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:Chimeric Antigen Receptor T-cell Therapy for Chronic Lymphocytic Leukemia: What is the supporting evidence so far?
Chimeric Antigen Receptor T-cell Therapy for Chronic Lymphocytic Leukemia: What is the supporting evidence so far?
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。
尽管承认新型疗法已提高慢性淋巴细胞白血病(CLL)患者的生存率,但具有高危疾病特征者治疗失败风险仍较高。传统上,异基因造血细胞移植(allo-HCT)曾作为高危 CLL 的一线巩固治疗;然而,随着布鲁顿酪氨酸激酶(BTK)和 B 细胞淋巴瘤 2(BCL-2)抑制剂等靶向疗法出现,allo-HCT 已被推迟至疾病后期。对 BTK 和 BCL-2 抑制剂均治疗失败的复发/难治性(R/R)CLL 患者,由于预后不良而构成治疗挑战。靶向 CD19 的CAR-T 细胞疗法已提高多种 R/R B 细胞非霍奇金淋巴瘤的缓解率和总生存期。目前尚无 CAR-T 细胞疗法获批用于 CLL。新出现的数据似乎显示 CAR-T 细胞疗法可使 R/R CLL 患者获益,即使患者此前接受 allo-HCT 后治疗失败亦然。
While acknowledging that newer therapies have improved survival rates in chronic lymphocytic leukemia (CLL), patients with high-risk disease features are at an increased risk of treatment failure. Allogeneic hematopoietic cell transplantation (allo-HCT) was traditionally offered as front-line consolidation in high-risk CLL; however, with the emergence of targeted therapies like Bruton tyrosine kinase (BTK) and B-cell lymphoma 2 (BCL-2) inhibitors, the role of allo-HCT has been relegated to later stages of the disease.
Patients with relapsed/refractory (R/R) CLL who have failed both BTK and BCL-2 inhibitors represent a therapeutic challenge owing to a poor prognosis. Chimeric antigen receptor T-cell (CAR T) therapies targeting CD19 have improved response rates and overall survival in various types of R/R B-cell non-Hodgkin lymphomas. For CLL, no approved CAR T-cell therapies are yet available. Emerging data appear to show a therapeutic benefit of CAR T-cell therapy in patients with R/R CLL, even after failing an allo-HCT.
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