医学
多发性骨髓瘤
药品
肿瘤科
重症监护医学
来那度胺
内科学
药理学
作者
Sofía I. Quezada-Ramírez,Luz Tarín‐Arzaga,Andrés Gómez‐De León,David Gómez‐Almaguer
标识
DOI:10.1080/17474086.2025.2490764
摘要
Discerning the best therapy sequence is a challenge for NDMM individuals. Minimal residual disease assessment is becoming a pivotal tool for guiding therapeutic approaches to enhance outcomes and tolerability. Emerging evidence supports early use of potent therapies - such as next-generation anti-CD38 antibodies and CELMoDs - to achieve deeper, more durable responses and possibly delay relapses. Immunotherapies like bispecific antibodies and CAR-T cells are also being explored in front-line settings, though reducing their infectious complications is still under investigation.
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