Suppr超能文献

复发/难治性多发性骨髓瘤中teclistamab剂量的降阶梯治疗:捷克骨髓瘤组真实世界证据分析

De-escalated Teclistamab dosing in relapsed/refractory multiple myeloma: Czech myeloma group real-world evidence analysis.

作者信息

Stork Martin, Radocha Jakub, Mihalyova Jana, Spicka Ivan, Pika Tomas, Jungova Alexandra, Boichuk Ivanna, Mensikova Klara, Straub Jan, Sedlak Frantisek, Minarik Jiri, Krhovska Petra, Novakova Denisa, Hornakova Michaela, Knechtova Zdenka, Sendlerova Nela, Dekojova Tereza, Maisnar Vladimir, Jelinek Tomas, Hajek Roman, Pour Ludek

机构信息

Department of Internal Medicine, Hematology and Oncology, Faculty of Medicine, University Hospital Brno, Masaryk University, Brno, Czech Republic.

Department of Internal Medicine - Hematology, Faculty of Medicine in Hradec Kralove, University Hospital Hradec Kralove, Charles University, Hradec Kralove, Czech Republic.

出版信息

Ann Hematol. 2025 Aug 18. doi: 10.1007/s00277-025-06529-1.

Abstract

Teclistamab, a BCMA×CD3 bispecific antibody, demonstrates high efficacy in relapsed/refractory multiple myeloma (RRMM). However, optimal dosing strategies outside clinical trials remain undefined. Thus, we performed a retrospective, multicentre analysis of 73 RRMM patients treated with teclistamab monotherapy at Czech Myeloma Group centres between 2023 and 2025. The study compared efficacy and safety between patients receiving standard weekly dosing and those with reduced-frequency dosing. The whole cohort had a median age of 67 years; 68.5% were penta-refractory. Dosing was de-escalated in 24.7% of patients, typically within one month of treatment initiation. Median progression-free survival (PFS) was 9.41 months and was comparable between weekly and non-weekly groups (9.1 vs. 11.3 months; p = 0.141), despite a significantly lower relative dose intensity in the latter (60.5% vs. 87.0%; p < 0.001). Infection rates and severe adverse events were similar between groups. A lower incidence of neutropenia was observed with less frequent dosing, but this did not translate into reduced infection burden. In conclusion, in real-world practice, early de-escalation of teclistamab dosing appears to maintain clinical efficacy. These findings support ongoing efforts to individualize treatment schedules with the aim of balancing effectiveness, tolerability, and patient-specific factors in BCMA-targeted therapy.

摘要

替西妥单抗是一种BCMA×CD3双特异性抗体,在复发/难治性多发性骨髓瘤(RRMM)中显示出高效性。然而,临床试验之外的最佳给药策略仍不明确。因此,我们对2023年至2025年间在捷克骨髓瘤集团中心接受替西妥单抗单药治疗的73例RRMM患者进行了一项回顾性多中心分析。该研究比较了接受标准每周给药的患者与减少给药频率的患者之间的疗效和安全性。整个队列的中位年龄为67岁;68.5%为五重难治性。24.7%的患者给药剂量降低,通常在治疗开始后一个月内。中位无进展生存期(PFS)为9.41个月,每周给药组和非每周给药组之间相当(9.1个月对11.3个月;p = 0.141),尽管后者的相对剂量强度显著较低(60.5%对87.0%;p < 0.001)。两组之间的感染率和严重不良事件相似。给药频率较低时观察到中性粒细胞减少的发生率较低,但这并未转化为感染负担的减轻。总之,在实际临床实践中,替西妥单抗给药的早期剂量降低似乎能维持临床疗效。这些发现支持了正在进行的个体化治疗方案的努力,旨在平衡BCMA靶向治疗的有效性、耐受性和患者特异性因素。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验