CAR T cells in multiple myeloma: lessons learned

被引:1
|
作者
Prasad, Vinay [1 ]
机构
[1] Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA 94115 USA
关键词
CIRCULATING TUMOR-CELLS; DYNAMIC DNA METHYLATION; RANDOMIZED PHASE-III; LUNG-CANCER SUBTYPES; NEUROENDOCRINE PHENOTYPE; 1ST-LINE THERAPY; PLUS ETOPOSIDE; AURORA KINASE; DOUBLE-BLIND; ES-SCLC;
D O I
10.1038/s41571-024-00898-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The question of whether chimeric antigen receptor (CAR) T cell therapies should be used in earlier lines (after 1-2 prior lines of therapy) in patients with relapsed and/or refractory multiple myeloma remains unanswered. Herein, I argue that the use of surrogate end points that lack a robust correlation with overall survival, as well as suboptimal control arms and use of post-progression therapies, limit the ability to make definitive conclusions on the basis of the available data.
引用
收藏
页码:563 / 564
页数:2
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