Addition of thalidomide to oral melphalan/prednisone in patients with multiple myeloma not eligible for transplantation: Results of a randomized trial from the Turkish Myeloma Study Group

dc.contributor.authorBeksaç, Meral
dc.contributor.authorHaznedar, Rauf
dc.contributor.authorTuğlular, Tulin Fıratlı
dc.contributor.authorÖzdoğu, Hakan
dc.contributor.authorAydoğdu, İsmet
dc.contributor.authorKonuk, Nahide
dc.contributor.authorSucak, Gülşan
dc.contributor.authorKaygusuz, Işık
dc.contributor.authorKarakuş, Sema
dc.contributor.authorKaya, Emin
dc.contributor.authorGülbaş, Zafer
dc.contributor.authorÖzet, Gülsüm
dc.contributor.authorGöker, Hakan
dc.contributor.authorÜndar, Levent
dc.contributor.buuauthorAli, Rıdvan
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Hematoloji Anabilim Dalıtr_TR
dc.contributor.scopusid7201813027tr_TR
dc.date.accessioned2022-03-11T08:29:33Z
dc.date.available2022-03-11T08:29:33Z
dc.date.issued2011-01
dc.description.abstractThe combination of melphalan-prednisone-thalidomide (MPT) has been investigated in several clinical studies that differed significantly with regard to patient characteristics and treatment schedules. This prospective trial differs from previous melphalan-prednisone (MP) vs. MPT trials by treatment dosing, duration, routine anticoagulation, and permission for a crossover. Newly diagnosed patients with multiple myeloma (MM) (n = 122) aged greater than 55 yr, not eligible for transplantation were randomized to receive 8 cycles of M (9 mg/m2/d) and P (60 mg/m2/d) for 4 d every 6 wk (n = 62) or MP and thalidomide (100 mg/d) continuously (n = 60). Primary endpoint was treatment response and toxicities following 4 and 8 cycles of therapy. Secondary endpoints were disease-free (DFS) and overall survival (OS). Overall, MPT-treated patients were younger (median 69 yr vs. 72 yr; P = 0.016) and had a higher incidence of renal impairment (RI, 19% vs. 7%, respectively; P = 0.057). After 4 cycles of treatment (n = 115), there were more partial responses or better in the MPT arm than in the MP arm (57.9% vs. 37.5%; P = 0.030). However, DFS and OS were not significantly different between the arms after a median of 23 months follow-up (median OS 26.0 vs. 28.0 months, P = 0.655; DFS 21.0 vs. 14.0 months, P = 0.342, respectively). Crossover to MPT was required in 11 patients, 57% of whom responded to treatment. A higher rate of grade 3-4 infections was observed in the MPT arm compared with the MP arm (22.4% vs. 7.0%; P = 0.033). However, none of these infections were associated with febrile neutropenia. Death within the first 3 months was observed more frequently in the MP arm (n = 8, 14.0%) than in the MPT arm (n = 2, 3.4%; P = 0.053). Long-term discontinuation and dose reduction rates were also analyzed (MPT: 15.5% vs. MP: 5.3%; P = 0.072). Although patients treated with MPT were relatively younger and had more frequent RI, better responses and less early mortality were observed in all age groups despite more frequent discontinuation.en_US
dc.description.sponsorshipERKİM İlaç A.Ş.tr_TR
dc.description.sponsorshipTürk Bilimler Akademisitr_TR
dc.identifier.citationBeksaç, M. vd. (2011). "Addition of thalidomide to oral melphalan/prednisone in patients with multiple myeloma not eligible for transplantation: Results of a randomized trial from the Turkish Myeloma Study Group". European Journal of Haematology, 86(1), 16-22.en_US
dc.identifier.endpage22tr_TR
dc.identifier.issn0902-4441
dc.identifier.issn1600-0609
dc.identifier.issue1tr_TR
dc.identifier.pubmed20942865tr_TR
dc.identifier.scopus2-s2.0-78650159700tr_TR
dc.identifier.startpage16tr_TR
