 Jul 6.Abstract
Although high-dose therapy and autologous stem cell transplant combined with novel agents continues to be the hallmark of first-line treatment in newly diagnosed transplant-eligible multiple myeloma patients, the impact of tandem autologous or autologous/reduced-intensity allogeneic transplant for patients with extramedullary disease (EMD) and high-risk cytogenetics is not yet defined. Here, we analyzed clinical and cytogenetic data from 488 adult myeloma patients with EMD undergoing single autologous (n = 373), tandem autologous (n = 84), or autologous-allogeneic transplant (n = 31) between 2003 and 2015. At least 1 high-risk abnormality was present in 41% (n = 202), with del(17p) (40%) and t(4;14) (45%) the most frequent. More than 1 high-risk abnormality was found in 54%. High-risk cytogenetics showed worse 4-year overall survival (OS) and progression-free survival (PFS) of 54% and 29%, respectively, versus 78% and 49% for standard-risk cytogenetics (P < .001). Co-segregation of high-risk abnormalities did not seem to affect outcome. Regarding transplant regimen, OS and PFS were 70% and 43% for single autologous versus 83% and 52% for tandem autologous and 88% and 58% for autologous-allogeneic (P=.06 and P =.30). In multivariate analysis high-risk cytogenetics were associated with worse survival (hazard ratio [HR.], 2.00; P = .003), whereas tandem autologous significantly improved outcome versus single autologous transplant (NRs,.46 and.64; P = .02 and P = .03). Autologous allogeneic transplant did not significantly differ in outcome but appeared to improve survival, but results were limited because of small population (HR, .31). In conclusion, high-risk cytogenetics is frequently observed in newly diagnosed myeloma with EMD and significantly worsens outcome after single autologous, whereas a tandem autologous transplant strategy may overcome onset poor prognosis.
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https://dx.doi.org/10.1016/j.bbmt.2019.07.004MeSH
Disease-Free SurvivalChromosome Aberrations
Aged
Autografts
Adult
Follow-Up Studies
Humans
Middle Aged
Male
Multiple Myeloma
Europe
Stem Cell Transplantation
Female
Societies, Medical
Risk Factors
Survival Rate
DeCS
AutoinjertosTasa de Supervivencia
Mieloma Múltiple
Femenino
Europa (Continente)
Sociedades Médicas
Masculino
Estudios de Seguimiento
Factores de Riesgo
Humanos
Persona de Mediana Edad
Anciano
Adulto
Aberraciones Cromosómicas
Trasplante de Células Madre
Supervivencia sin Enfermedad
This item appears in following Docusalut collections
Instituto de Investigación Sanitaria Islas Baleares - IDISBA > Comunicación científicaHospital Universitario Son Llàtzer - HUSLL > Comunicación científica