van de Donk Niels W C J, Moreau Philippe, San-Miguel Jesús F, Mateos Maria-Victoria, Dimopoulos Meletios A, Zweegman Sonja, Gay Francesca, Engelhardt Monika, Mina Roberto, Zamagni Elena, Delforge Michel, Beksac Meral, Spencer Andrew, Schjesvold Fredrik, Driessen Christoph, Kaiser Martin, Perrot Aurore, Wäsch Ralph, Korst Charlotte Lbm, Broijl Annemiek, Touzeau Cyrille, Manier Salomon, Hajek Roman, Ludwig Heinz, Fernandez de Larrea Carlos, Popat Rakesh, Musto Pellegrino, Rodriguez-Otero Paula, Yong Kwee, Rasche Leo, Terpos Evangelos, Raab Marc S, Boccadoro Mario, Sonneveld Pieter, Einsele Hermann
Department of Hematology, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, Netherlands; Cancer Biology and Immunology, Cancer Center Amsterdam, Amsterdam, Netherlands.
Department of Hematology, University Hospital Hôtel-Dieu, Nantes, France.
Lancet Haematol. 2025 Aug;12(8):e635-e649. doi: 10.1016/S2352-3026(25)00117-6. Epub 2025 Jun 25.
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.
新型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格局。在本综述中,欧洲骨髓瘤网络提供了优化T细胞免疫疗法安全性和有效性的建议。对于有资格接受CAR T细胞疗法和双特异性抗体治疗的患者,由于其高缓解率和持久的无进展生存期,以及生活质量的改善,我们建议首先使用CAR T细胞疗法。此外,先前的双特异性抗体治疗对CAR T细胞疗法的疗效有负面影响,并且有新证据表明,B细胞成熟抗原导向的CAR T细胞疗法后复发可以用双特异性抗体有效控制。在开始T细胞免疫疗法之前,及时转诊和规划对于优化治疗选择、进行充分的诊断测试(如排除潜伏感染)以及识别可改变的风险因素以改善临床结果至关重要。支持性护理对于所有接受T细胞免疫疗法的患者预防非复发死亡率至关重要。