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.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Efficacy and safety of CAR-T therapy targeting CLL1 in patients with extramedullary diseases of acute myeloid leukemia.
Efficacy and safety of CAR-T therapy targeting CLL1 in patients with extramedullary diseases of acute myeloid leukemia.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
我们的研究结果证明了 CLL1 CAR-T 疗法在治疗伴 EMD 的 AML 患者中的疗效,同时也表明并发症发生率可控,处于可耐受范围内。
急性髓系白血病(AML)患者中髓外病变(EMD)的发生率约为 10%–20%。与无 EMD 患者相比,这些患者在病因学、治疗应答和预后方面存在显著差异。CLL1 CAR-T 治疗复发/难治性 AML 已显示出令人满意的疗效和安全性,但髓外病灶是否会影响 CLL1 CAR-T 疗效仍引发担忧。
本研究共纳入 47 例患者,其中 27 例仅有 AML 在骨髓中的肿瘤浸润,20 例同时存在髓外和骨髓浸润。CLL1 CAR-T 细胞由天津市第一中心医院血液学实验室制备并严格质控。输注后评估疗效和不良反应,并密切监测 CAR-T 细胞扩增、细胞因子释放水平及其他指标。
在 20 例有 EMD 患者和 27 例无 EMD 患者中,分别有 65.00% 和 81.48% 达到骨髓完全缓解。在有 EMD 的患者中,评估 CLL1 CAR-T 对髓外病灶的疗效时,55.00% 达到完全缓解,10.00% 达到部分缓解。与无 EMD 患者相比,EMD 患者的总生存期、无进展生存期和缓解持续时间似乎更短,但差异未达到统计学显著性。两组并发症发生率相近;有无 EMD 患者的 CAR-T 细胞扩增水平及伴随的细胞因子释放也无显著差异。
本研究显示 CLL1 CAR-T 治疗伴 EMD 的 AML 患者有效,并发症发生率可管理且处于可耐受范围。无论是否存在 EMD,CLL1 CAR-T 均是 AML 患者的理想策略,可改善病情,使患者有机会接受根治性造血干细胞移植,并显著改善预后。
A total of 47 patients were enrolled in this study, including 27 patients with isolated AML tumor bone marrow infiltration and 20 patients with both extramedullary and bone marrow infiltration of AML. CLL1 CAR-T cells were manufactured and subjected to rigorous quality control in the hematology laboratory of Tianjin First Central Hospital. The efficacy and adverse reactions were assessed following CAR-T cell infusion, while expansion of CAR-T cells, levels of cytokines releasing, and other indicators were closely monitored.
Among the 20 patients with EMDs and the 27 individuals without EMDs, complete remission in bone marrow was achieved by 65.00% and 81.48% of patients, respectively. Meanwhile, among the patients with EMDs, 55.00% achieved complete remission while 10.00% achieved partial remission when assessing the efficacy of CLL1 CAR-T cells against extramedullary niduses. Although the overall survival, progression-free survival, and duration of remission period appeared to be shorter for patients with EMDs compared to those without EMDs, this difference did not reach statistical significance. The incidence rates of complications were comparable between both groups. Meanwhile, there were no significant differences observed in the levels of CAR-T cell expansion and accompanying cytokines release between patients with and without EMDs.
Our study findings have demonstrated the efficacy of CLL1 CAR-T therapy in the treatment of AML patients with EMDs, while also indicating manageable occurrence rates of complications within a tolerable range. The CLL1 CAR-T therapy, serving as an ideal strategy for AML patients irrespective of the presence of EMDs, effectively ameliorates the conditions of AML patients and provides them with an opportunity to undergo curative hematopoietic stem cell transplantation while significantly enhancing their prognosis.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
MEMBER ACCOUNT
登录成功会直接打开下一页。