Matching-adjusted indirect comparison of axi-cel and liso-cel in relapsed or refractory large B-cell lymphoma

被引:8
|
作者
Oluwole, Olalekan O. [1 ]
Chen, Jenny M. H. [2 ]
Chan, Keith [2 ]
Patel, Anik R. [3 ]
Jansen, Jeroen P. [4 ]
Keeping, Sam [2 ]
Zheng, Yan [3 ]
Snider, Julia T. [3 ]
Locke, Frederick L. [5 ]
机构
[1] Vanderbilt Ingram Canc Ctr, 1301 Med Ctr Dr,Suite 3903, Nashville, TN 37232 USA
[2] PRECISIONheor, Vancouver, BC, Canada
[3] Kite, Santa Monica, CA USA
[4] PRECISIONheor, Oakland, CA USA
[5] H Lee Moffitt Canc Ctr & Res Inst, Tampa, FL USA
关键词
Large B-cell lymphoma; axicabtagene ciloleucel; lisocabtagene maraleucel; CAR T-cell therapy; MAIC; comparative efficacy; GUIDELINES; MANAGEMENT; SURVIVAL; OUTCOMES;
D O I
10.1080/10428194.2022.2113526
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In the absence of a randomized head-to-head trial, an unanchored matching-adjusted indirect comparison was performed to estimate the relative treatment effects of axicabtagene ciloleucel (axi-cel; ZUMA-1) versus lisocabtagene maraleucel (liso-cel; TRANSCEND-NHL-001) for treatment of relapsed/refractory (R/R) large B-cell lymphoma (LBCL) after at least two lines of therapy. After matching, axi-cel and liso-cel had comparable objective response rates and duration. Compared to liso-cel, axi-cel was associated with improvements in overall survival (hazard ratio [HR]: 0.53 [95% CI: 0.34-0.82]) and progression-free survival (HR: 0.61 [95% CI: 0.40-0.92]). Axi-cel was associated with a higher rate of grade >= 3 cytokine release syndrome (odds ratio [OR]: 3.64 [95% CI: 1.04-12.76]) and neurological events (OR: 3.45 [95% CI: 1.65-7.19]), with smaller differences estimated in scenario analyses including ZUMA-1 safety management cohorts. Results suggest axi-cel improved survival compared to liso-cel but with increased odds of specific adverse events.
引用
收藏
页码:3052 / 3062
页数:11
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