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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.
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页码:563 / 564
页数:2
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