Elranatamab in Relapsed/Refractory Multiple Myeloma: A Multicenter Real-World Study from Türkiye
| dc.contributor.author | Bozdemir, Asli | |
| dc.contributor.author | Hacioglu, Sibel | |
| dc.contributor.author | Akgun Cagliyan, Gulsum | |
| dc.contributor.author | Alayvaz Aslan, Nevin | |
| dc.contributor.author | Uzun, Suleyman Utku | |
| dc.contributor.author | Kara, Kayihan | |
| dc.contributor.author | Guler, Nil | |
| dc.date.accessioned | 2026-09-08T07:11:44Z | |
| dc.date.issued | 2026 | |
| dc.department | Fırat Üniveristesi | |
| dc.description.abstract | Background: 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.doi | 10.3390/jcm15166232 | |
| dc.identifier.issn | 2077-0383 | |
| dc.identifier.issue | 16 | |
| dc.identifier.scopus | 2-s2.0-105048403973 | |
| dc.identifier.scopusquality | Q1 | |
| dc.identifier.uri | https://doi.org/10.3390/jcm15166232 | |
| dc.identifier.uri | https://hdl.handle.net/11508/65124 | |
| dc.identifier.volume | 15 | |
| dc.identifier.wos | WOS:001859170500001 | |
| dc.identifier.wosquality | Q1 | |
| dc.indekslendigikaynak | Web of Science | |
| dc.indekslendigikaynak | Scopus | |
| dc.language.iso | en | |
| dc.publisher | Mdpi | |
| dc.relation.ispartof | Journal of Clinical Medicine | |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.snmz | KA_WOS_20250903 | |
| dc.subject | Elranatamab | |
| dc.subject | Bispecific Antibody | |
| dc.subject | Multiple Myeloma | |
| dc.subject | Real-World Data | |
| dc.subject | Infectious Complications | |
| dc.title | Elranatamab in Relapsed/Refractory Multiple Myeloma: A Multicenter Real-World Study from Türkiye | |
| dc.type | Article |







