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brexucabtagene autoleucel 体内扩增与 BTKi 难治对套细胞淋巴瘤无进展生存期产生负面影响:CART-SIE 研究结果

英文原题:Brexucabtagene autoleucel in-vivo expansion and BTKi refractoriness have a negative influence on progression-free survival in mantle cell lymphoma: Results from CART-SIE study.

查看英文原题

Brexucabtagene autoleucel in-vivo expansion and BTKi refractoriness have a negative influence on progression-free survival in mantle cell lymphoma: Results from CART-SIE study.

PubMed 2024/12/22(内容时间) Br J Haematol Q2 · IF 3.6(JCR 2025)

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中文摘要

布瑞基奥仑赛(brexu-cel)彻底改变了套细胞淋巴瘤患者的治疗方式。在这项前瞻性、多中心观察性研究中,研究者评估了106名患者,并对其中61人的外周血brexu-cel动力学进行了纵向监测。临床结局和毒性与既往真实世界研究一致。

值得注意的是,除母细胞样变异和乳酸脱氢酶升高等已知不良预后因素外,布鲁顿酪氨酸激酶抑制剂(BTKi)难治状态和血小板计数也成为重要生存预测因素。

具体而言,BTKi难治患者的1年总生存率为56%,而BTKi治疗后复发患者为92%(p=0.0001)。研究还显示,体内监测brexu-cel扩增是可行的,且与无进展生存期和毒性相关。按brexu-cel峰值浓度分类,强扩增患者的1年无进展生存率为74%,弱扩增患者为54%(p=0.02)。

此外,体内扩增情况有助于识别输注后第90天评估时未应答(疾病进展或稳定)的高危患者(OR=4.7,95%置信区间:1.1–34,p=0.04);该组患者预后极差。结合其他临床因素监测brexu-cel扩增情况,或有助于识别早期复发高危患者。

展开英文摘要原文

Brexucabtagene autoleucel (brexu-cel) has revolutionized the treatment of patients affected by mantle cell lymphomas. In this prospective, observational multicentre study, we evaluated 106 patients, with longitudinal brexu-cel kinetics in peripheral blood monitored in 61 of them. Clinical outcomes and toxicities are consistent with previous real-world evidence studies.

Notably, beyond established poor prognostic factors-such as blastoid variant and elevated lactate dehydrogenase-Bruton tyrosine-kinase inhibitors (BTKi) refractoriness and platelet count emerged as significant predictors of survival. Specifically, the 1-year overall survival was 56% in BTKi-refractory patients compared to 92% in BTKi-relapsed patients (p = 0. 0001).

Our study also demonstrated that in-vivo monitoring of brexu-cel expansion is feasible and correlates with progression-free survival and toxicities. Progression-free survival at 1 year was 74% in patients categorized as strong expanders, based on brexu-cel peak concentration, versus 54% in poor expanders (p = 0. 02).

Furthermore, in-vivo expansion helped identify a high-risk group of non-responders, those with progressive or stable disease at the 90-day post-infusion evaluation (OR = 4. 7, 95% CI = 1. 1-34, p = 0. 04) characterized by dismal outcomes. When integrated with other clinical factors, monitoring brexu-cel expansion could assist in recognizing patients at high risk of early relapse.

论文信息

作者
Stella F、Chiappella A、Magni M、Bonifazi F、De Philippis C、Musso M、Cutini I、Ljevar S
单位
Hematology, School of Medicine, Università degli Studi di Milano, Milan, Italy.Italy
文献类型
多中心研究 · 观察性研究
期刊
British journal of haematology2025 Feb
原文标识
PubMed 39710966 · DOI 10.1111/bjh.19961