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:Chimeric antigen receptor T-cell infusion for large B-cell lymphoma in complete remission: a center for international blood and marrow transplant research analysis.
Chimeric antigen receptor T-cell infusion for large B-cell lymphoma in complete remission: a center for international blood and marrow transplant research analysis.
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靶向 CD19 的嵌合抗原受体(CAR)T 细胞疗法常用于复发/难治性大 B 细胞淋巴瘤(LBCL),但挽救或桥接治疗有时能使患者在 CAR-T 输注前达到完全缓解(CR)。针对输注时已处于 CR 患者的结局,相关研究有限。研究从 CIBMTR 登记库中识别出 134 例 CAR-T 输注前处于 CR 的 LBCL 患者,既往治疗线数中位数为 3(范围 2–9)。输注后 2 年无进展生存期概率为 43.5%(95% CI 34.4–52.8),总生存期概率为 63.8%(95% CI 54.4–72.6)。2 年非复发死亡及复发/进展累积发生率分别为 9.2%(95% CI 4.5–15.4)和 47.3%(95% CI 38.2–56.6)。3 级及以上 CRS 和 ICANS 发生率分别为 2.2% 和 8.2%。
总之,既往至少接受两线治疗、经重度预处理后 CAR-T 前已达 CR 的 LBCL 患者中,仍有一部分在 2 年时未发生进展。
此外,毒性谱令人鼓舞,3 级 CRS 和 ICANS 发生率均很低。
CD19 CAR T-cell (CAR-T) therapy is commonly administered to patients with relapsed or refractory large B-cell lymphomas (LBCL), but salvage or bridging therapy can sometimes lead to a complete response (CR) prior to infusion. Limited studies have assessed the outcomes of patients infused in CR. A total of 134 patients with LBCL in CR prior to CAR-T infusion were identified from the CIBMTR registry, with median prior lines of therapy of 3 (range 2-9). At two years post-infusion, the probability of progression-free survival was 43. 5% (95% CI 34. 4-52. 8) and the probability of overall survival was 63.
8% (95% CI 54. 4-72. 6). The cumulative incidence rates of non-relapse mortality and relapse/progression at two years were 9. 2% (95% CI 4. 5-15. 4) and 47. 3% (95% CI 38. 2-56. 6), respectively. The rate of grade 3 or higher cytokine release syndrome (CRS) and immune effector cell-associated neurotoxicity syndrome (ICANS) were 2.
2% and 8. 2%, respectively. In summary, CAR-T in heavily pretreated patients with LBCL who are in CR following two or more lines of prior therapy demonstrate that a subset of patients may remain free of progression at two years.
Additionally, the toxicity profile was impressive with very low rates of grade 3 CRS and ICANS.
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