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dc.contributor.authorBrowne, Paul
dc.contributor.authorAuner, Holger W.
dc.contributor.authorIacobelli, Simona
dc.contributor.authorSbianchi, Giulia
dc.contributor.authorKnol-Bout, Cora
dc.contributor.authorBlaise, Didier
dc.contributor.authorRussell, Nigel H.
dc.contributor.authorApperley, Jane F.
dc.contributor.authorPohlreich, David
dc.contributor.authorKobbe, Guido
dc.contributor.authorIsaksson, Cecilia
dc.contributor.authorLenhoff, Stig
dc.contributor.authorScheid, Christof
dc.contributor.authorTouzeau, Cyrille
dc.contributor.authorJantunen, Esa
dc.contributor.authorAnagnostopoulos, Achilles
dc.contributor.authorYakoub-Agha, Ibrahim
dc.contributor.authorTanase, Alina
dc.contributor.authorSchaap, Nicolaas
dc.contributor.authorWiktor-Jedrzejczak, Wieslaw
dc.contributor.authorKrejci, Marta
dc.contributor.authorSchönland, Stefan O.
dc.contributor.authorMorris, Curly
dc.contributor.authorGarderet, Laurent
dc.contributor.authorKröger, Nicolaus
dc.date.accessioned2019-10-29T15:18:24Z
dc.date.available2019-10-29T15:18:24Z
dc.date.issued2018
dc.date.submitted2018en
dc.identifier.citationAuner, H.W., Iacobelli, S., Sbianchi, G., Knol-Bout, C., Blaise, D., Russell, N.H., Apperley, J.F., Pohlreich, D., Browne, P.V., Kobbe, G., Isaksson, C., Lenhoff, S., Scheid, C., Touzeau, C., Jantunen, E., Anagnostopoulos, A., Yakoub-Agha, I., Tanase, A., Schaap, N., Wiktor-Jedrzejczak, W., Krejci, M., Schönland, S.O., Morris, C., Garderet, L. & Kröger, N. Melphalan 140 mg/m2or 200 mg/m2for autologous transplantation in myeloma: Results from the collaboration to collect autologous transplant outcomes in Lymphoma and Myeloma (CALM) study. A report by the EBMT chronic malignancies working party, Haematologica, 103, 3, 2018, 514-521en
dc.identifier.otherY
dc.description.abstractMelphalan at a dose of 200 mg/m2 is standard conditioning prior to autologous hematopoietic stem cell transplantation for multiple myeloma, but a dose of 140 mg/m2 is often used in clinical practice in patients perceived to be at risk of excess toxicity. To determine whether melphalan 200 mg/m2 and melphalan 140 mg/m2 are equally effective and tolerable in clinically relevant patient subgroups we analyzed 1964 first single autologous transplantation episodes using a series of Cox proportional-hazards models. Overall survival, progression-free survival, cumulative incidence of relapse, non-relapse mortality, hematopoietic recovery and second primary malignancy rates were not significantly different between the melphalan 140 mg/m2 (n=245) and melphalan 200 mg/m2 (n=1719) groups. Multivariable subgroup analysis showed that disease status at transplantation interacted with overall survival, progression-free survival, and cumulative incidence of relapse, with a significant advantage associated with melphalan 200 mg/m2 in patients transplanted in less than partial response (adjusted hazard ratios for melphalan 200 mg/m2 versus melphalan 140 mg/m2 : 0.5, 0.54, and 0.56). In contrast, transplantation in very good partial or complete response significantly favored melphalan 140 mg/m2 for overall survival (adjusted hazard ratio: 2.02). Age, renal function, prior proteasome inhibitor treatment, gender, or Karnofsky score did not interact with overall/progression-free survival or relapse rate in the melphalan dose groups. There were no significant survival or relapse rate differences between melphalan 200 mg/m2 and melphalan 140 mg/m2 patients with high-risk or standard-risk chromosomal abnormalities. In conclusion, remission status at the time of transplantation may favor the use of melphalan 200 mg/m2 or melphalan 140 mg/m2 for key transplant outcomes (NCT01362972).en
dc.format.extent514-521en
dc.language.isoenen
dc.relation.ispartofseriesHaematologica;
dc.relation.ispartofseries103;
dc.relation.ispartofseries3;
dc.rightsYen
dc.subjectMelphalanen
dc.subjectStem cell transplantationen
dc.titleMelphalan 140 mg/m2or 200 mg/m2for autologous transplantation in myeloma: Results from the collaboration to collect autologous transplant outcomes in Lymphoma and Myeloma (CALM) study. A report by the EBMT chronic malignancies working partyen
dc.typeJournal Articleen
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/brownpv
dc.identifier.rssinternalid188909
dc.identifier.doihttp://dx.doi.org/10.3324/haematol.2017.181339
dc.rights.ecaccessrightsopenAccess
dc.identifier.orcid_id0000-0001-5310-1487
dc.identifier.urihttp://www.haematologica.org/content/103/3/514
dc.identifier.urihttp://hdl.handle.net/2262/89934


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