Early mortality with bispecific antibody therapy in RRMM: an IMWG immunotherapy database real-world analysis

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Authors: Carlyn Rose Tan, Saad Z. Usmani, Andriy Derkach, Andre De Menezes Silva Corraes, Ricardo Parrondo, S. Ailawadhi, Sireesha Asoori, Mrugakshi Dave, Rakesh Popat, Oliver Morjaria, Roman Hajek, Jana Mihályová
+19 more Myo Htut, Murali Janakiram, Alissa Visram, Efstathios Kastritis, M A Dimopoulos, Joaquín Martínez-López, Chandramouli Nagarajan, Susan Bal, Luciano J. Costa, Hermann Einsele, Torsten Steinbrunn, Johannes M. Waldschmidt, Christine Riedhammer, Rahul Banerjee, Wee Joo Chng, Allison CY Tso, Yi Lin, Tom Martin, Hira Mian
Cited by: 2
References: 30

Abstract

ABSTRACT: Recent therapeutic advances, including bispecific antibodies (bsAbs), have improved outcomes for patients with relapsed/refractory multiple myeloma (RRMM). However, early mortality (EM) remains a significant challenge, even in the era of novel immunotherapies. We conducted a multicenter, retrospective analysis of real-world patients with RRMM treated with commercial bsAbs to evaluate the incidence and causes of EM. Between May 2022 and June 2025, a total of 441 patients were treated across 7 countries. EM, defined as death within 12 months of therapy initiation, occurred in 148 patients (34%), with a median time from bsAb initiation to death of 2.87 months (interquartile range, 1.38-6.85). The leading cause of EM was progressive disease (72%), followed by infection (13%); regardless of the cause of death, 82% had active disease at the time of death. Our findings highlight that despite encouraging efficacy, EM remains high among real-world bsAb recipients, emphasizing the need for improved disease control strategies and supportive care interventions.

Fields of Study & Subjects

Multiple Myeloma Research and Treatments Cancer Treatment and Pharmacology Monoclonal and Polyclonal Antibodies Research

Publication details

Journal / source
Blood Advances
Publisher
American Society of Hematology
Volume
10
Issue
9
Pages
2937–2946
Publication date
24 February 2026
Language
EN