Elranatamab in Relapsed/Refractory Multiple Myeloma: A Multicenter Real-World Study from Türkiye

dc.contributor.authorBozdemir, Asli
dc.contributor.authorHacioglu, Sibel
dc.contributor.authorAkgun Cagliyan, Gulsum
dc.contributor.authorAlayvaz Aslan, Nevin
dc.contributor.authorUzun, Suleyman Utku
dc.contributor.authorKara, Kayihan
dc.contributor.authorGuler, Nil
dc.date.accessioned2026-09-08T07:11:44Z
dc.date.issued2026
dc.departmentFırat Üniveristesi
dc.description.abstractBackground: Elranatamab, a bispecific antibody targeting BCMA and CD3, has demonstrated clinical activity in relapsed/refractory multiple myeloma. Real-world evidence regarding infectious complications and supportive care remains limited. We evaluated the early clinical activity, safety profile, infectious complications, and supportive care practices associated with relapsed/refractory multiple myeloma (RRMM). This study represents one of the first multicenter real-world evaluations of elranatamab in T & uuml;rkiye. Methods: This multicenter retrospective study included 87 patients with relapsed/refractory multiple myeloma treated with elranatamab. Clinical characteristics, treatment responses, immune-mediated toxicities, infectious complications, and supportive care practices were assessed. Overall response rate (ORR), progression-free survival (PFS), and overall survival (OS) were evaluated. Multivariable analyses were performed to identify factors associated with treatment response and clinical outcomes. Results: At 3 months, ORR was 47.1% in the ITT population, 54.7% in the mITT population, and 83.7% among evaluable patients; corresponding 6-month ORRs were 31.0%, 42.2%, and 81.8%, respectively. The high proportion of patients without landmark response assessments primarily reflected insufficient follow-up, early death, or disease progression. Elevated LDH remained independently associated with lower response probability and inferior clinical outcomes. Cytokine release syndrome (CRS) occurred in 69% of patients, with grade >= 3 events in 5.7%, whereas immune effector cell-associated neurotoxicity syndrome (ICANS) was infrequent (4.6%) and no grade >= 3 events occurred. Grade >= 3 infections occurred in 39% of patients, including CMV events requiring antiviral treatment in 24.1%. No HBV reactivation occurred among patients receiving antiviral prophylaxis. Median PFS and OS were 8.1 and 10.6 months, respectively. Conclusions: Elranatamab demonstrated early clinical activity and a manageable safety profile in a heavily pretreated real-world RRMM population. Infectious complications, including CMV events, remained clinically relevant, emphasizing the importance of supportive care. Longer follow-up is needed to characterize long-term outcomes.
dc.identifier.doi10.3390/jcm15166232
dc.identifier.issn2077-0383
dc.identifier.issue16
dc.identifier.scopus2-s2.0-105048403973
dc.identifier.scopusqualityQ1
dc.identifier.urihttps://doi.org/10.3390/jcm15166232
dc.identifier.urihttps://hdl.handle.net/11508/65124
dc.identifier.volume15
dc.identifier.wosWOS:001859170500001
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.language.isoen
dc.publisherMdpi
dc.relation.ispartofJournal of Clinical Medicine
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WOS_20250903
dc.subjectElranatamab
dc.subjectBispecific Antibody
dc.subjectMultiple Myeloma
dc.subjectReal-World Data
dc.subjectInfectious Complications
dc.titleElranatamab in Relapsed/Refractory Multiple Myeloma: A Multicenter Real-World Study from Türkiye
dc.typeArticle

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