不适合移植的大 B 细胞淋巴瘤二线使用 axicabtagene ciloleucel:ALYCANTE 最终分析
Second-line axicabtagene ciloleucel in large B-cell lymphoma ineligible for transplantation: ALYCANTE final analysis.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Outcomes of allogeneic hematopoietic stem cell transplantation for relapsed or refractory diffuse large B-cell lymphoma.
Outcomes of allogeneic hematopoietic stem cell transplantation for relapsed or refractory diffuse large B-cell lymphoma.
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异基因造血干细胞移植(allo-HSCT)由于固有的移植物抗淋巴瘤效应,是弥漫大B细胞淋巴瘤(DLBCL)的一种治愈性治疗方式。
然而,关于哪些复发/难治性DLBCL患者可能从allo-HSCT中获益,现有信息有限。我们回顾性分析了1268例接受allo-HSCT的DLBCL患者的数据。3年总生存率和无进展生存期(PFS)率分别为30.3%和21.6%。多因素分析显示,移植时疾病稳定或进展、男性患者、移植时体能状态较差以及距前次移植间隔较短与较低的PFS独立相关。采用四个预后因素构建了PFS预后指数,预测3年PFS分别为55.4%、43.7%、20.4%和6.6%。该预后模型相应地预测了allo-HSCT后的复发率(P < 0.0001),而未预测移植相关死亡率(P = 0.249)。该预后指数可以识别出从allo-HSCT中获益的DLBCL患者亚组,并且值得评估该模型是否也适用于在嵌合抗原受体工程T细胞治疗后复发接受allo-HSCT的患者,尽管随着新型免疫疗法的增加,allo-HSCT的应用正在减少。
Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is a currative treatment modality for diffuse large B-cell lymphoma (DLBCL) because of the intrinsic graft-versus-lymphoma effect.
However, limited information is available regarding which patients with relapsed or refractory DLBCL are likely to benefit from allo-HSCT.
We retrospectively analyzed data from 1268 DLBCL patients who received allo-HSCT. The overall survival and progression-free survival (PFS) rates were 30. 3% and 21. 6% at 3 years, respectively. Multivariate analysis revealed that stable or progressive disease at transplantation, male patient, poorer performance status at transplantation, and shorter intervals from previous transplantation were associated independently with a lower PFS. Four prognostic factors were used to construct a prognostic index for PFS, predicting 3-year PFS of 55. 4%, 43. 7%, 20.
4% and 6. 6%, respectively. The prognostic model predicted relapse rates following allo-HSCT accordingly (P < 0. 0001), whereas did not predict transplantation-related mortality (P = 0. 249).
The prognostic index can identify a subgroup of DLBCL patients who benefit from allo-HSCT and it is worthwhile to evaluate whether this model is also applicable to patients undergoing allo-HSCT in cases of relapse after chimeric antigen receptor engineered T-cell therapy, although the application of allo-HSCT has been declining with the increase of novel immunotherapies.
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