骨髓爆发和修改EASIX引导的凝血病风险分层以及复发/耐药B-ALL中CAR-T治疗后的结果
Yingying Li1, Jiachen Liu1, Lili Luo1
1Institute of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China; Hubei Clinical Medical Center of Cell Therapy for Neoplastic Disease, Wuhan, 430022, China; Hubei Clinical and Research Center of Thrombosis and Haemostasis, Wuhan, 430022, China.
一个新的模型预测了B-ALL患者的CAR T细胞相关凝血病 (CARAC) 风险. 高风险的CARAC,特别是DIC,表明生存结果明显较差.
科学领域:
- 血液学 血液学 血液学
- 在瘤学瘤学.
- 免疫治疗是一种免疫疗法.
背景情况:
- 化学抗原受体 (CAR) T细胞疗法是B细胞急性淋巴细胞白血病 (B-ALL) 复发/耐药的突破.
- 卡尔T细胞相关凝血病 (CARAC) 是一种严重的并发症,增加了出血和传播性血管内凝血 (DIC) 的风险.
研究的目的:
- 开发CARAC风险分层的预测模型.
- 评估CARAC对患者结果的影响,包括整体存活率 (OS) 和无进展存活率 (PFS).
主要方法:
- 一项针对接受CD19 CAR-T治疗的r/r B-ALL患者的多中心回顾性研究.
- 机器学习和物流回归被用来识别关键预测因素和构建预测模型.
- 使用ROC曲线,校准和临床决策曲线验证模型性能;生存分析评估结果.
主要成果:
- 骨髓爆发和修改的内皮激活和压力指数 (mEASIX) 是独立的CARAC预测指标.
- 开发了一个风险分层:低风险 (mEASIX<4.0),高风险的CARAC-nonDIC (mEASIX≥4.0,10-44%的爆发),以及高风险的CARAC-DIC (mEASIX≥4.0,≥44%的爆发).
- 与非CARAC患者相比,CARAC患者的OS和PFS明显恶化;随着CARAC风险的增加,结果逐渐恶化.
结论:
- 已经建立了一个有效的CARAC风险预测和分层模型.
- 高风险的CARAC,特别是CARAC-DIC,与明显较差的患者结局有关.
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