CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
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.
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.
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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。
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.
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