Optimising T-cell immunotherapy in patients with multiple myeloma: practical considerations from the European Myeloma Network

Prof Niels W C J van de Donk MD, Philippe Moreau MD, Jesús F San-Miguel MD, Maria-Victoria Mateos MD, Meletios A Dimopoulos MD, Sonja Zweegman MD, Francesca Gay MD, Monika Engelhardt MD, Roberto Mina MD, Elena Zamagni MD, Michel Delforge MD, Meral Beksac MD, Andrew Spencer MD, Fredrik Schjesvold MD, Christoph Driessen MD, Martin Kaiser MD, Aurore Perrot MD, Ralph Wäsch MD, Charlotte LBM Korst MD, Annemiek Broijl MD, Cyrille Touzeau MD, Salomon Manier MD, Roman Hajek MD, Heinz Ludwig MD, Carlos Fernandez de Larrea MD, Rakesh Popat MD, Pellegrino Musto MD, Paula Rodriguez-Otero MD, Kwee Yong MD, Leo Rasche MD, Evangelos Terpos MD, Marc S Raab MD, Mario Boccadoro MD, Pieter Sonneveld MD, Hermann Einsele MD, EMN Guidelines Committee
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Abstract

Novel T-cell immunotherapies (chimeric antigen receptor [CAR] T cells and T-cell redirecting bispecific antibodies) are changing the treatment landscape of relapsed or refractory multiple myeloma. In this Review, the European Myeloma Network provides recommendations to optimise both safety and efficacy of T-cell immunotherapy. In patients who are eligible for both CAR T-cell therapy and bispecific antibodies, we recommend using CAR T-cell therapy first due to the high response rate and durable progression-free survival, accompanied by improved quality of life. Furthermore, previous bispecific antibody treatment has a negative effect on the efficacy of CAR T-cell therapy, and there is emerging evidence that suggests that relapse after B-cell maturation antigen-directed CAR T-cell therapy can be effectively managed with bispecific antibodies. Timely referral and planning are crucial before initiating T-cell immunotherapy to optimise treatment selection, conduct adequate diagnostic tests (eg, excluding latent infections), and identify modifiable risk factors to improve clinical outcomes. Supportive care is crucial in all patients receiving T-cell immunotherapy to prevent non-relapse mortality.
优化多发性骨髓瘤患者的t细胞免疫治疗:来自欧洲骨髓瘤网络的实际考虑
新的T细胞免疫疗法(嵌合抗原受体(CAR) T细胞和T细胞重定向双特异性抗体)正在改变复发或难治性多发性骨髓瘤的治疗前景。在这篇综述中,欧洲骨髓瘤网络提供了优化t细胞免疫治疗的安全性和有效性的建议。对于同时适合CAR - t细胞治疗和双特异性抗体治疗的患者,我们建议首先使用CAR - t细胞治疗,因为它具有高反应率和持久的无进展生存期,并伴有生活质量的改善。此外,以前的双特异性抗体治疗对CAR - t细胞治疗的疗效有负面影响,并且有新的证据表明,b细胞成熟抗原导向的CAR - t细胞治疗后的复发可以用双特异性抗体有效地控制。在开始t细胞免疫治疗之前,及时转诊和规划至关重要,以优化治疗选择,进行充分的诊断测试(例如,排除潜伏感染),并确定可改变的风险因素,以改善临床结果。在所有接受t细胞免疫治疗的患者中,支持性护理对于预防非复发性死亡率至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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