CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:An Italian Delphi consensus on the current and future burden and clinical management of lenalidomide-refractory multiple myeloma.
An Italian Delphi consensus on the current and future burden and clinical management of lenalidomide-refractory multiple myeloma.
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本 Delphi 共识研究报告显示,针对 lenalidomide 难治性 MM,自二线治疗起即存在重大未满足的临床需求,亟需新近可用且可及的治疗方案。
因多发性骨髓瘤(MM)接受治疗的患者中来那度胺难治的发生率正在上升。探讨专家对来那度胺难治性MM疾病负担以及当前和未来治疗选择的看法,对于优化该类情况下的治疗至关重要。
2024年1月至7月,我们在意大利开展了一项纳入12名血液学专家的改良德尔菲研究。该项目遵循德尔菲研究的最佳实践,包括匿名性、迭代、受控反馈、共识的定义与分析。
需进行两轮方可完成德尔菲流程。所有临床医师均全程参与。专家一致认为,预计2026年意大利开始二线治疗的患者中将有超过80%对lenalidomide难治。专家组员达成完全共识(100%的专家组员),认为该患者群体的主要临床未满足需求是具有新作用机制的新型(免疫)疗法的获批与可及性。超过三分之二的专家组员还原则上同意,从二线治疗起即使用T细胞重定向疗法,包括CAR-T 和双特异性抗体。在lenalidomide难治MM患者的特定亚组中,未发现可指导治疗选择的明确患者特征。
Refractoriness to lenalidomide in patients treated for multiple myeloma (MM) is increasing. Exploring opinions of experts on the burden of lenalidomide-refractory MM and on current and future therapeutic options is critical for optimizing care in this setting.
From January to July 2024, we conducted a modified Delphi study involving 12 haematologists in Italy. The project followed the best practices for Delphi studies, including anonymity, iteration, controlled feedback, definition and analysis of consensus.
Two rounds were required to complete the Delphi process. Participation of clinicians was complete. Experts agreed that more than 80% of Italian patients starting second-line therapy are expected to be refractory to lenalidomide in 2026. Full consensus emerged (100% of panellists) that the main clinical unmet needs in this patient setting are the approval and access to novel (immuno)therapies with new mechanisms of action. More than two-thirds of panellists also agreed, in principle, to the use of T-cell redirecting therapies, including CAR-T and bispecific antibodies, from the second-line of treatment onwards. No clear patient characteristics emerged to drive therapeutic options in specific subgroups of subjects with lenalidomide-refractory MM.
This Delphi consensus study reported a major clinical unmet need of newly available and accessible therapeutic options for lenalidomide-refractory MM, already starting from the second-line of treatment.
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