医学
CD19
内科学
Blinatumoab公司
肿瘤科
累积发病率
年轻人
回顾性队列研究
队列
外周血
作者
Liora M. Schultz,Anne Eaton,Christina Baggott,Jenna Rossoff,Snehit Prabhu,Amy K. Keating,Christa Krupski,Holly Pacenta,Christine Philips,Julie‐An Talano,Amy Moskop,Susanne H.C. Baumeister,Gary Douglas Myers,Nicole Karras,Patrick A. Brown,Muna Qayed,Michelle L. Hermiston,Prakash Satwani,Rachel Wilcox,Cara A. Rabik
摘要
Nonresponse and relapse after CD19-chimeric antigen receptor (CAR) T-cell therapy continue to challenge survival outcomes. Phase II landmark data from the ELIANA trial demonstrated nonresponse and relapse rates of 14.5% and 28%, respectively, whereas use in the real-world setting showed nonresponse and relapse rates of 15% and 37%. Outcome analyses describing fate after post-CAR nonresponse and relapse remain limited. Here, we aim to establish survival outcomes after nonresponse and both CD19+ and CD19- relapses and explore treatment variables associated with inferior survival.
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