[自体造血干细胞移植对 CAR-T 治疗复发/难治性多发性骨髓瘤疗效的影响]。

M J Ding, X X Jie, H J Li, Z Y Xu, L Nian, K M Qi, Z L Yan, F Zhu, J Cao, H X Zhang, K L Xu, H Cheng, Z Y Li
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引用次数: 0

摘要

目的评估自体造血干细胞移植(ASCT)对嵌合抗原受体T细胞(CAR-T)疗法治疗复发/难治性多发性骨髓瘤(RRMM)的效果。研究方法回顾性队列研究。分析了2020年1月3日至2022年9月13日期间在徐州医科大学附属医院血液科接受CAR-T治疗的168例RRMM患者的临床数据。根据患者之前是否接受过ASCT,将其分为移植组(TG;n=47)和非移植组(NTG;n=121)。采用χ2检验、Kaplan-Meier法和独立样本t检验分析了客观反应率(ORR)、无进展生存期(PFS)、总生存期(OS)以及CAR-T输注前的CD3、CD4、CD8、CD19、CD56和自然杀伤(NK)细胞水平。结果在168例RRMM患者中,98例(58.3%)为男性。中位发病年龄为57岁(30-70岁)。接受CAR-T治疗后,NTG患者的ORR为89.3%(92/103),TG患者的ORR为72.9%(27/73)。NTG的ORR优于TG(χ2=5.71,P=0.017)。CAR-T治疗1年后,NTG的ORR为78.1%(75/96),TG的ORR为59.4%(19/32)。NTG的ORR优于TG(χ2=4.32,P=0.038)。NTG的中位OS和PFS明显长于TG(OS,30个月对20个月;PFS,26个月对12个月;Pt均=-2.15,P=0.034),TG和NTG的CD3、CD8、CD19、CD56和NK细胞计数无明显差异(均P>0.05)。结论在接受CAR-T治疗的RRMM患者中,未接受过ASCT治疗的患者的预后明显优于之前接受过ASCT治疗的患者,这可能与接受CAR-T治疗前的CD4水平有关。
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[Impact of autologous hematopoietic stem cell transplantation on the efficacy of CAR-T treatment of relapsed/refractory multiple myeloma].

Objective: To evaluate the effect of autologous hematopoietic stem cell transplantation (ASCT) on the treatment of relapsed/refractory multiple myeloma (RRMM) with chimeric antigen receptor T cell (CAR-T) therapy. Methods: A retrospective cohort study. The clinical data of 168 patients with RRMM who underwent CAR-T therapy at the Department of Hematology, Xuzhou Medical University Hospital from 3 January 2020 to 13 September 2022 were analyzed. Patients were classified into a transplantation group (TG; n=47) and non-transplantation group (NTG; n=121) based on whether or not they had undergone ASCT previously. The objective response rate (ORR), progression-free survival (PFS), overall survival (OS) and the levels of CD3, CD4, CD8, CD19, CD56 and natural killer (NK) cells before CAR-T infusion were analyzed by χ2 test, Kaplan-Meier method and independent sample t-test. Results: Among 168 patients with RRMM, 98 (58.3%) were male. The median age of onset was 57 (range 30-70) years. After CAR-T therapy, the ORR of patients was 89.3% (92/103) in the NTG and 72.9% (27/73) in the TG. The ORR of the NTG was better than that of the TG (χ2=5.71, P=0.017). After 1 year of CAR-T therapy, the ORR of the NTG was 78.1% (75/96), and that of the TG was 59.4% (19/32). The ORR of the NTG was better than that of the TG (χ2=4.32, P=0.038). The median OS and PFS in the NTG were significantly longer than those in the TG (OS, 30 vs. 20 months; PFS, 26 vs. 12 months; both P<0.05). The CD4 level before CAR-T infusion in the TG was significantly lower than that in the NTG (25.65±13.56 vs. 32.64±17.21; t=-2.15, P=0.034), and there were no significant differences in the counts of CD3, CD8, CD19, CD56, and NK cells between the TG and NTG (all P>0.05). Conclusion: Among patients suffering from RRMM who received CAR-T therapy, patients who did not receive ASCT had significantly better outcomes than those who had received ASCT previously, which may have been related to the CD4 level before receiving CAR-T therapy.

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