Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/37063
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dc.contributor.authorBeksac, M.-
dc.contributor.authorAydin, Y.-
dc.contributor.authorGoker, H.-
dc.contributor.authorTurgut, Mehmet-
dc.contributor.authorBesisik, S.K.-
dc.contributor.authorCagirgan, S.-
dc.contributor.authorTuglular, T.-
dc.date.accessioned2021-02-02T09:23:49Z-
dc.date.available2021-02-02T09:23:49Z-
dc.date.issued2020-
dc.identifier.issn2152-2650-
dc.identifier.urihttps://hdl.handle.net/11499/37063-
dc.identifier.urihttps://doi.org/10.1016/j.clml.2020.02.017-
dc.description.abstractBackground: In countries where frontline drug approval is limited to first-generation proteasome inhibitors or immunomodulatory drugs, relapses have been both more frequent and less durable. We investigated real world data on the efficacy and safety of daratumumab monotherapy among patients with relapsed refractory multiple myeloma (RRMM) from Turkey using a prospective early access program. Patients and Methods: A total of 42 patients with RRMM after a minimum of 3 previous lines of proteasome inhibitor/immunomodulatory drug-based treatments were included from 25 centers across Turkey. Daratumumab monotherapy was administered intravenously at a dose of 16 mg/kg weekly (cycles 1-2), on alternate weeks (cycles 3-6), and monthly thereafter. Results: The median daratumumab monotherapy duration was 5.5 months (range, 0.2-28.7 months). The overall response rate was 45.2%, including 14 (33.3%) partial responses, 4 (9.5%) very good partial responses, and 1 (2.4%) complete response. The median duration of response was 4.9 months. The median progression-free survival (PFS) was 5.5 (95% confidence interval, 2.6-8.4 months) with 12- and 18-month PFS rates of 35.7% and 31.0%, respectively. The median overall survival was not reached; the 12- and 18-month overall survival rates were 64.3% and 59.5%, respectively. The depth of response had a significant effect on PFS (log-rank test, P = .026). Overall, of the 76 adverse events reported, 33 (43.4%) were grade ? 3; only 4 (9.52%) were grade 3 infusion-related reactions. No infusion-related reactions or adverse events led to treatment discontinuation. Conclusion: The present findings from our daratumumab early access program have confirmed the efficacy and safety profile of daratumumab monotherapy in heavily pretreated Turkish patients with RRMM. The present study investigated the efficacy and safety profile of daratumumab monotherapy in 42 patients with relapsed refractory multiple myeloma through a Turkish early access program. The current findings have confirmed the efficacy of daratumumab monotherapy in heavily pretreated patients with refractory multiple myeloma because of the deep and durable responses and favorable safety and tolerability profile. © 2020 The Authorsen_US
dc.language.isoenen_US
dc.publisherElsevier Inc.en_US
dc.relation.ispartofClinical Lymphoma, Myeloma and Leukemiaen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectEAPen_US
dc.subjectEfficacyen_US
dc.subjectRRMMen_US
dc.subjectSafetyen_US
dc.subjectSurvivalen_US
dc.subjectbortezomiben_US
dc.subjectdaratumumaben_US
dc.subjectlenalidomideen_US
dc.subjectmelphalanen_US
dc.subjectpomalidomideen_US
dc.subjectprednisoloneen_US
dc.subjectthalidomideen_US
dc.subjectadulten_US
dc.subjectageden_US
dc.subjectanemiaen_US
dc.subjectArticleen_US
dc.subjectcancer diagnosisen_US
dc.subjectcancer fatigueen_US
dc.subjectcancer recurrenceen_US
dc.subjectclinical articleen_US
dc.subjectcohort analysisen_US
dc.subjectcontrolled studyen_US
dc.subjectcoughingen_US
dc.subjectdrug approvalen_US
dc.subjectdrug efficacyen_US
dc.subjectdrug safetyen_US
dc.subjectdrug tolerabilityen_US
dc.subjectdrug withdrawalen_US
dc.subjectdyspneaen_US
dc.subjectfemaleen_US
dc.subjectfeveren_US
dc.subjecthumanen_US
dc.subjectlower respiratory tract infectionen_US
dc.subjectmaleen_US
dc.subjectmiddle ageden_US
dc.subjectmonotherapyen_US
dc.subjectmultiple cycle treatmenten_US
dc.subjectmultiple myelomaen_US
dc.subjectnauseaen_US
dc.subjectneuropathyen_US
dc.subjectneutropeniaen_US
dc.subjectoverall survivalen_US
dc.subjectpneumoniaen_US
dc.subjectprogression free survivalen_US
dc.subjectprospective studyen_US
dc.subjectrashen_US
dc.subjectthroat irritationen_US
dc.subjectthrombocytopeniaen_US
dc.subjecttreatment durationen_US
dc.subjecttreatment responseen_US
dc.subjectupper respiratory tract infectionen_US
dc.titleEarly access program results from Turkey and a literature review on daratumumab monotherapy among heavily pretreated patients with relapsed/refractory myelomaen_US
dc.typeArticleen_US
dc.identifier.volume20en_US
dc.identifier.issue8en_US
dc.identifier.startpagee474-
dc.identifier.startpagee474en_US
dc.identifier.endpagee484en_US
dc.authorid0000-0003-0757-9206-
dc.identifier.doi10.1016/j.clml.2020.02.017-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.pmid32482539en_US
dc.identifier.scopus2-s2.0-85085602296en_US
dc.identifier.wosWOS:000552071100004en_US
dc.identifier.scopusqualityQ2-
dc.ownerPamukkale University-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextopen-
item.languageiso639-1en-
item.openairetypeArticle-
item.fulltextWith Fulltext-
item.cerifentitytypePublications-
crisitem.author.dept13.01. Private Law-
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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