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Review
. 2025 Apr 5;17(7):1235.
doi: 10.3390/cancers17071235.

Real-World Evidence Evaluating Teclistamab in Patients with Relapsed/Refractory Multiple Myeloma: A Systematic Literature Review

Affiliations
Review

Real-World Evidence Evaluating Teclistamab in Patients with Relapsed/Refractory Multiple Myeloma: A Systematic Literature Review

Benjamin Derman et al. Cancers (Basel). .

Abstract

Background: Teclistamab (TEC) is the first B-cell maturation antigen-directed bispecific antibody approved in 2022 by the European Medicines Agency and Food and Drug Administration for triple-class exposed relapsed/refractory multiple myeloma (RRMM). Objectives: As TEC is increasingly used in real-world (RW) settings, this study seeks to gather existing RW evidence on effectiveness, safety, healthcare resource utilization, and clinical practices associated with TEC. Methods: A systematic literature review was performed to identify RW observational studies of TEC-treated adults with RRMM from 2023 to June 2024. Results: Sixty-one records representing 41 unique studies were included; sample sizes ranged from 8 to 572 patients. Where reported, median follow-up ranged from 2.3 to 33.6 months, and >65% of the patients would have been ineligible for the pivotal trial of TEC (MajesTEC-1) in all but one study. In eight studies with ≥50 patients and ≥3 months follow-up, overall response rates were 59-66% and cytokine release syndrome (CRS) rates were 18-64%. Tocilizumab use for CRS management was reported in 14 studies, with two indicating CRS rates of 13% and 26% when used prophylactically. Survival and infection outcomes showed wide variability due to short follow-up in most studies. Conclusions: Overall, early RW effectiveness and safety outcomes of TEC were comparable to findings from MajesTEC-1.

Keywords: B-cell maturation antigen; bispecific antibodies; cytokine release syndrome; immune effector cell-associated neurotoxicity syndrome; real-world evidence; relapsed–refractory multiple myeloma; systematic literature review; teclistamab.

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Conflict of interest statement

B. Derman is an employee of UChicago Medicine and declares consulting services for Janssen Scientific Affairs, Cota Healthcare, Guidepoint Global, Gerson Lehrman Group, Precision AQ, Sanofi, and Canopy, as well as honoraria from OncLive/MJH Life Sciences, Plexus, and Multiple Myeloma Research Foundation and research funding from GlaxoSmithKline and Amgen. C. Tan is an employee of the Memorial Sloan Kettering Cancer Center and declares consulting services for Janssen Medical Affairs and Sanofi, honoraria from MJH Life Sciences, and may hold stock and other ownership interests in Johnson & Johnson/Janssen, Moderna Therapeutics, ImmunityBio, Nektar, and Pfizer and research funding from Janssen and Takeda. I. Steinfield, F.R. Wilson, and S. Keeping are employees of Precision AQ. D. Lin, B. Wu, M. Fernandez, J. Fowler, A. Paner-Straseviciute, N. Kim, M. Doyle, A. Marshall, and J. Cheadle are employees of Johnson & Johnson Innovative Medicine and may hold stock or stock options of Johnson & Johnson. J.J. Liu is an employee of the Illinois Cancer Care.

Figures

Figure 1
Figure 1
PRISMA flow diagram of included studies. Abbreviations: ASCO, American Society of Clinical Oncology; ASH, American Society for Hematology; EHA, European Hematology Association; HOPA, Hematology/Oncology Pharmacy Association; IMS, International Myeloma Society; LL&M, Lymphoma, Leukemia & Myeloma Congress; ONS, Oncology Nursing Society; SOHO, Society of Hematologic Oncology.

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