Davis Kuruvilla , Thien Huynh , Matthew Nester , Chloe Chose , Guston Zervoudakis , G.Douglas Letson , David M. Joyce , Odion T. Binitie , Nicholas B. Figura , James R. Costello , Ciara L. Freeman , Alexander L. Lazarides
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引用次数: 0
摘要
多发性骨髓瘤是一种由浆细胞引起的血液系统恶性肿瘤,在这种错综复杂的疾病中,骨病是一种重要的并发症,往往会使人衰弱。嵌合抗原受体 T 细胞(CAR-T)疗法的出现标志着治疗领域发生了关键性转变,为治疗多发性骨髓瘤,尤其是复发或难治性疾病提供了新的途径。这种创新的治疗模式不仅能精确地靶向恶性细胞,还能影响骨微环境,为患者治疗带来了挑战和机遇。在这篇综合综述中,我们旨在探讨多发性骨髓瘤患者同时接受 CAR-T 疗法时骨病的多方面问题,重点介绍其临床影响以及诊断方法和治疗干预措施的最新进展。文章旨在综合目前对骨髓瘤细胞、CAR-T 细胞和骨微环境之间相互作用的理解,并结合这一具有挑战性的独特患者群体的当前治疗策略。
Management of bone disease with concurrent chimeric antigen receptor T-cell therapy for multiple myeloma
In the intricate landscape of multiple myeloma, a hematologic malignancy of plasma cells, bone disease presents a pivotal and often debilitating complication. The emergence of Chimeric Antigen Receptor T-cell (CAR-T) therapy has marked a pivotal shift in the therapeutic landscape, offering novel avenues for the management of MM, particularly for those with relapsed or refractory disease. This innovative treatment modality not only targets malignant cells with precision but also influences the bone microenvironment, presenting both challenges and opportunities in patient care. In this comprehensive review, we aim to examine the multifaceted aspects of bone disease in patients with multiple myeloma and concurrent CAR-T therapy, highlighting its clinical ramifications and the latest advancements in diagnostic modalities and therapeutic interventions. The article aims to synthesize current understanding of the interplay between myeloma cells, CAR-T cells, and the bone microenvironment in the context of current treatment strategies in this challenging and unique patient population.
期刊介绍:
Critical Reviews in Oncology/Hematology publishes scholarly, critical reviews in all fields of oncology and hematology written by experts from around the world. Critical Reviews in Oncology/Hematology is the Official Journal of the European School of Oncology (ESO) and the International Society of Liquid Biopsy.