美国三级暴露和bcma暴露多发性骨髓瘤患者的真实世界治疗模式和临床结果

IF 1.2
EJHaem Pub Date : 2025-09-23 DOI:10.1002/jha2.70145
Hira S. Mian, Jennifer S. Harper, Hoa H. Le, Alex Z. Fu, Saurabh Patel, Xinke Zhang, Rafael Fonseca
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引用次数: 0

摘要

b细胞成熟抗原(BCMA)靶向免疫疗法是一种治疗重度预处理三级暴露多发性骨髓瘤(TCE MM)的新疗法。虽然暴露于TCE+ bcma的患者数量正在增长,但这一群体的实际数据有限。方法:我们使用美国索赔数据库Komodo's Healthcare Map提供了来自TCE+ bcma暴露的MM患者的真实数据,这些患者开始了后续治疗(LOT)。结果:我们确定了656例TCE+ bcma暴露患者;平均年龄66.5岁。从MM诊断到指数的时间为5.4年;平均先前批次数为5.9个。每个药物类别中接受的最普遍的既往治疗是达拉单抗(98.5%),泊马度胺(86.0%),卡非佐米(85.8%)和贝兰他单抗(74.5%)。在TCE+BCMA暴露后,总共观察到137种不同的后续治疗方案;最常见的方案是替司他单抗(10.4%)。在后续方案中,排名前三的靶向药物分别是卡非佐米(20.2%)、波马度胺(20.1%)和硼替佐米(16.6%)。在接受后续治疗的TCE+ bcma暴露人群中,到下一次治疗或死亡的中位时间为6.8个月(95% CI, 6.1-7.5);到停止治疗或死亡的时间为3.5个月(95% CI, 3.2-3.7)。结论:对重度预处理TCE+ bcma暴露MM患者的首次现实世界分析显示,临床结果较差,治疗再治疗频繁且无标准护理,突出了对新治疗方法的需求。临床试验注册:作者已确认本次提交不需要临床试验注册。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Real-World Treatment Patterns and Clinical Outcomes Among Patients With Triple-Class–Exposed and BCMA-Exposed Multiple Myeloma Within the United States

Real-World Treatment Patterns and Clinical Outcomes Among Patients With Triple-Class–Exposed and BCMA-Exposed Multiple Myeloma Within the United States

Introduction

A novel therapy for heavily pretreated triple-class–exposed multiple myeloma (TCE MM) is B-cell maturation antigen (BCMA)-targeted immunotherapy. While the number of TCE+BCMA-exposed patients is growing, real-world data for this group are limited.

Methods

We present real-world data from patients with TCE+BCMA-exposed MM who initiated a subsequent line of therapy (LOT) using a US-based claims database, Komodo's Healthcare Map.

Results

We identified 656 TCE+BCMA-exposed patients; mean age was 66.5 years. Time from MM diagnosis to index was 5.4 years; mean number of prior LOTs was 5.9. The most prevalent prior therapy received within each drug class was daratumumab (98.5%), pomalidomide (86.0%), carfilzomib (85.8%) and belantamab mafodotin (74.5%). A total of 137 different subsequent treatment regimens were observed following TCE+BCMA exposure; the most common regimen was teclistamab (10.4%). The top three targeted agents within the subsequent regimen were carfilzomib (20.2%), pomalidomide (20.1%) and bortezomib (16.6%). Among this TCE+BCMA-exposed population who received subsequent treatment, the median time to next treatment or death was 6.8 (95% CI, 6.1–7.5) months; time to treatment discontinuation or death was 3.5 (95% CI, 3.2–3.7) months.

Conclusion

This first real-world analysis of patients with heavily pretreated TCE+BCMA-exposed MM shows poor clinical outcomes, frequent therapy retreatment and no standard-of-care, highlighting the need for novel treatments.

Clinical Trial Registration

The authors have confirmed clinical trial registration is not needed for this submission.

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