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:Impact of Consolidative Unrelated Cord Blood Transplantation on Clinical Outcomes of Patients With Relapsed/Refractory Acute B Lymphoblastic Leukemia Entering Remission Following CD19 Chimeric Antigen Receptor T Cells.
Impact of Consolidative Unrelated Cord Blood Transplantation on Clinical Outcomes of Patients With Relapsed/Refractory Acute B Lymphoblastic Leukemia Entering Remission Following CD19 Chimeric Antigen Receptor T Cells.
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巩固性 UCBT 可在一定程度上改善 CD19 CAR-T 治疗后达到缓解的 R/R B-ALL 患者的临床结局,尤其是在治疗前复发次数较多、具有不良预后标志以及肿瘤负荷较高的患者中。UCBT 后发生 aGVHD 与更好的 RFS 相关。
尽管嵌合抗原受体(CAR)-T细胞疗法在血液系统恶性肿瘤中已广泛应用并取得显著缓解率,但其高复发率仍是需要克服的障碍。CAR-T 细胞介导缓解后巩固性移植的作用仍存在争议。我们开展了一项回顾性研究,通过亚组分析探讨桥接非血缘脐血移植(UCBT)能否改善不同特征患者在接受CAR-T 治疗后获得缓解的预后。
我们回顾了53例复发/难治性(R/R)B细胞急性淋巴细胞白血病(B-ALL)患者,这些患者成功输注了CD19 CAR-T 细胞并达到完全缓解(CR)。在本研究中,25例患者接受了巩固性UCBT(UCBT组),28例患者未接受任何干预直至复发(非UCBT组)。随后根据性别、年龄、既往复发次数、肿瘤负荷、不良预后标志物的存在以及CAR结构进行了预后亚组分析。
与非UCBT组相比,接受巩固性UCBT的患者具有更好的中位无事件生存期(EFS;12.3个月 vs. 6.2个月;P = 0.035)和无复发生存期(RFS;22.3个月 vs. 7.2个月;P = 0.046),而总生存期(OS;30.8个月 vs. 15.3个月;P = 0.118)无显著差异。随后的多因素分析显示,桥接至UCBT是RFS的保护因素(P = 0.048),但对EFS(P = 0.205)或OS(P = 0.541)无显著影响。在亚组分析中,UCBT对具有特定特征的患者有额外获益。经历2次复发或持续未缓解(NR)的患者在UCBT后表现出更好的RFS(P = 0.025)。具有不良预后标志物的患者观察到更好的EFS(P = 0.027)。在输注前微小残留病(MRD)5%或伴有髓外疾病(EMD)的亚组中,UCBT显著延长了EFS(P = 0.009)、RFS(P = 0.017)和OS(P = 0.026)。发生急性移植物抗宿主病(aGVHD)的患者似乎具有更长的缓解持续时间(P = 0.007)。
While chimeric antigen receptor (CAR)-T cell therapy is becoming widely used in hematological malignancies with remarkable remission rate, their high recurrence remains an obstacle to overcome. The role of consolidative transplantation following CAR-T cell-mediated remission remains controversial. We conducted a retrospective study to explore whether bridging to unrelated cord blood transplantation (UCBT) could improve the prognosis of patients entering remission after CAR-T therapy with different characteristics through subgroup analyses.
We reviewed 53 patients with relapsed/refractory (R/R) B-cell acute lymphoblastic leukemia (B-ALL) successfully infused with CD19 CAR-T cells and achieved complete remission (CR). In this study, 25 patients received consolidative UCBT (UCBT group) and 28 patients did not accept any intervention until relapse (non-UCBT group). Subgroup analysis on prognosis was then performed according to gender, age, number of previous relapses, tumor burden, presence of poor prognostic markers, and structure of CAR.
Compared with the non-UCBT group, patients who underwent consolidative UCBT had better median event-free survival (EFS; 12.3 months vs. 6.2 months; P = 0.035) and relapse-free survival (RFS; 22.3 months vs. 7.2 months; P = 0.046), while no significant difference was found in overall survival (OS; 30.8 months vs. 15.3 months; P = 0.118). Subsequent multivariate analysis revealed that bridging to UCBT was a protective factor for RFS (P = 0.048) but had no significant effect on EFS (P = 0.205) or OS (P = 0.541). In the subgroup analysis, UCBT has an added benefit in patients with specific characteristics. Patients who experienced 2 relapses or with sustained non-remission (NR) showed better RFS (P = 0.025) after UCBT. Better EFS was seen in patients with poor prognostic markers (P = 0.027). In the subgroup with pre-infusion minimal residual disease (MRD) 5% or with extramedullary disease (EMD), UCBT significantly prolonged EFS (P = 0.009), RFS (P = 0.017), and OS (P = 0.026). Patients with occurrence of acute graft-versus-host disease (aGVHD) appeared to have a longer duration of remission (P = 0.007).
Consolidative UCBT can, to some extent, improve clinical outcomes of patients with R/R B-ALL entering remission following CD19 CAR-T therapy, especially in patients with more recurrences before treatment, patients with poor prognostic markers, and patients with a higher tumor burden. The occurrence of aGVHD after UCBT was associated with better RFS.
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