Service de Maladies Infectieuses et Tropicales, Centre Hospitalo-universitaire (CHU) de Toulouse, France.
Service d'hématologie, Centre Hospitalo-universitaire (CHU) de Tours, France.
Clin Microbiol Infect. 2024 Jun;30(6):764-771. doi: 10.1016/j.cmi.2024.02.023. Epub 2024 Mar 1.
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.
双特异性抗体(BsAb)是一种用于治疗复发性或难治性多发性骨髓瘤的有效治疗方法。尽管安全性良好,但临床试验中似乎经常发生感染事件。仍需要来自真实世界的数据来描述接受 BsAb 治疗的患者的感染流行病学、特征、危险因素和结局。
这是一项在 2020 年 12 月至 2023 年 2 月期间在法国 14 个中心进行的接受 BsAb 治疗的多发性骨髓瘤患者的回顾性、多中心研究。主要目的是描述需要住院、特定治疗或调整 BsAb 给药的感染发生率。
在 229 名接受 BsAb 治疗的多发性骨髓瘤患者中,153 名(67%)接受了特卡利单抗,47 名(20%)接受了埃拉纳他单抗,29 名(13%)接受了塔卢卡单抗。我们共报告了 234 例感染,其中 123 例(53%)为≥3 级。主要感染影响呼吸道(n=116,50%),其次是菌血症(n=36,15%)。住院率为 56%(n=131),20 例(9%)感染导致死亡。所有患者的首次感染累积发生率为 70%,BCMA 靶向药物治疗的患者为 73%,GPRC5D 靶向 BsAb 治疗的患者为 51%。单因素分析发现,用于细胞因子释放综合征(CRS)/免疫效应细胞相关神经毒性综合征(ICANS)的皮质类固醇与首次感染风险增加相关(HR=2.13;95%CI,1.38-3.28),而 GPRC5D 靶向 BsAb 和抗细菌预防与较低的风险相关(HR=0.53;95%CI,0.3-0.94 和 HR=0.65;95%CI,0.46-0.9)。精细和灰色多变量模型发现,只有用于 CRS/ICANS 的皮质类固醇与首次感染风险增加相关(HR=2.01;95%CI,1.27-3.19)。
实施旨在降低 BsAb 下感染风险的预防措施至关重要,尤其是在接受 CRS/ICANS 皮质类固醇治疗的患者中。