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:Prognostic differences of refractory/relapsed nodal and extranodal diffuse large B-cell lymphoma in the chimeric antigen receptor T cell therapy era.
Prognostic differences of refractory/relapsed nodal and extranodal diffuse large B-cell lymphoma in the chimeric antigen receptor T cell therapy era.
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在接受 CAR-T 治疗的患者中,R/R EN-DLBCL 的临床结局比 R/R N-DLBCL 更差,而 ASCT + CAR-T 治疗是 R/R EN-DLBCL 患者一种有前景的替代治疗选择。
结外受累被认为是弥漫大B细胞淋巴瘤(DLBCL)的不良预后因素。然而,在CAR-T 细胞治疗时代,难治/复发(R/R)结内和结外DLBCL患者的预后差异仍不清楚。
本研究纳入18例R/R结内DLBCL(R/R N-DLBCL)和19例R/R结外DLBCL(R/R EN-DLBCL),比较临床结局。
中位随访时间为13(范围,1-47)个月,淋巴结和结外患者之间的1年无进展生存期(PFS;83.3% vs. 42.1%,P = 0.008)和1年总生存期(OS;94.4% vs. 63.2%,P = 0.020)存在显著差异。在多变量Cox回归分析中,与R/R N-DLBCL相比,R/R EN-DLBCL与更差的PFS(风险比[HR] = 4.263,P = 0.018)和OS(HR = 9.589,P = 0.034)相关。此外,与单独CAR-T 治疗相比,自体造血干细胞移植(ASCT)联合CAR-T 治疗(ASCT + CAR-T)与更好的PFS相关(HR = 0.164,P = 0.003)。
Extranodal involvement is recognized as a poor prognostic factor for diffuse large B-cell lymphoma (DLBCL). However, the prognostic differences of patients with refractory/relapsed (R/R) nodal and extranodal DLBCL in the chimeric antigen receptor T cell (CART) therapy era are still unclear.
In this study, 18 R/R nodal DLBCL (R/R N-DLBCL) and 19 R/R extranodal DLBCL (R/R EN-DLBCL) were enrolled to compare clinical outcomes.
The median follow-up time was 13 (range, 1-47) months and one-year progression-free survival (PFS; 83.3% vs. 42.1%, P = 0.008) and one-year overall survival (OS; 94.4% vs. 63.2%, P = 0.020) were significantly different between nodal and extranodal patients. In the multivariable Cox regression analysis, R/R EN-DLBCL was associated with worse PFS (hazard ratio [HR] = 4.263, P = 0.018) and OS (HR = 9.589, P = 0.034) compared to R/R N-DLBCL. Additionally, autologous hematopoietic stem cell transplantation (ASCT) combined with CART therapy (ASCT + CART) was correlated with better PFS (HR = 0.164, P = 0.003) compared to CART treatment alone.
The clinical outcomes of R/R EN-DLBCL were worse than R/R N-DLBCL in patients receiving CART therapy and ASCT + CART therapy is a promising alternative treatment for patients with R/R EN-DLBCL.
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