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:Analysis benefits of a second Allo-HSCT after CAR-T cell therapy in patients with relapsed/refractory B-cell acute lymphoblastic leukemia who relapsed after transplant.
Analysis benefits of a second Allo-HSCT after CAR-T cell therapy in patients with relapsed/refractory B-cell acute lymphoblastic leukemia who relapsed after transplant.
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我们的研究表明,CAR-T 治疗后续巩固性二次移植可显著改善移植后复发的 B-ALL 患者的长期生存。对于合适的患者应考虑二次移植,并建议在 CAR-T 治疗后 90 天内进行。
嵌合抗原受体(CAR)T细胞疗法已在B细胞急性淋巴细胞白血病(B-ALL)患者中显示出较高的初始完全缓解(CR)率,包括移植后复发的患者。然而,缓解持续时间仍需改善。CAR-T 疗法后桥接第二次异基因造血干细胞移植(allo-HSCT)能否改善长期生存仍存在争议。我们回顾性分析了移植后复发并接受CAR-T 疗法后续巩固性第二次allo-HSCT的B-ALL患者的长期随访数据,以探讨这种治疗顺序能否改善长期生存。
2017年10月至2022年3月期间进行了一项单中心回顾性研究,纳入95例在CAR-T 治疗后达到CR并接受巩固性二次移植的患者。
患者在接受第二次移植时的中位年龄为22.8岁(范围:3.3-52.8)。在第一次移植后,71例患者(74.7%)发生骨髓复发,16例患者(16.8%)发生髓外复发,5例患者(5.3%)同时发生骨髓和髓外复发,3/95例患者(3.2%)仅为微小残留病(MRD)阳性。患者接受了自体(n=57,60.0%)或异基因(n=28,29.5%)CAR-T 细胞,而10例患者(10.5%)情况未知。所有患者在CAR-T 治疗后均达到CR。在第二次HSCT前,86例患者(90.5%)为MRD阴性,9例(9.5%)为MRD阳性。所有第二次移植的供者均与第一次移植的供者不同。第二次HSCT后的中位随访时间为623天(范围:33-1901)。3年总生存期(OS)和无白血病生存(LFS)分别为55.3%(95%CI,44.3-66.1%)和49.8%(95%CI,38.7-60.9%)。3年复发率(RI)和非复发死亡率(NRM)分别为10.5%(95%CI,5.6-19.6%)和43.6%(95%CI,33.9-56.2%)。在多变量分析中,从CAR-T 到第二次HSCT的间隔90天与更优的LFS(HR,4.10,95%CI,1.64-10.24;p=0.003)和OS(HR,2.67,95%CI,1.24-5.74,p=0.012)相关,以及降低的NRM(HR,2.45,95%CI,1.14-5.24,p=0.021)。
Chimeric antigen receptor (CAR) T-cell therapy has demonstrated high initial complete remission (CR) rates in B-cell acute lymphoblastic leukemia (B-ALL) patients, including those who relapsed after transplant. However, the duration of remission requires improvements. Whether bridging to a second allogeneic hematopoietic stem cell transplant (allo-HSCT) after CAR-T therapy can improve long-term survival remains controversial. We retrospectively analyzed long-term follow-up data of B-ALL patients who relapsed post-transplant and received CAR-T therapy followed by consolidation second allo-HSCT to investigate whether such a treatment sequence could improve long-term survival.
A single-center, retrospective study was performed between October 2017 and March 2022, involving 95 patients who received a consolidation second transplant after achieving CR from CAR-T therapy.
The median age of patients was 22.8 years (range: 3.3-52.8) at the second transplant. After the first transplant, 71 patients (74.7%) experienced bone marrow relapse, 16 patients (16.8%) had extramedullary relapse, 5 patients (5.3%) had both bone marrow and extramedullary relapse and 3/95 patients (3.2%) had positive minimal residual disease (MRD) only. Patients received autologous (n=57, 60.0%) or allogeneic (n=28, 29.5%) CAR-T cells, while 10 patients (10.5%) were unknown. All patients achieved CR after CAR-T therapy. Before second HSCT, 86 patients (90.5%) were MRD-negative, and 9 (9.5%) were MRD-positive. All second transplant donors were different from the first transplant donors. The median follow-up time was 623 days (range: 33-1901) after the second HSCT. The 3-year overall survival (OS) and leukemia-free survival (LFS) were 55.3% (95%CI, 44.3-66.1%) and 49.8% (95%CI, 38.7-60.9%), respectively. The 3-year relapse incidence (RI) and non-relapse mortality (NRM) were 10.5% (95%CI, 5.6-19.6%) and 43.6% (95%CI, 33.9-56.2%), respectively. In multivariate analysis, the interval from CAR-T to second HSCT 90 days was associated with superior LFS(HR, 4.10, 95%CI,1.64-10.24; p =0.003) and OS(HR, 2.67, 95%CI, 1.24-5.74, p =0.012), as well as reduced NRM (HR, 2.45, 95%CI, 1.14-5.24, p =0.021).
Our study indicated that CAR-T therapy followed by consolidation second transplant could significantly improve long-term survival in B-ALL patients who relapsed post-transplant. The second transplant should be considered in suitable patients and is recommended to be performed within 90 days after CAR-T treatment.
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