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T 细胞 depleted 干细胞移植治疗高危成人急性淋巴细胞白血病:在首次完全缓解的患者中具有长期生存,移植物抗宿主病风险降低。

T cell-depleted stem cell transplantation for adults with high-risk acute lymphoblastic leukemia: long-term survival for patients in first complete remission with a decreased risk of graft-versus-host disease.

机构信息

Adult Bone Marrow Transplantation Service, Memorial Sloan-Kettering Cancer Center, New York, New York 10065, USA.

出版信息

Biol Blood Marrow Transplant. 2013 Feb;19(2):208-13. doi: 10.1016/j.bbmt.2012.09.003. Epub 2012 Sep 13.

Abstract

Consolidation with allogeneic hematopoietic stem cell transplantation (allo-HSCT) provides a survival benefit to patients with acute lymphoblastic leukemia (ALL). We have previously reported comparable survival and relapse rates after T cell-depleted (TCD) allo-HSCT compared with unmodified transplantations for acute myelogenous leukemia, myelodysplastic syndrome, and non-Hodgkin lymphoma with significantly decreased graft-versus-host disease (GVHD). We performed a 56-patient retrospective study to evaluate TCD allo-HSCT for the treatment of ALL after myeloablative total body irradiation-based therapy. The 2-year and 5-year overall survival rates for patients with ALL after TCD allo-HSCT were 0.39 (95% confidence interval [CI], 0.26-0.52) and 0.32 (95% CI, 0.19-0.44), respectively, and the 2-year and 5-year disease-free survival rates were 0.38 (95% CI, 0.25-0.50) and 0.32 (95% CI, 0.20-0.44). There was a trend toward improved survival of patients who underwent TCD allo-HSCT in first complete remission compared with those who did so in other remission states. The cumulative incidence of grade II-IV acute GVHD at 1 year was 0.20 (95% CI, 0.10-0.31), and no patients developed grade IV acute GVHD. The cumulative incidence of chronic GVHD in 41 evaluable patients at 2 and 5 years was 0.15 (95% CI, 0.04-0.26), and that of extensive chronic GVHD at 2 and 5 years was 0.05 (95% CI, 0-11.6). We demonstrate OS and DFS rates that compare favorably to unmodified allo-HSCT with lower rates of GVHD.

摘要

异基因造血干细胞移植(allo-HSCT)巩固治疗可为急性淋巴细胞白血病(ALL)患者带来生存获益。我们曾报道过,与未修饰的移植相比,T 细胞耗竭(TCD)allo-HSCT 用于治疗急性髓系白血病、骨髓增生异常综合征和非霍奇金淋巴瘤时,患者的存活率和复发率相当,但移植物抗宿主病(GVHD)的发生率显著降低。我们进行了一项 56 例患者的回顾性研究,以评估基于全身照射的清髓性预处理方案后,TCD allo-HSCT 治疗 ALL 的效果。接受 TCD allo-HSCT 的 ALL 患者 2 年和 5 年总生存率分别为 0.39(95%置信区间[CI],0.26-0.52)和 0.32(95% CI,0.19-0.44),2 年和 5 年无病生存率分别为 0.38(95% CI,0.25-0.50)和 0.32(95% CI,0.20-0.44)。与其他缓解状态相比,在首次完全缓解时接受 TCD allo-HSCT 的患者,其生存趋势有所改善。1 年时,Ⅱ-Ⅳ级急性 GVHD 的累积发生率为 0.20(95% CI,0.10-0.31),无患者发生 4 级急性 GVHD。在 41 例可评估患者中,2 年和 5 年时慢性 GVHD 的累积发生率分别为 0.15(95% CI,0.04-0.26),广泛型慢性 GVHD 的累积发生率分别为 0.05(95% CI,0-11.6)。我们的研究结果表明,OS 和 DFS 率与未修饰的 allo-HSCT 相当,但 GVHD 发生率较低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08b7/3963704/8f7fe804a550/nihms407656f1a.jpg

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