Characteristics and incidence of infections in patients with multiple myeloma treated by bispecific antibodies: a national retrospective study

医学 多发性骨髓瘤 内科学 入射(几何) 双特异性抗体 回顾性队列研究 抗体 免疫学 肿瘤科 单克隆抗体 数学 几何学
作者
Aurélie Jourdes,Elise Cellerin,Cyrille Touzeau,Stéphanie Harel,Blandine Denis,Guillaume Escure,Emmanuel Faure,Simon Jamard,François Danion,Cécile Sonntag,Florence Ader,Lionel Karlin,Sarah Souèges,Clarisse Cazelles,Clémentine de La Porte des Vaux,Laurent Frenzel,Fanny Lanternier,Xavier Brousse,Titouan Cazaubiel,Pierre Berger,Aude Collignon,Mathieu Blot,Andrea Pieragostini,Morgane Charles,Carine Chaleteix,Alexis Redor,Virginie Roland,Tom Cartau,Margaret Macro,Thomas Chalopin,Nicolas Vallet,Aurore Perrot,Guillaume Martin‐Blondel
出处
期刊:Clinical Microbiology and Infection [Elsevier]
卷期号:30 (6): 764-771 被引量:13
标识
DOI:10.1016/j.cmi.2024.02.023
摘要

Bispecific antibodies (BsAbs) are an effective treatment used in relapsed or refractory multiple myeloma. Despite a well-tolerated safety profile, infectious events appear to be frequent in clinical trials. Real-world data on epidemiology, characteristics, risk factors, and outcomes of infections in patients treated with BsAb are still needed. A retrospective, multicentre study in BsAb-treated patients with multiple myeloma was performed in 14 French centres from December 2020 to February 2023. The primary objective was to describe the incidence of infections that required hospitalization, specific treatment, or adaptation in BsAb administration. Among 229 patients with multiple myeloma treated with BsAb, 153 (67%) received teclistamab, 47 (20%) received elranatamab, and 29 (13%) talquetamab. We reported a total of 234 infections, including 123 (53%) of grade of ≥3. Predominant infections affected the respiratory tract (n = 116, 50%) followed by bacteraemias (n = 36, 15%). The hospitalization rate was 56% (n = 131), and 20 (9%) infections resulted in death. Global cumulative incidence of the first infection was 70% in all patients, 73% in patients treated with B-cell maturation antigen-targeting, and 51% with GPRC5D-targeting BsAb. In univariate analyses, corticosteroids for cytokine release syndrome (CRS)/immune effector cell-associated neurotoxicity syndrome (ICANS) were associated with a higher risk of first infection (HR = 2.13; 95% CI, 1.38-3.28), whereas GPRC5D-targeting BsAb and anti-bacterial prophylaxis were associated with a lower risk (HR = 0.53; 95% CI, 0.3-0.94 and HR = 0.65; 95% CI, 0.46-0.9). Fine and Gray multivariate model found that only corticosteroids for CRS/ICANS were correlated with a higher risk of first infection (HR = 2.01; 95% CI, 1.27-3.19). The implementation of preventive measures that aim to mitigate the risk of infection under BsAb is pivotal, notably in patients who received corticosteroids for CRS/ICANS.
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