dc.identifier.urihttps://doi.org/10.1111/j.1600-0609.2010.01524.x
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/10.1111/j.1600-0609.2010.01524.x
dc.identifier.urihttp://hdl.handle.net/11452/24950
dc.identifier.volume86tr_TR
dc.identifier.wos000285302200002tr_TR
dc.indexed.pubmedPubmeden_US
dc.indexed.scopusScopusen_US
dc.indexed.wosSCIEen_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.relation.collaborationYurt içitr_TR
dc.relation.collaborationSanayitr_TR
dc.relation.journalEuropean Journal of Haematologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectHematologyen_US
dc.subjectMultiple myelomaen_US
dc.subjectTreatmenten_US
dc.subjectMelphalanen_US
dc.subjectPrednisoneen_US
dc.subjectThalidomideen_US
dc.subjectPrednisone plus thalidomideen_US
dc.subjectElderly-patientsen_US
dc.subject.emtreeAcetylsalicylic aciden_US
dc.subject.emtreeLow molecular weight heparinen_US
dc.subject.emtreeMelphalanen_US
dc.subject.emtreePrednisoneen_US
dc.subject.emtreeThalidomideen_US
dc.subject.emtreeWarfarinen_US
dc.subject.emtreeAdd on therapyen_US
dc.subject.emtreeAdulten_US
dc.subject.emtreeAgeden_US
dc.subject.emtreeAnticoagulationen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeCancer mortalityen_US
dc.subject.emtreeCancer patienten_US
dc.subject.emtreeCancer survivalen_US
dc.subject.emtreeClinical trialen_US
dc.subject.emtreeConstipationen_US
dc.subject.emtreeControlled clinical trialen_US
dc.subject.emtreeControlled studyen_US
dc.subject.emtreeCrossover procedureen_US
dc.subject.emtreeDisease free survivalen_US
dc.subject.emtreeDrug dose comparisonen_US
dc.subject.emtreeDrug dose reductionen_US
dc.subject.emtreeDrug efficacyen_US
dc.subject.emtreeDrug megadoseen_US
dc.subject.emtreeDrug responseen_US
dc.subject.emtreeDrug safetyen_US
dc.subject.emtreeDrug withdrawalen_US
dc.subject.emtreeFebrile neutropeniaen_US
dc.subject.emtreeFemaleen_US
dc.subject.emtreeHeart diseaseen_US
dc.subject.emtreeHematologic diseaseen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeInfectionen_US
dc.subject.emtreeKidney diseaseen_US
dc.subject.emtreeLow drug doseen_US
dc.subject.emtreeLung embolismen_US
dc.subject.emtreeMajor clinical studyen_US
dc.subject.emtreeMaleen_US
dc.subject.emtreeMultiple cycle treatmenten_US
dc.subject.emtreeMultiple myelomaen_US
dc.subject.emtreeNeuropathyen_US
dc.subject.emtreeOverall survivalen_US
dc.subject.emtreePriority journalen_US
dc.subject.emtreeRandomized controlled trialen_US
dc.subject.emtreeSkin manifestationen_US
dc.subject.emtreeThrombosisen_US
dc.subject.emtreeThrombosis preventionen_US
dc.subject.emtreeTreatment durationen_US
dc.subject.emtreeTreatment outcomeen_US
dc.subject.emtreeVein thrombosisen_US
dc.subject.meshAge factorsen_US
dc.subject.meshAgeden_US
dc.subject.meshAged, 80 and overen_US
dc.subject.meshAntineoplastic combined chemotherapy protocolsen_US
dc.subject.meshCross-over studiesen_US
dc.subject.meshFemaleen_US
dc.subject.meshHumansen_US
dc.subject.meshKidney diseasesen_US
dc.subject.meshMaleen_US
dc.subject.meshMelphalanen_US
dc.subject.meshMiddle ageden_US
dc.subject.meshMultiple myelomaen_US
dc.subject.meshOpportunistic infectionsen_US
dc.subject.meshPrednisoneen_US
dc.subject.meshSurvival analysisen_US
dc.subject.meshThalidomideen_US
dc.subject.meshTreatment outcomeen_US
dc.subject.scopusIxazomib; Lenalidomide; Multiple Myelomaen_US
dc.subject.wosHematologyen_US
dc.titleAddition of thalidomide to oral melphalan/prednisone in patients with multiple myeloma not eligible for transplantation: Results of a randomized trial from the Turkish Myeloma Study Groupen_US
dc.typeArticle
dc.wos.quartileQ2en_US

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