Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/24950
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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.date.accessioned2022-03-11T08:29:33Z-
dc.date.available2022-03-11T08:29:33Z-
dc.date.issued2011-01-
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.issn0902-4441-
dc.identifier.issn1600-0609-
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.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.language.isoenen_US
dc.publisherWileyen_US
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.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.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.typeArticleen_US
dc.identifier.wos000285302200002tr_TR
dc.identifier.scopus2-s2.0-78650159700tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Hematoloji Anabilim Dalıtr_TR
dc.identifier.startpage16tr_TR
dc.identifier.endpage22tr_TR
dc.identifier.volume86tr_TR
dc.identifier.issue1tr_TR
dc.relation.journalEuropean Journal of Haematologyen_US
dc.contributor.buuauthorAli, Rıdvan-
dc.relation.collaborationYurt içitr_TR
dc.relation.collaborationSanayitr_TR
dc.identifier.pubmed20942865tr_TR
dc.subject.wosHematologyen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubmeden_US
dc.wos.quartileQ2en_US
dc.contributor.scopusid7201813027tr_TR
dc.subject.scopusIxazomib; Lenalidomide; Multiple Myelomaen_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
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