TY - JOUR
T1 - Optimising T-cell immunotherapy in patients with multiple myeloma
T2 - practical considerations from the European Myeloma Network
AU - van de Donk, Niels W.C.J.
AU - Moreau, Philippe
AU - San-Miguel, Jesús F.
AU - EMN Guidelines Committee
AU - Mateos, Maria Victoria
AU - Dimopoulos, Meletios A.
AU - Zweegman, Sonja
AU - Gay, Francesca
AU - Engelhardt, Monika
AU - Mina, Roberto
AU - Zamagni, Elena
AU - Delforge, Michel
AU - Beksac, Meral
AU - Spencer, Andrew
AU - Schjesvold, Fredrik
AU - Driessen, Christoph
AU - Kaiser, Martin
AU - Perrot, Aurore
AU - Wäsch, Ralph
AU - Korst, Charlotte LBM
AU - Broijl, Annemiek
AU - Touzeau, Cyrille
AU - Manier, Salomon
AU - Hajek, Roman
AU - Ludwig, Heinz
AU - Fernandez de Larrea, Carlos
AU - Popat, Rakesh
AU - Musto, Pellegrino
AU - Rodriguez-Otero, Paula
AU - Yong, Kwee
AU - Rasche, Leo
AU - Terpos, Evangelos
AU - Raab, Marc S.
AU - Boccadoro, Mario
AU - Sonneveld, Pieter
AU - Einsele, Hermann
N1 - Publisher Copyright: © 2025 Elsevier Ltd
PY - 2025/8
Y1 - 2025/8
N2 - 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.
AB - 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.
UR - https://www.scopus.com/pages/publications/105009111125
U2 - 10.1016/S2352-3026(25)00117-6
DO - 10.1016/S2352-3026(25)00117-6
M3 - Review article
C2 - 40580975
AN - SCOPUS:105009111125
SN - 2451-9960
VL - 12
SP - e635-e649
JO - The Lancet Haematology
JF - The Lancet Haematology
IS - 8
ER -